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首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >Fabrication of photostable ternary CdS/MoS2/MWCNTs hybrid photocatalysts with enhanced H-2 generation activity
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Fabrication of photostable ternary CdS/MoS2/MWCNTs hybrid photocatalysts with enhanced H-2 generation activity

机译:具有增强的H-2生成活性的光稳定三元CdS / MoS2 / MWCNTs杂化光催化剂的制备

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This article reports the synthesis and photocatalytic H-2-generation of pristine and CdS-based hybrid, photocatalysts. Acid-treated-multi-walled carbon nanotubes (a-MWCNTs) and colloids of the exfoliated two-dimensional MoS2 nanosheets were used for the preparation of binary CdS/a-MWCNTs and ternary CdS/MoS2/a-MWCNTs nanocomposites. Controlled exfoliation of as-synthesized bulk marigold flower-like MoS2 to few-layer MoS2 nanosheets shows a strong absorption and photoluminescence, indicating an indirect to direct bandgap transition. The visible-light photocatalytic H-2-evolution performance of the ternary nanocomposites was superior to that of the binary and pure photocatalysts. Transient photocurrent results revealed that the ternary nanocomposite exhibits a maximum photocurrent density of 11.12 mA/cm(2), which is 12 times higher than that of pristine CdS. This enhanced H-2-generation performance and photocurrent response is attributed to the CdS/MoS2 heterojunction, Which increases charge-separation efficiency of the composite. Furthermore, the presence of a-MWCNTs, as a co-catalyst/support, accounts for this excellent performance involving electron transfer from photoexcited CdS to MOS2 edges through a-MWCNTs; this transfer results in enhanced charge separation. This enhanced charge-separation efficiency and photostability was demonstrated using a suitable mechanism, which was evident from photocurrent measurements and photoluminescence data. In such ternary hybrids, metal co-catalysts showed H-2-evolution activity with the following order: Pd > Ni > Au > Ag > Cu. This work further highlights the role of MoS2/CNTs p-n junction embedded in CdS which serves as a promising heterojunction that promoted hydrogen production. (C) 2016 Elsevier B.V. All rights reserved.
机译:本文报道了原始和基于CdS的杂化光催化剂的合成和光催化H-2-生成。酸处理的多壁碳纳米管(a-MWCNT)和剥离的二维MoS2纳米片的胶体用于制备二元CdS / a-MWCNT和三元CdS / MoS2 / a-MWCNTs纳米复合材料。合成后的散装万寿菊花状MoS2到少数层MoS2纳米片的受控剥落显示出很强的吸收和光致发光,表明存在间接到直接的带隙跃迁。三元纳米复合材料的可见光光催化H-2-演化性能优于二元和纯光催化剂。瞬态光电流结果表明,三元纳米复合材料的最大光电流密度为11.12 mA / cm(2),比原始CdS高12倍。这种增强的H-2生成性能和光电流响应归因于CdS / MoS2异质结,该异质结提高了复合材料的电荷分离效率。此外,作为助催化剂/载体的a-MWCNT的存在解释了这种出色的性能,涉及电子通过a-MWCNT从光激发的CdS转移到MOS2边缘。这种转移导致电荷分离增强。使用合适的机制证明了这种增强的电荷分离效率和光稳定性,这从光电流测量和光致发光数据中可以明显看出。在这种三元杂化物中,金属助催化剂显示出H-2-演化活性,顺序如下:Pd> Ni> Au> Ag> Cu。这项工作进一步强调了嵌入CdS中的MoS2 / CNTs p-n结的作用,这是一个有希望的异质结,可促进氢的产生。 (C)2016 Elsevier B.V.保留所有权利。

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