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Thermodynamically driven self-formation of Ag nanoparticles in Zn-embedded carbon nanofibers for efficient electrochemical CO2reduction
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- Title
- Thermodynamically driven self-formation of Ag nanoparticles in Zn-embedded carbon nanofibers for efficient electrochemical CO2reduction
- DGIST Authors
- Lee, Gi-Baek ; Ahn, In-Kyoung ; Joo, Won-Hyo ; Lee, Jae-Chan ; Kim, Ji-Yong ; Hong, Deokgi ; Kim, Hyoung Gyun ; Lee, Jusang ; Kim, Miyoung ; Nam, Dae-Hyun ; Joo, Young-Chang
- Issued Date
- 2021-07
- Citation
- Lee, Gi-Baek. (2021-07). Thermodynamically driven self-formation of Ag nanoparticles in Zn-embedded carbon nanofibers for efficient electrochemical CO2reduction. doi: 10.1039/d1ra02463a
- Type
- Article
- Keywords
- Silver nanoparticles ; Zinc ; Zinc compounds ; Active material ; Ag nanoparticle ; Faradaic efficiencies ; Free-energy difference ; Gas diffusion electrodes ; Renewable fuels ; Self formation ; Thermal calcination ; Silver compounds ; Carbon monoxide ; Carbon nanofibers ; Diffusion in gases ; Electrolytes ; Free energy ; Gibbs free energy ; Metal nanoparticles ; Potassium hydroxide
- ISSN
- 2046-2069
- Abstract
-
The electrochemical CO2reduction reaction (CO2RR), which converts CO2into value-added feedstocks and renewable fuels, has been increasingly studied as a next-generation energy and environmental solution. Here, we report that single-atom metal sites distributed around active materials can enhance the CO2RR performance by controlling the Lewis acidity-based local CO2concentration. By utilizing the oxidation Gibbs free energy difference between silver (Ag), zinc (Zn), and carbon (C), we can produce Ag nanoparticle-embedded carbon nanofibers (CNFs) where Zn is atomically dispersed by a one-pot, self-forming thermal calcination process. The CO2RR performance of AgZn-CNF was investigated by a flow cell with a gas diffusion electrode (GDE). Compared to Ag-CNFs without Zn species (53% at −0.85 Vvs.RHE), the faradaic efficiency (FE) of carbon monoxide (CO) was approximately 20% higher in AgZn-CNF (75% at −0.82 Vvs.RHE) with 1 M KOH electrolyte. © The Royal Society of Chemistry 2021.
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- Publisher
- Royal Society of Chemistry
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