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arXiv:1906.02769 · Journal of Applied Physics

Signature of quantum entanglement in NH4CuPO4·H2O

Tanmoy Chakraborty, Harkirat Singh, Chiranjib Mitra

Published Jan 17, 2014• 15 citations
arXivHTMLPDF

Abstract

Entangled solid state systems have gained a great deal of attention due to their fruitful applications in modern quantum technologies. Herein, detection of entanglement content from experimental magnetic susceptibility and specific heat data is reported for NH4CuPO4·H2O in its solid state crystalline form. NH4CuPO4·H2O is a prototype of Heisenberg spin 1/2 dimer system. Temperature dependent magnetic susceptibility and specific data are fitted to an isolated dimer model and the exchange coupling constant is determined. Field dependent magnetization isotherms taken at different temperatures are plotted in a three dimensional plot. Subsequently, entanglement is detected both from susceptibility and specific heat through two different entanglement measures; entanglement witness and entanglement of formation. The temperature evolution of entanglement is studied and the critical temperature is determined up to which entanglement exists. Temperature dependent nature of entanglement extracted from susceptibility and specific heat shows good consistency with each other. Moreover, the field dependent entanglement is also investigated.

DOI
10.1063/1.4861732

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arXiv:2303.05372•New Journal of Physics•Sep 15, 2023•6 citations
Entangled solid state systems have gained a great deal of attention due to their fruitful applications in modern quantum technologies. Herein, detection of entanglement content from experimental magnetic susceptibility and specific heat data is reported for NH4CuPO4·H2O in its solid state crystalline form. NH4CuPO4·H2O is a prototype of Heisenberg spin 1/2 dimer system. Temperature dependent magnetic susceptibility and specific data are fitted to an isolated dimer model and the exchange coupling constant is determined. Field dependent magnetization isotherms taken at different temperatures are plotted in a three dimensional plot. Subsequently, entanglement is detected both from susceptibility and specific heat through two different entanglement measures; entanglement witness and entanglement of formation. The temperature evolution of entanglement is studied and the critical temperature is determined up to which entanglement exists. Temperature dependent nature of entanglement extracted from susceptibility and specific heat shows good consistency with each other. Moreover, the field dependent entanglement is also investigated.
A quantitative estimation of quantum discord is performed for a Heisenberg spin 1/2 dimer compound (NH4CuPO4, H2O) by means of experimental magnetic and thermal measurements. Magnetic susceptibility and specific heat data were collected for NH4CuPO4, H2O and analyzed within the framework of the Heisenberg isolated dimer model. Internal energy as a function of temperature is obtained by integrating the specific heat versus temperature data. Subsequently, quantum discord, total correlations and spin-spin correlation function are quantified from susceptibility and internal energy and plotted as a function of temperature. Violation of Bell's inequality is also tested for NH4CuPO4, H2O via both experimental susceptibility and specific heat data signifying the presence of entanglement.
Violation of Bell’s inequality test has been established as an efficient tool to determine the presence of entanglement in quantum spin 1/2 magnets. Herein, macroscopic thermodynamic quantities, namely, magnetic susceptibility and specific heat have been employed to perform Bell’s inequality test for [NH4CuPO4, H2O], a spin 1/2 antiferromagnet with nearest neighbor interactions. The mean value of the Bell operator is quantified and plotted as a function of temperature. The threshold temperature is determined above which the Bell’s inequality is not violated and a good consistency is found between the analyses done on magnetic and thermal data.
Low dimensional spin systems are a class of interacting many body systems which often can suitably be described by physical models with possible experimental realizations. A series of inorganic, organometallic and organic systems representing different spin ½ models have been synthesized and their thermodynamics have been investigated. In most of the cases, antiferromagnetic coupling is favored and the system can be well described by Heisenberg model where the unpaired spins interact isotropically to the nearest neighbor with an intrachain coupling constant (J). Isothermal heat capacity plots as a function of field at low temperature captures the Quantum Critical Point (QCP) experimentally, owing to change in symmetry of the ground state. This change of phase is associated with the occurrence of first order quantum phase transition in NH4CuPO4·H2O which has been established by studying field dependent behavior of magnetization and entanglement. On one hand entanglement being a nonlocal property of the spins takes its maximum value when the applied magnetic field is zero. On the other hand magnetization describing the local properties of the individual spins takes its maximum value upon reaching the saturation magnetic field at the expense of entanglement. It signifies a physical picture of quantum information sharing and gives an to opportunity capture the critical magnetic field. We have investigated this scenario in NH4CuPO4·H2O and determined the critical field which shows an excellent match with the value obtained from the field dependent specific heat data.
Entanglement has been extensively studied from the perspective of Quantum Information Processing for the last decade and various measures of entanglement, to quantify it are now available. Experimentally also it has been possible to measure entanglement in pure state, mostly in optics. However, in recent years there has been significant development in Quantum Condensed Matter systems, especially spin chains, where extraction of entanglement has been made possible through macroscopic witness operators like magnetic susceptibility. In this work, we have studied the magnetic properties of some spin chains, where the exchange interaction can be tuned by preparation technique and we have extracted a magnetic field and temperature dependence of entanglement from susceptibility and magnetization data taken at various temperatures and fields. The spin chains considered here fall in two categories, first one is an alternating dimer model and the second is an infinite spin chain. We have given the experimental plots of entanglement as a function of temperature and magnetic fields and compared them with the theoretical plots.
The absolute temperature (T) and magnetic field (B) dependent magnetization(M) and study of entanglement out of the experimental data is reported for dichloro(thiazole)copper(II), a Heisenberg spin chain system. The magnetic susceptibility (χ) vs. T plot assures the behavior of infinite spin chain. The M vs. B data has been taken at different temperature as long as the antiferromagnetic(AFM) correlations persist significantly. M, B and T have been plotted in a 3D plot showing explicitly the dependence of the three parameters on one another. Since the concurrence is a measure of entanglement, the value of concurrence is extracted from the χ vs. T data and that's how the information about entanglement is extracted from the macroscopic magnetic susceptibility.
Abstract In this paper, we used a theoretical measure known as distance between the states, , to determine the bipartite entanglement of a one dimensional magnetic dimer system. The calculation was compared with the well-known entanglement measure, concurrence, and found to be the same. was, then, expressed in terms of two thermodynamic quantities, namely, magnetic susceptibility and specific heat. Experimental verification of temperature variation of the bipartite entanglement measure in terms of magnetic susceptibility and specific heat was done on single crystals of copper acetate-an excellent one dimensional dimer system. The results showed the existence of bipartite entanglement till temperatures as high as room temperature! Large sized single crystals of copper acetate were grown by a new evaporation technique and characterised by thermogravimetric analysis, IR and Raman spectroscopy measurements. Density functional theory calculations were done to calculate the delocalisation index which showed much lower values of δ ( C u , C u ) than other bonds, implying that the probability of direct Cu–Cu exchange in copper acetate is very small. Band structure calculations revealed the presence of flat bands at the Fermi level implying very weak intermolecular interactions in copper acetate.