4.8 Article

A novel sulfur-assisted annealing method of g-C3N4 nanosheet compensates for the loss of light absorption with further promoted charge transfer for photocatalytic production of H2 and H2O2

期刊

APPLIED CATALYSIS B-ENVIRONMENTAL
卷 281, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.apcatb.2020.119539

关键词

g-C3N4; sulfur doping; Band structure regulation; Charge separation; Surface charge transfer

资金

  1. National Natural Science Foundation of China [51579096, 51521006, 51909089]
  2. Funds for Innovative Province Construction of Hunan Province [2019RS3012]
  3. Key Research and Development Program of Hunan Province of China
  4. National Innovative Talent Promotion Program of China [2017SK2241]
  5. National Program for Support of Top-Notch Young Professionals of China [2017RA2088]

向作者/读者索取更多资源

Sulfur doping can regulate the band structure of g-C3N4, enhance its optical absorption ability, introduce new absorption bands, and create local electron accumulation points, thereby improving charge separation efficiency and surface charge transfer ability.
Exfoliating g-C3N4 into 2D nanosheet to minimize the stacking layer for the improvement of charge transfer and separation is considered to be the effective measure to enhance its photocatalytic performance. However, no matter what method is used, the exfoliated g-C3N4 nanosheet shows decreased optical absorption compared to the pristine bulk-like one. In this work, a simple one-step sulfur doping method is proposed on the basis of exfoliated g-C3N4 nanosheet, which can directly regulate the band structure of g-C3N4 and enhance its optical absorption ability. The proposed sulfur doping method redshift the light absorption edge of g-C3N4 nanosheet to the level of pristine bulk-like g-C3N4, and even induce the generation of a new n ->pi* absorption band. In addition, the introduced sulfur doping site can form a local electron accumulation point, so that to further improve the charge separation efficiency and surface charge transfer ability of g-C3N4 nanosheets.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据