Ingenious design of ternary hollow nanosphere with shell hierarchical tandem heterojunctions toward optimized Visible-light photocatalytic reduction of U(VI)

光催化 三元运算 异质结 材料科学 化学工程 可见光谱 吸附 纳米技术 化学 光电子学 催化作用 物理化学 有机化学 计算机科学 工程类 程序设计语言
作者
Zhimin Dong,Zhibin Zhang,Ting Wang,Dongling Zeng,Zhongping Cheng,Yingcai Wang,Xiaohong Cao,Youqun Wang,Yunhai Liu,Xiaolin Fan
出处
期刊:Separation and Purification Technology [Elsevier BV]
卷期号:286: 120418-120418 被引量:37
标识
DOI:10.1016/j.seppur.2021.120418
摘要

TiO2 based photocatalytic reduction has been regarded as a promising technology for flexibility of uranium recovery from seawater, however, the use of sacrificing agents and protection gas are two major challenges for practical application. Herein, a ternary hybrid TiO2@[email protected] hollow nanosphere (TCA) was designed and synthesized for highly efficient photocatalytic reduction of U(VI). The designed ternary hollow nanosphere is composed of double heterojunctions: type-Z heterojunction generated between TiO2 with CdS and metal–semiconductor junction between CdS and Au NPs, which is contributive for the spatial separation and diffusion of photogenerated charges. Therefore, compared with loaded Pt or GOQDs, the superior photocatalytic reduction efficiency of TCA2 (Au NPs content of 0.8%) for U(VI) achieves 99.7% within 25 min and remains unchanged after five cycles in the presence of 3 mmol·L-1 NaHCO3 under air condition. Its photoreduction rate constant is 5.7 and 4.1 times as much as the CdS and hollow TiO2@CdS nanosphere. Additionally, in the absence of any protective gases and holes sacrificial agent, the soluble U(VI) adsorbed on the photocatalyst is reduced to insoluble α-U3O8 by photogenerated electrons and superoxide radical, which has been recognized as one of the most effective strategy for the separation and recovery U(VI) from polluted environment.
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