Co-sputtered CuNi heteroatomic electrocatalyst for enhanced 5-hydroxymethylfurfural selective electrochemical conversion

The electrochemical conversion of biomass-derived 5-hydroxymethylfurfural (HMF) represents a promising, economically viable, and environmentally sustainable approach for producing value-added chemicals using renewable energy and in situ hydrogen generated through water electrolysis. However, the electrochemical hydrogenation (ECH) of HMF remains challenging due to the inherently low catalytic activity and selectivity of the electrodes, compounded by competition with the kinetically favored hydrogen evolution reaction (HER) in aqueous electrolytes. In this work, we demonstrate that Cu<sub>x</sub>Ni<sub>100-x</sub> heteroatomic thin films, fabricated via direct current (DC) magnetron co-sputtering, achieve a more than one order of magnitude increase in the HMF to 2,5-Bis-hydroxymethylfuran (BHMF) conversion rate, with nearly 50% faradic efficiency (FE) for BHMF, when compared to pure Cu and Ni electrodes (~ 10% BHMF FE). Our results suggest that the synergistic interaction between Cu and Ni creates an optimal catalytic environment for both HMF and adsorbed hydrogen (H<sub>ads</sub>) species, thereby enhancing BHMF formation through the ECH pathway.

Authors

Institutions

Publication Details

Journal
Scientific Reports
Published
2025-12-13
DOI
https://doi.org/10.1038/s41598-025-32621-7
Primary Topic
Catalysis for Biomass Conversion
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Co-sputtered CuNi heteroatomic electrocatalyst for enhanced 5-hydroxymethylfurfural selective electrochemical conversion

Laura Ramos Rivera, Bijandra Kumar, Baleeswaraiah Muchharla, Abdennaceur Karoui et al.
Scientific Reports
Catalysis for Biomass Conversion
article

Co-sputtered CuNi heteroatomic electrocatalyst for enhanced 5-hydroxymethylfurfural selective electrochemical conversion

Laura Ramos Rivera, Bijandra Kumar, Baleeswaraiah Muchharla, Abdennaceur Karoui, Kishor Kumar Sadasivuni, A. Victor Adedeji, Sunita Sanwaria, Kapil Kumar, Moumita Dikshit, Sandeep Kumar
article en

Abstract

The electrochemical conversion of biomass-derived 5-hydroxymethylfurfural (HMF) represents a promising, economically viable, and environmentally sustainable approach for producing value-added chemicals using renewable energy and in situ hydrogen generated through water electrolysis. However, the electrochemical hydrogenation (ECH) of HMF remains challenging due to the inherently low catalytic activity and selectivity of the electrodes, compounded by competition with the kinetically favored hydrogen evolution reaction (HER) in aqueous electrolytes. In this work, we demonstrate that Cu<sub>x</sub>Ni<sub>100-x</sub> heteroatomic thin films, fabricated via direct current (DC) magnetron co-sputtering, achieve a more than one order of magnitude increase in the HMF to 2,5-Bis-hydroxymethylfuran (BHMF) conversion rate, with nearly 50% faradic efficiency (FE) for BHMF, when compared to pure Cu and Ni electrodes (~ 10% BHMF FE). Our results suggest that the synergistic interaction between Cu and Ni creates an optimal catalytic environment for both HMF and adsorbed hydrogen (H<sub>ads</sub>) species, thereby enhancing BHMF formation through the ECH pathway.

Scientific ReportsVol. 16(1)
Chhattisgarh Council of Science and Technology (IN), National Institute of Technology Delhi (IN), Qatar University (QA), Elizabeth City State University (US), Old Dominion University (US)
National Science Foundation, U.S. Department of Energy, National Nuclear Security Administration
Openalex Percentile: Top 61%
Catalysis for Biomass Conversion
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.