Identifying a Real Catalyst of [NiFe]-Hydrogenase Mimic for Exceptional H2 Photogeneration.
Xu-Zhe WangShu-Lin MengHongyan XiaoKe FengYang WangJing-Xin JianXu-Bing LiChen-Ho TungLi-Zhu WuPublished in: Angewandte Chemie (International ed. in English) (2020)
Inspired by the natural [NiFe]-H2 ase, we designed mimic 1, (dppe)Ni(μ-pdt)(μ-Cl)Ru(CO)2 Cl to realize effective H2 evolution under photocatalytic conditions. However, a new species 2 was captured in the course of photo-, electro-, and chemo- one-electron reduction. Experimental studies of in situ IR spectroscopy, EPR, NMR, X-ray absorption spectroscopy, and DFT calculations corroborated a dimeric structure of 2 as a closed-shell, symmetric structure with a RuI center. The isolated dimer 2 showed the real catalytic role in photocatalysis with a benchmark turnover frequency (TOF) of 1936 h-1 for H2 evolution, while mimic 1 worked as a pre-catalyst and evolved H2 only after being reduced to 2. The remarkably catalytic activity and unique dimer structure of 2 operated in photocatalysis unveiled a broad research prospect in hydrogenases mimics for advanced H2 evolution.
Keyphrases
- visible light
- high resolution
- highly efficient
- photodynamic therapy
- solid state
- density functional theory
- ionic liquid
- room temperature
- single molecule
- metal organic framework
- mass spectrometry
- ms ms
- carbon dioxide
- molecular dynamics simulations
- molecular docking
- computed tomography
- radiation therapy
- gold nanoparticles
- crystal structure
- high speed
- body composition
- drug delivery
- quantum dots