苯乙酮
电催化剂
催化作用
化学
固碳
固定(群体遗传学)
组合化学
有机化学
电化学
生物化学
二氧化碳
电极
物理化学
基因
作者
Anxiang Guan,Yueli Quan,Yangshen Chen,Zhengzheng Liu,Junbo Zhang,Miao Kan,Quan Zhang,Haoliang Huang,Linping Qian,Linjuan Zhang,Gengfeng Zheng
出处
期刊:Chinese Journal of Catalysis
[China Science Publishing & Media Ltd.]
日期:2022-11-09
卷期号:43 (12): 3134-3141
被引量:10
标识
DOI:10.1016/s1872-2067(22)64116-0
摘要
The electrocarboxylation reaction is an attractive means to convert CO 2 into valuable chemicals under ambient conditions, while it still suffers from low efficiency due to the high stability of CO 2 . In this work, we report a double activation strategy for simultaneously activating CO 2 and acetophenone by silver-doped CeO 2 (Ag-CeO 2 ) nanowires, featuring as an effective electrocatalyst for electrocarboxylation of acetophenone with CO 2 . Compared to the Ag foil, Ag nanoparticles and CeO 2 nanowires, the Ag-CeO 2 nanowire catalyst allowed to reduce the onset potential difference between CO 2 and acetophenone activation, thus enabling efficient electrocarboxylation to form 2-phenyllactic acid. The Faradaic efficiency for producing 2-phenyllactic acid reached 91% at −1.8 V versus Ag/AgI. This double activation strategy of activating both CO 2 and organic substrate molecules can benefit the catalyst design to improve activities and selectivities in upgrading CO 2 fixation for higher-value electrocarboxylation. This paper realizes the important role of minimizing the overpotential difference between CO 2 and organic substrate molecules in the CO 2 -involved electrocarboxylation reaction.
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