Activating Lattice Oxygen in Perovskite Oxide by B‐Site Cation Doping for Modulated Stability and Activity at Elevated Temperatures
Abstract Doping perovskite oxide with different cations is used to improve its electro‐catalytic performance for various energy and environment devices. In this work, an activated lattice oxygen activity in Pr0.4Sr0.6CoxFe0.9−xNb0.1O3−δ (PSCxFN, x = 0, 0.2, 0.7) thin film model system by B‐site cati...
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oai:doaj.org-article:ace7fc5cdee54b3ebf69254b6fe30c962021-11-17T08:40:31ZActivating Lattice Oxygen in Perovskite Oxide by B‐Site Cation Doping for Modulated Stability and Activity at Elevated Temperatures2198-384410.1002/advs.202102713https://doaj.org/article/ace7fc5cdee54b3ebf69254b6fe30c962021-11-01T00:00:00Zhttps://doi.org/10.1002/advs.202102713https://doaj.org/toc/2198-3844Abstract Doping perovskite oxide with different cations is used to improve its electro‐catalytic performance for various energy and environment devices. In this work, an activated lattice oxygen activity in Pr0.4Sr0.6CoxFe0.9−xNb0.1O3−δ (PSCxFN, x = 0, 0.2, 0.7) thin film model system by B‐site cation doping is reported. As Co doping level increases, PSCxFN thin films exhibit higher concentration of oxygen vacancies (Vo••) as revealed by X‐ray diffraction and synchrotron‐based X‐ray photoelectron spectroscopy. Density functional theory calculation results suggest that Co doping leads to more distortion in FeO octahedra and weaker metaloxygen bonds caused by the increase of antibonding state, thereby lowering Vo•• formation energy. As a consequence, PSCxFN thin film with higher Co‐doping level presents larger amount of exsolved particles on the surface. Both the facilitated Vo•• formation and B‐site cation exsolution lead to the enhanced hydrogen oxidation reaction (HOR) activity. Excessive Co doping until 70%, nevertheless, results in partial decomposition of thin film and degrades the stability. Pr0.4Sr0.6(Co0.2Fe0.7Nb0.1)O3 with moderate Co doping level displays both good HOR activity and stability. This work clarifies the critical role of B‐site cation doping in determining the Vo•• formation process, the surface activity, and structure stability of perovskite oxides.Huijun ChenChaesung LimMengzhen ZhouZuyun HeXiang SunXiaobao LiYongjian YeTing TanHui ZhangChenghao YangJeong Woo HanYan ChenWileyarticlecation dopingFeO octahedrametaloxygen bondoxygen vacancyperovskite oxideScienceQENAdvanced Science, Vol 8, Iss 22, Pp n/a-n/a (2021) |
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cation doping FeO octahedra metaloxygen bond oxygen vacancy perovskite oxide Science Q |
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cation doping FeO octahedra metaloxygen bond oxygen vacancy perovskite oxide Science Q Huijun Chen Chaesung Lim Mengzhen Zhou Zuyun He Xiang Sun Xiaobao Li Yongjian Ye Ting Tan Hui Zhang Chenghao Yang Jeong Woo Han Yan Chen Activating Lattice Oxygen in Perovskite Oxide by B‐Site Cation Doping for Modulated Stability and Activity at Elevated Temperatures |
description |
Abstract Doping perovskite oxide with different cations is used to improve its electro‐catalytic performance for various energy and environment devices. In this work, an activated lattice oxygen activity in Pr0.4Sr0.6CoxFe0.9−xNb0.1O3−δ (PSCxFN, x = 0, 0.2, 0.7) thin film model system by B‐site cation doping is reported. As Co doping level increases, PSCxFN thin films exhibit higher concentration of oxygen vacancies (Vo••) as revealed by X‐ray diffraction and synchrotron‐based X‐ray photoelectron spectroscopy. Density functional theory calculation results suggest that Co doping leads to more distortion in FeO octahedra and weaker metaloxygen bonds caused by the increase of antibonding state, thereby lowering Vo•• formation energy. As a consequence, PSCxFN thin film with higher Co‐doping level presents larger amount of exsolved particles on the surface. Both the facilitated Vo•• formation and B‐site cation exsolution lead to the enhanced hydrogen oxidation reaction (HOR) activity. Excessive Co doping until 70%, nevertheless, results in partial decomposition of thin film and degrades the stability. Pr0.4Sr0.6(Co0.2Fe0.7Nb0.1)O3 with moderate Co doping level displays both good HOR activity and stability. This work clarifies the critical role of B‐site cation doping in determining the Vo•• formation process, the surface activity, and structure stability of perovskite oxides. |
format |
article |
author |
Huijun Chen Chaesung Lim Mengzhen Zhou Zuyun He Xiang Sun Xiaobao Li Yongjian Ye Ting Tan Hui Zhang Chenghao Yang Jeong Woo Han Yan Chen |
author_facet |
Huijun Chen Chaesung Lim Mengzhen Zhou Zuyun He Xiang Sun Xiaobao Li Yongjian Ye Ting Tan Hui Zhang Chenghao Yang Jeong Woo Han Yan Chen |
author_sort |
Huijun Chen |
title |
Activating Lattice Oxygen in Perovskite Oxide by B‐Site Cation Doping for Modulated Stability and Activity at Elevated Temperatures |
title_short |
Activating Lattice Oxygen in Perovskite Oxide by B‐Site Cation Doping for Modulated Stability and Activity at Elevated Temperatures |
title_full |
Activating Lattice Oxygen in Perovskite Oxide by B‐Site Cation Doping for Modulated Stability and Activity at Elevated Temperatures |
title_fullStr |
Activating Lattice Oxygen in Perovskite Oxide by B‐Site Cation Doping for Modulated Stability and Activity at Elevated Temperatures |
title_full_unstemmed |
Activating Lattice Oxygen in Perovskite Oxide by B‐Site Cation Doping for Modulated Stability and Activity at Elevated Temperatures |
title_sort |
activating lattice oxygen in perovskite oxide by b‐site cation doping for modulated stability and activity at elevated temperatures |
publisher |
Wiley |
publishDate |
2021 |
url |
https://doaj.org/article/ace7fc5cdee54b3ebf69254b6fe30c96 |
work_keys_str_mv |
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