Issue 1, 2020

Recent advances in the mechanisms of the hydrogen evolution reaction by non-innocent sulfur-coordinating metal complexes

Abstract

Efficient hydrogen generation from aqueous protons through direct conversion of solar energy is an essential prerequisite of a future hydrogen economy and easily accessible renewable energy. For achieving this goal, the effective synthesis of a catalyst that can promote the hydrogen evolution reaction (HER) is in demand. Several mononuclear non-noble metal complexes carrying non-innocent S donating ligands have been reported as efficient photocatalysts and electrocatalysts for proton reduction. A thorough understanding of the elementary steps of hydrogen formation allows one to derive structure–property relationships that can guide future catalyst design. In this review, we highlight the mechanisms of the homogeneous HER for these catalysts in the light of photocatalytic, electrocatalytic and computational data with the main concern of elucidating the interplay between the localization of the electron density and the hydrogen evolution reaction pathway. In addition, the effects of π-conjugation, heteroatoms and electron accepting/donating moieties on the basicity of the metal center and catalyst overpotential are discussed to rationalize the formation of a metal or ligand hydrid intermediate. Moreover, some suggestions are provided for future use in the design of effective HER catalysts.

Graphical abstract: Recent advances in the mechanisms of the hydrogen evolution reaction by non-innocent sulfur-coordinating metal complexes

Article information

Article type
Review Article
Submitted
30 aug 2019
Accepted
31 okt 2019
First published
01 nov 2019
This article is Open Access
Creative Commons BY license

Inorg. Chem. Front., 2020,7, 37-71

Recent advances in the mechanisms of the hydrogen evolution reaction by non-innocent sulfur-coordinating metal complexes

M. Drosou, F. Kamatsos and C. A. Mitsopoulou, Inorg. Chem. Front., 2020, 7, 37 DOI: 10.1039/C9QI01113G

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