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The shuttling behavior and slow conversion kinetics of the intermediate lithium polysulfides are the severe obstacles for the application of lithium‐sulfur (Li‐S) batteries over a wide temperature range. Here, an engineered lamellar yolk–shell structure of In2O3@void@carbon for the Li‐S battery cathode is developed for the first time to construct a powerful barrier that effectively inhibits the shuttling of polysulfides. On the basis of the unique nanochannel‐containing morphology, the continuous kinetic transformation of sulfur and polysulfides is confined in a stable framework, which is demonstrated by using X‐ray nanotomography. The constructed Li‐S battery exhibits a high cycling capability over 1000 cycles at 1.0 C with a capacity decay rate as low as 0.038% per cycle, good rate performance, and temperature tolerance at −10, 25, and 50 °C. A nondestructive in situ monitoring method of the interfacial reaction resistance in different cycling stages is proposed, which provides a new analysis perspective for the development of emerging electrochemical energy‐storage systems. [ABSTRACT FROM AUTHOR]

Self‐healing and flexibility are significant for many emerging applications of secondary batteries, which have attracted broad attention. Herein, a self‐healing flexible quasi‐solid Zn‐ion battery composing of flexible all‐in‐one cathode (VS2 nanosheets growing on carbon cloth) and anode (electrochemically deposited Zn nanowires), and a self‐healing hydrogel electrolyte, is presented. The free‐standing all‐in‐one electrodes enable a high capacity and robust structure during flexible transformation of the battery, and the hydrogel electrolyte possesses a good self‐healing performance. The presented battery remains as a high retention potential even after healing from being cut into six pieces. When bending at 60°, 90°, and 180°, the battery capacities remain 124, 125, and 114 mAh g−1, respectively, cycling at a current density of 50 mA g−1. Moreover, after cutting and healing twice, the battery still delivers a stable capacity, indicating a potential use of self‐healing and wearable electronics. [ABSTRACT FROM AUTHOR]

Magnesium batteries have been considered promising candidates for next‐generation energy storage systems owing to their high energy density, good safety without dendrite formation, and low cost of magnesium resources. However, high‐performance cathodes with stable capacity, good conductivity, and fast ions transport are needed, since many conventional cathodes possess a low performance and poor preparation controllability. Herein, a liquid‐driven coaxial flow focusing (LDCFF) approach for preparing a novel microcapsule system with controllable size, high loading, and stable magnesium‐storage performance is presented. Taking the MoS2‐infilled microcapsule as a case study, the magnesium battery cathode based on the microcapsules displays a capacity of 100 mAh g−1 after 100 cycles. High capacity retention is achieved at both low and high temperatures of −10, ‒5, and 45 °C, and a stable rate‐performance is also obtained. The influences of the liquid flow rates on the size and shell thickness of the microcapsules are investigated; and electron and ion diffusion properties are also studied by first‐principle calculations. The presented LDCFF method is quite general, and the high performance of the microcapsules enables them to find broad applications for making emerging energy‐storage materials and secondary battery systems. [ABSTRACT FROM AUTHOR]