Abstract

For efficient water splitting, it is essential to develop inexpensive and super-efficient electrocatalysts for the oxygen evolution reaction (OER). Herein, we report a phosphate-based electrocatalyst [Fe3Co(PO4)4@reduced-graphene-oxide(rGO)] showing outstanding OER performance (much higher than state-of-the-art Ir/C catalysts), the design of which was aided by first-principles calculations. This electrocatalyst displays low overpotential (237 mV at high current density 100 mA cm−2 in 1 M KOH), high turnover frequency (TOF: 0.54 s−1), high Faradaic efficiency (98%), and long-term durability. Its remarkable performance is ascribed to the optimal free energy for OER at Fe sites and efficient mass/charge transfer. When a Fe3Co(PO4)4@rGO anodic electrode is integrated with a Pt/C cathodic electrode, the electrolyzer requires only 1.45 V to achieve 10 mA cm−2 for whole water splitting in 1 M KOH (1.39 V in 6 M KOH), which is much smaller than commercial Ir-C//Pt-C electrocatalysts. This cost-effective powerful oxygen production material with carbon-supporting substrates offers great promise for water splitting.

Details

Title
Superb water splitting activity of the electrocatalyst Fe3Co(PO4)4 designed with computation aid
Author
Sultan, Siraj 1   VIAFID ORCID Logo  ; Ha, Miran 2 ; Kim, Dong Yeon 1   VIAFID ORCID Logo  ; Tiwari, Jitendra N 1 ; Chang Woo Myung 1   VIAFID ORCID Logo  ; Meena, Abhishek 1 ; Shin, Tae Joo 3   VIAFID ORCID Logo  ; Chae, Keun Hwa 4   VIAFID ORCID Logo  ; Kim, Kwang S 1   VIAFID ORCID Logo 

 Center for Superfunctional Materials, Department of Chemistry, Ulsan National Institute of Science and Technology (UNIST), Ulsan, Korea 
 Center for Superfunctional Materials, Department of Chemistry, Ulsan National Institute of Science and Technology (UNIST), Ulsan, Korea; Department of Energy and Chemical Engineering, UNIST, Ulsan, Korea 
 UNIST Central Research Facilities, UNIST, Ulsan, Korea 
 Advanced Analysis Center, Korea Institute of Science and Technology, Seoul, Korea 
Pages
1-9
Publication year
2019
Publication date
Nov 2019
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2314766856
Copyright
© 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.