双金属片
固氮酶
光催化
光化学
电子转移
配体(生物化学)
可见光谱
金属有机骨架
固氮
金属
材料科学
化学
催化作用
氮气
组合化学
有机化学
吸附
光电子学
生物化学
受体
冶金
作者
Ke An,Hanjie Ren,Dong Yang,Zhanfeng Zhao,Yuchen Gao,Yao Chen,Jiangdan Tan,Wenjing Wang,Zhongyi Jiang
标识
DOI:10.1016/j.apcatb.2021.120167
摘要
Inspired by nitrogenase, we designed a kind of metal-organic framework (MOF) photocatalysts, U(Zr-Hf)-X, composed of bimetallic Zr-Hf nodes and different functional ligands. In the Zr-Hf bimetallic cluster, the Zr species serves as the active site of nitrogen fixation, while the Hf species acts as electron buffer tank to optimize electron transfer and utilization. In the organic ligands, the light absorption and utilization of MOFs is improved via introducing target functional groups to efficiently generate electrons. Notably, the organic ligand containing two thiol groups (-SH) can extend the absorption edge to the visible region. The optimal U(0.5Hf)-2SH (metal nodes: 0.5Zr: 0.5Hf; linkers: TPA-2SH) photocatalyst exhibits nitrogen fixation rate up to 116.1 μmol g−1 h−1 under visible-light, attributed to the ligand-to-metal-to-metal electron transfer (LMMET) pathway and Zr-based π-backbonding mechanism. Our nitrogenase-inspired strategy establishes a novel paradigm for rational design of visible-light-driven nitrogen fixation catalysts.
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