Highly stable single Pt atomic sites anchored on aniline-stacked graphene for hydrogen evolution reaction-Reference-Cited by-同舟云学术

Highly stable single Pt atomic sites anchored on aniline-stacked graphene for hydrogen evolution reaction

Published:2019 Issue:3 Volume:12 Page:1000-1007
ISSN:1754-5692
Container-title:Energy & Environmental Science
language:en
Short-container-title:Energy Environ. Sci.

Author:

Ye Shenghua¹²³⁴,Luo Feiyan¹²³⁴,Zhang Qianling¹²³⁴,Zhang Pingyu¹²³⁴^ORCID,Xu Tingting¹²³⁴,Wang Qi⁵⁶³⁷,He Dongsheng⁸⁹³⁴,Guo Licheng¹²³⁴,Zhang Yu¹²³⁴,He Chuanxin¹²³⁴^ORCID,Ouyang Xiaoping¹⁰¹¹¹²⁴,Gu Meng⁵⁶³⁷^ORCID,Liu Jianhong¹²³⁴,Sun Xueliang¹³¹⁴¹⁵¹⁶¹⁷^ORCID

Affiliation:

1. College of Chemistry and Environmental Engineering

2. Shenzhen University

3. Shenzhen

4. P. R. China

5. Department of Materials Science and Engineering

6. Southern University of Science and Technology

7. China

8. Materials Characterization and Preparation Center

9. South University of Science and Technology of China

10. School of Materials Science and Engineering

11. Xiangtan University

12. Xiangtan

13. Department of Mechanical and Materials Engineering

14. University of Western Ontario

15. London

16. Ontario N6A 5B9

17. Canada

Abstract

Single-atom Pt sites stabilized by aniline stacked on graphene exhibit excellent electrocatalytic activity and durability for the hydrogen evolution reaction.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Guangdong Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Nuclear Energy and Engineering,Renewable Energy, Sustainability and the Environment,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/EE/C8EE02888E

Reference63 articles.

1. Porous Molybdenum Phosphide Nano-Octahedrons Derived from Confined Phosphorization in UIO-66 for Efficient Hydrogen Evolution

2. Porous molybdenum carbide nano-octahedrons synthesized via confined carburization in metal-organic frameworks for efficient hydrogen production