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Abstract Spin excitations, including magnons and spinons, can carry thermal energy and spin information. Studying spin‐mediated thermal transport is crucial for spin caloritronics, enabling efficient heat dissipation in microelectronics and advanced thermoelectric applications. However, designing quantum materials with controllable spin transport is challenging. Here, highly textured spin‐chain compound Ca₂CuO₃is synthesized using a solvent‐cast cold pressing technique, aligning 2D nanostructures with spin chains perpendicular to the pressing direction. The sample exhibits high thermal conductivity anisotropy and an excellent room‐temperature thermal conductivity of 12 ± 0.7 W m⁻¹K⁻¹, surpassing all polycrystalline quantum magnets. Such a high value is attributed to the significant spin‐mediated thermal conductivity of 10 ± 1 W m⁻¹K⁻¹, the highest reported among all polycrystalline quantum materials. Analysis through a 1D kinetic model suggests that near room‐temperature, spinon thermal transport is dominated by coupling with high‐frequency phonons, while extrinsic spinon‐defect scattering is negligible. Additionally, this method is used to prepare textured La₂CuO₄, exhibiting highly anisotropic magnon thermal transport and demonstrating its broad applicability. A distinct role of defect scattering in spin‐mediated thermal transport is observed in two spin systems. These findings open new avenues for designing quantum materials with controlled spin transport for thermal management and energy conversion. 

In this paper, we propose a method for bounding the probability that a stochastic differential equation (SDE) system violates a safety specification over the infinite time horizon. SDEs are mathematical models of stochastic processes that capture how states evolve continuously in time. They are widely used in numerous applications such as engineered systems (e.g., modeling how pedestrians move in an intersection), computational finance (e.g., modeling stock option prices), and ecological processes (e.g., population change over time). Previously the safety verification problem has been tackled over finite and infinite time horizons using a diverse set of approaches. The approach in this paper attempts to connect the two views by first identifying a finite time bound, beyond which the probability of a safety violation can be bounded by a negligibly small number. This is achieved by discovering an exponential barrier certificate that proves exponentially converging bounds on the probability of safety violations over time. Once the finite time interval is found, a finite-time verification approach is used to bound the probability of violation over this interval. We demonstrate our approach over a collection of interesting examples from the literature, wherein our approach can be used to find tight bounds on the violation probability of safety properties over the infinite time horizon. 

Axially chiral enamides bearing a N–C axis have been recently studied and were proposed to be valuable chiral building blocks, but a stereoselective synthesis has not been achieved. Here, we report the first enantioselective synthesis of axially chiral enamides via a highly efficient, catalytic approach. In this approach, C(sp 2 )–N bond formation is achieved through an iridium-catalyzed asymmetric allylation, and then in situ isomerization of the initial products through an organic base promoted 1,3-H transfer, leading to the enamide products with excellent central-to-axial transfer of chirality. Computational and experimental studies revealed that the 1,3-H transfer occurs via a stepwise deprotonation/re-protonation pathway with a chiral ion-pair intermediate. Hydrogen bonding interactions with the enamide carbonyl play a significant role in promoting both the reactivity and stereospecificity of the stepwise 1,3-H transfer. The mild and operationally simple formal N -vinylation reaction delivered a series of configurationally stable axially chiral enamides with good to excellent yields and enantioselectivities.