Tuning proton-coupled electron transfer by crystal orientation for efficient water oxidization on double perovskite oxides

Yunmin Zhu, Zuyun He, YongMan Choi*, Huijun Chen, Xiaobao Li, Bote Zhao, Yi Yu, Hui Zhang, Kelsey A. Stoerzinger, Zhenxing Feng, Yan Chen*, Meilin Liu*

*此作品的通信作者

研究成果: Article同行評審

98 引文 斯高帕斯(Scopus)

摘要

Developing highly efficient and cost-effective oxygen evolution reaction (OER) electrocatalysts is critical for many energy devices. While regulating the proton-coupled electron transfer (PCET) process via introducing additive into the system has been reported effective in promoting OER activity, controlling the PCET process by tuning the intrinsic material properties remains a challenging task. In this work, we take double perovskite oxide PrBa0.5Sr0.5Co1.5Fe0.5O5+δ (PBSCF) as a model system to demonstrate enhancing OER activity through the promotion of PCET by tuning the crystal orientation and correlated proton diffusion. OER kinetics on PBSCF thin films with (100), (110), and (111) orientation, deposited on single crystal LaAlO3 substrates, were investigated using electrochemical measurements, density functional theory (DFT) calculations, and synchrotron-based near ambient X-ray photoelectron spectroscopy. The results clearly show that the OER activity and the ease of deprotonation depend on orientation and follow the order of (100) > (110) > (111). Correlated with OER activity, proton diffusion is found to be the fastest in the (100) film, followed by (110) and (111) films. Our results point out a way of boosting PCET and OER activity, which can also be successfully applied to a wide range of crucial applications in green energy and environment.
原文English
文章編號4299
頁數10
期刊Nature Communications
11
發行號1
DOIs
出版狀態Published - 27 8月 2020

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