Cu-based Polyoxometalate Catalyst for Efficient Catalytic Hydrogen Evolution

被引:54
|
作者
Lv, Hongjin [1 ]
Gao, Yuanzhe [1 ,4 ]
Guo, Weiwei [1 ]
Lauinger, Sarah M. [1 ]
Chi, Yingnan [1 ]
Bacsa, John [2 ]
Sullivan, Kevin P. [1 ]
Wieliczko, Marika [1 ]
Musaev, Djamaladdin G. [3 ]
Hill, Craig L. [1 ]
机构
[1] Emory Univ, Dept Chem, 1515 Dickey Dr, Atlanta, GA 30322 USA
[2] Emory Univ, Xray Crystallog Ctr, 1515 Dickey Dr, Atlanta, GA 30322 USA
[3] Emory Univ, Cherry L Emerson Ctr Sci Computat, 1515 Dickey Dr, Atlanta, GA 30322 USA
[4] Hebei Normal Univ, Coll Chem & Mat Sci, 20 Rd East Second Ring South, Shijiazhuang 050024, Hebei, Peoples R China
关键词
NOBLE-METAL-FREE; EFFECTIVE CORE POTENTIALS; WATER OXIDATION CATALYST; VISIBLE-LIGHT; MOLECULAR CALCULATIONS; RUTHENIUM(II) COMPLEXES; HOMOGENEOUS CATALYST; ELECTRO-CATALYST; PHOTO-REDUCTION; ACETIC-ACID;
D O I
10.1021/acs.inorgchem.6b01032
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Copper-based complexes have been largely neglected as potential water reduction catalysts. This article reports the synthesis and characterization of a tetra-copper-containing polyoxotungstate, Na3K7[Cu-4(H2O)(2)(B-alpha-PW9O34)(2)]center dot 30H(2)O (Na3K7-Cu4P2). Cu4P2 is a water-compatible catalyst for efficient visible-light-driven hydrogen evolution when coupled to (4,4'-di-tert-butyl-2,2'-dipyridyl)-bis(2-phenylpyridine(1H))-iridium(III) hexafluorophosphate ([Ir(ppy)(2)(dtbbpy)][PF6]) as a light absorber and triethanolamine (TEOA) as sacrificial electron donor. Under minimally optimized conditions, a turnover number (TON) of similar to 1270 per Cu4P2 catalyst is obtained after 5 h of irradiation (light-emitting diode; lambda = 455 nm; 20 mW); a photochemical quantum efficiency of as high as 15.9% is achieved. Both oxidative and reductive quenching pathways are observed by measuring the luminescence intensity of excited state [Ir(ppy)(2)(dtbbpy)](+)* in the presence of Cu4P2 or TEOA, respectively. Many stability studies (e.g., UV-vis absorption, FT-IR, dynamic light scattering, transmission electron microscopy, and scanning electron microscopy/energy-dispersive X-ray spectroscopy) show that catalyst Cu4P2 undergoes slow decomposition under turnover conditions; however, both the starting Cu4P2 as well as its molecular decomposition products are the dominant catalytically active species for H-2 evolution not Cu or CuOx particles. Considering the high. abundance and low cost of copper, the present work provides considerations for the design and synthesis of efficient, molecular, water-compatible Cu-based water reduction catalysts.
引用
收藏
页码:6750 / 6758
页数:9
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