<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">WJCMP</journal-id><journal-title-group><journal-title>World Journal of Condensed Matter Physics</journal-title></journal-title-group><issn pub-type="epub">2160-6919</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/wjcmp.2012.24042</article-id><article-id pub-id-type="publisher-id">WJCMP-25050</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Physics&amp;Mathematics</subject></subj-group></article-categories><title-group><article-title>
 
 
  Effect of the Variable B-Field on the Dynamic of a Central Electron Spin Coupled to an Anti-Ferromagnetic Qubit Bath
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>artin</surname><given-names>Tchoffo</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Georges</surname><given-names>Collince Fouokeng</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Siaka</surname><given-names>Massou</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ngwa</surname><given-names>Engelbert Afuoti</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Issofa</surname><given-names>Nsangou</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Lukong</surname><given-names>Cornelius Fai</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Alex</surname><given-names>Ghislain Tchouadeu</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Jean-Pierre</surname><given-names>Kenné</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib></contrib-group><aff id="aff4"><addr-line>Department of Mechanical Engineering, Laboratory of Integrated Production Technologies, University of Québec, Québec, Canada</addr-line></aff><aff id="aff3"><addr-line>Department of Physics, Laboratory of Mesoscopic and Multilayer Structures, University of Dschang, Dschang, Cameroon; Department of Thermal Engineering and Energetics, Douala University Institute of Technology, Douala, Cameroun</addr-line></aff><aff id="aff2"><addr-line>De- partment of Physics, Faculty of Sciences and Technics, University of Abomey-Calavi, Cotonou, Benin</addr-line></aff><aff id="aff1"><addr-line>Department of Physics, Laboratory of Mesoscopic and Multilayer Structures, University of Dschang, Dschang, Cameroon</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>mtchoffo2000@yahoo.fr(AT)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>15</day><month>11</month><year>2012</year></pub-date><volume>02</volume><issue>04</issue><fpage>246</fpage><lpage>256</lpage><history><date date-type="received"><day>September</day>	<month>5th,</month>	<year>2012</year></date><date date-type="rev-recd"><day>October</day>	<month>7th,</month>	<year>2012</year>	</date><date date-type="accepted"><day>October</day>	<month>19th,</month>	<year>2012</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  This present issue is an extension of the work of Y. Xiao-Zhong 
  et al. who investigated the influence of constant external magnetic field on the decoherence of a central electron spin of atom coupled to an anti-ferromagnetic environment. We have shown in this work that the character variability of the field induces oscillations amongst the eigen modes of the environment. This observation is made via the derivation of the transition probability density of state, a manner by which critical parameters (parameters where transition occur) of the system could be obtained as it shows resonance peak. We equally observed that the two different magnons modes resulting from the frequency splitting via the application of the time-varying external B-Field, exhibit each a resonant peak of similar amplitude at different temperature ranges. This additional information shows that the probability for the central spin system to remain in its initially prepared diabatic state is enhanced for some temperature ranges for the corresponding two magnon modes. Hence, these temperature ranges where the probability density is maximum could save as decoherence free environment; an important requirement for the implementation of quantum computation and information processing in solid state circuitry. The theoretical and numerical results presented for the decoherence time and the probability density are that of a decohered central electron spin coupled to an anti-ferromagnetic spin bath. The theory is based on a spin wave approximation and on the density matrix using both transformations of Bloch, Primakov and Bogoliobuv in the adiabatic limit.
 
</p></abstract><kwd-group><kwd>Decoherence; Spin Wave; Anti-Ferromagnetic Environment; Central Spin; Variable B-Field</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>The interaction between quantum systems induced decoherence is commonly studied in the weak coupling and the strong coupling limits. Quantum decoherence is nowadays considered as the key concept in the description of the transition from the quantum to the classical world [<xref ref-type="bibr" rid="scirp.25050-ref1">1</xref>]. Various classical analogs have been developed and treated within the perturbation theory in the weak coupling regime [<xref ref-type="bibr" rid="scirp.25050-ref2">2</xref>]. Examples of the effects of weak coupling are changes in atomic decay rates [<xref ref-type="bibr" rid="scirp.25050-ref3">3</xref>] (Purcell effect) and F&#246;rster energy transfer [<xref ref-type="bibr" rid="scirp.25050-ref4">4</xref>] between a donor and acceptor atom and molecule. F&#246;rster energy transfer assumes that the transfer rate from donor to acceptor is smaller than the relaxation rate of the acceptor. This assumption ensures that once the energy is transferred to the acceptor, there is little or no feedback effect to the donor. On the other hand, as the interaction energy becomes sufficiently large, a feedback effect on the donor becomes possible thus a signature of the strong coupling regime. In this limit, it is no longer possible to distinguish between donor and acceptor. i.e. the system is seen as part of a large system including the environment. The excitation becomes delocalized, and we view the pair as one system. A characteristic feature of the strong coupling regime is energy level splitting, a property that can be well understood from a classical perspective [<xref ref-type="bibr" rid="scirp.25050-ref5">5</xref>]. The Hamiltonian of the total system provides a coupling between the apriori factorized two Hilbert spaces of the system and the environment, so that quantum evolution usually determines entanglement of the subsystems with the environment states. A key problem is to understand the characteristics of the environment and its full influence on the system. It is widely accepted that a rapid loss of coherence caused by the coupling to environmental degrees of freedom is at the root of the non-observation of superposition of macroscopically distinct quantum states.