4.7 Article

The activation of inert NiFe Prussian Blue analogues to boost oxygen evolution reaction activity

期刊

JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 607, 期 -, 页码 967-977

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2021.09.114

关键词

Active Mo sites; Inert sites; NiFe Prussian Blue Analogue; Reaction energy barrier; Oxygen evolution reaction

资金

  1. National Key Research and Development Program of China [2018YFB1502700]
  2. Provincial Nature Science Foundation of Sichuan [2017CC0017, 2018FZ0105, 2019YJ0025]
  3. Research and Development Program of Chengdu [2019-YF05-01193-SN]
  4. Fundamental Research Funds for the Central Universities [20826041E4280]
  5. Sichuan University Postdoctoral Interdisciplinary Innovation Fund

向作者/读者索取更多资源

In this study, Mo substituted Fe sites and S doped in Prussian Blue Analogues (PBA) were successfully designed and synthesized to enhance the OER activity and structural stability. PBA-SMo/NF showed superior activity and durability, providing valuable guidance for the application of PBA in electrocatalysis.
The inert sites of Prussian Blue Analogue (PBA) seriously affected its electrocatalytic activity and application, how to activate inert sites in PBA to fulfill effective oxygen evolution reduction (OER) is a major challenge. Herein, Mo substituted Fe sites and S doped in inert PBA were designed and synthesized by hydrothermal method to enhance structural stability and OER activity. PBA-SMo/NF shows the optimum activity with a low overpotential of 252 and 294 mV for harvesting current density 20 and 100 mA cm(-2), respectively, and exhibits excellent durability under high current density. Theoretical calculation of H2O adsorption energy and Bader charges reveals that Mo sites in PBA-SMo possess favourable H2O adsorption kinetics. More important, Gibbs free energy diagram and DOS show PBA-SMo have lower energy barriers for OER and better conductivity. This work provides a kind of guidance for the design and optimization of PBA for broad applications. (C) 2021 Published by Elsevier Inc.

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