Post-synthetic exchange (PSE) of UiO-67 frameworks with Ru/Rh half-sandwich units for visible-light-driven H2 evolution and CO2 reduction

被引:91
作者
Liao, Wei-Ming [1 ]
Zhang, Jian-Hua [1 ]
Wang, Zheng [1 ]
Yin, Shao-Yun [1 ]
Pan, Mei [1 ]
Wang, Hai-Ping [1 ]
Su, Cheng-Yong [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Sch Chem, Lehn Inst Funct Mat, MOE Lab Bioinorgan & Synthet Chem, Guangzhou 510275, Guangdong, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
关键词
METAL-ORGANIC FRAMEWORKS; CARBON-DIOXIDE REDUCTION; RUTHENIUM(II) COMPLEX; HYDROGEN-PRODUCTION; MOLECULAR CATALYST; WATER; PHOTOCATALYSIS; LIGANDS; RU(II); MOF;
D O I
10.1039/c8ta02962h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Electron-deficient Ru/Rh half-sandwich units are optoelectronical, stereochemical, and redox and catalytically active in nature. Four different species of these units were designed and successfully incorporated into UiO-67 frameworks by post-synthetic exchange (PSE) method and employed for photocatalytic H-2 evolution and CO2 reduction. Among them, the PSE-MOF catalysts containing [M-OH2] (M = Rh or Ru) groups show higher photocatalytic activity than those with [M-Cl], providing a new example of the exploitation of H2O molecules as small ancillary ligands for the construction of Ru/Rh half-sandwich units and subsequent incorporation into MOFs as photocatalytic centers. The application of TEOA (triethanolamine) and DMA (N,N-dimethylaniline) as sacrificial agents leads to different catalytic mechanisms and durations. A long-term hydrogen evolution lasting for 174 h without significant decrease in efficiency was achieved in the RhOH2@UiO-DMA system, showing the advantage of PSE-MOFs as highly stable photocatalytic platforms with superior self-protective properties.
引用
收藏
页码:11337 / 11345
页数:9
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