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Development of a Dinitrosyl Iron Complex Molecular Catalyst into a Hydrogen Evolution Cathode
Author(s) -
Chiou TzungWen,
Lu TsaiTe,
Wu YingHao,
Yu YiJu,
Chu LiKang,
Liaw WenFeng
Publication year - 2015
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201508351
Subject(s) - catalysis , chemistry , cathode , combinatorial chemistry , homogeneous , aqueous solution , hydrogen , electrocatalyst , water splitting , redox , inorganic chemistry , electrochemistry , chemical engineering , electrode , organic chemistry , physics , photocatalysis , engineering , thermodynamics
Despite extensive efforts, the electrocatalytic reduction of water using homogeneous/heterogeneous Fe, Co, Ni, Cu, W, and Mo complexes remains challenging because of issues involving the development of efficient, recyclable, stable, and aqueous‐compatible catalysts. In this study, evolution of the de novo designed dinitrosyl iron complex DNIC‐PMDTA from a molecular catalyst into a solid‐state hydrogen evolution cathode, considering all the parameters to fulfill the electronic and structural requirements of each step of the catalytic cycle, is demonstrated. DNIC‐PMDTA reveals electrocatalytic reduction of water at neutral and basic media, whereas its deposit on electrode preserves exceptional longevity, 139 h. This discovery will initiate a systematic study on the assembly of [Fe(NO) 2 ] motif into current collector for mass production of H 2 , whereas the efficiency remains tailored by its molecular precursor [(L)Fe(NO) 2 ].