Reconstruction of the surface Bi3+ oxide layer on Bi2O2CO3: Facilitating electron transfer for enhanced photocatalytic degradation performance of antibiotics in water

被引:0
作者
Fang, Yu [1 ]
Hong, Liu [1 ]
Dai, Yang [1 ]
Xiang, Qing [1 ]
Zhang, Nianbing [1 ]
Li, Jiaojiao [1 ]
机构
[1] Guizhou Normal Univ, Sch Mat & Construct Engn, Guiyang 550025, Peoples R China
关键词
Tetracycline hydrochloride; Catalytic system; Oxidized Bi3+ structure; Charge transport; MICROSPHERES; EFFICIENT; INACTIVATION; NANOSHEETS;
D O I
10.1016/j.ceramint.2024.10.132
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The advancement and meticulous design of functional photocatalysts exhibiting exceptional photocatalytic redox activity represent a pivotal approach to mitigating the dual challenges of environmental pollution and energy scarcity. In this study, we elucidate the construction of a Bi2O2CO3 catalytic system capable of inhibiting oxidative electron transfer through the attenuation of homogeneous Bi0 particle formation, achieved through the judicious modulation of solvent ratios. This innovative architecture possesses a distinctive active site and enhances interfacial Bi-O electron transfer pathways via exposure to oxidized Bi3+. Upon photoexcitation, the Bi2O2CO3 catalytic system undergoes structural distortions in its excited state that facilitate forbidden radiative relaxation, thereby fostering long-lived charge separation states. Remarkable catalytic activity was demonstrated in the remediation of pollutants, encompassing auto-oxidation and the catalytic degradation of superoxide radicals (center dot O2-) and holes (h+). Notably, the effective degradation of tetracycline hydrochloride (TCH) in aqueous media reached an impressive 86 % under simulated visible light irradiation, accompanied by a reaction rate constant 3.08 times superior to that of the 5-Bi/Bi2O2CO3 counterpart. Theoretical analyses revealed that the oxidized state of Bi2O2CO3 exhibits a crystal structure with significant electron trapping capability, undergoing pronounced apparent relaxation phenomena on its surface while demonstrating an enhanced adsorption affinity for H2O and O2. The potential degradation mechanisms were rigorously investigated through High-performance liquid chromatography (HPLC-MS), elucidating the photodegradation pathways and intermediates of TC. This work may serve as a distinct paradigm for the rational design of novel photocatalysts aimed at fostering sustainable environmental remediation and advancing energy innovation.
引用
收藏
页码:52788 / 52796
页数:9
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