4.7 Article

Sandwich-Structured MXene/Carbon Hybrid Support Decorated with Pt Nanoparticles for Oxygen Reduction Reaction

Journal

ACS APPLIED ENERGY MATERIALS
Volume 5, Issue 12, Pages 14957-14965

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsaem.2c02479

Keywords

proton-exchange membrane fuel cells; MXene; three-dimensional support; oxygen reduction reaction; enhanced stability

Funding

  1. National Natural Science Foundation of China [21673064, 51802059, 21905070, 22075062]
  2. Shenzhen Science and Technology Program [JCYJ20210324120400002, SGDX20210823103803017]
  3. Key Research and Development Program of Shandong Province [2022CXGC010305]
  4. Heilongjiang Touyan Team [HITTY-20190033]
  5. Fundamental Research Funds for the Central Universities [FRFCU5710051922]

Ask authors/readers for more resources

A three-dimensional (3D) support hybridized by MXene and Ketjen Black was developed, and a 3D Pt/MCM catalyst was obtained. The catalyst exhibited high specific surface area, exposed active sites, excellent ORR activity, and ultrahigh durability.
Carbon supports for cathodic catalysts in proton-exchange membrane fuel cells suffer from rapid corrosion and instability; therefore, alternative supports with a stable structure and a high electric conductivity are highly required. In this paper, a three-dimensional support hybridized by MXene and Ketjen Black is developed, in which Ketjen Black is sandwiched between MXene nanosheets (MCM). After decorating with Pt nanoparticles by a facile wet-chemical approach, a three-dimensional (3D) Pt/MCM catalyst is obtained. The intercalated Ketjen Black prevents the stacking of MXene nanosheets, thus increasing the specific surface area of the catalyst and exposing the active sites. The strong interaction between functionalized MXene nanosheets and Pt nanoparticles further enhances its intrinsic electrocatalytic activity. Pt/MCM demonstrated encouraging ORR activity with the half-wave potential and specific activity of 0.892 V and 0.377 mA center dot cm-2, respectively, surpassing the state-of-the-art Pt/C catalysts. Especially, Pt/MCM achieves ultrahigh durability with a 1 mV decrease in half-wave potential and a 1.73% decrease in mass activity after an accelerated durability test. Given the performance and structure-activity relationships of Pt/MCM, it holds great potential for various energy and catalysis-related applications.

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