氧还原反应
透视图(图形)
共价键
氧还原
化学
还原(数学)
纳米技术
组合化学
材料科学
电化学
计算机科学
电极
有机化学
物理化学
数学
人工智能
几何学
作者
Rui Qiao,Jinyan Wang,Hongyin Hu,Shuanglong Lu
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2024-05-30
卷期号:29 (11): 2563-2563
被引量:13
标识
DOI:10.3390/molecules29112563
摘要
Hydrogen peroxide (H2O2) is an environmentally friendly oxidant with a wide range of applications, and the two-electron pathway (2e−) of the oxygen reduction reaction (ORR) for H2O2 production has attracted much attention due to its eco-friendly nature and operational simplicity in contrast to the conventional anthraquinone process. The challenge is to design electrocatalysts with high activity and selectivity and to understand their structure–activity relationship and catalytic mechanism in the ORR process. Covalent organic frameworks (COFs) provide an efficient template for the construction of highly efficient electrocatalysts due to their designable structure, excellent stability, and controllable porosity. This review firstly outlines the design principles of COFs, including the selection of metallic and nonmetallic active sites, the modulation of the electronic structure of the active sites, and the dimensionality modulation of the COFs, to provide guidance for improving the production performance of H2O2. Subsequently, representative results are summarized in terms of both metallic and metal-free sites to follow the latest progress. Moreover, the challenges and perspectives of 2e− ORR electrocatalysts based on COFs are discussed.
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