Khursheed Ahmad, Waseem Raza, Mohd Quasim Khan, Rais Ahmad Khan
{"title":"基于掺钨 MoS2 的纳米结构在可见光下光催化氢气进化","authors":"Khursheed Ahmad, Waseem Raza, Mohd Quasim Khan, Rais Ahmad Khan","doi":"10.1007/s11144-024-02627-9","DOIUrl":null,"url":null,"abstract":"<div><p>In this work, we introduced a simple approach to boost the photocatalytic activity of MoS<sub>2</sub> by introducing transition metal (W) doping. The W-MoS<sub>2</sub> (10 mg) exhibited a substantial enhancement in photocatalytic activity for H<sub>2</sub> production, achieving an impressive rate of approximately 925 µmol g<sup>−1</sup> after 6 h, which is 1.5-fold higher than bare MoS<sub>2</sub>. The highest H<sub>2</sub> production activity of 1740 µmol g<sup>−1</sup> after 6 h was obtained for 50 mg W-MoS<sub>2</sub> photocatalyst. The observed increase in activity can be ascribed to the formation of a Schottky barrier at the heterojunction interface, along with advantageous properties of improved active sites resulting from tungsten doping into MoS<sub>2</sub>. Furthermore, the enhanced activity of W-MoS<sub>2</sub> may be attributed to the promotion of catalytic kinetics by tungsten and molybdenum sites, exhibiting commendable activity for water dissociation and higher efficiency in H<sup>+</sup> adsorption. These factors contribute significantly to the overall improved performance of the W-MoS<sub>2</sub> photocatalyst. Further, platinum (Pt) was also used as cocatalyst and enhanced photocatalytic activity of 2145 µmol g<sup>−1</sup> after 6 h was observed for W-MoS<sub>2</sub> + 5 wt% Pt.</p></div>","PeriodicalId":750,"journal":{"name":"Reaction Kinetics, Mechanisms and Catalysis","volume":"137 4","pages":"2363 - 2374"},"PeriodicalIF":1.7000,"publicationDate":"2024-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Tungsten-doped MoS2-based nanostructure for photocatalytic hydrogen evolution under visible light\",\"authors\":\"Khursheed Ahmad, Waseem Raza, Mohd Quasim Khan, Rais Ahmad Khan\",\"doi\":\"10.1007/s11144-024-02627-9\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>In this work, we introduced a simple approach to boost the photocatalytic activity of MoS<sub>2</sub> by introducing transition metal (W) doping. The W-MoS<sub>2</sub> (10 mg) exhibited a substantial enhancement in photocatalytic activity for H<sub>2</sub> production, achieving an impressive rate of approximately 925 µmol g<sup>−1</sup> after 6 h, which is 1.5-fold higher than bare MoS<sub>2</sub>. The highest H<sub>2</sub> production activity of 1740 µmol g<sup>−1</sup> after 6 h was obtained for 50 mg W-MoS<sub>2</sub> photocatalyst. The observed increase in activity can be ascribed to the formation of a Schottky barrier at the heterojunction interface, along with advantageous properties of improved active sites resulting from tungsten doping into MoS<sub>2</sub>. Furthermore, the enhanced activity of W-MoS<sub>2</sub> may be attributed to the promotion of catalytic kinetics by tungsten and molybdenum sites, exhibiting commendable activity for water dissociation and higher efficiency in H<sup>+</sup> adsorption. These factors contribute significantly to the overall improved performance of the W-MoS<sub>2</sub> photocatalyst. Further, platinum (Pt) was also used as cocatalyst and enhanced photocatalytic activity of 2145 µmol g<sup>−1</sup> after 6 h was observed for W-MoS<sub>2</sub> + 5 wt% Pt.</p></div>\",\"PeriodicalId\":750,\"journal\":{\"name\":\"Reaction Kinetics, Mechanisms and Catalysis\",\"volume\":\"137 4\",\"pages\":\"2363 - 2374\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2024-05-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Reaction Kinetics, Mechanisms and Catalysis\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s11144-024-02627-9\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reaction Kinetics, Mechanisms and Catalysis","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11144-024-02627-9","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Tungsten-doped MoS2-based nanostructure for photocatalytic hydrogen evolution under visible light
In this work, we introduced a simple approach to boost the photocatalytic activity of MoS2 by introducing transition metal (W) doping. The W-MoS2 (10 mg) exhibited a substantial enhancement in photocatalytic activity for H2 production, achieving an impressive rate of approximately 925 µmol g−1 after 6 h, which is 1.5-fold higher than bare MoS2. The highest H2 production activity of 1740 µmol g−1 after 6 h was obtained for 50 mg W-MoS2 photocatalyst. The observed increase in activity can be ascribed to the formation of a Schottky barrier at the heterojunction interface, along with advantageous properties of improved active sites resulting from tungsten doping into MoS2. Furthermore, the enhanced activity of W-MoS2 may be attributed to the promotion of catalytic kinetics by tungsten and molybdenum sites, exhibiting commendable activity for water dissociation and higher efficiency in H+ adsorption. These factors contribute significantly to the overall improved performance of the W-MoS2 photocatalyst. Further, platinum (Pt) was also used as cocatalyst and enhanced photocatalytic activity of 2145 µmol g−1 after 6 h was observed for W-MoS2 + 5 wt% Pt.
期刊介绍:
Reaction Kinetics, Mechanisms and Catalysis is a medium for original contributions in the following fields:
-kinetics of homogeneous reactions in gas, liquid and solid phase;
-Homogeneous catalysis;
-Heterogeneous catalysis;
-Adsorption in heterogeneous catalysis;
-Transport processes related to reaction kinetics and catalysis;
-Preparation and study of catalysts;
-Reactors and apparatus.
Reaction Kinetics, Mechanisms and Catalysis was formerly published under the title Reaction Kinetics and Catalysis Letters.