Boosting hydrogen evolution activity of vanadyl pyrophosphate nanosheets for electrocatalytic overall water splitting-Reference-Cited by-同舟云学术

Boosting hydrogen evolution activity of vanadyl pyrophosphate nanosheets for electrocatalytic overall water splitting

Published:2019 Issue:71 Volume:55 Page:10511-10514
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Zhang Chaoxiong¹²³⁴⁵,Liu Haoxuan¹²³⁴⁵^ORCID,He Jia¹²³⁴⁵,Hu Guangzhi⁶⁷⁸⁹^ORCID,Bao Haihong¹²³⁴⁵,Lü Fang¹²³⁴⁵,Zhuo Longchao³¹⁰¹¹⁹,Ren Junqiang¹²¹³¹⁴⁹,Liu Xijun¹²³⁴⁵^ORCID,Luo Jun¹²³⁴⁵

Affiliation:

1. Center for Electron Microscopy

2. Institute for New Energy Materials and Low-Carbon Technologies

3. School of Materials Science and Engineering

4. Tianjin University of Technology

5. Tianjin 300384

6. School of Chemical Science and Technology

7. Yunnan University

8. Kunming 650091

9. China

10. Xi’an University of Technology

11. Xi’an 710048

12. State Key Laboratory of Advanced Processing and Recycling of Nonferrous Metals

13. Lanzhou University of Technology

14. Lanzhou 730050

Abstract

Herein, vanadyl pyrophosphate nanosheets have been firstly reported as a novel catalyst for hydrogen evolution with superb catalytic activity, and also exhibited outstanding performance for overall water splitting in an alkaline electrolyte.

Funder

National Natural Science Foundation of China

National Basic Research Program of China

Tianjin Science and Technology Committee

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2019/CC/C9CC04481G

Reference38 articles.

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4. Ultrathin bismuth nanosheets from in situ topotactic transformation for selective electrocatalytic CO2 reduction to formate

5. Potential-Cycling Synthesis of Single Platinum Atoms for Efficient Hydrogen Evolution in Neutral Media

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