Li Lingwei, Feng Hange, Dong Zibo, Yang Tiantian, Xue Shaolin
College of Science, Donghua University, Shanghai 201620, China.
College of Science, Donghua University, Shanghai 201620, China; College of Information Science and Technology, Donghua University, Shanghai 201620, China.
J Colloid Interface Sci. 2023 Nov;649:10-21. doi: 10.1016/j.jcis.2023.06.067. Epub 2023 Jun 14.
Designing heterojunction photocatalysts with strong interfacial interactions is an effective way to reduce the recombination of photogenerated charge carriers. Here, silver phosphate (AgPO) nanoparticles are coupled with hollow flower-like indium selenide (InSe) microspheres by a facile Ostwald ripening and in-situ growth method, resulting in the construction of InSe/AgPO hollow microsphere step-scheme (S-scheme) heterojunction with a large contact interface. The flower-like InSe with hollow and porous structure provides a large specific surface area and numerous active sites for photocatalytic reactions to take place. The photocatalytic activity was tested by measuring the hydrogen evolution from antibiotic wastewater, and the H evolution rate of InSe/AgPO reached 4206.4 µmol gh under visible light, which is approximately 2.8 times greater than that of InSe. In addition, the amount of tetracycline (TC) degradation when it was used as a sacrificial agent is about 54.4% after 1 h. On the one hand, Se-P chemical bonds act as electron transfer channels in the S-scheme heterojunctions, which can facilitate the migration and separation of photogenerated charge carriers. On the other hand, the S-scheme heterojunctions can retain the useful holes and electrons with higher redox capacities, which is very favorable for the generation of more •OH radicals and the photocatalytic activity is greatly enhanced. This work provides an alternative design approach for photocatalysts toward hydrogen evolution in antibiotic wastewater.
设计具有强界面相互作用的异质结光催化剂是减少光生载流子复合的有效方法。在此,通过简便的奥斯特瓦尔德熟化和原位生长方法,将磷酸银(AgPO)纳米颗粒与中空花状硒化铟(InSe)微球耦合,从而构建了具有大接触界面的InSe/AgPO中空微球阶梯型(S型)异质结。具有中空和多孔结构的花状InSe为光催化反应提供了大的比表面积和众多活性位点。通过测量抗生素废水的析氢量来测试光催化活性,InSe/AgPO在可见光下的析氢速率达到4206.4 μmol g⁻¹ h⁻¹,约为InSe的2.8倍。此外,当使用四环素(TC)作为牺牲剂时,1小时后其降解量约为54.4%。一方面,Se-P化学键在S型异质结中充当电子转移通道,可促进光生载流子的迁移和分离。另一方面,S型异质结可以保留具有更高氧化还原能力的有用空穴和电子,这非常有利于生成更多的•OH自由基,光催化活性大大增强。这项工作为光催化剂用于抗生素废水析氢提供了一种替代设计方法。