杂原子
电催化剂
过渡金属
催化作用
分解水
电化学
材料科学
纳米技术
金属有机骨架
配体(生物化学)
化学工程
化学
有机化学
吸附
物理化学
电极
戒指(化学)
受体
工程类
光催化
生物化学
作者
Liming Cao,Jia Zhang,Liwen Ding,Zi‐Yi Du,Chun‐Ting He
标识
DOI:10.1016/j.jechem.2021.12.006
摘要
It is critical to synthesize high-efficiency electrocatalysts to boost the performance of water splitting to meet the requirements of industrial applications. Metal-organic frameworks (MOFs) can function as ideal molecular platforms for the design of highly reactive transition metal phosphides (TMPs), a kind of candidates for high-efficiently electrocatalytic water splitting. The intrinsic activity of the electrocatalysts can be greatly improved via modulating the electronic structure of the catalytic center through the MOF precursors/templates. Moreover, the carbon layer converted in-situ by the organic ligands can not only protect the TMPs from being degraded in the harsh electrochemical environments, but also avoid agglomeration of the catalysts, thereby promoting their activities and stabilities. Furthermore, heteroatom-containing ligands can incorporate N, S or P, etc. atoms into the carbon matrixes after conversion, regulating the coordination microenvironments of the active centers as well as their electronic structures. In this review, we first summarized the latest developments in MOF-derived TMPs by the unique advantages in metal, organic ligand, and morphology regulations for electrocatalytic water splitting. Secondly, we concluded the critical scientific issues currently facing for designing state-of-the-art TMP-based electrocatalysts. Finally, we presented an outlook on this research area, encompassing electrocatalyst construction, catalytic mechanism research, etc.
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