Exploring Oxygen Vacancy Effect in 1D Structural SnIP for CO2 Electro-Reduction to Formate

被引:0
|
作者
Bang, Hyeon-Seok [1 ,2 ,3 ]
Jeon, Jiho [1 ,4 ]
Kang, Jinsu [2 ]
Ko, Young-Jin [1 ]
Oh, Cheoulwoo [1 ]
Kim, Hyunchul [1 ]
Zhang, Xiaojie [2 ]
Choi, Kyung Hwan [4 ]
Woo, Chaeheon [2 ]
Dong, Xue [4 ]
Yu, Hak Ki [5 ,6 ]
Lee, Woong Hee [1 ]
Choi, Jae-Young [1 ,2 ,3 ,4 ]
Oh, Hyung-Suk [1 ,2 ,3 ]
机构
[1] Korea Inst Sci & Technol, Clean Energy Res Ctr, Hwarang Ro 14-Gil 5, Seoul 02792, South Korea
[2] Sungkyunkwan Univ SKKU, Sch Adv Mat Sci & Engn, Suwon 16419, South Korea
[3] Sungkyunkwan Univ SKKU, KIST SKKU Carbon Neutral Res Ctr, Suwon 16419, South Korea
[4] Sungkyunkwan Univ, SKKU Adv Inst Nano Technol SAINT, Suwon 16419, South Korea
[5] Ajou Univ, Dept Mat Sci & Engn, Suwon 16499, South Korea
[6] Ajou Univ, Dept Energy Syst Res, Suwon 16499, South Korea
基金
新加坡国家研究基金会;
关键词
1D structure; CO2; reduction; electrocatalysts; formate; oxygen vacancy; ELECTROCHEMICAL REDUCTION; HYDROGEN EVOLUTION; EFFICIENT; TIN; CATALYSTS; ELECTROREDUCTION; ELECTROCATALYST; NANOPARTICLES; ACID;
D O I
10.1002/smll.202404343
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
1D nanostructures exhibit a large surface area and a short network distance, facilitating electron and ion transport. In this study, a 1D van der Waals material, tin iodide phosphide (SnIP), is synthesized and used as an electrocatalyst for the conversion of CO2 to formate. The electrochemical treatment of SnIP reconstructs it into a web-like structure, dissolves the I and P components, and increases the number of oxygen vacancies. The resulting oxygen vacancies promote the activity of the CO2 reduction reaction (CO2RR), increasing the local pH of the electrode surface and maintaining the oxidative metal site of the catalyst despite the electrochemically reducing environment. This strategy, which stabilizes the oxidation state of the catalyst, also helps to improve the durability of CO2RR. In practice, 1D structured SnIP catalyst exhibits outstanding performance with >92% formate faradaic efficiency (FEformate) at 300 mA cm(-2), a maximum partial current density for formate of 343 mA cm(-2), and excellent long-term stability (>100 h at 100 mA cm(-2) with >86% FEformate). This study introduced a method to easily generate oxygen vacancies on the catalyst surface by utilizing 1D materials and a strategy to improve the durability of CO2RR by stabilizing the oxidation state of the catalyst.
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页数:9
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