</p><p>Ford et al. (henceforth abbreviated as FLO) in its recent publication [<xref ref-type="bibr" rid="scirp.25050-ref5">5</xref>], discuss a thought experiment in which a Brownian particle initially in thermal equilibrium with its environment is subjected to a double-slit position measurement, giving rise to an interference pattern. Analyzing the decay of this pattern, they derive a decoherence time that is much shorter than that suggested by previous calculations [<xref ref-type="bibr" rid="scirp.25050-ref6">6</xref>]. Because the decoherence time calculated by FLO remains finite even in the absence of any coupling to the environment, they describe their result as “decoherence without dissipation [<xref ref-type="bibr" rid="scirp.25050-ref7">7</xref>]”.</p><p>The usual physical picture of decoherence [2,8] is the averaging over the unobserved degrees of freedom (the “environment”) that leads to non-unitary time evolution, with a consequent loss of information. If there is no coupling to the environment, there will be no such lost. We remark that the transition from the quantum to the classical regime due to decoherence is different from the semiclassical limit, where the classical behavior is recovered by exploiting the smallness of Planck’s constant. There are three relevant main differences to this regard: First, decoherence requires an open system, second, decoherence acts at the length-scale of the interference pattern, whereas a typical semi-classical procedure consists in evaluating a macroscopic observable on a fast oscillating probability distribution, third, decoherence is a dynamical effect; it grows with time [<xref ref-type="bibr" rid="scirp.25050-ref9">9</xref>]. In spite of its recognized relevance, there are still few rigorous results on decoherence, both from the analytical [<xref ref-type="bibr" rid="scirp.25050-ref10">10</xref>] and the numerical [<xref ref-type="bibr" rid="scirp.25050-ref11">11</xref>] point of view. The coupled oscillator model was previously studied by Lukas Novotny [<xref ref-type="bibr" rid="scirp.25050-ref12">12</xref>] in the strong coupling regime with mechanical model oscillators. Xiao-Zhong Yuan et al. [<xref ref-type="bibr" rid="scirp.25050-ref13">13</xref>] gave a quantum mechanical representation of the oscillators where the oscillators are constituted by a central spin atom coupled to an anti-ferromagnetic environment under the influence of a constant magnetic field. This model is an intuitive and popular model for many phenomena, including electromagnetically induced transparency [<xref ref-type="bibr" rid="scirp.25050-ref14">14</xref>], level repulsion [<xref ref-type="bibr" rid="scirp.25050-ref15">15</xref>] nonadiabatic processes [<xref ref-type="bibr" rid="scirp.25050-ref16">16</xref>], and rapid adiabatic passage [<xref ref-type="bibr" rid="scirp.25050-ref17">17</xref>].</p><p>In this paper we investigate the mechanism of decoherence in the simplest model of a quantum mechanically coupled oscillators, as a canonical example of the strong coupling regime characterized by frequency splitting. The conditions for the appearance of decoherence, adiabatic and non-diabatic transitions are investigated. The system of interacting oscillators is the central spin of a couple to an anti-ferromagnetic environment and subjected to a variable external magnetic field. Maintaining sufficient quantum coherence and quantum superposition properties is one of the most important requirements for applications in quantum computing and information processing, quantum teleportation [18,19], quantum cryptography [<xref ref-type="bibr" rid="scirp.25050-ref20">20</xref>] quantum dense coding [<xref ref-type="bibr" rid="scirp.25050-ref21">21</xref>], and telecloning [<xref ref-type="bibr" rid="scirp.25050-ref22">22</xref>]. Therefore it is imperative to understand and mitigate the possible mechanisms of decoherence that hinder the realization of the above goals.</p><p>This work is structured as follows; the model Hamiltonian of the central spin in the dual action of the antiferromagnetic bath and a parallel magnetic field is presented in Section 2. One of the most important observations in this section is frequency splitting of the antiferromagnetic spin bath due to the presence of external magnetic field, a situation where we can simulate the behavior of the system to that of a two level system a characteristic feature of the Landau-Zener scenario. The influence of the environment on the central spin dynamics is captured in the decohence factor and is evaluated in Section 3. We derive the transition probability of state in Section 4 and finally end with the conclusion.</p></sec><sec id="s2"><title>2. Model Hamiltonian</title><p>We study a single central spin atom coupled to an antiferromagnetic spin bath environment subjected to a time dependent magnetic field. Without the external magnetic field, an anti-ferromagnetic crystal has in any elementary chain two network of spin orientation; anti-parallel spin oriented in <img src="15-4800142\7bc324a4-b6d8-4c10-9155-afafe20311d0.jpg" /> direction and in <img src="15-4800142\dfc0cd5e-1726-41bc-906c-4150543ded3b.jpg" /> direction and an anisotropy field,<img src="15-4800142\da88fdb2-8e5d-496e-9371-2f626c0f9320.jpg" />. In the presence of the external magnetic field the Hamiltonian is given for example by Equation 2.6.2 in ref. [<xref ref-type="bibr" rid="scirp.25050-ref23">23</xref>] The Hamiltonian of the environment used in this work is the Ising type model.</p><disp-formula id="scirp.25050-formula38255"><label>(2.1)</label><graphic position="anchor" xlink:href="15-4800142\b45823b1-2633-4afd-986d-b56a477bd72f.jpg"  xlink:type="simple"/></disp-formula><p>In an anti-ferromagnetic environment contrary to the ferromagnetic environment, the coupling factor <img src="15-4800142\740795a6-2d71-4d15-9163-75bd667907e7.jpg" /> is positive.