Selective electrosynthesis of 1,3-butadiene by tailoring the coverage of acetylene and water

Chuanqi Cheng, Jiajun Wang, Fanpeng Chen, Yanran Han, Yichen He, Bin Zhang () and Bo-Hang Zhao ()
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Chuanqi Cheng: Tianjin University
Jiajun Wang: Tianjin University
Fanpeng Chen: Tianjin University
Yanran Han: Tianjin University
Yichen He: Tianjin University
Bin Zhang: Tianjin University
Bo-Hang Zhao: Tianjin University

Nature Communications, 2025, vol. 16, issue 1, 1-11

Abstract: Abstract 1,3-Butadiene (C4H6), the main raw material for producing important chemicals (nylon, synthetic resin, rubber), relies on petroleum cracking with intensive carbon emissions. The electrocatalytic dimeric hydrogenation of natural gas/coal-derived C2H2 to C4H6 provides a nonpetroleum pathway. However, C4H6, as a byproduct of C2H2 hydrogenation, is usually neglected because of its very low Faradaic efficiency. Here, we theoretically and experimentally report a mechanism comprising acetylene dimerization and subsequent hydrogenation. The first dimerization process can be accelerated under appropriate coverage of acetylene and water. A ligand-modifying strategy is subsequently proposed to regulate the wettability of Cu nanoarrays to enable suitable coverages. The optimized 1-dodecanethiol-modified Cu nanoarrays deliver a 65.3% C4H6 Faradaic efficiency at 100 mA cm−2. The C4H6 formation kinetics become sluggish at the two ends of the surface C2H2/H2O ratios, and moderate C2H2/H2O coverage accelerates the C‒C coupling process to promote C4H6 production. Moreover, life cycle assessment demonstrates its sustainability.

Date: 2025
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DOI: 10.1038/s41467-025-60881-4

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