电合成
催化作用
电化学
选择性
纳米技术
材料科学
Atom(片上系统)
化学
过氧化氢
电催化剂
电子结构
组合化学
电极
光化学
电子转移
物理化学
计算化学
有机化学
计算机科学
嵌入式系统
作者
Jingjing Liu,Zhichao Gong,Minmin Yan,Guanchao He,Haisheng Gong,Gonglan Ye,Huilong Fei
出处
期刊:Small
[Wiley]
日期:2021-11-02
卷期号:18 (3)
被引量:71
标识
DOI:10.1002/smll.202103824
摘要
Abstract Electrochemical synthesis of hydrogen peroxide (H 2 O 2 ) via the 2‐electron oxygen reduction reaction (ORR) has emerged as a promising alternative to the energy‐intensive anthraquinone process and catalysts combining high selectivity with superior activity are crucial for enhancing the efficiency of H 2 O 2 electrosynthesis. In recent years, single‐atom catalysts (SACs) with the merits of maximum atom utilization efficiency, tunable electronic structure, and high mass activity have attracted extensive attention for the selective reduction of O 2 to H 2 O 2 . Although considerable improvements are made in the performance of SACs toward the 2‐electron ORR process, the principles for modulating the catalytic properties of SACs by adjusting the electronic structure remain elusive. In this review, the regulation strategies for optimizing the 2‐electron ORR activity and selectivity of SACs by different methods of electronic structure tuning, including the altering of the central metal atoms, the modulation of the coordinated atoms, the substrate effect, and alloy engineering are summarized. Finally, the challenges and future prospects of advanced SACs for H 2 O 2 electrosynthesis via the 2‐electron ORR process are proposed.
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