Deprotonated of layered double hydroxides during electrocatalytic water oxidation for multi-cations intercalation

Bowen Jin, Jianxiong Gao, Yunqi Zhang, Mingfei Shao
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Abstract

Aqueous rechargeable batteries using abundant multi-ion cations have received increasing attention in the energy storage field for their high safety and low cost. Layered double hydroxides (LDHs) possess a two-dimensional structure and exhibit great potential as cathodes for multi-ion intercalation. However, the insufficient active sites of LDHs result in low capacities in the discharging process. Interestingly, the LDHs after the deprotonation process exhibit favorable electrochemical performance of multi-cation intercalation. The deprotonation process of LDHs has been widely found in the oxygen evolution reaction and energy storage field, where LDHs lose H in laminates and converts to deprotonated γ-phase MOOHs (MOOs). Herein, we take a comprehensive overview of the dynamics structure transformation of the deprotonation process of LDHs. Furthermore, the development of advanced aqueous battery cathode and metal battery anode based on deprotonated LDHs for energy storage is explored and summarized. Finally, the perspective of deprotonated LDHs in the energy storage field is discussed.

Abstract Image

多阳离子插层电催化水氧化过程中层状双氢氧化物的去质子化
使用丰富的多离子阳离子的水性可充电电池因其安全性高、成本低而在储能领域受到越来越多的关注。层状双氢氧化物(LDHs)具有二维结构,具有作为多离子插层阴极的巨大潜力。然而,由于 LDHs 的活性位点不足,导致其在放电过程中容量较低。有趣的是,经过去质子化过程的 LDHs 在多离子插层方面表现出良好的电化学性能。LDHs 的去质子化过程在氧进化反应和储能领域被广泛发现,LDHs 在层状结构中失去 H,转化为去质子化的 γ 相 MOOHs(MOOs)。在此,我们将全面概述 LDHs 去质子化过程的动力学结构转变。此外,还对基于去质子化 LDHs 的先进水电池正极和金属电池负极的储能开发进行了探讨和总结。最后,讨论了去质子化 LDHs 在储能领域的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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