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...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: 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
Formato: article
Lenguaje:EN
Publicado: Wiley 2021
Materias:
Q
Acceso en línea:https://doaj.org/article/ace7fc5cdee54b3ebf69254b6fe30c96
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:ace7fc5cdee54b3ebf69254b6fe30c96
record_format dspace
spelling 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 FeO octahedra and weaker metaloxygen 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 dopingFeO octahedrametaloxygen bondoxygen vacancyperovskite oxideScienceQENAdvanced Science, Vol 8, Iss 22, Pp n/a-n/a (2021)
institution DOAJ
collection DOAJ
language EN
topic cation doping
FeO octahedra
metaloxygen bond
oxygen vacancy
perovskite oxide
Science
Q
spellingShingle cation doping
FeO octahedra
metaloxygen 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 FeO octahedra and weaker metaloxygen 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 AT huijunchen activatinglatticeoxygeninperovskiteoxidebybsitecationdopingformodulatedstabilityandactivityatelevatedtemperatures
AT chaesunglim activatinglatticeoxygeninperovskiteoxidebybsitecationdopingformodulatedstabilityandactivityatelevatedtemperatures
AT mengzhenzhou activatinglatticeoxygeninperovskiteoxidebybsitecationdopingformodulatedstabilityandactivityatelevatedtemperatures
AT zuyunhe activatinglatticeoxygeninperovskiteoxidebybsitecationdopingformodulatedstabilityandactivityatelevatedtemperatures
AT xiangsun activatinglatticeoxygeninperovskiteoxidebybsitecationdopingformodulatedstabilityandactivityatelevatedtemperatures
AT xiaobaoli activatinglatticeoxygeninperovskiteoxidebybsitecationdopingformodulatedstabilityandactivityatelevatedtemperatures
AT yongjianye activatinglatticeoxygeninperovskiteoxidebybsitecationdopingformodulatedstabilityandactivityatelevatedtemperatures
AT tingtan activatinglatticeoxygeninperovskiteoxidebybsitecationdopingformodulatedstabilityandactivityatelevatedtemperatures
AT huizhang activatinglatticeoxygeninperovskiteoxidebybsitecationdopingformodulatedstabilityandactivityatelevatedtemperatures
AT chenghaoyang activatinglatticeoxygeninperovskiteoxidebybsitecationdopingformodulatedstabilityandactivityatelevatedtemperatures
AT jeongwoohan activatinglatticeoxygeninperovskiteoxidebybsitecationdopingformodulatedstabilityandactivityatelevatedtemperatures
AT yanchen activatinglatticeoxygeninperovskiteoxidebybsitecationdopingformodulatedstabilityandactivityatelevatedtemperatures
_version_ 1718425690117767168