{"title":"In Situ Photodeposition of Au Nanoparticle Plasma: Enhanced Defect-State g-C3N4 Photocatalytic Hydrogen Evolution","authors":"Yahao Zhao, Wen Liu, Peng Liu, Qian Fu, Difu Zhan, Furong Ye, Zhengwang Cheng, Jiayi Tian, Yizhong Huang and Changcun Han*, ","doi":"10.1021/acs.cgd.4c00584","DOIUrl":null,"url":null,"abstract":"<p >To further enhance the hydrogen evolution activity of g-C<sub>3</sub>N<sub>4</sub>, Au nanoparticle (NP)-modified defective-state g-C<sub>3</sub>N<sub>4</sub> nanosheet photocatalysts (Au/HCN) were successfully prepared through in situ photodeposition in this study. The prepared Au/HCN exhibited an excellent photocatalytic hydrogen evolution activity. Under full spectrum, the hydrogen production rate of Au/HCN (7289 μmol·g<sup>–1</sup>·h<sup>–1</sup>) was 1.6 times higher than that of Au NPs-modified pure g-C<sub>3</sub>N<sub>4</sub> nanosheets (Au/CN) (4437 μmol·g<sup>–1</sup>·h<sup>–1</sup>) and 4.3 times higher than that of Au NPs-modified bulk g-C<sub>3</sub>N<sub>4</sub> (Au/BCN) (1664 μmol·g<sup>–1</sup>·h<sup>–1</sup>). The photoluminescence and steady-state photovoltage spectra indicate that Au/HCN has the highest ability for photogenerated charge separation and photogenerated electron transfer efficiency. The ultraviolet–visible spectrophotometer (DRS) spectra revealed an additional light absorption peak at 520 nm for Au/HCN. The above results indicate that the defects can effectively inhibit the recombination of photogenerated charges from HCN. In addition, the synergistic interaction between Au NPs and HCN, as well as the surface plasmon resonance effect of Au NPs, promoted photocatalytic hydrogen evolution.</p>","PeriodicalId":34,"journal":{"name":"Crystal Growth & Design","volume":null,"pages":null},"PeriodicalIF":3.2000,"publicationDate":"2024-06-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Crystal Growth & Design","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.cgd.4c00584","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
To further enhance the hydrogen evolution activity of g-C3N4, Au nanoparticle (NP)-modified defective-state g-C3N4 nanosheet photocatalysts (Au/HCN) were successfully prepared through in situ photodeposition in this study. The prepared Au/HCN exhibited an excellent photocatalytic hydrogen evolution activity. Under full spectrum, the hydrogen production rate of Au/HCN (7289 μmol·g–1·h–1) was 1.6 times higher than that of Au NPs-modified pure g-C3N4 nanosheets (Au/CN) (4437 μmol·g–1·h–1) and 4.3 times higher than that of Au NPs-modified bulk g-C3N4 (Au/BCN) (1664 μmol·g–1·h–1). The photoluminescence and steady-state photovoltage spectra indicate that Au/HCN has the highest ability for photogenerated charge separation and photogenerated electron transfer efficiency. The ultraviolet–visible spectrophotometer (DRS) spectra revealed an additional light absorption peak at 520 nm for Au/HCN. The above results indicate that the defects can effectively inhibit the recombination of photogenerated charges from HCN. In addition, the synergistic interaction between Au NPs and HCN, as well as the surface plasmon resonance effect of Au NPs, promoted photocatalytic hydrogen evolution.
期刊介绍:
The aim of Crystal Growth & Design is to stimulate crossfertilization of knowledge among scientists and engineers working in the fields of crystal growth, crystal engineering, and the industrial application of crystalline materials.
Crystal Growth & Design publishes theoretical and experimental studies of the physical, chemical, and biological phenomena and processes related to the design, growth, and application of crystalline materials. Synergistic approaches originating from different disciplines and technologies and integrating the fields of crystal growth, crystal engineering, intermolecular interactions, and industrial application are encouraged.