4.8 Article

Breaking Platinum Nanoparticles to Single-Atomic Pt-C4 Co-catalysts for Enhanced Solar-to-Hydrogen Conversion

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 60, 期 5, 页码 2541-2547

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202013206

关键词

co-catalyst; H-2 generation; photocatalysis; single-atom doping; water splitting

资金

  1. National Key Research Program of China [2017YFA0204800, 2016YFA0202403]
  2. Natural Science Foundation of China [22072081]
  3. Changjiang Scholar and Innovative Research Team [IRT_14R33]
  4. 111 Project [B14041]
  5. Chinese National 1000-Talent-Plan program
  6. National Key Research and Development Program of China [2017YFA0403400]

向作者/读者索取更多资源

Effective transfer and utilization of photogenerated electrons is crucial for achieving highly efficient H-2 generation through photocatalytic water splitting. Single-atom Pt-doped CN as the co-catalyst to CuS demonstrates enhanced photocatalytic performance, reducing overpotential and interfacial resistance for improved water splitting efficiency.
Effective transfer and utilization of the photogenerated electrons are a key factor for achieving highly efficient H-2 generation by photocatalytic water splitting. Apart from the activity of the co-catalyst, the interface between the co-catalyst and semiconductor is of particular importance. Guided by DFT calculations, single-atom (SA) Pt doped carbon nitride (CN) is successfully synthesized for use as the co-catalyst to the semiconducting CuS. The catalyst system (Pt1-CN@CuS) exhibits an enhanced photocatalytic performance for water splitting with a H-2 production rate of 25.4 mu mol h(-1) and an apparent quantum yield (AQY) of 50.3 % under the illumination of LED-530. Solar-to-hydrogen (STH) conversion efficiency is calculated to be 0.5 % under AM 1.5 illumination. This is the very first investigation of SA as the co-catalyst, which decreases the overpotential of CN during the water splitting and lowers interfacial resistance of the catalyst/co-catalyst and co-catalyst/electrolyte.

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