Cu-based Polyoxometalate Catalyst for Efficient Catalytic Hydrogen Evolution
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- 作者：Hongjin Lv ; Yuanzhe Gao ; Weiwei Guo ; Sarah M. Lauinger ; Yingnan Chi ; John Bacsa ; Kevin P. Sullivan ; Marika Wieliczko ; Djamaladdin G. Musaev ; Craig L. Hill
- 刊名：Inorganic Chemistry
- 出版年：2016
- 出版时间：July 5, 2016
- 年：2016
- 卷：55
- 期：13
- 页码：6750-6758
- 全文大小：586K
- 年卷期：0
- ISSN：1520-510X
文摘
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[Cu4(H2O)2(B-α-PW9O34)2]·30H2O (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 ∼1270 per Cu4P2 catalyst is obtained after 5 h of irradiation (light-emitting diode; λ = 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 H2 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.