材料科学
电催化剂
纳米晶材料
循环伏安法
析氧
无定形固体
化学工程
钙钛矿(结构)
电化学
无机化学
氧化物
表层
图层(电子)
催化作用
玻璃碳
表面工程
表面改性
透射电子显微镜
贵金属
纳米技术
氧化锡
X射线吸收光谱法
兴奋剂
纳米颗粒
分析化学(期刊)
扫描电子显微镜
纳米晶
纳米尺度
作者
Takuya Katsumata,Soma Kobata,Yusuke Watase,Ryotaro Aso,Shunsuke Yagi,Yuta Kimura,Koji Amezawa,Takashi Nakamura
标识
DOI:10.1021/acsanm.5c03435
摘要
Perovskite oxides have emerged as promising noble metal-free catalysts for oxygen evolution reaction (OER) in alkaline water electrolysis. Anion doping and surface modification have attracted attention as developing strategies for highly active OER catalyst materials. Here, we report an original electrochemical F-doping technique that simultaneously controls anion composition and nanoscale surface structure to enhance the OER activity. 20 mol % F-doped La 0.5 Sr 0.5 CoO 3-δ (LSC55) samples with different surface states were prepared by changing the current density, which corresponds to the F-doping rate. Low-rate F-doping (60 μA g –1 ) created a thin amorphous surface layer (∼3 nm), while high-rate doping (3000 μA g –1 ) created a thick F-enriched nanocrystalline layer (∼20 nm). Both of the F-doped samples exhibited significantly enhanced OER activity compared to the pristine LSC55 sample. The high-rate sample showed the highest activity among the samples tested in this work. Remarkably, the OER activity of all of the samples was improved with increasing cyclic voltammetry cycles. Scanning transmission electron microscopy analyses revealed progressive amorphization by surface reconstruction in all of the samples during the OER. Soft X-ray absorption spectroscopy revealed that F remained in the reconstructed amorphous surface layer of the F-doped samples even after the OER measurements. These results indicated that the highly active F-containing surface layer was reconstructed on the high-rate F-doped LSC55. This study demonstrates the utility of nanoscale surface engineering by electrochemical anion doping, providing pathways for advanced electrocatalyst development.
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