Photocatalytic CO2 Reduction to Formate Using a Mn(I) Molecular Catalyst in a Robust Metal-Organic Framework

被引:290
作者
Fei, Honghan [1 ]
Sampson, Matthew D. [1 ]
Lee, Yeob [1 ]
Kubiak, Clifford P. [1 ]
Cohen, Seth M. [1 ]
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
基金
美国国家科学基金会;
关键词
CARBON-DIOXIDE REDUCTION; WATER OXIDATION; RHENIUM(I) COMPLEX; N-DONOR; MANGANESE; FUNCTIONALIZATION; PHOTOCHEMISTRY; RUTHENIUM; UIO-67; TRIETHANOLAMINE;
D O I
10.1021/acs.inorgchem.5b00752
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A manganese bipyridine complex, Mn(bpydc)-(CO)(3)Br (bpydc 5,5'-dicarboxylate-2,2'-bipyridine), has been incorporated into a highly robust Zr(IV)-based metal-organic framework (MOF) for use as a CO2 reduction photocatalyst. In conjunction with [Ru(dmb)(3)](2+) (dmb = 4,4'-dirnethyl-2,2'-bipyridine) as a photosensitizer and 1-benzyl-1,4-dihydronicotinamide (BNAH) as a sacrificial reductant, Mn-incorporated MOFs efficiently catalyze CO2 reduction to formate in DMF/triethanol-amine under visible-light irradiation. The photochemical performance of the Mn-incorporated MOP reached a turnover number of approximately 110 in 18 h, exceeding that of the homogeneous reference systems. The increased activity of the MOF-incorporated Mn catalyst is ascribed to the struts of the framework providing isolated active sites, which stabilize the catalyst and inhibit dimerization Of the singly reduced Mn complex. The MOF catalyst largely retained its crystallinity throughout prolonged catalysis and was successfully reused over several catalytic runs.
引用
收藏
页码:6821 / 6828
页数:8
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