Yuan Lang, Yin Yihang, Xiang Peng, Shao Yugui, Gao Jie, Liu Jianan, Meng Huiyuan, Li Li, Xie Ying, Xiao Xudong, Jiang Baojiang
College of Modern Agriculture and Ecological Environment, Heilongjiang University, Harbin, China.
Heilongjiang Provincial Key Laboratory of Environmental Nanotechnology, School of Chemistry and Materials Science, Heilongjiang University, Harbin, China.
Front Chem. 2024 Feb 2;12:1340955. doi: 10.3389/fchem.2024.1340955. eCollection 2024.
Designing and developing photocatalysts with excellent performance in order to achieve efficient hydrogen production is an important strategy for addressing future energy and environmental challenges. Traditional single-phase photocatalytic materials either have a large bandgap and low visible light response or experience rapid recombination of the photogenerated carriers with low quantum efficiency, seriously hindering their photocatalytic applications. To solve these issues, an important solution is to construct well-matched heterojunctions with highly efficient charge separation capabilities. To this end, an sulfurization reaction was adopted after the deposition of Bi supramolecular complex on a layered supramolecular precursor of tubular carbon nitride (TCN). X-ray diffraction (XRD) patterns confirmed that the as-prepared sample has a good crystalline structure without any other impurities, while high-resolution transmission electron microscopy (HR-TEM) revealed that the heterojunction possesses a 2D structure with a layer of nano-array on its surface. Combined Fourier-transform infrared (FT-IR) spectra and energy-dispersive X-ray spectroscopy (EDX) revealed the interfacial interactions. Owing to the formation of the Z-scheme heterojunction, the visible light adsorption and the separation efficiency of the photo-generated carriers are both obviously enhanced, leaving the high energy electrons and high oxidative holes to participate in the photocatalytic reactions. As a result, the photocatalytic hydrogen evolution rate of BiS-TCN achieves 65.2 μmol g·h. This proposed green and environmentally benign route can also be applied to construct other sulfides with 2D TCN, providing some important information for the design and optimization of novel carbon-nitride-based semiconductors.
设计和开发具有优异性能的光催化剂以实现高效产氢是应对未来能源和环境挑战的重要策略。传统的单相光催化材料要么具有较大的带隙和低可见光响应,要么光生载流子快速复合且量子效率低,严重阻碍了它们的光催化应用。为了解决这些问题,一个重要的解决方案是构建具有高效电荷分离能力的良好匹配的异质结。为此,在管状氮化碳(TCN)的层状超分子前驱体上沉积Bi超分子配合物后采用了硫化反应。X射线衍射(XRD)图谱证实所制备的样品具有良好的晶体结构且无任何其他杂质,而高分辨率透射电子显微镜(HR-TEM)显示该异质结具有二维结构,其表面有一层纳米阵列。傅里叶变换红外(FT-IR)光谱和能量色散X射线光谱(EDX)相结合揭示了界面相互作用。由于形成了Z型异质结,可见光吸附和光生载流子的分离效率均明显提高,使得高能电子和高氧化性空穴参与光催化反应。结果,BiS-TCN的光催化析氢速率达到65.2 μmol g·h。这种提出的绿色环保路线也可应用于构建其他与二维TCN的硫化物,为新型氮化碳基半导体的设计和优化提供一些重要信息。