Ag2S/CdS-Heterostructured Nanorod Synthesis by L-Cysteine-Mediated Reverse Microemulsion Method

被引:2
|
作者
Liu, Jing [1 ]
Shan, Dongyu [1 ]
Zhang, Tingting [1 ]
Li, Yunhe [1 ]
Wang, Ran [1 ]
Liu, Meiying [1 ]
机构
[1] Liaoning Normal Univ, Sch Chem & Chem Engn, Dalian 116029, Liaoning, Peoples R China
来源
CHEMISTRYSELECT | 2019年 / 4卷 / 35期
基金
中国国家自然科学基金;
关键词
Metal sulfide; L-cysteine; reverse microemulsion; photocatalytic H-2-evolution; visible light; PHOTOCATALYTIC HYDROGEN-PRODUCTION; H-2; EVOLUTION; CDS; COCATALYST; EXCHANGE; GENERATION; SURFACE;
D O I
10.1002/slct.201902171
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Highly-efficient charge separation is of significant importance for the improvement of photocatalytic performance towards solar H-2 production. Here, Ag2S/CdS hetero nanorods with intimate contact were fabricated at ambient temperature by L-cysteine-assisted method involving a Triton X-100/cyclohexane/hexanol/water quaternary W/O reverse microemulsion process. The formation of Ag2S/CdS nanojunction is verified by XRD, TEM, HRTEM, EDS as well as XPS technique, while the photocatalytic activity of Ag2S/CdS hetero nanorod is assessed by water photo-reduction to H-2 in the presence of S2-/SO32- as sacrificial agents under visible-light irradiation. It is demonstrated that Ag2S/CdS hetero nanorod exhibits an about 480-fold enhancement in the H-2-evolution rate relative to that of pristine CdS. In combination with UV-vis absorption and photoluminescence spectra, the synergistic effects stemmed from the extended light-absorption and facilitated charge-separation between the interfaces largely contribute to boosting the photocatalytic H-2-evolution activity of CdS nanorod. This work offers a novel strategy to in-situ construct CdS-based heterostructured photocatalysts with good performance and low cost.
引用
收藏
页码:10219 / 10224
页数:6
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