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Preparation of Bi2MoO6/Ti3C2 MXene heterojunction photocatalysts for fast tetracycline degradation and Cr(VI) reduction
Inorganic Chemistry Frontiers ( IF 7 ) Pub Date : 2020-06-16 , DOI: 10.1039/d0qi00540a
Danxia Zhao 1, 2, 3, 4 , Chun Cai 1, 2, 3, 4
Affiliation  

In this work, a new artificial photocatalytic system has been designed based on the two-dimensional (2D) heterojunction of bismuth molybdate (Bi2MoO6)/Ti3C2 MXenes. The strong interface contact and short charge transport distance between Bi2MoO6 and Ti3C2 ensure extraordinary surface and interface charge transfer abilities. The optimized photocatalyst Bi2MoO6/Ti3C2 exhibited the highest photocatalytic activity, and its removal rates for tetracycline hydrochloride (TC) and heavy metal ion Cr(VI) were about 8.8 and 11.2 times that of pristine Bi2MoO6, respectively. DFT simulation calculations revealed that the stronger interaction promotes the polarization charge distribution of Bi2MoO6/Ti3C2, thereby further enhancing the separation and transfer of photoinduced electrons and holes. Meanwhile, Bi2MoO6/Ti3C2 could provide new adsorption sites, which are conducive to the interaction between pollutant molecules and the catalyst. This indicates that efficient charge separation and excellent adsorption in heterojunction photocatalysts play a key role in improving photocatalytic performance.

中文翻译:

用于快速四环素降解和Cr(VI)还原的Bi2MoO6 / Ti3C2 MXene异质结光催化剂的制备

在这项工作中,基于钼酸铋(Bi 2 MoO 6)/ Ti 3 C 2 MXenes的二维(2D)异质结,设计了一种新的人工光催化系统。Bi 2 MoO 6和Ti 3 C 2之间的牢固的界面接触和短的电荷传输距离确保了出色的表面和界面电荷转移能力。优化的光催化剂Bi 2 MoO 6 / Ti 3 C 2表现出最高的光催化活性,并且对四环素盐酸盐(TC)和重金属离子Cr(VI)分别是原始Bi 2 MoO 6的8.8倍和11.2倍。DFT模拟计算表明,较强的相互作用促进了Bi 2 MoO 6 / Ti 3 C 2的极化电荷分布,从而进一步增强了光致电子和空穴的分离和转移。同时,Bi 2 MoO 6 / Ti 3 C 2可以提供新的吸附位,有利于污染物分子与催化剂之间的相互作用。这表明异质结光催化剂中有效的电荷分离和出色的吸附作用在改善光催化性能方面起着关键作用。
更新日期:2020-07-28
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