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Oxide‐Derived Bismuth as an Efficient Catalyst for Electrochemical Reduction of Flue Gas

Post‐combustion flue gas (mainly containing 5–40% CO2 balanced by N2) accounts for about 60% global CO2 emission. Rational conversion of flue gas into value‐added chemicals is still a formidable challenge. Herein, this work reports a β‐Bi2O3‐derived bismuth (OD‐Bi) catalyst with surface coordinated...

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Published in:Small (Weinheim an der Bergstrasse, Germany) Germany), 2023-07, Vol.19 (30), p.e2300417-n/a
Main Authors: Yang, Fangqi, Liang, Caihong, Zhou, Weizhen, Zhao, Wendi, Li, Pengfei, Hua, Zhengyu, Yu, Haoming, Chen, Shixia, Deng, Shuguang, Li, Jing, Lam, Yeng Ming, Wang, Jun
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cited_by cdi_FETCH-LOGICAL-c3737-bc5637a47155f448574b341e0829baacfb85b4e738143e95de5d53a306324c633
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container_title Small (Weinheim an der Bergstrasse, Germany)
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creator Yang, Fangqi
Liang, Caihong
Zhou, Weizhen
Zhao, Wendi
Li, Pengfei
Hua, Zhengyu
Yu, Haoming
Chen, Shixia
Deng, Shuguang
Li, Jing
Lam, Yeng Ming
Wang, Jun
description Post‐combustion flue gas (mainly containing 5–40% CO2 balanced by N2) accounts for about 60% global CO2 emission. Rational conversion of flue gas into value‐added chemicals is still a formidable challenge. Herein, this work reports a β‐Bi2O3‐derived bismuth (OD‐Bi) catalyst with surface coordinated oxygen for efficient electroreduction of pure CO2, N2, and flue gas. During pure CO2 electroreduction, the maximum Faradaic efficiency (FE) of formate reaches 98.0% and stays above 90% in a broad potential of 600 mV with a long‐term stability of 50 h. Additionally, OD‐Bi achieves an ammonia (NH3) FE of 18.53% and yield rate of 11.5 µg h−1 mgcat−1 in pure N2 atmosphere. Noticeably, in simulated flue gas (15% CO2 balanced by N2 with trace impurities), a maximum formate FE of 97.3% is delivered within a flow cell, meanwhile above 90% formate FEs are obtained in a wide potential range of 700 mV. In‐situ Raman combined with theory calculations reveals that the surface coordinated oxygen species in OD‐Bi can drastically activate CO2 and N2 molecules by selectively favors the adsorption of *OCHO and *NNH intermediates, respectively. This work provides a surface oxygen modulation strategy to develop efficient bismuth‐based electrocatalysts for directly reducing commercially relevant flue gas into valuable chemicals. β‐Bi2O3‐derived bismuth (OD‐Bi) catalyst with surface coordinated oxygen species is prepared via a facile in situ electrochemical reduction approach. The OD‐Bi catalyst exhibits superior electroreduction performance using pure CO2, N2, and flue gas as feedstocks. The surface coordinated oxygen species can drastically improve the catalytic activities.
doi_str_mv 10.1002/smll.202300417
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Rational conversion of flue gas into value‐added chemicals is still a formidable challenge. Herein, this work reports a β‐Bi2O3‐derived bismuth (OD‐Bi) catalyst with surface coordinated oxygen for efficient electroreduction of pure CO2, N2, and flue gas. During pure CO2 electroreduction, the maximum Faradaic efficiency (FE) of formate reaches 98.0% and stays above 90% in a broad potential of 600 mV with a long‐term stability of 50 h. Additionally, OD‐Bi achieves an ammonia (NH3) FE of 18.53% and yield rate of 11.5 µg h−1 mgcat−1 in pure N2 atmosphere. Noticeably, in simulated flue gas (15% CO2 balanced by N2 with trace impurities), a maximum formate FE of 97.3% is delivered within a flow cell, meanwhile above 90% formate FEs are obtained in a wide potential range of 700 mV. In‐situ Raman combined with theory calculations reveals that the surface coordinated oxygen species in OD‐Bi can drastically activate CO2 and N2 molecules by selectively favors the adsorption of *OCHO and *NNH intermediates, respectively. This work provides a surface oxygen modulation strategy to develop efficient bismuth‐based electrocatalysts for directly reducing commercially relevant flue gas into valuable chemicals. β‐Bi2O3‐derived bismuth (OD‐Bi) catalyst with surface coordinated oxygen species is prepared via a facile in situ electrochemical reduction approach. The OD‐Bi catalyst exhibits superior electroreduction performance using pure CO2, N2, and flue gas as feedstocks. 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In‐situ Raman combined with theory calculations reveals that the surface coordinated oxygen species in OD‐Bi can drastically activate CO2 and N2 molecules by selectively favors the adsorption of *OCHO and *NNH intermediates, respectively. This work provides a surface oxygen modulation strategy to develop efficient bismuth‐based electrocatalysts for directly reducing commercially relevant flue gas into valuable chemicals. β‐Bi2O3‐derived bismuth (OD‐Bi) catalyst with surface coordinated oxygen species is prepared via a facile in situ electrochemical reduction approach. The OD‐Bi catalyst exhibits superior electroreduction performance using pure CO2, N2, and flue gas as feedstocks. 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In‐situ Raman combined with theory calculations reveals that the surface coordinated oxygen species in OD‐Bi can drastically activate CO2 and N2 molecules by selectively favors the adsorption of *OCHO and *NNH intermediates, respectively. This work provides a surface oxygen modulation strategy to develop efficient bismuth‐based electrocatalysts for directly reducing commercially relevant flue gas into valuable chemicals. β‐Bi2O3‐derived bismuth (OD‐Bi) catalyst with surface coordinated oxygen species is prepared via a facile in situ electrochemical reduction approach. The OD‐Bi catalyst exhibits superior electroreduction performance using pure CO2, N2, and flue gas as feedstocks. 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source Wiley-Blackwell Read & Publish Collection
subjects Ammonia
bismuth
Bismuth oxides
Bismuth trioxide
Carbon dioxide
Catalysts
Chemical reduction
CO 2 reduction
Electrocatalysts
Electrowinning
Flue gas
flue gas reduction
N 2 reduction
Nanotechnology
Oxygen
Trace impurities
title Oxide‐Derived Bismuth as an Efficient Catalyst for Electrochemical Reduction of Flue Gas
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