{"title":"Ni3N/g-C3N4上连续气水裂解光热催化制氢","authors":"Zhonghao Han, Zhiying Yang, Yingpeng Xie, Ludong Yi, Xi Yang, Guangwen Xu","doi":"10.1002/cctc.202500128","DOIUrl":null,"url":null,"abstract":"<p>The initiation of the water splitting reaction necessitates a considerable energy input and the associated energy barrier can be notably mitigated through the utilization of appropriate catalysts. Ni<sub>3</sub>N/g-C<sub>3</sub>N<sub>4</sub> catalyst was synthesized through a combination of thermal decomposition and hydrothermal synthesis techniques for photothermal water splitting reaction. The catalyst was characterized using XRD, HRTEM, UV–vis, XPS, electrochemical impedance spectroscopy (EIS), and photoluminescence (PL). It was observed that the Ni<sub>3</sub>N promoter is uniformly dispersed on the g-C<sub>3</sub>N<sub>4</sub> exerting no discernible influence on the surface structure and crystal phase of the g-C<sub>3</sub>N<sub>4</sub>.The incorporation of Ni<sub>3</sub>N effectively decreases the resistance of g-C<sub>3</sub>N<sub>4</sub>, enhances the photocurrent intensity, facilitates the transfer of photogenerated electrons from g-C<sub>3</sub>N<sub>4</sub> to Ni<sub>3</sub>N, and suppresses the recombination of photogenerated carriers. Additionally, the findings from the photothermal water splitting experiments revealed that g-C<sub>3</sub>N<sub>4</sub> decreased the activation energy to 71.23 kJ·mol<sup>−1</sup>, while the Ni<sub>3</sub>N promoter further lowered it to 19.73 kJ·mol<sup>−1</sup>.</p>","PeriodicalId":141,"journal":{"name":"ChemCatChem","volume":"17 8","pages":""},"PeriodicalIF":3.8000,"publicationDate":"2025-02-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Photothermalcatalytic Hydrogen Production by Continuous Gaseous Water Splitting over Ni3N/g-C3N4\",\"authors\":\"Zhonghao Han, Zhiying Yang, Yingpeng Xie, Ludong Yi, Xi Yang, Guangwen Xu\",\"doi\":\"10.1002/cctc.202500128\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The initiation of the water splitting reaction necessitates a considerable energy input and the associated energy barrier can be notably mitigated through the utilization of appropriate catalysts. Ni<sub>3</sub>N/g-C<sub>3</sub>N<sub>4</sub> catalyst was synthesized through a combination of thermal decomposition and hydrothermal synthesis techniques for photothermal water splitting reaction. The catalyst was characterized using XRD, HRTEM, UV–vis, XPS, electrochemical impedance spectroscopy (EIS), and photoluminescence (PL). It was observed that the Ni<sub>3</sub>N promoter is uniformly dispersed on the g-C<sub>3</sub>N<sub>4</sub> exerting no discernible influence on the surface structure and crystal phase of the g-C<sub>3</sub>N<sub>4</sub>.The incorporation of Ni<sub>3</sub>N effectively decreases the resistance of g-C<sub>3</sub>N<sub>4</sub>, enhances the photocurrent intensity, facilitates the transfer of photogenerated electrons from g-C<sub>3</sub>N<sub>4</sub> to Ni<sub>3</sub>N, and suppresses the recombination of photogenerated carriers. Additionally, the findings from the photothermal water splitting experiments revealed that g-C<sub>3</sub>N<sub>4</sub> decreased the activation energy to 71.23 kJ·mol<sup>−1</sup>, while the Ni<sub>3</sub>N promoter further lowered it to 19.73 kJ·mol<sup>−1</sup>.</p>\",\"PeriodicalId\":141,\"journal\":{\"name\":\"ChemCatChem\",\"volume\":\"17 8\",\"pages\":\"\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2025-02-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ChemCatChem\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/cctc.202500128\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemCatChem","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cctc.202500128","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Photothermalcatalytic Hydrogen Production by Continuous Gaseous Water Splitting over Ni3N/g-C3N4
The initiation of the water splitting reaction necessitates a considerable energy input and the associated energy barrier can be notably mitigated through the utilization of appropriate catalysts. Ni3N/g-C3N4 catalyst was synthesized through a combination of thermal decomposition and hydrothermal synthesis techniques for photothermal water splitting reaction. The catalyst was characterized using XRD, HRTEM, UV–vis, XPS, electrochemical impedance spectroscopy (EIS), and photoluminescence (PL). It was observed that the Ni3N promoter is uniformly dispersed on the g-C3N4 exerting no discernible influence on the surface structure and crystal phase of the g-C3N4.The incorporation of Ni3N effectively decreases the resistance of g-C3N4, enhances the photocurrent intensity, facilitates the transfer of photogenerated electrons from g-C3N4 to Ni3N, and suppresses the recombination of photogenerated carriers. Additionally, the findings from the photothermal water splitting experiments revealed that g-C3N4 decreased the activation energy to 71.23 kJ·mol−1, while the Ni3N promoter further lowered it to 19.73 kJ·mol−1.
期刊介绍:
With an impact factor of 4.495 (2018), ChemCatChem is one of the premier journals in the field of catalysis. The journal provides primary research papers and critical secondary information on heterogeneous, homogeneous and bio- and nanocatalysis. The journal is well placed to strengthen cross-communication within between these communities. Its authors and readers come from academia, the chemical industry, and government laboratories across the world. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and is supported by the German Catalysis Society.