Self-Decoupled Oxygen Electrocatalysis for Ultrastable Rechargeable Zn-Air Batteries with Mild-Acidic Electrolyte.

Rechargeable zinc-air batteries (ZABs) have been considered promising as next-generation sustainable energy storage devices; however, their large-scale deployment is hampered by the unsatisfactory cyclic lifespan. Employing neutral and mild-acidic electrolytes is effective in extending the cyclability, but the rapid performance degradation of the bifunctional catalysts owing to different microenvironmental requirements of the alternative oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is still a serious limitation of their cyclic life. Herein, we propose a "self-decoupling" strategy to significantly improve the stability of the bifunctional catalysts by constructing a smart interface in the bifunctional air electrode. This smart interface, containing a resistance-switchable sulfonic acid doped polyaniline nanoarray interlayer, is nonconductive at high potential but conductive at low potential, which enables spontaneous electrochemical decoupling of the bifunctional catalyst for the ORR and OER, respectively, and thus protects it from degradation. The resulting self-decoupled mild-acidic ZAB delivers stable cyclic performances in terms of a negligible energy efficiency loss of 0.015% cycle-1 and 3 times longer cycle life (∼1400 h) compared with the conventional mild-acidic ZAB using a normal bifunctional air electrode and the same low-cost ZnCo phosphide/nitrogen-doped carbon bifunctional catalyst. This work provides an effective strategy for tolerating alternative oxidation-reduction reactions and emphasizes the importance of smart nanostructure design for more sustainable batteries.

A self-decoupled 32-channel receive array for human-brain MRI at 10.5 T.

PURPOSE: Receive array layout, noise mitigation, and B0 field strength are crucial contributors to SNR and parallel-imaging performance. Here, we investigate SNR and parallel-imaging gains at 10.5 T compared with 7 T using 32-channel receive arrays at both fields. METHODS: A self-decoupled 32-channel receive array for human brain imaging at 10.5 T (10.5T-32Rx), consisting of 31 loops and one cloverleaf element, was co-designed and built in tandem with a 16-channel dual-row loop transmitter. Novel receive array design and self-decoupling techniques were implemented. Parallel imaging performance, in terms of SNR and noise amplification (g-factor), of the 10.5T-32Rx was compared with the performance of an industry-standard 32-channel receiver at 7 T (7T-32Rx) through experimental phantom measurements. RESULTS: Compared with the 7T-32Rx, the 10.5T-32Rx provided 1.46 times the central SNR and 2.08 times the peripheral SNR. Minimum inverse g-factor value of the 10.5T-32Rx (min[1/g] = 0.56) was 51% higher than that of the 7T-32Rx (min[1/g] = 0.37) with R = 4 × 4 2D acceleration, resulting in significantly enhanced parallel-imaging performance at 10.5 T compared with 7 T. The g-factor values of 10.5 T-32 Rx were on par with those of a 64-channel receiver at 7 T (eg, 1.8 vs 1.9, respectively, with R = 4 × 4 axial acceleration). CONCLUSION: Experimental measurements demonstrated effective self-decoupling of the receive array as well as substantial gains in SNR and parallel-imaging performance at 10.5 T compared with 7 T.

Hydrogen-exchange kinetics studied through analysis of self-decoupling of nuclear magnetic resonance.

Hydrogen exchange between solute and water molecules occurs across a wide range of timescales. Rapid hydrogen-exchange processes can effectively diminish 1H-15N scalar couplings. We demonstrate that the self-decoupling of 15N nuclear magnetic resonance can allow quantitative investigations of hydrogen exchange on a micro- to millisecond timescale, which is relatively difficult to analyze with other methods. Using a Liouvillian matrix incorporating hydrogen exchange as a mechanism for scalar relaxation, the hydrogen exchange rate can be determined from 15N NMR line shapes recorded with and without 1H decoupling. Self-decoupling offers a simple approach to analyze the kinetics of hydrogen exchange in a wide range of timescale.

Research on the parallel load sharing principle of a novel self-decoupled piezoelectric six-dimensional force sensor.

This paper presents a novel integrated piezoelectric six-dimensional force sensor which can realize dynamic measurement of multi-dimensional space load. Firstly, the composition of the sensor, the spatial layout of force-sensitive components, and measurement principle are analyzed and designed. There is no interference of piezoelectric six-dimensional force sensor in theoretical analysis. Based on the principle of actual work and deformation compatibility coherence, this paper deduces the parallel load sharing principle of the piezoelectric six-dimensional force sensor. The main effect factors which affect the load sharing ratio are obtained. The finite element model of the piezoelectric six-dimensional force sensor is established. In order to verify the load sharing principle of the sensor, a load sharing test device of piezoelectric force sensor is designed and fabricated. The load sharing experimental platform is set up. The experimental results are in accordance with the theoretical analysis and simulation results. The experiments show that the multi-dimensional and heavy force measurement can be realized by the parallel arrangement of the load sharing ring and the force sensitive element in the novel integrated piezoelectric six-dimensional force sensor. The ideal load sharing effect of the sensor can be achieved by appropriate size parameters. This paper has an important guide for the design of the force measuring device according to the load sharing mode.