Photochemical H2 Evolution from Bis(diphosphine)nickel Hydrides Enables Low-Overpotential Electrocatalysis
Author:
Affiliation:
1. Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-3290, United States
2. Department of Chemistry, North Carolina State University, Raleigh, North Carolina 27695-8204, United States
Funder
Division of Chemistry
Basic Energy Sciences
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.1c10628
Reference62 articles.
1. Molecular Photoelectrocatalysts for Light-Driven Hydrogen Production
2. Efficient homogeneous photochemical water gas shift reaction catalysed under extremely mild conditions by novel iridium(III) complexes: [(η5-Me5C5)Ir(bpy)Cl]+, [(η5-Me5C5)Ir(bpy)H]+, and [(η5-Me5C5)Ir(phen)Cl]+(bpy = 2,2′-bipyridine; phen = 1,10-phenanthroline)
3. Synthesis and molecular structure of a new family of iridium-(III) and rhodium(III) complexes: [(η5-Me5C5)Ir(LL)X]+ and [(η5-Me5C5)Rh(LL)Cl]+; LL = 2,2′-bipyridine or 1,10-phenanthroline; X = Cl or H. Single crystal structures of [(η5-Me5C5)Ir(bpy)Cl]Cl and [(η5-Me5C5)Rh(phen)Cl]ClO4
4. Spectroscopic behavior of a new family of mixed-ligand iridium(III) complexes
5. Photocatalysis of the Homogeneous Water-Gas Shift Reaction under Ambient Conditions by Cationic Iridium(III) Complexes
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