2D Conjugated Metal–Organic Frameworks as Electrocatalysts for Boosting Glycerol Upgrading Coupled with Hydrogen Production

Y Yutong Luo M Michael Beerbaum (Center for Advanced Systems Understanding 1 , 02826 Görlitz,) S Stefan Röher (Chair of Electrochemistry Technische Universität Dresden Zellescher Weg 19 01069 Dresden Germany) S Sara Amanzadeh Salout (Chair of Chemistry Technische Universität Dresden Bergstraße 66 01069 Dresden Germany) V Volodymyr Bon (Chair of Inorganic Chemistry I) Y Yang Lu L Leonid Shupletsov (Inorganic Chemistry I Technische Universität Dresden Dresden Germany) A Ankita De (Chair of Inorganic Chemistry I, Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, Bergstraße 66, 01069 Dresden, Germany) X Xinliang Feng I Inez M. Weidinger (Chair of Electrochemistry) T Thomas D. Kühne (CASUS - Center for Advanced Systems Understanding, Helmholtz-Zentrum Dresden-Rossendorf E.V. (HZDR), Untermarkt 20, Görlitz D-02826, Germany) A Arafat Hossain Khan I Irena Senkovska (Chair of Inorganic Chemistry I) S Stefan Kaskel (Chair of Inorganic Chemistry I)

Abstract

Abstract The valorisation of glycerol using renewable electricity is recognised as an effective and attractive approach for producing high‐value compounds from biomass byproducts. 2D conjugated metal–organic frameworks (2D c‐MOFs) have emerged as promising electrocatalysts due to their tunable structures, high electronic conductivity, and efficient utilisation of well‐defined active centres. In this study, we report the first systematic investigation of 2D c‐MOFs containing Ni‐X 4 (X = O or N) moieties for the glycerol oxidation reaction (GOR), examining key factors influencing both electrocatalytic activity and selectivity. In situ 13 C electrochemical nuclear magnetic resonance and Raman spectroscopies provide insights into the GOR mechanism and confirm that Ni–O 4 sites are the primary active centres. Theoretical calculations further reveal that [Ni 3 (HHTQ) 2 ] n (HHTQ = 2,3,7,8,12,13‐hexahydroxytricycloquinazoline) exhibits superior GOR activity due to strong adsorption of reaction intermediates and weak interlayer interactions. This work highlights the potential of 2D c‐MOFs as highly efficient GOR catalysts, paving the way for the rational design of advanced electrocatalysts and contributing to the development of sustainable energy conversion and storage technologies.

Article Details

Volume / Issue Vol. 64, Issue 27
Published July 01, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (14)

Y

Yutong Luo

M

Michael Beerbaum

Center for Advanced Systems Understanding 1 , 02826 Görlitz,

S

Stefan Röher

Chair of Electrochemistry Technische Universität Dresden Zellescher Weg 19 01069 Dresden Germany

S

Sara Amanzadeh Salout

Chair of Chemistry Technische Universität Dresden Bergstraße 66 01069 Dresden Germany

V

Volodymyr Bon

Chair of Inorganic Chemistry I

Y

Yang Lu

L

Leonid Shupletsov

Inorganic Chemistry I Technische Universität Dresden Dresden Germany

A

Ankita De

Chair of Inorganic Chemistry I, Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, Bergstraße 66, 01069 Dresden, Germany

X

Xinliang Feng

I

Inez M. Weidinger

Chair of Electrochemistry

T

Thomas D. Kühne

CASUS - Center for Advanced Systems Understanding, Helmholtz-Zentrum Dresden-Rossendorf E.V. (HZDR), Untermarkt 20, Görlitz D-02826, Germany

A

Arafat Hossain Khan

I

Irena Senkovska

Chair of Inorganic Chemistry I

S

Stefan Kaskel

Chair of Inorganic Chemistry I