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

乙炔 材料科学 电合成 分析化学(期刊) 结晶学 化学 物理化学 电化学 有机化学 电极
作者
Bin Zhang,Chuanqi Cheng,Jiajun Wang,Fanpeng Chen,Yanbing Han,Yichen He,Bo‐Hang Zhao
出处
期刊:Research Square - Research Square
标识
DOI:10.21203/rs.3.rs-5240353/v1
摘要

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.

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