Enhanced photocatalytic Cr(VI) reduction and H2 production of CdSe quantum dots supported on Co-encapsulated N-doped carbon

被引:7
|
作者
Chen, Meng [1 ,2 ]
Fang, Huawei [1 ,2 ]
Wang, Chao [1 ,2 ]
Xu, Jixiang [1 ,2 ]
Wang, Lei [1 ,3 ]
机构
[1] Qingdao Univ Sci & Technol, Key Lab Ecochem Engn, Taishan Scholar Advantage & Characterist Disciplin, Qingdao 266042, Peoples R China
[2] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, Qingdao 266042, Peoples R China
[3] Qingdao Univ Sci & Technol, Coll Environm & Safety Engn, Qingdao 266042, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
CdSe QDs; Co nanoparticle; N-doped carbon; Cr(VI) reduction; H-2; evolution; METAL-ORGANIC FRAMEWORKS; PERSPECTIVES; CONVERSION; COMPOSITE; COBALT; HOLLOW;
D O I
10.1016/j.jtice.2023.104798
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Background: Solar-driven water splitting is regarded as one promising green way to produce H-2. Photo-reduction of hexavalent chromium (Cr(VI)) to hypotoxic Cr(III) can control the Cr(VI)-induced pollution. A key in these processes is to develop a photocatalyst with high specific surface area, good light absorption and efficient charge carrier separation. Methods: A Co-encapsulated N-doped carbon (Co@NC) was prepared by pyrolysis ZIF-8@ZIF-67 precursor to modify CdSe quantum dots (QDs). The obtained catalyst was used to reduce Cr(VI) and split water under visible light irradiation. Significant findings: Modification CdSe with Co@NC made obtained Co@NC/CdSe possessing enhanced visible-light absorption and photoexcited charge separation. The optimal 2%Co@NC/CdSe exhibited the excellent Cr (VI) reduction performance with a rate constant of 0.28 min(-1) in the absence of sacrificial agent, as well as high H-2 evolution rate of 6.48 mmol g(-1) h(-1) in 10% lactic acid solution. The H2O2 and electrons were the active species to reduce Cr(VI). This work gives a beneficial insight for improving the photocatalytic activity of QDs.
引用
收藏
页数:7
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