腙
铜
析氧
共价键
电催化剂
金属
材料科学
金属有机骨架
电化学
光化学
化学
纳米技术
组合化学
有机化学
冶金
电极
物理化学
吸附
作者
Chao Lin,Huayun Ma,Jun‐Ru He,Qing Xu,Meng Song,Cheng‐Xing Cui,Yong Chen,Chunxiang Li,Mingli Jiao,Lipeng Zhai
出处
期刊:Small
[Wiley]
日期:2024-07-01
卷期号:20 (44): e2403775-e2403775
被引量:11
标识
DOI:10.1002/smll.202403775
摘要
Despite the challenges associated with the synthesis of flexible metal-covalent organic frameworks (MCOFs), these offer the unique advantage of maximizing the atomic utilization efficiency. However, the construction of flexible MCOFs with flexible building units or linkages has rarely been reported. In this study, novel flexible MCOFs are constructed using flexible building blocks and copper clusters with hydrazone linkages. The heterometallic frameworks (Cu, Co) are prepared through the hydrazone linkage coordination method and evaluated as catalysts for the oxygen evolution reaction (OER). Owing to the spatial separation and functional cooperation of the heterometallic MCOF catalysts, the as-synthesized MCOFs exhibited outstanding catalytic activities with an overpotential of 268.8 mV at 10 mA cm-2 for the OER in 1 M KOH, which is superior to those of the reported covalent organic frameworks (COFs)-based OER catalysts. Theoretical calculations further elucidated the synergistic effect of heterometallic active sites within the linkages and frameworks, contributing to the enhanced OER activity. This study thus introduces a novel approach to the fundamental design of flexible MCOF catalysts for the OER, emphasizing their enhanced atomic utilization efficiency.
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