Mesoporous PdAg Nanospheres for Stable Electrochemical CO2 Reduction to Formate

被引:171
|
作者
Zhou, Yuan [1 ]
Zhou, Rui [1 ]
Zhu, Xiaorong [2 ]
Han, Na [1 ]
Song, Bin [1 ]
Liu, Tongchao [3 ]
Hu, Guangzhi [4 ]
Li, Yafei [2 ]
Lu, Jun [3 ]
Li, Yanguang [1 ]
机构
[1] Soochow Univ, Inst Funct Nano & Soft Mat FUNSOM, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Suzhou 215123, Peoples R China
[2] Nanjing Normal Univ, Coll Chem & Mat Sci, Nanjing 210023, Peoples R China
[3] Argonne Natl Lab, Chem Sci & Engn Div, Lemont, IL 60439 USA
[4] Yunnan Univ, Sch Ecol & Environm Sci, Inst Ecol Res & Pollut Control Plateau Lakes, Kunming 650504, Yunnan, Peoples R China
基金
中国国家自然科学基金;
关键词
electrochemical CO(2)reduction; formate; mesoporous nanospheres; palladium-silver alloys; stability; CARBON-DIOXIDE; ELECTROREDUCTION; CONVERSION; CATALYSIS; ACID;
D O I
10.1002/adma.202000992
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Palladium is a promising material for electrochemical CO(2)reduction to formate with high Faradaic efficiency near the equilibrium potential. It unfortunately suffers from problematic operation stability due to CO poisoning on surface. Here, it is demonstrated that alloying is an effective strategy to alleviate this problem. Mesoporous PdAg nanospheres with uniform size and composition are prepared from the co-reduction of palladium and silver precursors in aqueous solution using dioctadecyldimethylammonium chloride as the structure-directing agent. The best candidate can initiate CO(2)reduction at zero overpotential and achieve high formate selectivity close to 100% and great stability even at <-0.2 V versus reversible hydrogen electrode. The high selectivity and stability are believed to result from the electronic coupling between Pd and Ag, which lowers the d-band center of Pd and thereby significantly enhances its CO tolerance, as evidenced by both electrochemical analysis and theoretical simulations.
引用
收藏
页数:6
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