Constructing highly active surface-nanostructured core/bi-shell La1.2Sr0.8Ni0.5Mn0.5O4+δ cathode for protonic ceramic fuel cells

被引:30
作者
Hou, Jie [1 ,2 ]
Gong, Junyi [1 ]
Luo, Jing-Li [2 ]
机构
[1] Univ South China, Sch Resource Environm & Safety Engn, Hengyang 421001, Peoples R China
[2] Shenzhen Univ, Coll Mat Sci & Engn, Guangdong Res Ctr Interfacial Engn Funct Mat, Key Lab Polymer Sci & Technol, Shenzhen 518055, Peoples R China
关键词
PCFC; Core; bi-shell; La1; 2Sr0; 8Ni0; 5Mn0; Dopant segregation; Proton migration; RUDDLESDEN-POPPER SERIES; ELECTROCHEMICAL PERFORMANCE; ELECTRICAL-PROPERTIES; SYSTEM LA2-XSRXNIO4+DELTA; OXYGEN NONSTOICHIOMETRY; CATALYTIC-OXIDATION; COMPOSITE CATHODES; PEROVSKITE OXIDES; STATE; STABILITY;
D O I
10.1016/j.cej.2023.141459
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Development of highly-active electrodes is essential yet challenging for the designs of low-temperature protonic ceramic fuel cells (LT-PCFCs). Herein, a core/bi-shell surface-nanostructure on base of K2NiF4-type La1.2Sr0.8Ni0.5Mn0.5O4+delta (LSNM) is developed. With the occurence of dopant segregation during atom arrange-ment in powder calcination process, the core/bi-shell is formed, accompanied by the formations of B-site defi-cient K2NiF4 phase and perovskite separately existing in two shell-regions, which could promote oxygen reduction and proton migration, thus extending the cathode reaction. The DFT simulation also provides further evidence of easily proton transfer for facilely rotating and jumping. This unique LSNM cathode attains an impressive power approaching 1.1 W cm-2 at 650 degrees C, outperforming other Ln2NiO4-based cathodes in the literature. On balance, the predominant cell performance coupled with good durability suggests that the core/bi-shell LSNM is a preferential alternative for LT-PCFCs. This work provides a new strategy to design highly-active electrode materials via decorating surface structure, which would be beneficial to the related electrocatalytic fields.
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页数:11
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