萤石
光催化
纳米晶材料
微晶
材料科学
金红石
分解水
带隙
氢
无机化学
化学工程
化学
纳米技术
冶金
光电子学
催化作用
有机化学
工程类
生物化学
作者
Srijita Nundy,Dalibor Tatar,Jelena Bijelić,Habib Ullah,Aritra Ghosh,Tapas K. Mallick,Rafael Meinusch,Bernd Smarsly,Asif Ali Tahir,Igor Djerdj
标识
DOI:10.1002/adsu.202200067
摘要
Abstract Five different rare‐earth‐based nanocrystalline high entropy oxides (HEOs) with fluorite structure and average crystallite sizes between 6 and 8 nm are prepared and their photocatalytic behavior toward azo dye degradation and photoelectrochemical water splitting for hydrogen generation is examined. The cationic site in the fluorite lattice consists of five equimolar elements selected from the group of rare‐earth elements including La, Ce, Pr, Eu, and Gd and second‐row transition metals, Y and Zr. The studied HEOs exhibit bandgaps in the range from 1.91 to 3.0 eV and appropriate valence and conduction bands for water splitting. They reveal high photocatalytic activity that is mostly attributed to the accessibility of more photocatalytic active sites, which provide radicals responsible for the azo dye degradation. The materials successfully produce hydrogen by photocatalytic water splitting, suggesting the potential of HEOs as new photocatalysts. The photocatalytic performances of all studied HEOs outperform the single fluorite oxides or equivalent mixed oxides. The Ce 0.2 Zr 0.2 La 0.2 Pr 0.2 Y 0.2 O 2 (CZLPY) engender hydrogen in 9.2 µmol mg −1 per hour that is much higher content than for pristine CeO 2 material which amounts to 0.8 µmol mg −1 per hour.
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