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Selective Partial Substitution of B‐Site with Phosphorus in Perovskite Electrocatalysts for Highly Efficient Oxygen Evolution Reaction
Author(s) -
Zhang Wenhua,
Zhou Wulan,
Zhang Zhenbao,
Chen Zilong,
Tan Shaozao,
Chen Dengjie
Publication year - 2019
Publication title -
chemnanomat
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.947
H-Index - 32
ISSN - 2199-692X
DOI - 10.1002/cnma.201800387
Subject(s) - perovskite (structure) , valence (chemistry) , oxygen evolution , oxygen , inorganic chemistry , doping , chemistry , catalysis , conductivity , materials science , crystallography , electrochemistry , electrode , biochemistry , optoelectronics , organic chemistry
Perovskite oxides are promising electrocatalysts for the oxygen evolution reaction (OER). However, the activity and stability of perovskite oxides still needs to be improved to efficiently utilize renewable and clean energy resources. Herein, we selectively introduced phosphorus (P) into SrCo 0.8 Fe 0.2 O 3‐δ (SCF) to form modified perovskite oxides, i. e., SrCo 0.8 Fe 0.15 P 0.05 O 3‐δ , SrCo 0.75 Fe 0.2 P 0.05 O 3‐δ and Sr(Co 0.8 Fe 0.2 ) 0.95 P 0.05 O 3‐δ . An improved OER activity and stability compared to un‐doped SCF was clearly observed. Meanwhile, the specific surface area, oxygen vacancy content and electronic conductivity increased due to the P doping. Moreover, a lower valence state of B‐site cations induced by the high‐valence P 5+ was detected, which may contribute to the better activity and stability. Among them, the dual‐site substitution to form Sr(Co 0.8 Fe 0.2 ) 0.95 P 0.05 O 3‐δ stands out when evaluating the activity and stability in alkaline solution. The results suggest that the P doping could be an effective strategy to develop perovskite electrocatalysts with high electrocatalytic activity and stability.