The cross-coupling between magnetic and ferroelectric orders in spin-driven organic multiferroics provides great potential for realizing multi-state logic memory. Creating strong magnetoelectric coupling around room-temperature is the key to eliminate the main roadblock for practical application. Herein, quantum correlation controlled means are employed to tune the transition temperature TC = 300 K, as the optimal operating temperature. After that, based on the magnetocaloric or electrocaloric effect, a temperature mediated mechanism is proposed to enhance magnetoelectric coupling within an isentropic rather than an isothermal process. Furthermore, a moderate magnetic field combined with a relatively weak electric field can jointly control and dramatically enhance the isentropic magnetoelectric coupling around room-temperature.
We study the magnetocaloric effect and the critical behavior of a periodic Anderson-like organic polymer using Green's function theory, in which the localized f orbitals hybridize with the conduction orbitals at even sites. The field-induced metal-insulator transitions with the magnetic Grüneisen parameter showing |Γh|∼T(-1) power-law critical behaviour are revealed, which provides a new thermodynamic means for probing quantum phase transitions. It is found that the competition of up-spin and down-spin hole excitations is responsible for the double peak structure of magnetic entropy change (-ΔS) for the dominant Kondo coupling case, implying a double magnetic cooling process via demagnetization, which follows a power law dependence of the magnetic field h: -ΔS∼h(n). The local exponent n tends to 1 and 2 below and above TC, while has a minimum of 0.648 at TC, which is in accordance with the experimental observation of perovskite manganites Pr0.55Sr0.45MnO3 and Nd0.55Sr0.45MnO3 (J. Y. Fan et al., Appl. Phys. Lett., 2011, 98, 072508; Europhys. Lett., 2015, 112, 17005) corresponding to the conventional ferromagnets within the mean field theory -ΔS∼h(2/3). At TC, the -ΔS∼h curves with a convex curvature superpose each other for small V values, which are separated by the large V case, distinguishing the RKKY interaction and Kondo coupling explicitly. Furthermore, the critical scaling law n(TC) = 1 + (β- 1)/(β + γ) = 1 + 1/δ(1 - 1/β) is related to the critical exponents (β, γ, and δ) extracted from the Arrott-Noakes equation of state and the Kouvel-Fisher method, which fulfill the Widom scaling relation δ = 1 + γβ(-1), indicating the self-consistency and reliability of the obtained results. In addition, based on the scaling hypothesis through checking the scaling analysis of magnetization, the M-T-h curves collapse into two independent universal branches below and above TC.
Up to now, probing the quantum phase transition (QPT) and quantum critical (QC) phenomena at finite temperatures in one-dimensional (1D) spin systems still lacks an in-depth understanding. Herein, we study the QPT and thermodynamics of 1D spin-1/2 anisotropic Heisenberg antiferromagnetic chains by Green’s function theory. The quantum phase diagram is renormalized by the anisotropy (∆), which manifests a quantum critical point (QCP) hc = 1 + ∆ signaling the transition from gapless Tomonaga–Luttinger liquid (TLL) to gapped ferromagnetic (FM) state, demonstrated by the magnetic entropy and thermal Drude weight. At low temperatures, it is shown that two crossover temperatures fan out a QC regime and capture the QCP via the linear extrapolation to zero temperature. In addition, around QCP, the QC scaling is performed by analyzing the entropy and thermal Drude weight to extract the critical exponents (α, δ, and β) that fulfill the Essamm–Fisher scaling law, which provides a novel thermodynamic means to detect QPT for experiment. Furthermore, scaling hypothesis equations with two rescaled manners are proposed to testify the scaling analysis, for which all the data points fall on a universal curve or two independent branches for the plot against rescaled field or temperature, implying the self-consistency and reliability of the obtained critical exponents.
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