</p><disp-formula id="scirp.25050-formula38256"><label>(2.2)</label><graphic position="anchor" xlink:href="15-4800142\c6c1ed28-a456-435b-bcef-3e0f07bb2cca.jpg"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.25050-formula38257"><label>(2.3)</label><graphic position="anchor" xlink:href="15-4800142\f86872c7-ea2c-4131-8c4c-ca6766566e68.jpg"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.25050-formula38258"><label>(2.4)</label><graphic position="anchor" xlink:href="15-4800142\dcf1f420-9c54-42a6-bf48-28118b00eb61.jpg"  xlink:type="simple"/></disp-formula><p>and the magnetic moment of each atom</p><disp-formula id="scirp.25050-formula38259"><label>(2.5)</label><graphic position="anchor" xlink:href="15-4800142\2f440b03-3488-4974-ae3c-524cfea239ef.jpg"  xlink:type="simple"/></disp-formula><p>where g is the gyromagnetic factor, <img src="15-4800142\8fb0b779-5467-4121-be07-c7c45b68ecce.jpg" />is the Bohr magneton, <img src="15-4800142\eb097708-b2b0-4b76-ac8a-c53a6de7cc1f.jpg" />the coupling constant, <img src="15-4800142\71464290-a62e-421f-8c19-c2a7147d16dc.jpg" />the exchange interaction. We consider only nearest neighbor interaction. We assumed that the spin structure of the environment may be divided into two interpenetrating sublattices <img src="15-4800142\290ad35e-9dc4-4b73-9693-c0ee3ed10bb6.jpg" /> and <img src="15-4800142\1467109f-527c-4e82-a020-6874ccafa0d6.jpg" /> with the property that all nearest neighbor of an atom of <img src="15-4800142\ac0b21dd-a1f2-4ad3-961f-8a7dcde00cab.jpg" /> lie on <img src="15-4800142\2c17d02d-6aff-4682-9429-989d385233ca.jpg" /> and vice versa. <img src="15-4800142\7958c159-04cf-4782-ab77-67b5a2b48314.jpg" />and <img src="15-4800142\fc34513c-053c-4969-8aad-ee90cdc909ca.jpg" /> represents spin operators of <img src="15-4800142\77c67860-be2b-45f3-92f1-776138c32e51.jpg" /> and <img src="15-4800142\11255f05-840d-4885-bc6b-a58e365f4938.jpg" /> atom on sublattice a and b, each sublattice contains <img src="15-4800142\37738f1b-da3b-4006-9ebc-326b6e339a9e.jpg" /> atoms. <img src="15-4800142\94c472fe-56bb-4210-b25c-8b312d9dea23.jpg" />is the applied external magnetic field in the z-direction. <img src="15-4800142\655dca05-cf36-48ec-ba58-e9aab67da67b.jpg" />is the anisotropy field, assumed to be positive which approximates the effect of the crystal anisotropic energy with the property of turning for positive magnetic moment, <img src="15-4800142\cc0527e8-8e19-400a-9287-eeacc6d111a5.jpg" />, to align the spins on sublattice <img src="15-4800142\9fbbb319-3f58-4cf3-932e-af54c43bb274.jpg" /> in the positive z-direction and spins on sublattice <img src="15-4800142\3022cd3e-3a62-4cdc-b884-2c1403485da1.jpg" /> in the negative z-direction. In ref. [<xref ref-type="bibr" rid="scirp.25050-ref24">24</xref>] is analyzed the crossover factor,<img src="15-4800142\9de2b11e-ab9a-43b1-be71-3059a54547d1.jpg" />; the vector that connect(connects) atom on site <img src="15-4800142\3eb65857-1da1-4b6a-8e33-bd228970b213.jpg" /> or <img src="15-4800142\be03be86-0111-4b5d-a125-53d1eeecd976.jpg" /> with its nearest neighbor. To map the spin operators of the environment to bosonic operators, we use the Holstein-Primakoff transformation,</p><disp-formula id="scirp.25050-formula38260"><label>(2.6.a)</label><graphic position="anchor" xlink:href="15-4800142\396ae608-7723-4266-976c-832c71b04dcb.jpg"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.25050-formula38261"><label>(2.6.b)</label><graphic position="anchor" xlink:href="15-4800142\6cf39911-dd6f-4e1c-92bf-969389908eb8.jpg"  xlink:type="simple"/></disp-formula><p>and</p><disp-formula id="scirp.25050-formula38262"><label>(2.6.c)</label><graphic position="anchor" xlink:href="15-4800142\94d5c19f-6dcf-4da2-976d-f889b570a4ab.jpg"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.25050-formula38263"><label>(2.6.d)</label><graphic position="anchor" xlink:href="15-4800142\e9081d67-0d8a-4c8a-8939-4a9419ee346a.jpg"  xlink:type="simple"/></disp-formula><p>From where we have</p><disp-formula id="scirp.25050-formula38264"><label>(2.7)</label><graphic position="anchor" xlink:href="15-4800142\60b1646f-b19c-4e1a-8951-9345d3eb4948.jpg"  xlink:type="simple"/></disp-formula><p>with <img src="15-4800142\208c9315-ac1b-417f-9e15-9b27932f5343.jpg" /> the eigen value of spin Hence Equation (2.3) defines the Heisenberg Hamiltonian plus the external magnetic field in the Ising model. It is impossible to solve it exactly but conveniently when full advantage of the translational symmetry is considered. We need creation operators which create Bloch-like non localized excitations, in order to take translational symmetry into account. We consider one atom per unit cell and,<img src="15-4800142\16540b40-810e-43b7-870d-7ef29d14b326.jpg" />’s creates localized spin deviations at a single site. We use the spin wave approximation at low temperatures and we may expect the spin deviation quantum number to be rather small. Let <img src="15-4800142\39fa2704-969c-4185-a39f-0604d7e2d060.jpg" /> and <img src="15-4800142\1fcc011e-c40d-40c1-aced-6efb5c51719f.jpg" /> to reduce Equation (2.5) and (2.6); if we neglect the product of four operators and denote by <img src="15-4800142\8d2b2e15-e74b-4f1c-8189-b359fee2e7e1.jpg" /> the number of nearest neighbor, the Hamiltonian of the bath follows thus</p><disp-formula id="scirp.25050-formula38265"><label>(2.8)</label><graphic position="anchor" xlink:href="15-4800142\d76d3bda-721c-46db-8c8d-0921d662f71f.jpg"  xlink:type="simple"/></disp-formula><p>where <img src="15-4800142\71054ab2-eb0e-466f-b908-077098f83f0d.jpg" /> is the free Hamiltonian of the environment and <img src="15-4800142\05bdcda4-cfd4-4209-8eed-c6971633c69a.jpg" /> the Hamiltonian describing the excited state of the environment</p><disp-formula id="scirp.25050-formula38266"><label>(2.9)</label><graphic position="anchor" xlink:href="15-4800142\a93a9547-3fa8-4a4b-992b-a3ec0a78b43d.jpg"  xlink:type="simple"/></disp-formula><p>The Hamiltonian <img src="15-4800142\22c80399-ce4e-4dd2-9ad3-ee55ff51acdf.jpg" /> is made (up) of two parts</p><disp-formula id="scirp.25050-formula38267"><label>(2.10)</label><graphic position="anchor" xlink:href="15-4800142\8afc8b8f-f59a-49a1-8842-62c79f6d40c4.jpg"  xlink:type="simple"/></disp-formula><p>where the first part <img src="15-4800142\a0617851-68ce-4c10-a1df-addb41a58f2b.jpg" /> is the quantified Hamiltonian of the two magnons without interaction and <img src="15-4800142\c29d9af0-7eaa-44c4-96ba-ff73286261b1.jpg" /> the interacting Hamiltonian of the two magnons with expressions:</p><disp-formula id="scirp.25050-formula38268"><label>(2.11)</label><graphic