Shi Hong-Long, Zou Bin, Li Zi-An, Luo Min-Ting, Wang Wen-Zhong
School of Science, Minzu University of China, Beijing 100081, People's Republic of China, Tel. +861068930809.
Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190, People's Republic of China, Tel. +861082648001.
Beilstein J Nanotechnol. 2019 Jul 18;10:1434-1442. doi: 10.3762/bjnano.10.141. eCollection 2019.
The prominent role of oxygen vacancies in the photocatalytic performance of bismuth tungsten oxides is well recognized, while the underlying formation mechanisms remain poorly understood. Here, we use the transmission electron microscopy to investigate the formation of oxygen vacancies and the structural evolution of BiWO under in situ electron irradiation. Our experimental results reveal that under 200 keV electron irradiation, the breaking of relatively weak Bi-O bonds leads to the formation of oxygen vacancies in BiWO. With prolonged electron irradiation, the reduced Bi cations tend to form Bi clusters on the nanoflake surfaces, and the oxygen atoms are released from the nanoflakes, while the W-O networks reconstruct to form WO. A possible mechanism that accounts for the observed processes of Bi cluster formation and oxygen release under energetic electron irradiation is also discussed.
氧空位在铋钨氧化物光催化性能中所起的重要作用已得到广泛认可,但其潜在的形成机制仍知之甚少。在此,我们利用透射电子显微镜研究了原位电子辐照下铋钨氧化物中氧空位的形成及结构演变。我们的实验结果表明,在200 keV电子辐照下,相对较弱的Bi-O键断裂导致铋钨氧化物中形成氧空位。随着电子辐照时间延长,还原后的Bi阳离子倾向于在纳米片表面形成Bi团簇,氧原子从纳米片中释放出来,同时W-O网络重构形成WO。本文还讨论了一种可能的机制,该机制解释了在高能电子辐照下观察到的Bi团簇形成和氧释放过程。