前言:金属有机框架的自优化重构介绍了过氧化氢选择性电合成的阳离子空位

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引用次数: 0

摘要

在他们的研究文章(e202501930)中,赵国华和同事报告了一种利用mof的自优化重组行为来构建阳离子空位的新策略,该策略有效地抑制了氧活化过程中O─O键的过度裂解。这种策略促进了2e -途径生成H2O2(右),而不是4e -途径生成H2O(左)。通过采用固态电解质电池,实现了超高浓度H2O2水溶液(> 8wt %)的直接合成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Frontispiece: Self-Optimized Reconstruction of Metal–Organic Frameworks Introduces Cation Vacancies for Selective Electrosynthesis of Hydrogen Peroxide

Frontispiece: Self-Optimized Reconstruction of Metal–Organic Frameworks Introduces Cation Vacancies for Selective Electrosynthesis of Hydrogen Peroxide

In their Research Article (e202501930), Guohua Zhao and co-workers report a novel strategy utilizing the self-optimizing restructuring behavior of MOFs to construct cation vacancies, which effectively suppresses excessive O─O bond cleavage during oxygen activation. This strategy promotes the 2e pathway for H2O2 production (right) over the 4e pathway generating H2O (left). By employing a solid-state electrolyte cell, direct synthesis of ultrahigh-concentration H2O2 aqueous solution (>8 wt%) is achieved.

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来源期刊
Angewandte Chemie
Angewandte Chemie 化学科学, 有机化学, 有机合成
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