Near 100% Conversion of Acetylene to High‐purity Ethylene at Ampere‐Level Current

Author:

Wu Zeliang12ORCID,Zhang Jinqiang2,Guan Qihui3,Liu Xing3,Xiong Hanting3,Chen Shixia3,Hong Wei3,Li Dongfang2,Lei Yaojie2,Deng Shuguang4ORCID,Wang Jun3ORCID,Wang Guoxiu2ORCID

Affiliation:

1. School of Resources and Environmental Nanchang University Nanchang 330031 China

2. Centre for Clean Energy Technology School of Mathematical and Physical Sciences Faculty of Science University of Technology Sydney Sydney NSW 2007 Australia

3. School of Chemistry and Chemical Engineering Nanchang University Nanchang 330031 China

4. School for Engineering of Matter Transport and Energy Arizona State University 551 E. Tyler Mall Tempe AZ 85287 USA

Abstract

AbstractDirect production of high‐purity ethylene from acetylene using renewable energy through electrocatalytic semi‐hydrogenation presents a promising alternative to traditional thermocatalytic processes. However, the low conversion of acetylene results in a significant amount of acetylene impurities in the product, necessitating additional purification steps. Herein, a tandem electrocatalytic system that integrates acetylene electrolyzer and zinc‐acetylene battery units for high‐purity ethylene production is designed. The ultrathin CuO nanoribbons with enriched oxygen vacancies (CuO1‐x NRs) as electrocatalysts achieve a remarkable 93.2% Faradaic efficiency of ethylene at an ampere‐level current density of 1.0 A cm−2 in an acetylene electrolyzer, and the power density reaches 3.8 mW cm−2 in a zinc‐acetylene battery under acetylene stream. Moreover, the tandem electrocatalysis system delivers a single‐pass acetylene conversion of 99.998% and ethylene selectivity of 96.1% at a high current of 1.4 A. Experimental data and calculations demonstrate that the presence of oxygen vacancies accelerates water dissociation to produce active hydrogen atoms while preventing the over‐hydrogenation of ethylene. Furthermore, techno‐economic analysis reveals that the tandem system can dramatically reduce the overall ethylene production cost compared to the conventional thermocatalytic processes. A novel strategy for complete acetylene‐to‐ethylene conversion under mild conditions, establishing a non‐petroleum route for the production of ethylene is reported.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Jiangxi Province

China Scholarship Council

Australian Research Council

Publisher

Wiley

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