Double boosting single atom Fe–N4 sites for high efficiency O2 and CO2 electroreduction
Autor: | Zhi-You Zhou, Wei Xiao, Bin Cao, Wang Shengbao, Xifei Li, Huijuan Yang, Xingpu Wang, Jingchun Jia, Jian Qin, Chi Xiao, Hirbod Maleki Kheimeh Sari, Jihu Liu, Pengyang Zhang |
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Rok vydání: | 2021 |
Předmět: |
Materials science
Metal ions in aqueous solution Proton exchange membrane fuel cell 02 engineering and technology General Chemistry 010402 general chemistry 021001 nanoscience & nanotechnology Electrocatalyst 01 natural sciences 0104 chemical sciences Catalysis Metal Chemical engineering visual_art visual_art.visual_art_medium General Materials Science Density functional theory 0210 nano-technology Mesoporous material Power density |
Zdroj: | Carbon. 182:109-116 |
ISSN: | 0008-6223 |
DOI: | 10.1016/j.carbon.2021.05.038 |
Popis: | Metal-N4 single-atom catalysts have emerged as the frontier of catalysis. However, the low metal loading and abundance of single atoms embedded in carbon skeleton hinder their practical application. Herein, we report an effective “trapping and exposing” strategy for constructing single-atom Fe–N4 catalysts with high density of single-atom active sites. The strategy involves the strong binding of metal ions to sucrose (trapping) to prevent the migration and agglomeration of Fe3+, followed by the introduction of a mesoporous structure using an SBA-15 template to achieve sufficient exposure of the Fe–N4 sites (exposing). The as-prepared catalyst comprises Fe–N4 moieties (10.8 wt%) with a hierarchical structure. Density functional theory calculations reveal that the chelating reaction between sucrose and Fe3+ ions has a low free energy, resulting in the formation of highly dispersed Fe–N4 single atoms. The single-atom catalyst displays a high peak power density of 0.784 W cm−2 in a H2–O2 proton exchange membrane fuel cell and achieves an impressive CO current density of 109 A g−1 at negligible overpotentials in a flow cell. This work provides an efficient strategy for designing high-performance single-atom catalysts for practical electrocatalysis applications. |
Databáze: | OpenAIRE |
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