A porous TiC supported nanostructured complex metal oxide ceramic electrode for oxygen evolution reaction

Developing low-cost and high-performance electrodes with a customized size is greatly demanded to satisfy the industrial requirement of electrochemical water splitting. To meet this challenge, a novel binder-free electrode consisted of perovskite Sr2Fe1.4Ni0.1Mo0.5O6-δ (SFNMO) nanofibers or spinel N...

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Main Authors: Yang, Jianye, Wu, Kai, Li, Xing, Wang, Xuejiao, Pi, Guangguang, Fang, Wei, Yan, Qingyu
Other Authors: School of Materials Science and Engineering
Format: Article
Language:English
Published: 2023
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Online Access:https://hdl.handle.net/10356/172305
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1723052023-12-05T06:57:57Z A porous TiC supported nanostructured complex metal oxide ceramic electrode for oxygen evolution reaction Yang, Jianye Wu, Kai Li, Xing Wang, Xuejiao Pi, Guangguang Fang, Wei Yan, Qingyu School of Materials Science and Engineering Engineering::Materials Ceramic Electrode Electrocatalyst Developing low-cost and high-performance electrodes with a customized size is greatly demanded to satisfy the industrial requirement of electrochemical water splitting. To meet this challenge, a novel binder-free electrode consisted of perovskite Sr2Fe1.4Ni0.1Mo0.5O6-δ (SFNMO) nanofibers or spinel NiCo2O4 (NCO) nanosheets tightly bonded on a porous TiC substrate has been developed to catalyze the oxygen evolution reaction in alkaline water electrolysis. The optimal SFNMO/TiC electrode requires a stable overpotential of ∼380 mV to achieve a current density of 30 mA cm−2 within 20 h of operation. The competitive OER performance of such electrode can be attributed to its unique large finger-like straight pore structure, which favors the mass transfer of electrolyte solution as well as produced oxygen bubbles. Furthermore, the strong adhesion between metal oxide catalysts and TiC substrate is derived from the interfacial reaction (form a TiCxOy solid solution), thus lowering the contact resistance of catalyst/substrate interface and promoting the charge transfer kinetics of electrodes, which leads to an outstanding catalytic performance. This work was financially supported by the National Natural Science Foundation of China (No. 22208171), Ningbo Natural Science Foundation (No. 20221JCGY010458), Ningbo Yongjiang Talent Introduction Programme (No. 2021A-141-G). 2023-12-05T06:57:57Z 2023-12-05T06:57:57Z 2023 Journal Article Yang, J., Wu, K., Li, X., Wang, X., Pi, G., Fang, W. & Yan, Q. (2023). A porous TiC supported nanostructured complex metal oxide ceramic electrode for oxygen evolution reaction. Ceramics International, 49(16), 27662-27667. https://dx.doi.org/10.1016/j.ceramint.2023.05.275 0272-8842 https://hdl.handle.net/10356/172305 10.1016/j.ceramint.2023.05.275 2-s2.0-85161345867 16 49 27662 27667 en Ceramics International © 2023 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Materials
Ceramic Electrode
Electrocatalyst
spellingShingle Engineering::Materials
Ceramic Electrode
Electrocatalyst
Yang, Jianye
Wu, Kai
Li, Xing
Wang, Xuejiao
Pi, Guangguang
Fang, Wei
Yan, Qingyu
A porous TiC supported nanostructured complex metal oxide ceramic electrode for oxygen evolution reaction
description Developing low-cost and high-performance electrodes with a customized size is greatly demanded to satisfy the industrial requirement of electrochemical water splitting. To meet this challenge, a novel binder-free electrode consisted of perovskite Sr2Fe1.4Ni0.1Mo0.5O6-δ (SFNMO) nanofibers or spinel NiCo2O4 (NCO) nanosheets tightly bonded on a porous TiC substrate has been developed to catalyze the oxygen evolution reaction in alkaline water electrolysis. The optimal SFNMO/TiC electrode requires a stable overpotential of ∼380 mV to achieve a current density of 30 mA cm−2 within 20 h of operation. The competitive OER performance of such electrode can be attributed to its unique large finger-like straight pore structure, which favors the mass transfer of electrolyte solution as well as produced oxygen bubbles. Furthermore, the strong adhesion between metal oxide catalysts and TiC substrate is derived from the interfacial reaction (form a TiCxOy solid solution), thus lowering the contact resistance of catalyst/substrate interface and promoting the charge transfer kinetics of electrodes, which leads to an outstanding catalytic performance.
author2 School of Materials Science and Engineering
author_facet School of Materials Science and Engineering
Yang, Jianye
Wu, Kai
Li, Xing
Wang, Xuejiao
Pi, Guangguang
Fang, Wei
Yan, Qingyu
format Article
author Yang, Jianye
Wu, Kai
Li, Xing
Wang, Xuejiao
Pi, Guangguang
Fang, Wei
Yan, Qingyu
author_sort Yang, Jianye
title A porous TiC supported nanostructured complex metal oxide ceramic electrode for oxygen evolution reaction
title_short A porous TiC supported nanostructured complex metal oxide ceramic electrode for oxygen evolution reaction
title_full A porous TiC supported nanostructured complex metal oxide ceramic electrode for oxygen evolution reaction
title_fullStr A porous TiC supported nanostructured complex metal oxide ceramic electrode for oxygen evolution reaction
title_full_unstemmed A porous TiC supported nanostructured complex metal oxide ceramic electrode for oxygen evolution reaction
title_sort porous tic supported nanostructured complex metal oxide ceramic electrode for oxygen evolution reaction
publishDate 2023
url https://hdl.handle.net/10356/172305
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