Tunable metal-reduced graphene oxide hybrid materials for electric field-driven catalytic hydrogenation

Abstract Efficient hydrogenation catalysts operating under mild conditions are essential for sustainable chemical synthesis. Herein, reduced graphene oxide (rGO) supported Ni, Pd, Cu, and Zn catalysts were investigated for the hydrogenation of 1-octene under an applied external electric field (EEF). Paired ON/OFF experiments demonstrate that the EEF significantly enhances hydrogenation activity in a catalyst-dependent manner. Notably, Cu–rGO exhibits the highest activity under EEF, revealing an activity trend distinct from conventional thermal hydrogenation. Density functional theory (DFT) calculations provide complementary insight into intrinsic electronic structures while highlighting the limitations of static models for describing EEF-driven catalysis. Graphical abstract

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Publication Details

Journal
MRS Communications
Published
2026-02-23
DOI
https://doi.org/10.1557/s43579-026-00944-9
Primary Topic
Nanomaterials for catalytic reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Tunable metal-reduced graphene oxide hybrid materials for electric field-driven catalytic hydrogenation

Fazira Ilyana Abdul Razak, Suhaila Sapari, Yee Shi Wee, Emelda Raymond
MRS Communications
Nanomaterials for catalytic reactions
article

Tunable metal-reduced graphene oxide hybrid materials for electric field-driven catalytic hydrogenation

Fazira Ilyana Abdul Razak, Suhaila Sapari, Yee Shi Wee, Emelda Raymond
article en

Abstract

Abstract Efficient hydrogenation catalysts operating under mild conditions are essential for sustainable chemical synthesis. Herein, reduced graphene oxide (rGO) supported Ni, Pd, Cu, and Zn catalysts were investigated for the hydrogenation of 1-octene under an applied external electric field (EEF). Paired ON/OFF experiments demonstrate that the EEF significantly enhances hydrogenation activity in a catalyst-dependent manner. Notably, Cu–rGO exhibits the highest activity under EEF, revealing an activity trend distinct from conventional thermal hydrogenation. Density functional theory (DFT) calculations provide complementary insight into intrinsic electronic structures while highlighting the limitations of static models for describing EEF-driven catalysis. Graphical abstract

MRS Communications
Universitas Airlangga (ID), University of Technology Malaysia (MY)
Ministry of Higher Education, Malaysia, Universiti Teknologi Malaysia
Responsible consumption and production
Openalex Percentile: Top 45%
Nanomaterials for catalytic reactions
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