光催化
羟基自由基
化学
X射线光电子能谱
羟基化
煅烧
光化学
偶极子
氧气
激进的
催化作用
化学工程
有机化学
工程类
酶
作者
Zhuang Yang,Zengshou Qiang,Jian Wang,Yajun Wang,Wenqing Yao
标识
DOI:10.1002/sstr.202300339
摘要
The hydroxyl groups generated by hydrolysis are grafted onto the surface of BiPO 4 , and a stable surface hydroxylation structure is formed during the subsequent calcination process. This would facilitate the formation of a new hydroxyl functional structure on the surface of the parent photocatalyst without damaging its intrinsic structure. Synchronous illumination X‐Ray photoelectron spectroscopy shows that the hydroxyl functional ultrafine BiPO 4 can realize the conversion of defective oxygen to lattice oxygen, which is more conducive in improving the photocatalytic efficiency. The process of filling hydroxyl oxygen vacancies and forming a stable structure is explored using in‐ situ infrared spectroscopy. The induced dipole moment promotes the separation of photogenerated electron–hole pairs, which is beneficial for the enhancement of photocatalytic activity. The dipole moment of the hydroxyl functional‐modified ultrafine BiPO 4 is −1.409 D compared to −1.385 D for ordinary BiPO 4 . The results of this study indicate that hydroxyl functional structure and reduced sample granularity are effective strategies to improve the photocatalytic performance of BiPO 4 .
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