Impact of Organo‐Functionalization on the Light‐Driven Hydrogen Evolution Reactivity of Molecular Molybdenum Sulfides

Molecular molybdenum sulfides, or thiomolybdates, are well-established noble-metal free molecular catalysts for the hydrogen evolution reaction (HER). To-date, there is a knowledge-gap regarding the impact of organo-functionalization on reactivity, stability and heterogenization of this compound class. Here, we report the development of synthetic routes for controlled introduction of organic N-donor ligands as a first step toward establishing structure-property-reactivity relationships in this new compound class. Photophysical studies combined with computational modelling are used to rationalize trends in the observed light-driven homogeneous HER activity. This work lays the foundation to develop organo-functionalized thiomolybdate HER catalysts suitable for covalent or supramolecular linkage to photosensitizers and for anchoring on heterogeneous supports, e.g. photocathodes.

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Journal
Chemistry - A European Journal
Published
2026-05-23
DOI
https://doi.org/10.1002/chem.71178
Primary Topic
Metalloenzymes and iron-sulfur proteins
Type
article
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article

Impact of Organo‐Functionalization on the Light‐Driven Hydrogen Evolution Reactivity of Molecular Molybdenum Sulfides

Mariet Sibi Puthanagady, Luis Kammerer, Luca Schleicher, Moritz Jahn et al.
Chemistry - A European Journal
Metalloenzymes and iron-sulfur proteins
article

Impact of Organo‐Functionalization on the Light‐Driven Hydrogen Evolution Reactivity of Molecular Molybdenum Sulfides

Mariet Sibi Puthanagady, Luis Kammerer, Luca Schleicher, Moritz Jahn, Stephan Kupfer, Sven Rau, Amelie Meyer, Alexander K. Mengele, Carsten Streb, Benjamin Dietzek‐Ivanšić
article en

Abstract

Molecular molybdenum sulfides, or thiomolybdates, are well-established noble-metal free molecular catalysts for the hydrogen evolution reaction (HER). To-date, there is a knowledge-gap regarding the impact of organo-functionalization on reactivity, stability and heterogenization of this compound class. Here, we report the development of synthetic routes for controlled introduction of organic N-donor ligands as a first step toward establishing structure-property-reactivity relationships in this new compound class. Photophysical studies combined with computational modelling are used to rationalize trends in the observed light-driven homogeneous HER activity. This work lays the foundation to develop organo-functionalized thiomolybdate HER catalysts suitable for covalent or supramolecular linkage to photosensitizers and for anchoring on heterogeneous supports, e.g. photocathodes.

Chemistry - A European Journal
Universität Ulm (DE), Johannes Gutenberg University Mainz (DE), Leibniz Institute of Photonic Technology (DE), Institute of Inorganic Chemistry of the Slovak Academy of Sciences (SK), Leibniz Institute of Surface Engineering (DE), Technische Hochschule Ulm (DE), Friedrich Schiller University Jena (DE)
Openalex Percentile: Top 15%
Metalloenzymes and iron-sulfur proteins
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Impact of Organo‐Functionalization on the Light‐Driven Hydrogen Evolution Reactivity of Molecular Molybdenum Sulfides — Mariet Sibi Puthanagady, Luis Kammerer, et al. · Chemistry - A European Journal (2026) | TGRS Research Map | TGRS