光催化
氧化剂
光化学
纳米颗粒
电子转移
材料科学
吸附
降级(电信)
羟基自由基
化学
电化学
锆
催化作用
化学工程
激进的
无机化学
纳米技术
有机化学
电极
物理化学
电信
计算机科学
工程类
作者
Tianqiao Yang,Tianzhu Ma,Lixia Yang,Weili Dai,Shuqu Zhang,Shenglian Luo
标识
DOI:10.1016/j.apsusc.2021.148928
摘要
In situ growth of UiO-66 on zirconium (Zr) substrate was performed to construct a self-supporting photocatalyst through a mild electrochemical method with 1,4-benzenedicarboxylic acid as organic ligand. The as-prepared three-dimensional UiO-66 nanoparticles have abundant pores and corners, providing an ideal interface with large surface area for subsequent decoration of Pd nanoparticles (NPs). The resultant Pd/UiO-66 can efficiently degrade tetracycline (TC) via hydroxyl radical (•OH) and superoxide radical (•O2–) governing pathway, exhibiting outstanding photocatalytic performance due to fast mass transport endowed by well-dispersed Pd NPs. Under the simulated sunlight irradiation, the electrons of UiO-66 are transferred to Pd NPs, promoting the effective separation of photogenerated electron-hole pairs. Transient fluorescence spectra show that the lifetime of electrons is decreased from 5.08 ns to 3.60 ns with the assistance of Pd NPs, indicating that photogenerated electrons can transfer rapidly. Electrons gathering on the Pd/UiO-66 can react with O2 to produce •O2–, and plenty of holes left in UiO-66 host generate •OH by oxidizing the adsorbed H2O, producing abundant active species for photocatalytic degradation of tetracycline.
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