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Branched Polyethylenimine Improves Hydrogen Photoproduction from a CdSe Quantum Dot/[FeFe]‐Hydrogenase Mimic System in Neutral Aqueous Solutions
Author(s) -
Liang WenJing,
Wang Feng,
Wen Min,
Jian JingXin,
Wang XuZhe,
Chen Bin,
Tung ChenHo,
Wu LiZhu
Publication year - 2015
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201406361
Subject(s) - polyethylenimine , hydrogenase , aqueous solution , photochemistry , chemistry , catalysis , photocatalysis , artificial photosynthesis , ascorbic acid , water splitting , coordination sphere , hydrogen production , inorganic chemistry , organic chemistry , ion , transfection , biochemistry , food science , gene
Nature uses hydrogenase enzyme to catalyze proton reduction at pH 7 with overpotentials and catalytic efficiencies that rival platinum electrodes. Over the past several years, [FeFe]‐hydrogenase ([FeFe]‐H 2 ase) mimics have been demonstrated to be effective catalysts for light‐driven H 2 evolution. However, it remains a significant challenge to realize H 2 production by such an artificial photosynthetic system in neutral aqueous solution. Herein, we report a new system for photocatalytic H 2 evolution working in a broad pH range, especially under neutral conditions. This unique system is consisted of branched polyethylenimine (PEI)‐grafted [FeFe]‐H 2 ase mimic (PEI‐ g ‐Fe 2 S 2 ), MPA‐CdSe quantum dots (MPA=mercaptopropionic acid), and ascorbic acid (H 2 A) in water. Due to the secondary coordination sphere of PEI, which has high buffering capacity and stabilizing ability, the system is able to produce H 2 under visible‐light irradiation with turnover number of 10 600 based on the Fe 2 S 2 active site in PEI‐ g ‐Fe 2 S 2 . The stability and activity are much better than that of the same system under acidic or basic conditions and they are, to the best of our knowledge, the highest known to date for photocatalytic H 2 evolution from a [FeFe]‐H 2 ase mimic in neutral aqueous solution.