Photocatalytic Aqueous Reforming of Methyl Formate

D Dongxu Zuo (Department of Chemistry University of Bayreuth Universitatsstraße 30 95447 Bayreuth Germany) S Suman Pradhan (Department of Chemistry University of Bayreuth Bayreuth Germany) M Manami Banerjee (Department of Chemistry, University of Bayreuth, Universitätsstraße 30, 95447 Bayreuth, Germany) N Nils Rockstroh S Stephan Bartling A Abdallah I.M. Rabee (Leibniz‐Institut für Katalyse e.V. (LIKAT Rostock) Albert‐Einstein‐Str. 29a 18059 Rostock Germany) X Xinxin Tian (Leibniz-Institut für Katalyse) A Alina Skorynina (ALBA Synchrotron Light Facility, Carrer de la Llum 2−26, Barcelona, Cerdanyola del Vallès 08290, Spain) A Aleksander Jaworski (Department of Chemistry) L Laura Simonelli (CELLS─ALBA Synchrotron Radiation Facility, Carrer de la Llum 2-26, Cerdanyola del Vallès 08290, Spain) J Jabor Rabeah (Magnetic Resonance and X-ray Methods) H Haijun Jiao (Leibniz-Institut für Katalyse) M Matthias Beller (Leibniz-Institut für Katalyse) S Shoubhik Das (Department of Chemistry, University of Bayreuth, Universitätsstraße 30, 95447 Bayreuth, Germany)

Abstract

Abstract Green hydrogen is critical to establish a sustainable energy future as it offers a clean, renewable, and a versatile alternative for decarbonizing industries, transportation, and power generation. However, the limitations of current methods significantly restrict the scope and hinder many of the envisioned applications. This study aims to report on the first example of a 3d‐metal‐based (Cu) heterogeneous photocatalytic system to produce green hydrogen via dehydrogenation of methyl formate (MF), a reaction previously known to require 4d/5d transition metals. Employing a Cu‐based atomically dispersed heterogeneous photocatalyst supported on aryl‐amino‐substituted graphitic carbon nitride (d‐gC 3 N 4 ), the protocol offers numerous key advantages, including the recyclability of the photocatalyst for >10 cycles without significant activity loss, sustained hydrogen production (>15 days!) with high hydrogen yield (19.8 mmol g cat −1 ) and negligible CO emission, following an operationally simple, sustainable, and efficient catalytic pathway. Furthermore, the photocatalyst is characterized (using HAADF‐STEM, SS‐NMR, XAS, EPR, and XPS), all of which clearly demonstrated the presence of single atomic Cu‐site. Additionally, comprehensive mechanistic investigations together with DFT calculations allow for a thorough mechanistic rationale for this reaction. It is strongly believed that this atomically dispersed heterogeneous photocatalytic approach will open new avenues for establishing liquid organic hydrogen career (LOHC) technologies.

Article Details

Volume / Issue Vol. 37, Issue 39
Published October 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (14)

D

Dongxu Zuo

Department of Chemistry University of Bayreuth Universitatsstraße 30 95447 Bayreuth Germany

S

Suman Pradhan

Department of Chemistry University of Bayreuth Bayreuth Germany

M

Manami Banerjee

Department of Chemistry, University of Bayreuth, Universitätsstraße 30, 95447 Bayreuth, Germany

N

Nils Rockstroh

S

Stephan Bartling

A

Abdallah I.M. Rabee

Leibniz‐Institut für Katalyse e.V. (LIKAT Rostock) Albert‐Einstein‐Str. 29a 18059 Rostock Germany

X

Xinxin Tian

Leibniz-Institut für Katalyse

A

Alina Skorynina

ALBA Synchrotron Light Facility, Carrer de la Llum 2−26, Barcelona, Cerdanyola del Vallès 08290, Spain

A

Aleksander Jaworski

Department of Chemistry

L

Laura Simonelli

CELLS─ALBA Synchrotron Radiation Facility, Carrer de la Llum 2-26, Cerdanyola del Vallès 08290, Spain

J

Jabor Rabeah

Magnetic Resonance and X-ray Methods

H

Haijun Jiao

Leibniz-Institut für Katalyse

M

Matthias Beller

Leibniz-Institut für Katalyse

S

Shoubhik Das

Department of Chemistry, University of Bayreuth, Universitätsstraße 30, 95447 Bayreuth, Germany