In situ growth of Cd0.5Zn0.5S nanorods on Ti3C2 MXene nanosheet for efficient visible-light-driven photocatalytic hydrogen evolution

纳米棒 原位 化学 材料科学 纳米技术 有机化学
作者
Qin Li,Huihui Zhang,Huajun Gu,Yuanyuan Cui,Ruihua Gao,Wei‐Lin Dai
出处
期刊:Acta Physico-chimica Sinica [Peking University Press]
卷期号:41 (4): 100031-100031 被引量:16
标识
DOI:10.3866/pku.whxb202402016
摘要

Against the backdrop of energy scarcities and ecological concerns, the process of photocatalytic hydrogen evolution emerges as a critical method for transforming solar energy into chemical energy. Central to this technology is the crafting of photocatalysts that are not only efficient and durable but also economically viable. The key to creating photocatalysts that boast superior hydrogen production capabilities lies in enhancing the separation and transfer of photo-generated electrons and holes. This study introduces a binary heterojunction photocatalyst, featuring a combination of Cd 0.5 Zn 0.5 S and Ti 3 C 2 MXene , synthesized via an in situ hydrothermal method . In the composite, slender Cd 0.5 Zn 0.5 S nanorods are uniformly coated over the surface of single layer Ti 3 C 2 nanosheets , forming a Schottky heterojunction at the material interface . This structure enhances the separation efficiency of photo-generated electrons and holes, thereby improving the utilization of light. With 0.5 wt % (mass fraction) of Ti 3 C 2 MXene incorporated, we observed a peak photocatalytic H 2 generation rate of 15.56 mmol g −1 h −1 , outperforming the baseline Cd 0.5 Zn 0.5 S by 2.56 times. Notably, the photocatalytic efficiency remained largely unchanged after five cycles. This composite achieved the highest apparent quantum efficiency (AQE) of 18.4 % when exposed to 350 nm UV light . Various characterization techniques, including in situ X-ray photoelectron spectroscopy (XPS) and femtosecond transient absorption (fs-TA) spectroscopy, along with density functional theory (DFT) calculations, have further substantiated that the formation of a Schottky heterojunction at the interface is crucial for enhancing the photocatalytic hydrogen evolution performance of the composite material. This paper demonstrates the effectiveness of the novel carbon based material MXene as a co-catalyst for improving the performance of photocatalysts and offers a viable approach for the construction of MXene-containing photocatalytic hydrogen evolution catalysts.
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