| Unlocking Bifunctional Electrocatalytic Activity for CO2 Reduction Reaction by Win-Win Metal-Oxide Cooperation | |
| Cai, Zhao1,2,3; Wu, Yueshen2,3; Wu, Zishan2,3; Yin, Lichang4; Weng, Zhe2,3; Zhong, Yiren2,3; Xu, Wenwen1,2,3; Sun, Xiaoming1,5; Wang, Hailiang2,3 | |
| Corresponding Author | Yin, Lichang(lcyin@imr.ac.cn) ; Sun, Xiaoming(sunxm@mail.buct.edu.cn) ; Wang, Hailiang(hailiang.wang@yale.edu) |
| 2018-11-01 | |
| Source Publication | ACS ENERGY LETTERS
 |
| ISSN | 2380-8195 |
| Volume | 3Issue:11Pages:2816-2822 |
| Abstract | Understanding how remarkable properties of materials emerge from complex interactions of their constituents and designing advanced material structures to render desired properties are grand challenges. Metal-oxide interactions are frequently utilized to improve catalytic properties but are often limited to situations where only one component is facilitated by the other. In this work, we demonstrate highly cooperative win-win metal-oxide interactions that enable unprecedented catalytic functionalities for electrochemical CO2 reduction reactions. In a single SnOx/Ag catalyst, the oxide promotes the metal in the CO production mode, and meanwhile the metal promotes the oxide in the HCOOH production mode, achieving potential-dependent bifunctional CO2 conversion to fuels and chemicals with H-2 evolution suppressed in the entire potential window. Spectroscopic studies and computational simulations reveal that electron transfer from Ag to SnOx and dual-site cooperative binding for reaction intermediates at the SnOx/Ag interface are responsible for stabilizing the key intermediate in the CO pathway, changing the potential-limiting step in the HCOOH pathway, and increasing the kinetic barrier in the H-2 evolution pathway, together leading to highly synergistic CO2 electroreduction. |
| Funding Organization | National Science Foundation ; Doctoral New Investigator grant from ACS Petroleum Research Fund ; National Science Fund of China ; Special Program for Applied Research on Super Computation of the NSFC-Guangdong Joint Fund (second phase) |
| DOI | 10.1021/acsenergylett.8b01767 |
| Indexed By | SCI |
| Language | 英语 |
| Funding Project | National Science Foundation[CHE-1651717] ; Doctoral New Investigator grant from ACS Petroleum Research Fund ; National Science Fund of China[51472249] ; Special Program for Applied Research on Super Computation of the NSFC-Guangdong Joint Fund (second phase)[U1501501] |
| WOS Research Area | Chemistry ; Electrochemistry ; Energy & Fuels ; Science & Technology - Other Topics ; Materials Science |
| WOS Subject | Chemistry, Physical ; Electrochemistry ; Energy & Fuels ; Nanoscience & Nanotechnology ; Materials Science, Multidisciplinary |
| WOS ID | WOS:000450374600023 |
| Publisher | AMER CHEMICAL SOC |
| Citation statistics | |
| Document Type | 期刊论文 |
| Identifier | http://ir.imr.ac.cn/handle/321006/130337 |
| Collection | 中国科学院金属研究所 |
| Corresponding Author | Yin, Lichang; Sun, Xiaoming; Wang, Hailiang |
| Affiliation | 1.Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, Beijing 100029, Peoples R China 2.Yale Univ, Dept Chem, West Haven, CT 06516 USA 3.Yale Univ, Energy Sci Inst, West Haven, CT 06516 USA 4.Chinese Acad Sci, Shenyang Natl Lab Mat Sci, Inst Met Res, Shenyang 110016, Liaoning, Peoples R China 5.Beijing Univ Chem Technol, Coll Energy, Beijing 100029, Peoples R China |
| Recommended Citation GB/T 7714 | Cai, Zhao,Wu, Yueshen,Wu, Zishan,et al. Unlocking Bifunctional Electrocatalytic Activity for CO2 Reduction Reaction by Win-Win Metal-Oxide Cooperation[J]. ACS ENERGY LETTERS,2018,3(11):2816-2822. |
| APA | Cai, Zhao.,Wu, Yueshen.,Wu, Zishan.,Yin, Lichang.,Weng, Zhe.,...&Wang, Hailiang.(2018).Unlocking Bifunctional Electrocatalytic Activity for CO2 Reduction Reaction by Win-Win Metal-Oxide Cooperation.ACS ENERGY LETTERS,3(11),2816-2822. |
| MLA | Cai, Zhao,et al."Unlocking Bifunctional Electrocatalytic Activity for CO2 Reduction Reaction by Win-Win Metal-Oxide Cooperation".ACS ENERGY LETTERS 3.11(2018):2816-2822. |
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