材料科学
电子能量损失谱
薄膜
价(化学)
外延
电催化剂
氧化物
兴奋剂
光谱学
扫描透射电子显微镜
高分辨率透射电子显微镜
透射电子显微镜
分析化学(期刊)
结晶学
电化学
纳米技术
化学
物理化学
电极
冶金
物理
量子力学
有机化学
光电子学
色谱法
图层(电子)
作者
Le Wang,Krishna Prasad Koirala,Shuhang Wu,Jueli Shi,Hsin-Mei Kao,Andrew Ho,Min‐Ju Choi,Alexander B. C. Mantilla,Dongchen Qi,Anton Tadich,Mark Bowden,Bethany E. Matthews,Hua Zhou,Yang Yang,Chih‐Hung Chang,Zihua Zhu,Chongmin Wang,Yingge Du
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-08-11
卷期号:25 (33): 12719-12727
标识
DOI:10.1021/acs.nanolett.5c03196
摘要
High-entropy oxides (HEOs) offer exceptional compositional flexibility and structural stability, making them promising materials for energy and catalytic applications. Here, we investigate Sr doping effects on B-site cation oxidation states, local composition, and structure in epitaxial La1-xSrx(Cr0.2Mn0.2Fe0.2Co0.2Ni0.2)O3 thin films. X-ray spectroscopies reveal that Sr doping preferentially promotes Cr oxidation from Cr3+ to Cr6+, partially oxidizes Co and Ni, while leaving Mn4+ and Fe3+ unchanged. Atomic-resolution scanning transmission electron microscopy with energy-dispersive X-ray spectroscopy shows pronounced Cr segregation, with depletion at the interface and enrichment at the surface, along with partial amorphization in heavily Sr-doped samples. This segregation is likely driven by oxidation-induced migration of smaller, high-valence Cr cations during growth. These findings highlight the critical interplay between charge compensation, local strain, and compositional fluctuations in HEOs, indicating that precise control over growth conditions is critical for tuning their surface composition and electronic structure toward more robust electrocatalyst design.
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