position="anchor" xlink:href="15-4800142\5e0358d8-9e4f-4b6a-a0b4-b892d7402345.jpg"  xlink:type="simple"/></disp-formula><p>and</p><disp-formula id="scirp.25050-formula38269"><label>(2.12)</label><graphic position="anchor" xlink:href="15-4800142\095a2aeb-769d-4854-a6e5-4c6670dabe7f.jpg"  xlink:type="simple"/></disp-formula><p>To find the total number of magnons, we do the Fourier transformation of the total Hamiltonian with the Bloch operators:</p><disp-formula id="scirp.25050-formula38270"><label>(2.13.a)</label><graphic position="anchor" xlink:href="15-4800142\c7298dc0-df0d-4c1c-a29d-7fa10dae9ac7.jpg"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.25050-formula38271"><label>(2.13.b)</label><graphic position="anchor" xlink:href="15-4800142\b7b1fcd6-d790-4023-b498-0edf63d1e1d6.jpg"  xlink:type="simple"/></disp-formula><p>where <img src="15-4800142\e8e5fe7a-282e-4f07-942f-3a0abeafe0b8.jpg" /> is the vector of the primitive cell, k the wave vector. Let’s consider the restriction to the first Brillion zone and taking the inverse transformation of Equations (2.13.a) and (2.13.b)</p><disp-formula id="scirp.25050-formula38272"><label>(2.14.a)</label><graphic position="anchor" xlink:href="15-4800142\eb7eb5b1-3f25-43c3-80c8-5242e3067865.jpg"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.25050-formula38273"><label>(2.14.b)</label><graphic position="anchor" xlink:href="15-4800142\f7d13373-d2a8-4648-90b6-788d0015943b.jpg"  xlink:type="simple"/></disp-formula><p>The total number of magnons equals the total spin deviation quantum number of magnons in mode<img src="15-4800142\45bd757a-07e8-4544-a0d7-fecfb3caf3f5.jpg" />. The spin wave variable <img src="15-4800142\4c0f6e86-a116-4f92-ad22-f86e42d4c0bf.jpg" /> is substituted as</p><disp-formula id="scirp.25050-formula38274"><label>(2.15)</label><graphic position="anchor" xlink:href="15-4800142\9be94951-9e19-447a-bd38-5ee6ad138d5d.jpg"  xlink:type="simple"/></disp-formula><p>where <img src="15-4800142\cae5319e-9042-4e6a-9a57-a2bf13fbf207.jpg" /> is the occupation number operator for the number of magnons in mode k, <img src="15-4800142\943a0fa0-5d9c-4d8d-9a68-79bc28327c68.jpg" />is the number of particles in each sublattice and</p><disp-formula id="scirp.25050-formula38275"><label>(2.16)</label><graphic position="anchor" xlink:href="15-4800142\64cec077-eaf3-463f-8b58-7ee133bdb381.jpg"  xlink:type="simple"/></disp-formula><p>the Fourier transform coupling constant. The operators<img src="15-4800142\bc6212df-6415-4f2e-b793-822353f3ab9e.jpg" />, <img src="15-4800142\f1264289-7dfe-4574-901c-2bf334f4d34e.jpg" />, <img src="15-4800142\d72c246e-fb09-4a40-ae74-ae60dbc73ec2.jpg" />, <img src="15-4800142\2dbc14fa-f955-4123-a619-98deea35f6cb.jpg" />are the creation and annihilation operators of sublattices <img src="15-4800142\4dc7636a-dc6e-4bb5-a3d4-6c6bd01a4c1c.jpg" /> and <img src="15-4800142\6f1c6f3c-55b8-410a-97ba-18ba5d6ff9f6.jpg" /> respectively.</p><p>The Hamiltonian Equation (2.9) can then be transformed using the Bogoliubov transformation:</p><disp-formula id="scirp.25050-formula38276"><label>(2.17.a)</label><graphic position="anchor" xlink:href="15-4800142\b1b93395-d0c7-4a14-937e-9cae1dbb4349.jpg"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.25050-formula38277"><label>(2.17.b)</label><graphic position="anchor" xlink:href="15-4800142\af75f811-9761-4502-a257-66310a42d094.jpg"  xlink:type="simple"/></disp-formula><p>where the coefficients <img src="15-4800142\35b48a60-1477-463c-ae45-9e0c35fb3f27.jpg" /> and <img src="15-4800142\3b5e5ec8-3676-4e27-9013-2ea76ec921d4.jpg" /> are real and also the new operators obey the boson commutation rules:</p><disp-formula id="scirp.25050-formula38278"><label>(2.18)</label><graphic position="anchor" xlink:href="15-4800142\88480269-dda4-4f95-8536-933d6e9c4dd8.jpg"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.25050-formula38279"><label>(2.19)</label><graphic position="anchor" xlink:href="15-4800142\51c20845-f584-4ac3-8624-3f0d8fe0400a.jpg"  xlink:type="simple"/></disp-formula><p>which leads to the constraint,<img src="15-4800142\0b65edbc-1152-454b-9219-5b34ea88d118.jpg" />. The Hamiltonians respectively in Equation (2.1)-(2.3) becomes</p><disp-formula id="scirp.25050-formula38280"><label>(2.20)</label><graphic position="anchor" xlink:href="15-4800142\ecc2b473-ab5a-40fd-8f44-e121c7b5c656.jpg"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.25050-formula38281"><label>(2.21)</label><graphic position="anchor" xlink:href="15-4800142\a44f68c6-ddc1-442a-ba2c-8cf442ed255d.jpg"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.25050-formula38282"><label>(2.22)</label><graphic position="anchor" xlink:href="15-4800142\f1c3ad2f-0a4a-456e-9c54-a5da48c09d50.jpg"  xlink:type="simple"/></disp-formula><p><img src="15-4800142\2cf6a167-c797-44ed-9f7d-a04b14ff7f94.jpg" />is the energy of the free harmonic oscillator. The frequency of the two magnons at the symmetric position given by the site <img src="15-4800142\9c65cae3-6b92-4a32-a89c-a9f57e938e0b.jpg" />and the site <img src="15-4800142\1708156c-8565-4c4c-86bb-60b7109a7e71.jpg" /> of the system is:</p><disp-formula id="scirp.25050-formula38283"><label>(2.23)</label><graphic position="anchor" xlink:href="15-4800142\8c8b71d3-c6cd-4102-ac8f-975ffb4e65ed.jpg"  xlink:type="simple"/></disp-formula><p>In an anti-ferromagnet Cristal, the excitation of one magnon of a wave vector k lead to a change either of + 1/N, or of –1/N for the ensemble of the two anti-parallel spins of the elementary network link. There exist then two modes, <img src="15-4800142\d18b1ef5-5837-4646-ab6c-aeafd32bac64.jpg" />and <img src="15-4800142\c90de11d-bce2-428c-b753-d46b6b856036.jpg" /> which are degenerates if the contribution of the external magnetic field is neglected. These states, up and down correspond respectively to the eigen frequencies</p><disp-formula id="scirp.25050-formula38284"><label>(2.24.a)</label><graphic position="anchor" xlink:href="15-4800142\843d15c3-13fc-4370-91b7-6d341bcfe436.jpg"  xlink:type="simple"/></disp-formula><p>and</p><disp-formula id="scirp.25050-formula38285"><label>(2.24.b)</label><graphic position="anchor" xlink:href="15-4800142\8f8f44a4-583c-4304-853d-929edcdd8883.jpg"  xlink:type="simple"/></disp-formula><p>From the given expressions Equations (2.24.a) and (2.24.b), we see that the magnetic state of spin “up” or “down” depends at the same time on the excitation of the modes <img