Direct Z-scheme Heterojunction CeO2@NiAl-LDHs for Photodegradation of Rhodamine B and Photocatalytic Hydrogen Evolution: Performance and Mechanism

被引:3
|
作者
Zhang Lian-Yang [1 ]
Wu Jun-jie [2 ,3 ]
Meng Yue [4 ]
Xia Sheng-Jie [5 ]
机构
[1] Shaoxing Univ, Coll Text & Garment, Key Lab Clean Dyeing & Finishing Technol Zhejiang, Shaoxing 312000, Zhejiang, Peoples R China
[2] Hangzhou Binjiang Real Estate Grp Co Ltd, Hangzhou 310018, Peoples R China
[3] Hangzhou Janda Aoti Real Estate Co Ltd, Hangzhou 310016, Peoples R China
[4] Huzhou Univ, Sch Life Sci, Huzhou 313000, Zhejiang, Peoples R China
[5] Zhejiang Univ Technol, Coll Chem Engn, Hangzhou 310014, Peoples R China
关键词
layered double hydroxides; photocatalysis; heterojunction; build-in electronic field; rhodamine B; hydrogen evolution; LAYERED DOUBLE HYDROXIDES; CATALYTIC PERFORMANCE; DEGRADATION; EFFICIENCY;
D O I
10.11862/CJIC.2021.053
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Herein, a direct Z-scheme heterojunction CeO2@NiAl-LDHs (LDHs=layered double hydroxides) with core-shell structure was constructed. It shows high oxidative degradation of rhodamine B (36.91 mg.g(-1).h(-1)) and hydrogen production by photoreduction (14.08 mmol.g(-1).h(-1)). Density functional theory (DFT) calculation shows that there was a built-in electric field in the heterojunction, which promotes the electron transfer from LDHs to CeO2. Surface photovoltage spectroscopy (SPV) and transient photovoltage spectra (TPV) confirmed that the presence of heterojunction accelerated the number of electron transfer, and the recombination of electron and hole was obviously inhibited, so as to participate in oxidation and reduction more. Thus, it makes CeO2@NiAl-LDHs heterojunction photocatalyst have high photocatalytic activity for photodegr , adation of rhodamine B and hydrogen production from water.
引用
收藏
页码:316 / 326
页数:11
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