高效稳定的掺钾g-C3N4/Zn0.5Cd0.5S量子点异质结析氢光催化剂

Chenxi Ye, Peiyuan Guo, Xiya Chen, Zining Zhang, Yudong Guo, Zhenjun Chen, Huakang Yang, Dongxiang Luo, Xiao Liu
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引用次数: 0

摘要

高效、稳定的水裂解光催化剂的发展是清洁氢能源可持续生产的关键。本研究介绍了一种新型光催化剂,通过原位水热生长方法将0D Zn0.5Cd0.5S量子点(ZCS QDs)集成到二维K+掺杂石墨氮化碳(K- cn)微带上。对制备的光催化剂的光学特性、结构属性和电荷转移效率进行了综合表征。我们的研究结果表明,K+离子的加入有效地调节了g-C3N4的带隙和价带位置,促进了与ZCS量子点的最佳能级对齐。此外,ZCS量子点的集成提高了光子捕获能力,同时降低了光生载流子的重组率。优化后的ZCS 51%/K-CN光催化剂的模拟日光驱动产氢速率为9.606 mmol·h−1·g−1,比原始ZCS量子点的产氢速率提高了近3倍,无需贵金属辅助催化剂。最值得注意的是,该光催化剂在五个光催化循环中始终保持其析氢性能,强调了其稳定性。K-CN和ZCS量子点之间形成了ii型异质结,促进了电荷的分离和转移。本研究代表了通过将量子点与g-C3N4相结合来设计异质结光催化剂的重要一步,为光催化制氢提供了一种高效、持久的解决方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Highly Efficient and Stable Potassium-Doped g-C3N4/Zn0.5Cd0.5S Quantum Dot Heterojunction Photocatalyst for Hydrogen Evolution

Highly Efficient and Stable Potassium-Doped g-C3N4/Zn0.5Cd0.5S Quantum Dot Heterojunction Photocatalyst for Hydrogen Evolution

The advancement of efficient and robust photocatalysts for water splitting is pivotal for the sustainable production of clean hydrogen energy. This study introduces a novel photocatalyst, synthesized by integrating 0D Zn0.5Cd0.5S quantum dots (ZCS QDs) onto 2D K+-doped graphitic carbon nitride (K-CN) microribbons, via an in-situ hydrothermal growth method. A comprehensive characterization was performed to assess the optical characteristics, structural attributes, and charge transfer efficacy of the prepared photocatalysts. Our findings reveal that the incorporation of K+ ions effectively modulates the bandgap and valence band positions of g-C3N4, facilitating an optimal energy level alignment with ZCS QDs. Moreover, the integration of ZCS QDs improves the photon capture ability and concurrently diminishes the recombination rate of photogenerated charge carriers. The optimized ZCS 51%/K-CN photocatalyst demonstrates a promising simulated sunlight-driven hydrogen production rate of 9.606 mmol·h−1·g−1, surpassing that of pristine ZCS QDs by nearly three times, without the need for noble metal co-catalysts. Most notably, the photocatalyst maintains its hydrogen evolution performance consistently over five photocatalytic cycles, underscoring its stability. The remarkable photocatalytic activity is primarily ascribed to the formation of a type-II heterojunction between K-CN and ZCS QDs, which enhances charge separation and transfer. This research represents a significant step forward in the design of heterojunction photocatalysts by merging QDs with g-C3N4, offering a highly effective and durable solution for photocatalytic hydrogen production.

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