Comparison of H2 photogeneration by [FeFe]-hydrogenase mimics with CdSe QDs and Ru(bpy)3Cl2 in aqueous solution. Issue 6 (27th April 2016)

• Record Type: Journal Article
• Authors: Jian, Jing-Xin; Ye, Chen; Wang, Xu-Zhe; Wen, Min; Li, Zhi-Jun; Li, Xu-Bing; Chen, Bin; Tung, Chen-Ho; Wu, Li-Zhu
• Is Part Of: Energy & environmental science. Volume 9:Issue 6(2016)
• Page Start: 2083
• Page End: 2089
• Publication Date: 2016-04-27
• Subjects: Energy conversion -- Periodicals; Fuel switching -- Periodicals; Environmental sciences -- Periodicals; Environmental chemistry -- Periodicals; 333.79
• DOI: 10.1039/c6ee00629a
• Languages: English
• ISSNs: 1754-5692

Abstract

Abstract : Two simple water soluble [FeFe]-H2 ase mimic systems (I and II) were designed to understand the basic principles governing photocatalytic H2 evolution. Abstract : Two water soluble [FeFe]-hydrogenase ([FeFe]-H2 ase) mimics, Fe2 S2 -2SO3 Na (1 ) and Fe2 S2 -SO3 Na (2 ), were designed to compare the performance of photocatalytic H2 evolution systems using quantum dots (QDs) and the molecular photosensitizer [Ru(bpy)3 ] 2+ in water. Under the same conditions, the resulting systems showed that CdSe QDs display much higher activity than [Ru(bpy)3 ] 2+, meanwhile, the turnover numbers (TONs) of 2.65 × 10 4 (1 ) and 1.88 × 10 4 (2 ) for CdSe QD systems and 178 (1 ) and 114 (2 ) for [Ru(bpy)3 ] 2+ systems were comparable with the highest reported H2 evolution systems using the same photosensitizers. Spectroscopic and electrochemical analyses revealed that the excited [Ru(bpy)3 ] 2+ undergoes reductive-quenching while the excited CdSe QDs proceed via oxidative-quenching during the catalytic process. The greater free energy change and faster electron transfer rate in the CdSe QD system made the electron transfer between the photosensitizer and [FeFe]-H2 ase mimics more efficient, which was subsequently corroborated by emission quenching and transient absorption experiments. The reduced [FeFe]-H2 ase mimics generated from the CdSe QDs were demonstrated to react with protons at a rate of 1.17 × 10 7 M −1 s −1 for1 and 8.62 × 10 6 M −1 s −1 for2 .