src="15-4800142\c0ba1b76-04ef-4101-96bc-e3de7011ebf4.jpg" /> and <img src="15-4800142\85fe5820-a281-42a7-ae85-e205a4838d78.jpg" /> and to the population <img src="15-4800142\0a7cce38-99a8-4319-922d-3c8ec5d422b7.jpg" /> and <img src="15-4800142\de257904-e56b-4745-8798-93cea515e268.jpg" /> or of <img src="15-4800142\29b1f408-f276-4586-aec3-92dc7a2f0456.jpg" /> and<img src="15-4800142\cf046d40-2bff-436e-a568-2501f6d1e962.jpg" />. Using the kinetic energy expression of the system, the effective mass <img src="15-4800142\ed4882c3-da3e-4d7c-881f-9eb5b0e08879.jpg" /> of magnon is found,</p><disp-formula id="scirp.25050-formula38286"><label>(2.25)</label><graphic position="anchor" xlink:href="15-4800142\337d6367-6845-406d-bda7-db1caf50cc86.jpg"  xlink:type="simple"/></disp-formula><p>From where we have</p><disp-formula id="scirp.25050-formula38287"><label>(2.26)</label><graphic position="anchor" xlink:href="15-4800142\e4e7bff2-e75d-4abb-908a-0a64aa323fbd.jpg"  xlink:type="simple"/></disp-formula><p>Equation (2.26) gives the effective mass of a quasiparticle moving in the crystal with frequencies <img src="15-4800142\a121045c-9af8-4e43-b0bc-68aae38c34ef.jpg" /> in mode <img src="15-4800142\b51c96da-eced-4920-a2b5-d77425d4c74a.jpg" /> where a, b, c, <img src="15-4800142\4da94804-ed69-4800-a214-a2fbc389f8e2.jpg" />are the constants of system. The result of Equation (2.24.a) is not a good approximation to the situation of the spin wave [<xref ref-type="bibr" rid="scirp.25050-ref25">25</xref>]: We don’t take into account the processes which give in return their half-life. It has been calculated by some authors [26,27]. The critical magnetic field B<sub>c</sub> (the corresponding external field that corresponds to field with the energy equals to the energy of the environment) is evaluated; that is when the mode <img src="15-4800142\bcb508b2-1027-4f19-bec0-544915a3dc19.jpg" /> and at the finite oscillating time,</p><p><img src="15-4800142\609af973-9218-4192-96cd-a3d6c44283e8.jpg" />, and taking<img src="15-4800142\071ef7d2-3fd2-454e-8c09-6714ca04acbb.jpg" />:</p><disp-formula id="scirp.25050-formula38288"><label>(2.27)</label><graphic position="anchor" xlink:href="15-4800142\ab9f969e-5e3f-4859-9012-1099f73ef02e.jpg"  xlink:type="simple"/></disp-formula><p>Equation (2.27) is the critical magnetic field obtained as for the constant external magnetic field in [<xref ref-type="bibr" rid="scirp.25050-ref28">28</xref>]. In analogy to the dressed atom picture [<xref ref-type="bibr" rid="scirp.25050-ref29">29</xref>], the eigen frequencies <img src="15-4800142\0f135ed4-2741-400b-b240-677761f65adc.jpg" /> can be associated with dressed states, that is, the oscillator frequencies of state <img src="15-4800142\8068ff68-bf9c-4d92-874f-0ce414883c67.jpg" /> and <img src="15-4800142\3cd4fe4e-a45a-4186-8a1f-cab096927e75.jpg" /> (that are the states respectively with oscillator frequencies<img src="15-4800142\c928170d-6fa3-49c9-b398-ca0a5d3679dc.jpg" />,<img src="15-4800142\bb4626b8-4c95-4923-a94d-bf9780deb7c8.jpg" />), in the presence of mutual coupling.</p><p>In Figures 1-3 are plotted the frequencies of the two oscillators. In <xref ref-type="fig" rid="fig1">Figure 1</xref> the two curves intersect at <img src="15-4800142\59f34f97-96be-477d-aae6-ea4407167d63.jpg" /> and later diverge. The dynamics of the eigen modes frequencies as function of time shows oscillations depicting the character variability of the external magnetic field <xref ref-type="fig" rid="fig2">Figure 2</xref>, it appears that the two curves intersect at <img src="15-4800142\e3a543f3-bb91-48c4-97cd-11e3f6994d49.jpg" /></p><p>The dash curve corresponds to the frequency <img src="15-4800142\f8f01a6e-923e-44ab-8c6a-1729fbdfc89d.jpg" /> and the solid curve to the frequency<img src="15-4800142\629f1100-fe27-411e-8238-15bc76b3cd96.jpg" />.</p><p>There is a characteristic anti-crossing with a frequency splitting of</p><disp-formula id="scirp.25050-formula38289"><label>(2.28)</label><graphic position="anchor" xlink:href="15-4800142\a251d605-ca9a-4d50-8ef9-1690925553ec.jpg"  xlink:type="simple"/></disp-formula><p>with<img src="15-4800142\1e06610e-9d3f-4ca9-af9d-157ac2f125d5.jpg" />. As<img src="15-4800142\7ad39eaf-ccd8-4538-8198-cb0f73b728a5.jpg" />, the splitting increases with the external field. Anti-crossing is a characteristic fingerprint of strong coupling.</p><p>The eigen modes of the oscillators with frequencies <img src="15-4800142\7c55d01c-9918-41c6-bed3-ee78dfa9ac2d.jpg" /> translate the system to that of a two level system</p><p>coupled by a constant magnetic field as analogous to the case in [<xref ref-type="bibr" rid="scirp.25050-ref30">30</xref>] where the coupling is via a spring constant, whereby in the light of Landau-Zener scenario, the frequency difference of the oscillator changes linearly in time, the probability for level crossing (diabatic transition) at infinite large time is</p><disp-formula id="scirp.25050-formula38290"><label>(2.29)</label><graphic position="anchor" xlink:href="15-4800142\db1e1c6a-f56b-4530-b24d-0c13a07b2fad.jpg"  xlink:type="simple"/></disp-formula><p>where <img src="15-4800142\903b7449-642e-408d-802a-80ff07577f62.jpg" /> is the transition speed and is given by the dispersion relation<img src="15-4800142\7cc63188-57ba-40e1-848a-1e7a355d649e.jpg" />, where <img src="15-4800142\0d7db9c1-adab-4fc4-9dba-8e5911e01b68.jpg" /> is the wave vector.</p><p>Equation (2.29) is the probability that the anti-ferromagnetic bath mode remains in the initially prepared state<img src="15-4800142\b599c027-05b0-479a-903c-2a91b0d5fa68.jpg" />. The characteristic Gaussian shape of this transition is shown in <xref ref-type="fig" rid="fig3">Figure 3</xref>(a) a signature that the antiferromagnetic spin bath described by the two frequency modes interact via the magnetic field with the subsequent collapse of population with frequency mode <img src="15-4800142\00bfcec3-cde4-4a0a-9ced-a07fbc411966.jpg" /> (red solid curve) and raising of population with frequency mode <img src="15-4800142\248ca572-de43-4d2a-b3a7-d94cb9edaf1b.jpg" /> (green solid curve). This implies the magnetic field provides means by which the anti-ferromagnetic spin bath could be tailored.