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Register a new userControl and Local Measurement of the Spin Chemical Potential in a Magnetic Insulator
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The spin chemical potential characterizes the tendency of spins to diffuse. Probing the spin chemical potential could provide insight into materials such as magnetic insulators and spin liquids and aid optimization of spintronic devices. Here, we introduce single-spin magnetometry as a generic platform for non-perturbative, nanoscale characterization of spin chemical potentials. We use this platform to investigate magnons in a magnetic insulator, surprisingly finding that the magnon chemical potential can be efficiently controlled by driving the systems ferromagnetic resonance. We introduce a symmetry-based two-fluid theory describing the underlying magnon processes, realize the first experimental determination of the local thermomagnonic torque, and illustrate the detection sensitivity using electrically controlled spin injection. Our results open the way for nanoscale control and imaging of spin transport in mesoscopic spin systems.
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Many proposed experiments involving topological insulators (TIs) require spatial control over time-reversal symmetry and chemical potential. We demonstrate reconfigurable micron-scale optical control of both magnetization (which breaks time-reversal symmetry) and chemical potential in ferromagnetic thin films of Cr-(Bi,Sb)$_2$Te$_3$ grown on SrTiO$_3$. By optically modulating the coercivity of the films, we write and erase arbitrary patterns in their remanent magnetization, which we then image with Kerr microscopy. Additionally, by optically manipulating a space charge layer in the underlying SrTiO$_3$ substrates, we control the local chemical potential of the films. This optical gating effect allows us to write and erase p-n junctions in the films, which we study with photocurrent microscopy. Both effects are persistent and may be patterned and imaged independently on a few-micron scale. Dynamic optical control over both magnetization and chemical potential of a TI may be useful in efforts to understand and control the edge states predicted at magnetic domain walls in quantum anomalous Hall insulators.
We develop a linear-response transport theory of diffusive spin and heat transport by magnons in magnetic insulators with metallic contacts. The magnons are described by a position dependent temperature and chemical potential that are governed by diffusion equations with characteristic relaxation lengths. Proceeding from a linearized Boltzmann equation, we derive expressions for length scales and transport coefficients. For yttrium iron garnet (YIG) at room temperature we find that long-range transport is dominated by the magnon chemical potential. We compare the models results with recent experiments on YIG with Pt contacts [L.J. Cornelissen, et al., Nat. Phys. 11, 1022 (2015)] and extract a magnon spin conductivity of $sigma_{m}=5times10^{5}$ S/m. Our results for the spin Seebeck coefficient in YIG agree with published experiments. We conclude that the magnon chemical potential is an essential ingredient for energy and spin transport in magnetic insulators.
We report that Bi$_2$Se$_3$ thin films can be epitaxially grown on SrTiO$_{3}$ substrates, which allow for very large tunablity in carrier density with a back-gate. The observed low field magnetoconductivity due to weak anti-localization (WAL) has a very weak gate-voltage dependence unless the electron density is reduced to very low values. Such a transition in WAL is correlated with unusual changes in longitudinal and Hall resistivities. Our results suggest much suppressed bulk conductivity at large negative gate-voltages and a possible role of surface states in the WAL phenomena. This work may pave a way for realizing three-dimensional topological insulators at ambient conditions.
We observe an unusual behavior of the spin Hall magnetoresistance (SMR) measured in a Pt ultra-thin film deposited on a ferromagnetic insulator, which is a tensile-strained LaCoO3 (LCO) thin film with the Curie temperature Tc=85K. The SMR displays a strong magnetic-field dependence below Tc, with the SMR amplitude continuing to increase (linearly) with increasing the field far beyond the saturation value of the ferromagnet. The SMR amplitude decreases gradually with raising the temperature across Tc and remains measurable even above Tc. Moreover, no hysteresis is observed in the field dependence of the SMR. These results indicate that a novel low-dimensional magnetic system forms on the surface of LCO and that the Pt/LCO interface decouples magnetically from the rest of the LCO thin film. To explain the experiment, we revisit the derivation of the SMR corrections and relate the spin-mixing conductances to the microscopic quantities describing the magnetism at the interface. Our results can be used as a technique to probe quantum magnetism on the surface of a magnetic insulator.
The interaction energy for the indirect-exchange or Ruderman-Kittel-Kasuva-Yosida (RKKY) interaction between magnetic spins localized on lattice sites of the $alpha$-${cal T}_3$ model is calculated using linear response theory. In this model, the $texttt{AB}$-honeycomb lattice structure is supplemented with $texttt{C}$ atoms at the centers of the hexagonal lattice. This introduces a parameter $alpha$ for the ratio of the hopping integral from hub-to-rim and that around the rim of the hexagonal lattice. A valley and $alpha$-dependent retarded Greens function matrix is used to form the susceptibility. Analytic and numerical results are obtained for undoped $alpha$-${cal T}_3$, when the chemical potential is finite and also in the presence of an applied magnetic field. We demonstrate the anisotropy of these results when the magnetic impurities are placed on the $texttt{A,B}$ and $texttt{C}$ sublattice sites. Additionally, comparison of the behavior of the susceptibility of $alpha$-${cal T}_3$ with graphene shows that there is a phase transition at $alpha=0$.
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