Highly Dispersed Platinum on Honeycomb-like NiO@Ni Film as a Synergistic Electrocatalyst for the Hydrogen Evolution Reaction

Platinum (Pt) is well-known as the best-performing catalyst for the hydrogen evolution reaction (HER), but its practical application is severely hindered by its prohibitively high cost and problematic performance in alkaline electrolyte. Herein, we report that the issues of intrinsic activity and co...

Full description

Saved in:
Bibliographic Details
Published inACS catalysis Vol. 8; no. 9; pp. 8866 - 8872
Main Authors Chen, Zheng-Jun, Cao, Guo-Xuan, Gan, Li-Yong, Dai, Hao, Xu, Ning, Zang, Ming-Jie, Dai, Hong-Bin, Wu, Hui, Wang, Ping
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 07.09.2018
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Platinum (Pt) is well-known as the best-performing catalyst for the hydrogen evolution reaction (HER), but its practical application is severely hindered by its prohibitively high cost and problematic performance in alkaline electrolyte. Herein, we report that the issues of intrinsic activity and cost concern of Pt can be simultaneously addressed by employing a combination of concerted catalysis and nanoengineering strategies. Motivated by our density functional theory (DFT) calculations that the cooperative catalysis between Pt and NiO would lead to a better HER activity in comparison to Pt solely in alkaline solution, we successfully synthesized a Pt/NiO@Ni/NF nanocomposite catalyst by depositing highly dispersed Pt nanoclusters/nanoparticles on a honeycomb-like NiO@Ni film supported on Ni foam (NF). The resulting Pt/NiO@Ni/NF catalyst outperforms the commercial Pt/C catalyst with a high and stable HER activity in alkaline solution and, more impressively, with an economical Pt content as low as ∼0.1 mg cm–2.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Z.-J.C. and G.-X.C. contributed equally.
ISSN:2155-5435
2155-5435
DOI:10.1021/acscatal.8b02212