Toward Industrial Electrosynthesis of Ethylene: Energy‐Efficient and Stable Acetylene Semi‐Hydrogenation on a Copper Phosphide/MXene Electrocatalyst

Z Zeliang Wu (School of Chemistry and Chemical Engineering Nanchang University Nanchang 330031 China) Q Qihui Guan (School of Chemistry and Chemical Engineering Nanchang University Nanchang 330031 China) T Tao Wang D Dongfang Li (Centre for Clean Energy Technology, Faculty of Science) M Ming Lei (State Key Laboratory of Chemical Resource Engineering, Institute of Computational Chemistry, College of Science) W Wei Hong S Shixia Chen (School of Chemistry and Chemical Engineering Nanchang University Nanchang 330031 China) S Shijian Wang (Centre for Clean Energy Technology, Faculty of Science) G Guoxiu Wang (Center for Clean Energy Technology, School of Mathematical and Physical Sciences, Faculty of Science) J Jun Wang

Abstract

Abstract Electrocatalytic semi‐hydrogenation of acetylene to ethylene (EHAE) using renewable electricity represents a promising alternative approach for ethylene production. However, its relatively low energy efficiency (EE) and insufficient electrocatalyst stability hinder its industrial applications. The conduct a techno‐economic analysis indicates that the EHAE process becomes profitable when the EE exceeds 22.8% at an industrial current density of 0.2 A cm −2 . Herein, we report a novel electrocatalyst featuring firmly immobilized copper phosphide (Cu 3 P) nanoparticles on MXene nanosheets (Ti 3 C 2 /Cu 3 P) for a stable EHAE process at industrial currents using membrane electrode assembly (MEA) system. Specifically, the Ti 3 C 2 /Cu 3 P electrocatalyst achieves an EE of 23.0% at 0.2 A cm −2 , demonstrating its potential for practical application and economic viability. The strong interactions between Cu 3 P and Ti 3 C 2 MXene prevent the agglomeration and dissolution of Cu 3 P nanoparticles during long‐term EHAE process. Notably, in a 4 cm 2 MEA, Ti 3 C 2 /Cu 3 P catalysts can sustain high performance for 100 h at 1.0 A with an ethylene Faradaic efficiency decay of only 0.051% per hour. Quasi in situ electron paramagnetic resonance spectroscopy and theoretical calculations indicate that Ti 3 C 2 /Cu 3 P facilitates water dissociation and synergistically enhances the adsorption of acetylene and active hydrogen (H * ), thereby accelerating the kinetics of EHAE process.

Article Details

Volume / Issue Vol. 65, Issue 9
Published February 23, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

Z

Zeliang Wu

School of Chemistry and Chemical Engineering Nanchang University Nanchang 330031 China

Q

Qihui Guan

School of Chemistry and Chemical Engineering Nanchang University Nanchang 330031 China

T

Tao Wang

D

Dongfang Li

Centre for Clean Energy Technology, Faculty of Science

M

Ming Lei

State Key Laboratory of Chemical Resource Engineering, Institute of Computational Chemistry, College of Science

W

Wei Hong

S

Shixia Chen

School of Chemistry and Chemical Engineering Nanchang University Nanchang 330031 China

S

Shijian Wang

Centre for Clean Energy Technology, Faculty of Science

G

Guoxiu Wang

Center for Clean Energy Technology, School of Mathematical and Physical Sciences, Faculty of Science

J

Jun Wang