分层 C@ZnCdS/ZnS/MoS2 的光稳定性和可见光驱动的光活性增强

Qihong Lu, Ning Yang, Lei Zuo, Wenjian Fang, Jing Dong, Xianghua Zeng
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摘要

硫化锌镉固体(ZnxCd1-xS)相关复合材料因其可调带隙和较强的可见光吸收范围而在光催化制氢领域受到极大关注。但硫化物基金属材料普遍存在光腐蚀问题。因此,构建具有高效活性和光稳定性的光催化剂用于制氢就显得尤为重要。在此,我们先后制备了ZnCdS/ZnS(ZCS/ZS)异质结构、用MoS2量子点装饰ZCS/ZS的ZnCdS/ZnS/MoS2(ZCS/ZS/M)异质结构,然后得到了用碳层封装ZCS/ZS和ZCS/ZS/M的x-C@ZCS/ZS和x-C@ZCS/ZS/M异质结构。光催化制氢的性能表明,0.05-C@ZCS/ZS/M 样品与不含贵金属的助催化剂的光催化氢气进化率达到了 15.231 mmol-h-1-g-1。该速率是原始 ZCS/ZS 光催化剂的约 21 倍。光催化活性的提高归功于 ZCS/ZS 和 MoS2 形成的独特异质结结构。此外,碳膜在空间上分隔了氧化还原反应的位点,从而抑制了光生电子-空穴对的重组,在提供出色稳定性方面发挥了关键作用。
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Photostability and visible-light-driven photoactivity enhancement of hierarchical C@ZnCdS/ZnS/MoS2
Zinc cadmium sulfide solid (Zn x Cd1−x S) related composites received great attention in photocatalytic hydrogen production because of their tunable bandgap and strong visible light absorption range. But sulfide-based metal materials commonly suffer from photo-corrosion issues. It is very important to construct the photocatalysts with high efficient activity and photostability for H2 production. Herein, we successively prepared ZnCdS/ZnS (ZCS/ZS) heterostructures, ZnCdS/ZnS/MoS2 (ZCS/ZS/M) heterostructures decorated ZCS/ZS with MoS2 quantum dots, then we obtained x-C@ZCS/ZS and x-C@ZCS/ZS/M heterostructures encapsulated ZCS/ZS and ZCS/ZS/M with carbon layer. The performance of the photocatalytic hydrogen production showed that sample 0.05-C@ZCS/ZS/M has a remarkable photocatalytic H2 evolution rate of 15.231 mmol·h−1·g−1 with noble metal-free co-catalysts. This rate was approximately 21 times higher than that of the pristine ZCS/ZS photocatalyst. The optimized sample reveals an excellent stability, without activity losses after 10 h. The improved photocatalytic activity can be attributed to the unique heterojunction structure formed by ZCS/ZS and MoS2. Additionally, the carbon films played a crucial role in providing excellent stability by spatially separating the sites for redox reactions, thereby inhibiting the recombination of photo-generated electron–hole pairs.
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