CeOx Promoted Electrocatalytic CO2 Reduction to Formate by Assisting in the Critical Hydrogenation Step

被引:15
|
作者
Yu, Rongxing [1 ,2 ]
Qiu, Chen [1 ]
Lin, Zedong [1 ,3 ]
Liu, Hongzhi [1 ]
Gao, Jinqiang [1 ]
Li, Simeng [1 ]
Yao, Youwei [2 ]
Yu, Jun [1 ]
Yang, Shihe [1 ,3 ]
机构
[1] Peking Univ, Shenzhen Grad Sch, Sch Chem Biol & Biotechnol, Guangdong Key Lab Nanomicro Mat Res, Shenzhen 518055, Peoples R China
[2] Tsinghua Univ, Shenzhen Int Grad Sch, Shenzhen 518071, Peoples R China
[3] Shenzhen Bay Lab, Inst Biomed Engn, Shenzhen 518107, Peoples R China
来源
ACS MATERIALS LETTERS | 2022年 / 4卷 / 09期
关键词
HIGHLY EFFICIENT; SITES; PHASE;
D O I
10.1021/acsmaterialslett.2c00512
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Bismuth oxide is one of the best-known formate production catalysts from electrocatalytic reduction of CO2. It came as a surprise here that its hybridization with CeOx drastically boosted the catalytic activity and stability on CO2 reduction toward formate formation. Specifically, the formate faradaic efficiency of Bi2O3-CeOx exceeds 85% starting from -0.3 V vs reversible hydrogen electrode (RHE) and remains above 90% from -0.5 V to -1.1 V vs RHE, outperforming the pure Bi2O3 and most other reported formate catalysts. Experimental and computational results suggest that the significantly enhanced catalytic activity arises from the electronic synergy between Bi2O3 and CeOx. The electronic synergy results in abundant defects in CeOx favorable for CO2 activation and adsorption. Moreover, CeOx promotes water dissociation to form H* but with a large energy barrier to H-2, which can easily react with CO2 and accelerate the rate-determining step of hydrogenation step. The generality of the CeOx-promoted catalysis for CO2 reduction to formate is also demonstrated for In2O3. This work opens up a new avenue for the design of efficient CO2RR electrocatalysts.
引用
收藏
页码:1749 / 1755
页数:7
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