Breaking the Conversion Limit in an Intercalation-Type Cathode by Loosening Aqueous Cation Coordination.

Intercalation-type cathodes continue to dominate aqueous multivalent ion storage, despite higher theoretical capacities being available from conversion reactions involving multiple electron transfer. Pushing intercalation-type cathodes into conversion is certainly desirable, conventionally with great sacrificing cycling-stability, kinetics, and discharge potential. To date, limited progress has been achieved in overcoming this longstanding and formidable performance trade-off.

Sulfamoylbenzoic Acid Derivatives as Molecular Additives through Fine Dipole Moment Regulation for Highly Reproducible Perovskite Solar Cells.

An excellent reproducibility of high-quality perovskite thin films is imperative for the commercialization of perovskite solar cells. Multifunctional additive engineering is a promising strategy to tackle this challenge as it facilitates simultaneous control over crystallization processes and defect passivation. Here, an innovative strategy is proposed, leveraging -OH, -NH, and -Cl to precisely tune the dipole moment and electronic configuration of multifunctional modified 4-chloro-3-sulfonamide benzoic acid (CSBA) through substituent inductive and conjugation effects.

Electron Donors in the Intertwined Interface Restore Oxy-Substituted Selenides.

Nature chose selenium as the antioxidant element center in proteins, permitting the reversible conversion of organic bioenzymes between oxidized and selenized forms. Despite the importance of such antielectronegativity reversibility, it has not yet been demonstrated in inorganic selenides. We report an unexpected example showing that oxy-substituted sites in metal selenides can be restored to selenized forms reversibly by mild electrochemical manipulation in a copper aqueous solution.

Tailoring Synergistic Ion Environment for Copper Telluride toward High-Capacity and Ultrastable Acidic Multivalent-Ion Batteries.

Acidic batteries permit a reliable energy supply at low temperatures with low cost and intrinsic safety, yet the development of stable acid-resistant electrodes with high capacity and a reliable lifespan is still challenging. Herein, nonstoichiometric copper telluride (CuTe) nanosheets are first explored as high-performance electrodes for acidic batteries to provide a stable capacity release of 409 mAh g with a record-breaking lifespan of 40 000 cycles and excellent kinetics, enabling operation at a high current density of 20 A g. In contrast to the inherent perception of corrosive destruction of electrode materials by strongly acidic environments, the electrolyte environment enriched with copper ions and hydrogen ions synergistically stabilizes the CuTe electrode and drives reversible multielectron transfer asymmetric deep conversion, which is confirmed by in situ synchrotron X-ray diffraction, X-ray absorption spectroscopy, first-principal calculations, and composite electrochemical characterization.

Reversible multivalent carrier redox exceeding intercalation capacity boundary.

Compared with widely established monovalent-ion batteries, aqueous multivalent-ion batteries promise higher capacity release by achieving multiple electron-transfer events per ion intercalation in the host material. Despite plausibility, this high-capacity dream is untenable with the total tolerable redox charge-transfer limit of the host material for all carrier species equally, which is historically assumed to depend on the material rather than the guest carrier itself, and the kinetic hysteresis induced by larger charge/radius ratios induced kinetic hysteresis further enlarges the divide. Herein, we report that copper carrier redox in vanadium sulfide (VS) exceeds the intrinsic intercalation capacity boundary, with the highest capacity release as 675 mAh g at 0.

Self-Adaptive Activation of DNAzyme Nanoassembly for Synergistically Combined Gene Therapy.

DNAzyme represents a promising gene silencing toolbox yet is obstructed by the poor substrate accessibility in specific cells. Herein, a compact DNA nanoassembly, incorporating multimeric therapeutic DNAzyme, was prepared for selective delivery of gene-silencing DNAzyme with requisite cofactors and auxiliary chemo-drugs. By virtue of the sequence-conservative duplex-specific nuclease, the endogenous miRNA catalyzes the successive and site-specific cleavage of DNA nanoassembly substrate (nominated as the localized RNA walking machine) and thus ensures the liberation/activation of therapeutic agents with high accuracy and efficacy.

Accelerating AutoDock Vina with GPUs.

AutoDock Vina is one of the most popular molecular docking tools. In the latest benchmark CASF-2016 for comparative assessment of scoring functions, AutoDock Vina won the best docking power among all the docking tools. Modern drug discovery is facing a common scenario of large virtual screening of drug hits from huge compound databases.

Wearable on-device deep learning system for hand gesture recognition based on FPGA accelerator.

Gesture recognition is critical in the field of Human-Computer Interaction, especially in healthcare, rehabilitation, sign language translation, etc. Conventionally, the gesture recognition data collected by the inertial measurement unit (IMU) sensors is relayed to the cloud or a remote device with higher computing power to train models. However, it is not convenient for remote follow-up treatment of movement rehabilitation training.