Affiliation:
1. Key Laboratory of Photochemical Conversion and Optoelectronic Materials Technical Institute of Physics and Chemistry Chinese Academy of Sciences Beijing 100190 China
2. Center of Materials Science and Optoelectronics Engineering University of Chinese Academy of Sciences Beijing 100049 China
3. School of Materials Science and Engineering University of Science and Technology Beijing Beijing 100083 China
4. School of Chemical Sciences The University of Auckland Auckland 1142 New Zealand
Abstract
AbstractElectrochemical acetylene reduction (EAR) is a promising strategy for removing acetylene from ethylene‐rich gas streams. However, suppressing the undesirable hydrogen evolution is vital for practical applications in acetylene‐insufficient conditions. Herein, Cu single atoms are immobilized on anatase TiO2 nanoplates (Cu‐SA/TiO2) for electrochemical acetylene reduction, achieving an ethylene selectivity of ≈97% with a 5 vol% acetylene gas feed (Ar balance). At the optimal Cu‐single‐atom loading, Cu‐SA/TiO2 is able to effectively suppress HER and ethylene over‐hydrogenation even when using dilute acetylene (0.5 vol%) or ethylene‐rich gas feeds, delivering a 99.8% acetylene conversion, providing a turnover frequency of 8.9 × 10−2 s−1, which is superior to other EAR catalysts reported to date. Theoretical calculations show that the Cu single atoms and the TiO2 support acted cooperatively to promote charge transfer to adsorbed acetylene molecules, whilst also inhibiting hydrogen generation in alkali environments, thus allowing selective ethylene production with negligible hydrogen evolution at low acetylene concentrations.
Funder
National Natural Science Foundation of China
Natural Science Foundation of Beijing Municipality
Subject
Mechanical Engineering,Mechanics of Materials,General Materials Science
Cited by
21 articles.
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