</p><p>In <xref ref-type="fig" rid="fig3">Figure 3</xref>(b) supposing<img src="15-4800142\8fc89efc-a2f9-4dac-9dbf-5738c485b00f.jpg" />, the plot shows the range of values of the phase angle <img src="15-4800142\e5053648-a991-42d5-b757-aa67ddf3d959.jpg" /> that the survival transition amplitude is maximum as it exhibits a resonant peak. There is shrinkage in the width of this resonant peak for large value of the magnetic field</p><p>amplitude implying the initially prepared state of the environmental frequency mode could be tailored with precision if a certain value of the magnetic field amplitude and phase angle is used. <xref ref-type="fig" rid="fig4">Figure 4</xref> is the plot of the frequency versus the wave vector for some system parameters. The dotted curve represents the behavior of the frequency, <img src="15-4800142\dacdf3f8-d5a8-4428-80e8-c5b0c70a3877.jpg" />and the solid curve that of the frequency, <img src="15-4800142\e3e1c10c-be88-40a1-9154-261a41ce9499.jpg" />as the wave vector is varied. These curves show a basin-like behavior. It proceeds two extreme values (or minima) corresponding to the high cut-off frequency and the low cut-off frequency. Thus, any wave which is propagated with a frequency not included in this domain vanishes. Note that we have ignored damping of the magnons in the analysis of the coupled oscillators. When the external magnetic field exceeds B<sub>c</sub>, we have<img src="15-4800142\3ec9600c-ea78-4f10-bbf8-6e3e10b92adf.jpg" />. This indicates that, this branch of magnon is no longer stable due to the externally applied magnetic field.</p><p>As a result, the anti-ferromagnetic polarization ﬂips perpendicular to the field, i.e., the magnetic field induces spin flop transition. The spin-flop transition demonstrates a significant change of the spin configuration in the anti-ferromagnetic environment. This phenomenon has been observed and investigated for many different materials [31-33]. The spin wave theory is known to describe well the low-excitation and low-temperature properties of anti-ferromagnetic materials.</p><p>Despite this low-excitation approximation, the spin wave theory also describes well the physics for <img src="15-4800142\5e09688d-f92c-4680-9f86-6146f8de49c5.jpg" /> and the value of the critical magnetic field of the spin-flop transition in anti-ferromagnetic materials [<xref ref-type="bibr" rid="scirp.25050-ref28">28</xref>]. We will thus use the spin wave theory to discuss the decoherence time of the central spin under the influence of the anti-ferromagnetic environment when the external magnetic field is tuned to approach <img src="15-4800142\ed738a65-bd38-496d-89ad-051184e68b6b.jpg" /> from below (i.e.</p><p><img src="15-4800142\75ad7184-6836-4117-a2e2-59647646e2e6.jpg" />for<img src="15-4800142\b8439a6a-d67b-4944-b98c-1d3dbb6f578c.jpg" />). It will be shown that an analytic expression for the decoherence time can be evaluated.</p></sec><sec id="s3"><title>3. Decoherence Time</title><p>In this section, using the time evolution of the off-diagonal elements of the reduced density matrix for the central spin, we calculate the decoherence time. We assumed factorized initial state of the density matrix of the total systems, i.e.<img src="15-4800142\627e019e-8bfb-46fe-91e9-70745ca9e934.jpg" />. The initial state of the central spin is described by<img src="15-4800142\c42e5c07-f122-453f-bd17-d94492f12f53.jpg" />. The density matrix of the environment is assumed to be in thermal equilibrium, that is<img src="15-4800142\660d4d57-162e-4bb0-a004-ed57e9720ae9.jpg" />, where Z is the partition function. We are interested in the dynamics of the off-diagonal elements of the reduced density matrix as they carry information on the phase coherence of the system. This is equivalent to calculating the time evolution of the spin-flip operator, <img src="15-4800142\9f9eb286-ca01-4958-b00c-99704a3fd2b2.jpg" />, where <img src="15-4800142\a979effb-f414-4d29-8201-ecc62ea256a0.jpg" /> and <img src="15-4800142\640ac933-a409-4f8e-b01e-f29219801d92.jpg" /> are respectively the lower and upper eigen states of<img src="15-4800142\677d8695-631d-47e8-a517-78369a1f9eb9.jpg" />. By tracing out the environmental degrees of freedom, the time evolution of <img src="15-4800142\1261fe2f-7ee5-4f93-8e20-78fdb9843f9f.jpg" /> can be written as:</p><disp-formula id="scirp.25050-formula38291"><label>(3.30)</label><graphic position="anchor" xlink:href="15-4800142\2eaff424-a285-479d-8d99-b624e3bdbcdd.jpg"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.25050-formula38292"><label>(3.30)</label><graphic position="anchor" xlink:href="15-4800142\35f6d629-a4da-4ade-8887-391e453fbcd4.jpg"  xlink:type="simple"/></disp-formula><p>the decoherence factor <img src="15-4800142\4580c256-c7d7-4890-aca4-123127606539.jpg" /> can be found using the time evolution</p><disp-formula id="scirp.25050-formula38293"><label>(3.31)</label><graphic position="anchor" xlink:href="15-4800142\5ba43b4c-c686-4dac-b435-088e331d4ab3.jpg"  xlink:type="simple"/></disp-formula><p>From Equation (2.3) the decoherence factor yields</p><disp-formula id="scirp.25050-formula38294"><label>(3.32)</label><graphic position="anchor" xlink:href="15-4800142\6f96f3b4-473f-436d-a149-34cafef4e155.jpg"  xlink:type="simple"/></disp-formula><p>where</p><disp-formula id="scirp.25050-formula38295"><label>(3.33.a)</label><graphic position="anchor" xlink:href="15-4800142\86923619-ef14-4cb0-aee0-2d3a9afbfd49.jpg"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.25050-formula38296"><label>(3.34.b)</label><graphic position="anchor" xlink:href="15-4800142\30fb5944-57a8-4506-ad45-e4c0d77ac21e.jpg"  xlink:type="simple"/></disp-formula><p>The decoherence factor of the system in the volume <img src="15-4800142\b833bc43-adc5-461f-b566-3805c84d10c2.jpg" /> of environment is found at low temperature; that is for<img src="15-4800142\c295edc7-ff86-46e7-ba28-cd138d82e18c.jpg" />, where <img src="15-4800142\fc57a7b4-8ca3-46b3-8af6-bcce2356f29a.jpg" /> is the temperature,</p><disp-formula id="scirp.25050-formula38297"><label>(3.35)</label><graphic position="anchor" xlink:href="15-4800142\f3ab1f66-85d2-40d6-9591-08b978e365a4.jpg"  xlink:type="simple"/></disp-formula><p>Then in the thermodynamic limit, i.e.