Issue 2, 2018

Synthesis of ultrathin platinum nanoplates for enhanced oxygen reduction activity

Abstract

Ultrathin Pt nanostructures exposing controlled crystal facets are highly desirable for their superior activity and cost-effectiveness in the electrocatalytic oxygen reduction reaction (ORR), and they are conventionally synthesized by epitaxial growth of Pt on a limited range of templates, such as Pd nanocrystals, resulting in a high cost and less structural diversity of the ultrathin Pt nanostructures. To solve this problem, we demonstrate that ultrathin Pt nanostructures can be synthesized by templating conveniently available Ag nanocrystals without involving galvanic replacement, which enables a much-reduced cost and controllable new morphologies, such as ultrathin Pt nanoplates that expose the {111} facets. The resulting ultrathin Pt nanoplates are ∼1–2 nm in thickness, which show an ∼22-fold increase in specific activity (5.3 mA cm−2), an ∼9.5-fold increase in mass activity (1.62 A mg−1) and significantly enhanced catalytic stability in the ORR, compared with the commercial Pt/C catalyst. We believe this strategy opens a door to a highly extendable family of ultrathin noble metal nanostructures, thus promising excellent activity and stability in a broad range of catalytic applications.

Graphical abstract: Synthesis of ultrathin platinum nanoplates for enhanced oxygen reduction activity

Supplementary files

Article information

Article type
Edge Article
Submitted
08 Jul 2017
Accepted
27 Oct 2017
First published
30 Oct 2017
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2018,9, 398-404

Synthesis of ultrathin platinum nanoplates for enhanced oxygen reduction activity

H. Liu, P. Zhong, K. Liu, L. Han, H. Zheng, Y. Yin and C. Gao, Chem. Sci., 2018, 9, 398 DOI: 10.1039/C7SC02997G

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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