College of Materials and Chemical Engineering, Key Laboratory of Inorganic Nonmetallic Crystalline and Energy Conversion Materials, China Three Gorges University, Yichang, Hubei 443002, PR China; Hubei Three Gorges Laboratory, Yichang, Hubei 443007, PR China.
College of Materials and Chemical Engineering, Key Laboratory of Inorganic Nonmetallic Crystalline and Energy Conversion Materials, China Three Gorges University, Yichang, Hubei 443002, PR China; Hubei Three Gorges Laboratory, Yichang, Hubei 443007, PR China.
J Colloid Interface Sci. 2023 Sep;645:429-438. doi: 10.1016/j.jcis.2023.04.146. Epub 2023 May 3.
Optimize the separation and transport mechanism of photogenerated carriers in heterojunction composites, and make full use of the active sites of each material are key factors to enhance photocatalytic activity. Herein, we successfully synthesize defective CdLaS@La(OH)@CoS (CLS@LOH@CS) Z-scheme heterojunction photocatalysts through a facile solvothermal method, which show broad-spectrum absorption and excellent photocatalytic activity. La(OH) nanosheets not only greatly increase the specific surface area of photocatalyst, but also can be coupled with CdLaS (CLS) and form Z-scheme heterojunction by converting irradiation light. In addition, CoS with photothermal properties is obtained by in-situ sulfurization method, which can release heat to improve the mobility of photogenerated carriers, and also be used as a cocatalyst for hydrogen production. Most importantly, the formation of CoS leads to a large number of sulfur vacancy defects in CLS, and thus improving the separation efficiency of photogenerated electrons and holes, and increasing the catalytic active sites. Consequently, the maximum hydrogen production rate of CLS@LOH@CS heterojunctions can reach 26.4 mmol gh, which is 293 times than pristine CLS (0.09 mmol gh). This work will provide a new horizon for synthesizing high efficiency heterojunction photocatalysts through switching the separation and transport modes of photogenerated carrier.
优化异质结复合材料中光生载流子的分离和输运机制,充分利用各材料的活性位是提高光催化活性的关键因素。在此,我们通过简便的溶剂热法成功合成了具有缺陷的 CdLaS@La(OH)@CoS(CLS@LOH@CS)Z 型异质结光催化剂,其具有宽光谱吸收和优异的光催化活性。La(OH)纳米片不仅极大地增加了光催化剂的比表面积,而且还可以通过将照射光转化为与 CdLaS(CLS)耦合形成 Z 型异质结。此外,通过原位硫化法获得了具有光热性能的 CoS,其可以释放热量以提高光生载流子的迁移率,并且还可以用作产氢的助催化剂。最重要的是,CoS 的形成导致 CLS 中形成大量的硫空位缺陷,从而提高了光生电子和空穴的分离效率,并增加了催化活性位。因此,CLS@LOH@CS 异质结的最大产氢速率可达到 26.4 mmol gh,是原始 CLS(0.09 mmol gh)的 293 倍。这项工作将通过改变光生载流子的分离和输运方式为合成高效异质结光催化剂提供新的思路。