<img src="15-4800142\c03dfa35-65ec-435d-8776-018a83f12075.jpg" />, <img src="15-4800142\41f86fd8-66e0-445c-aca4-dd31b781136f.jpg" />it is obvious that <img src="15-4800142\2628d033-736e-49bd-a1d3-c1eec1fe2310.jpg" /> as<img src="15-4800142\bb34c80f-c07f-40c9-ac10-dd8d98f915d9.jpg" />. To find the relation between <img src="15-4800142\9cae68a6-b35e-437a-9a3a-1a772f4394df.jpg" /> and <img src="15-4800142\a3932bb6-212b-44f8-af5c-05f33e96d079.jpg" /> in the thermodynamic limit, we calculate:</p><disp-formula id="scirp.25050-formula38298"><label>(3.36)</label><graphic position="anchor" xlink:href="15-4800142\dbdbba1a-4395-40b2-8e32-b068a426c346.jpg"  xlink:type="simple"/></disp-formula><p>The absolute value of the decoherence factor in the thermodynamic limit can be expressed:</p><disp-formula id="scirp.25050-formula38299"><label>(3.37)</label><graphic position="anchor" xlink:href="15-4800142\88863268-4bd9-4192-b004-cf8bd7ad194e.jpg"  xlink:type="simple"/></disp-formula><p>where</p><disp-formula id="scirp.25050-formula38300"><label>(3.38)</label><graphic position="anchor" xlink:href="15-4800142\db8b081a-448b-4fd3-ae66-61fffc56870e.jpg"  xlink:type="simple"/></disp-formula><p>We obtained these results analytically for the case of a variable magnetic field. It indicates that the decoherence factor displays a Gaussian decay with time (see Equation (3.37)). The factor <img src="15-4800142\610f9976-3926-4ad4-85a6-b10aef80e65f.jpg" /> in the exponent is different from the Markovian approximation which usually shows a linear decay in time in the exponent thus portraying nonMarkovianity a signature of strong coupling between system and environment.</p><p>In <xref ref-type="fig" rid="fig5">Figure 5</xref> we see that the decoherence time decreases monotonically to zero with the external magnetic field. The opposite is observed in <xref ref-type="fig" rid="fig6">Figure 6</xref> where the</p><p>decoherence time increases exponentially with the anisotropy field. This behavior shows the fact that the anisotropy gives rise to stronger polarization of the environmental spin and reduces the effect of the external field on the decoherence of the central spin.</p><p>As discussed in[<xref ref-type="bibr" rid="scirp.25050-ref13">13</xref>] the field-dependent decoherence behavior may be inferred from the effective Hamiltonian, Equations (2.24)-(2.26). From the interaction Hamiltonian, Equation (2.25), we see that the larger the difference in the magnon excitation number between the magnon <img src="15-4800142\bff37e96-2a89-44b3-8ffb-02f02d9e4e5f.jpg" /> and magnon<img src="15-4800142\209223a8-ffe5-440c-8db1-8891013d37a1.jpg" />, the stronger the effect of the environment on the central spin. At a given temperature, the average thermal excitation number may be the same for the two magnons, but the ﬂuctuation in the excitations for each individual magnon may not be the same at the same time. If the external magnetic field is increased, the magnon frequency <img src="15-4800142\a8a2a6f9-3c3d-419b-a163-ff4da968e24a.jpg" /> decreases but <img src="15-4800142\ca82fc93-9377-4a6e-a4c7-909869fefd57.jpg" /> increases. Consequently, the magnon mode <img src="15-4800142\a60e0d87-e4a3-476c-b137-58f44a062202.jpg" /> is easier to be excited than the magnon mode <img src="15-4800142\333c55f2-09cf-43c0-8929-c066d56290ff.jpg" /> at a given anisotropy field, temperature and time. This results in a larger magnon excitation number difference and ﬂuctuation, and thus a stronger decoherence effect.</p><p>An alternative way to understand the field-dependent decoherence time may be in terms of quantum correlations. There is a kind of trade-off between the external magnetic field and the anisotropy field. The anisotropy field renders the anti-ferromagnetic environment stable. On the other hand, the external magnetic field tends to reduce the anti-ferromagnetic order of the environment. Therefore the stronger the external magnetic field is, the smaller the anti-ferromagnetic order. On the contrary, the larger the anisotropy field is, the stronger the correlation of the anti-ferromagnetic environment. If the constituents (spins) of the environment maintain appreciable correlations or entanglement between themselves, then there is a restriction on the entanglement between the central spin and the environment [34,35]. As a consequence, this sets a restriction on the amount that the central spin may decohered [32,33,36]. Thus as far as the decoherence of the central spin is concerned, the anisotropy field has a similar effect on the exchange interaction strength between the constituents (spins) of the anti-ferromagnetic environment. Strong intra-environmental interaction results in a strong anti-ferromagnetic correlation, thus an effective decoupling of the central spin from the environment and a suppression of decoherence [32,33]. Therefore the decoherence time increases with the increase of the anisotropy field but decreases with the increase of the strength of the external magnetic field.</p><p>In the subsequent section we find the transition probability of state in the system, considering that the density matrix of the environment is in thermal equilibrium.</p></sec><sec id="s4"><title>4. Probability Density of State</title><p>At thermodynamic equilibrium, the density state of the system is expressed as</p><disp-formula id="scirp.25050-formula38301"><label>(4.39)</label><graphic position="anchor" xlink:href="15-4800142\ee4598ac-5557-4d6b-ab86-64ae23ec0e30.jpg"  xlink:type="simple"/></disp-formula><p>H is the total Hamiltonian and T the Boltzmann temperature. Let’s evaluate the partition function of the system, at the thermodynamic equilibrium</p><disp-formula id="scirp.25050-formula38302"><label>(4.40)</label><graphic position="anchor" xlink:href="15-4800142\ca3a7780-e36a-4d5a-8ea9-acfdb3775f27.jpg"  xlink:type="simple"/></disp-formula><p>Here, g is the gyromagnetic factor, E<sub>0</sub> the energy of the free harmonic oscillator.</p><p>If we let<img src="15-4800142\d6fedb73-9b00-4e38-9410-36d5d8bd5844.jpg" />, <img src="15-4800142\06f63b8d-ee74-4acd-bbeb-d016eab73e8c.jpg" />the number of magnon for the different creation operator <img src="15-4800142\4447c330-4c64-4230-b3af-7bb36843c6e8.jpg" /> and <img src="15-4800142\d1b6930c-c428-45b6-b6a9-f15303107e15.jpg" /> respectively</p><disp-formula id="scirp.25050-formula38303"><label>(4.41)</label><graphic position="anchor" xlink:href="15-4800142\c0ae3f7d-e822-43f8-9e7d-1251dec2283c.jpg"  xlink:type="simple"/></disp-formula><p>Then we have the mean value of the probability density of state.