Phase transition guided V2O5/β-Bi2O3 Z-scheme heterojunctions for efficient photocatalytic Hg0 oxidation

被引:4
|
作者
Xie, Yibing [1 ]
Wu, Huihui [1 ]
Luo, Jianfei [1 ]
Zhang, Shao [1 ]
Wang, Langlang [1 ]
Wang, Xueqian [1 ]
Ma, Yixing [1 ]
Ning, Ping [1 ]
机构
[1] Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China
基金
中国国家自然科学基金;
关键词
Thermal phase transition; Photocatalytic Hg-0 oxidation; Vanadium loading; Z-Scheme heterojunction; V2O5/beta-Bi2O3; nanosheets; CHARGE-TRANSFER; FLUE-GAS; IN-SITU; ELEMENTAL MERCURY; OXYGEN VACANCY; DOPED TIO2; REMOVAL; SURFACE; FTIR; FE;
D O I
10.1016/j.seppur.2023.125318
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The incorporation of vanadium during the synthesis process induced a spontaneous and complete thermal phase transition from alpha-Bi2O3 to beta-Bi2O3. This phase transition facilitated the development of intrinsic electric field at the interface between V2O5 and beta-Bi2O3, consequently establishing a novel carrier transfer pathway. As a result, the fabricated V2O5/beta-Bi2O3 heterojunction exhibited an outstanding removal efficiency of over 98 % for gaseous mercury (Hg-0) under UV light, and this efficiency of 95.0 % even after 35 h of testing. Introducing vanadium enhanced the light absorption capacity in the ultraviolet region and effectively separated photoinduced charge carriers. As revealed by density functional theory calculations, the photoinduced electron-hole transfer in the V2O5/beta-Bi2O3 heterojunction followed the Z-scheme mechanism. This mechanism significantly contributed to the long-term stability of photocatalytic Hg-0 removal, even when H2O and NO were present. This study presents a novel material composited by a thermal phase transition technique, aimed at the highly effective and green removal of Hg-0 in the environment.
引用
收藏
页数:11
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