TY - JOUR
T1 - An excellent OER electrocatalyst of cubic SrCoO3-δ prepared by a simple F-doping strategy
AU - Wang, Wanhua
AU - Yang, Yi
AU - Huan, Daoming
AU - Wang, Likun
AU - Shi, Nai
AU - Xie, Yun
AU - Xia, Changrong
AU - Peng, Ranran
AU - Lu, Yalin
N1 - Funding Information:
This work was nancially supported by the Natural Science Foundation of China (51872276), the National Key Research and Development Program of China (2016YFA0401004), the External Cooperation Program of BIC, Chinese Academy of Sciences (211134KYSB20130017), the Hefei Science Center CAS (2016HSC-IU004), and the Fundamental Research Funds for the Central Universities (WK3430000004). We acknowledge the Supercomputing Center at the University of Science and Technology of China (USTC) for providing computational resources.
Publisher Copyright:
© 2019 The Royal Society of Chemistry.
PY - 2019
Y1 - 2019
N2 - Driven by the increasing global energy demand, the development of innovative energy conversion and storage systems is becoming more and more urgent. As one of the attractive means, water splitting has attracted widespread attention because of its great potential in storing electricity in the form of chemical fuel which also makes it a promising solution to the utilization of non-grid electricity generated by solar or wind. The oxygen evolution reaction (OER) is generally deemed as the key rate-limiting step of water splitting, and thus studying efficient OER electrocatalysts with a low overpotential and good stability is of vital importance. Here, we successfully prepared an OER catalyst with excellent electrochemical performance through a simple anion doping. Firstly, a stable cubic perovskite SrCoO3-δ was prepared by anion F-doping instead of traditional A and/or B site doping. Secondly, SrCoO2.85-δF0.15 demonstrates excellent OER activity superior to its parent hexagonal compound H-Sr2Co2O5 and those perovskites prepared via complicated A- and/or B-site doping. DFT calculations and XPS investigations reveal that the cubic structure and the highly oxidative oxygen species (O22-/O-) via F- doping jointly contribute to the better OER properties of SrCoO2.85-δF0.15. Our work brings forth a promising strategy to stabilize cubic structures from hexagonal ones via a simple anion doping strategy, which may open a new avenue for the development of even more effective OER catalysts and may be applied in many other fields related to structure transformation, in addition to energy and catalysis fields.
AB - Driven by the increasing global energy demand, the development of innovative energy conversion and storage systems is becoming more and more urgent. As one of the attractive means, water splitting has attracted widespread attention because of its great potential in storing electricity in the form of chemical fuel which also makes it a promising solution to the utilization of non-grid electricity generated by solar or wind. The oxygen evolution reaction (OER) is generally deemed as the key rate-limiting step of water splitting, and thus studying efficient OER electrocatalysts with a low overpotential and good stability is of vital importance. Here, we successfully prepared an OER catalyst with excellent electrochemical performance through a simple anion doping. Firstly, a stable cubic perovskite SrCoO3-δ was prepared by anion F-doping instead of traditional A and/or B site doping. Secondly, SrCoO2.85-δF0.15 demonstrates excellent OER activity superior to its parent hexagonal compound H-Sr2Co2O5 and those perovskites prepared via complicated A- and/or B-site doping. DFT calculations and XPS investigations reveal that the cubic structure and the highly oxidative oxygen species (O22-/O-) via F- doping jointly contribute to the better OER properties of SrCoO2.85-δF0.15. Our work brings forth a promising strategy to stabilize cubic structures from hexagonal ones via a simple anion doping strategy, which may open a new avenue for the development of even more effective OER catalysts and may be applied in many other fields related to structure transformation, in addition to energy and catalysis fields.
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U2 - 10.1039/c9ta03099a
DO - 10.1039/c9ta03099a
M3 - Article
AN - SCOPUS:85065918496
SN - 2050-7488
VL - 7
SP - 12538
EP - 12546
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 20
ER -