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

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<sup>-2</sup>. Herein, we report a novel electrocatalyst featuring firmly immobilized copper phosphide (Cu<sub>3</sub>P) nanoparticles on MXene nanosheets (Ti<sub>3</sub>C<sub>2</sub>/Cu<sub>3</sub>P) for a stable EHAE process at industrial currents using membrane electrode assembly (MEA) system. Specifically, the Ti<sub>3</sub>C<sub>2</sub>/Cu<sub>3</sub>P electrocatalyst achieves an EE of 23.0% at 0.2 A cm<sup>-2</sup>, demonstrating its potential for practical application and economic viability. The strong interactions between Cu<sub>3</sub>P and Ti<sub>3</sub>C<sub>2</sub> MXene prevent the agglomeration and dissolution of Cu<sub>3</sub>P nanoparticles during long-term EHAE process. Notably, in a 4 cm<sup>2</sup> MEA, Ti<sub>3</sub>C<sub>2</sub>/Cu<sub>3</sub>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<sub>3</sub>C<sub>2</sub>/Cu<sub>3</sub>P facilitates water dissociation and synergistically enhances the adsorption of acetylene and active hydrogen (H<sup>*</sup>), thereby accelerating the kinetics of EHAE process.

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Journal
Angewandte Chemie International Edition
Published
2026-01-19
DOI
https://doi.org/10.1002/anie.202518909
Primary Topic
Ammonia Synthesis and Nitrogen Reduction
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article
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article

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

Qihui Guan, Shixia Chen, Guoxiu Wang, Dongfang Li et al.
Angewandte Chemie International Edition
Ammonia Synthesis and Nitrogen Reduction
article

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

Qihui Guan, Shixia Chen, Guoxiu Wang, Dongfang Li, Shijian Wang, Wei Liang Hong, Jun Wang, Zeliang Wu, Ming Lei, Tao Wang
article en

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<sup>-2</sup>. Herein, we report a novel electrocatalyst featuring firmly immobilized copper phosphide (Cu<sub>3</sub>P) nanoparticles on MXene nanosheets (Ti<sub>3</sub>C<sub>2</sub>/Cu<sub>3</sub>P) for a stable EHAE process at industrial currents using membrane electrode assembly (MEA) system. Specifically, the Ti<sub>3</sub>C<sub>2</sub>/Cu<sub>3</sub>P electrocatalyst achieves an EE of 23.0% at 0.2 A cm<sup>-2</sup>, demonstrating its potential for practical application and economic viability. The strong interactions between Cu<sub>3</sub>P and Ti<sub>3</sub>C<sub>2</sub> MXene prevent the agglomeration and dissolution of Cu<sub>3</sub>P nanoparticles during long-term EHAE process. Notably, in a 4 cm<sup>2</sup> MEA, Ti<sub>3</sub>C<sub>2</sub>/Cu<sub>3</sub>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<sub>3</sub>C<sub>2</sub>/Cu<sub>3</sub>P facilitates water dissociation and synergistically enhances the adsorption of acetylene and active hydrogen (H<sup>*</sup>), thereby accelerating the kinetics of EHAE process.

Angewandte Chemie International EditionVol. 65(9)
University of Technology Sydney (AU), Nanchang University (CN)
Affordable and clean energy
Openalex Percentile: Top 84%
Ammonia Synthesis and Nitrogen Reduction
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