光催化
光化学
可见光谱
氢化酶
光敏剂
催化作用
光谱学
化学
制氢
氢
电子顺磁共振
电化学
材料科学
光电子学
物理化学
有机化学
电极
核磁共振
物理
量子力学
作者
Philipp Buday,Chizuru Kasahara,Elisabeth Hofmeister,Daniel Kowalczyk,Micheal K. Farh,Saskia Riediger,Martin Schulz,Maria Wächtler,Shunsuke Furukawa,Masaichi Saito,Dirk Ziegenbalg,Stefanie Gräfe,Peter Bäuerle,Stephan Kupfer,Benjamin Dietzek,Wolfgang Weigand
标识
DOI:10.1002/anie.202202079
摘要
Inspired by the active center of the natural [FeFe] hydrogenases, we designed a compact and precious metal-free photosensitizer-catalyst dyad (PS-CAT) for photocatalytic hydrogen evolution under visible light irradiation. PS-CAT represents a prototype dyad comprising π-conjugated oligothiophenes as light absorbers. PS-CAT and its interaction with the sacrificial donor 1,3-dimethyl-2-phenylbenzimidazoline were studied by steady-state and time-resolved spectroscopy coupled with electrochemical techniques and visible light-driven photocatalytic investigations. Operando EPR spectroscopy revealed the formation of an active [FeI Fe0 ] species-in accordance with theoretical calculations-presumably driving photocatalysis effectively (TON≈210).
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