</p><disp-formula id="scirp.25050-formula38304"><label>(4.42)</label><graphic position="anchor" xlink:href="15-4800142\fc5838fc-929f-4534-8a62-31d50222c356.jpg"  xlink:type="simple"/></disp-formula><p>where</p><disp-formula id="scirp.25050-formula38305"><label>(4.43)</label><graphic position="anchor" xlink:href="15-4800142\047c06cf-0426-419d-b54a-6e7310d4005f.jpg"  xlink:type="simple"/></disp-formula><disp-formula id="scirp.25050-formula38306"><label>(4.44)</label><graphic position="anchor" xlink:href="15-4800142\20ac6832-4b7d-4686-a001-1573c89d0ab0.jpg"  xlink:type="simple"/></disp-formula><p>The solid curve represents the vibration mode with frequency <img src="15-4800142\7956d09a-bfd2-414f-82c8-eed080ba4725.jpg" /> and the dot curve the mode with frequency<img src="15-4800142\acdaec07-f46e-4340-8bd3-626bf6e2a794.jpg" />. Here, <img src="15-4800142\22101bfb-6027-4d09-91e7-ec03297544c8.jpg" />is the gap between the two vibrational modes where looking at Equation (2.28), it results that <img src="15-4800142\45f58c65-6e11-4bf6-9e0f-8dfbc4fe794f.jpg" /> and may be interpreted as the energy necessary for spin transition from low spin energy state to high energy spin state.</p><p>Figures 7-9 show plots of the probability density of state as a function of temperature. The plots demonstrate a resonance peak within some temperature range. This provides us with additional information on the range of values of the temperature, anisotropy field, magnetic field and other system parameters for which the central spin system is sensitive to and possibly undergoes transition. Transforming temperature into frequency via the Matsubara relation, we could talk of triple resonance comprising of the driving field frequency, anisotropy field frequency and the environmental eigen modes frequency. The resonance peak in the plot of the probability density of state for the two vibrational modes corresponds to minimum decoherence effect of the environment and the driving field on the central spin. In <xref ref-type="fig" rid="fig7">Figure 7</xref>, it is seen that two different peaks having the same magnitude arises for the two eigen modes frequencies<img src="15-4800142\0218e11c-1827-414e-b6c6-2394cd4cd10f.jpg" />, <img src="15-4800142\56a36412-f84c-404f-9d3b-20a315a6ca5a.jpg" />at different temperatures. We see that the two different modes enhance the probability density of state with each doing so at different temperature ranges. In the same figure <img src="15-4800142\02702cd5-e8a8-440d-982a-b66be00bd18d.jpg" /> is the gap between the two vibrational modes where by looking at Equation</p><p>(2.29), it results that <img src="15-4800142\c31b7c1b-c45f-4366-a645-eca62dd7cf64.jpg" /> and may be interpreted as the energy necessary for spin to make transition from its low energy state (with frequency mode<img src="15-4800142\848b1a8b-0c4e-4a0d-a9b6-c9d5c9043278.jpg" />) to its high energy state (with frequency mode<img src="15-4800142\2deff424-d9ae-46f2-8dc0-108f9d1b4ac2.jpg" />) and vice versa. In <xref ref-type="fig" rid="fig8">Figure 8</xref> it is seen that the variable external magnetic field reduces the probability density of state as compared to the constant magnetic field. The character variability of the external magnetic field with its frequency is used to control the dynamic of the hold system. This is because the variable field induces oscillations amongst the magnon modes with alternate collapse and revival of the modes. In <xref ref-type="fig" rid="fig9">Figure 9</xref>, the anisotropy field plays the inverse rule as compared to the external magnetic field.</p><p>That is, the stronger the anisotropy field, the stronger the decoherence of the central spin system.</p><p>The solid and dash curves are the plot considering the external magnetic field constant whereas the dotted curve is the plot of the probability density of state subjected to a variable magnetic field.</p><p>We observed from <xref ref-type="fig" rid="fig8">Figure 8</xref> that increasing the anisotropic magnetic field intensity leads to an increase in the amplitude of the probability density. This shows that the anisotropy field provides to the central spin a decoherence free environment. This behavior is not surprising as the decoherence time increases with increase in anisotropy (see <xref ref-type="fig" rid="fig6">Figure 6</xref>).</p></sec><sec id="s5"><title>5. Conclusion and Perspective</title><p>We have studied the decoherence of a central spin coupled to an anti-ferromagnetic environment in the presence of a variable external magnetic field. The results, obtained using the spin wave approximation in the thermodynamic limit, show that the decoherence factor displays a Gaussian decay with time. It is shown that the probability density of state occurs at some critical values of magnetic field and temperatures. The probability density as a function of temperature is characterized by a resonant peak corresponding to some critical parameters of the system which here are the critical external magnetic field, anisotropy field and temperatures. The probability of the central spin to remain in the initially prepared state is maximum at these values and spin-flop transition is suppressed. Out of these parameter range spin-flop transition occurs, consistent with the QPT as studied in [37-39]. It is equally seen that strong anisotropy field enhances the probability density and reduces decoherence of the anti-ferromagnetic environment of the central spin. Therefore, in order to reduce the loss of coherence of the central spin, we could decrease the environmental temperature, choose variable magnetic field with high amplitude (which) could lead to dark state of the environment, and choose the anti-ferromagnetic surrounding or underlying anti-ferromagnetic materials with a strong crystal anisotropy field. The frequency eigen mode dependence on the phase angle as shown in (<xref ref-type="fig" rid="fig3">Figure 3</xref>(b)) suggest to us that the transition amplitude strongly depend on the phase angle and shall be one of the aspects for our future investigation.</p></sec><sec id="s6"><title>REFERENCES</title></sec><sec id="s7"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.25050-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">D. Guilini, E. Joos, C. Kiefer, J. Kupsch, I. O. Stamatescu and H. D. Zeh, “World in Quantum Theory,” Springer-Verlag, Berlin Heidelberg, 1996.</mixed-citation></ref><ref id="scirp.25050-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">R. R. Chance, A. Prock and R. Silbey, “Molecular Fluorescence and Energy Transfer near Metal Interfaces,” Advances in Chemical Physics, Vol. 37, 1978, pp. 1-65. 
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