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Exploring Oxygen Vacancy Effect in 1D Structural SnIP for CO2 Electro-Reduction to Formateoa mark
  • Bang, Hyeon Seok ;
  • Jeon, Jiho ;
  • Kang, Jinsu ;
  • Ko, Young Jin ;
  • Oh, Cheoulwoo ;
  • Kim, Hyunchul ;
  • Zhang, Xiaojie ;
  • Choi, Kyung Hwan ;
  • Woo, Chaeheon ;
  • Dong, Xue ;
  • Yu, Hak Ki ;
  • Lee, Woong Hee ;
  • Choi, Jae Young ;
  • Oh, Hyung Suk
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Publication Year
2024-12-05
Publisher
John Wiley and Sons Inc
Citation
Small, Vol.20
Keyword
1D structureCO2 reductionelectrocatalystsformateoxygen vacancy
Mesh Keyword
1-d structural1-D structures1D nanostructuresCO 2 reductionElectro reductionFormateOxidation stateReduction reactionVacancy effects]+ catalyst
All Science Classification Codes (ASJC)
BiotechnologyChemistry (all)BiomaterialsMaterials Science (all)Engineering (miscellaneous)
Abstract
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.
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/34350
DOI
https://doi.org/10.1002/smll.202404343
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Type
Article
Funding
H.-S.B., J.J., and J.K. contributed equally to this work. This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIT) (RS-2023-00302697, RS-2024-00431568).H.\u2010S.B., J.J., and J.K. contributed equally to this work. This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIT) (RS\u20102023\u201000302697, RS\u20102024\u201000431568).
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Yu, Hak Ki류학기
Department of Materials Science Engineering
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