Suppressed Manganese Oxides Shuttling in Acidic Electrolytes Extends Shelf‐Life of Electrolytic Proton Batteries

电解质 材料科学 质子 氧化锰 无机化学 化学工程 电极 冶金 化学 物理 物理化学 量子力学 工程类
作者
Sicheng Wu,Haocheng Guo,Zhen Su,Chen Jia,Xinyi Zhang,Shuhao Wang,Tingwen Zhao,Quentin Meyer,Chuan Zhao
出处
期刊:Advanced Functional Materials [Wiley]
卷期号:34 (28) 被引量:9
标识
DOI:10.1002/adfm.202315706
摘要

Abstract Aqueous proton batteries are promising candidates for the harvest and utilization of renewable yet intermittent energies. The redox couple of MnO 2 /Mn 2+ is one of the most competitive cathodes to enable proton batteries with high voltage. However, electrolytic products of the MnO 2 /Mn 2+ reactions tend to disperse into acidic electrolytes, and the composition of the electrolytic products as well as their influences on the counter electrode and the overall batteries are still unclear. Herein, the behaviors of the manganese electrolysis are studied with electrolytes of different proton concentrations and under variant current densities. The electrolytic products are disclosed to be ɛ‐MnO 2 regardless of the acidities of electrolytes and report, for the first time, the dispersed MnO 2 can chemically oxidize or dissolve the anode materials and subsequently induce self‐discharging. A membrane‐assisted protection strategy is proposed to prevent the free‐shuttle of MnO 2 particles and mitigate the battery self‐discharging. Accordingly, a much‐enhanced shelf‐life performance (61.3% capacity retention over a one‐week rest) is achieved for pyrene‐4,5,9,10‐tetraone//MnO 2 full‐cell. Furthermore, a customized device is developed with Nafion membrane, reaching excellent cycling stability (3000 cycles, 54 days) and a low self‐discharging rate. The findings and strategies for mitigating the self‐discharging issues are anticipated to advance the MnO 2 /Mn 2+ ‐based aqueous batteries and beyond.
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