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Functional Role of Fe, Cu-Doping in Ni-Based Perovskite Electrocatalysts for Oxygen Evolution Reaction.

Authors :
Hou, Bingxue
Wang, Cheng Cheng
Tang, Rui
Zhang, Qi
Tan, Zanxiong
Fan, Xincan
Cui, Xumei
Source :
NANO; Jun2020, Vol. 15 Issue 6, pN.PAG-N.PAG, 10p
Publication Year :
2020

Abstract

Water electrolysis is of vital importance to store renewable energy and the development of efficient, inexpensive and stable electrocatalysts for oxygen evolution reaction (OER) is essential, which requires much more understanding of the structural and the element classification. Here, a series of LaNi 0. 8 Fe<subscript>x</subscript> Cu 0. 2 − x O 3 − δ perovskites have been assessed as potential noble-metal-free OER electrocatalysts prepared by sol–gel method. Moreover, the functional role of Cu and Fe amount on the B-site of perovskites for OER electrocatalytic performance was evaluated. LaNi 0. 8 Fe 0. 2 O 3 − δ materials exhibited the highest intrinsic activities in 0.1 M KOH for OER with an onset potential of 1.56 V, a Tafel slope of 76 mV dec − 1 , slightly lower than that of benchmark perovskite-type electrocatalyst Ba 0. 5 Sr 0. 5 C O 0. 8 Fe 0. 2 O<subscript>3</subscript> (BSCF). The above results demonstrate that Cu element in the B-site of perovskites had little effect on the OER performance, and LaNi 0. 8 Fe 0. 2 O 3 − δ is a potential alternative electrocatalyst for OER application. LaNi<subscript>0.8</subscript>Fe<subscript>x</subscript>Cu<subscript>0.2–x</subscript>O<subscript>3– δ </subscript> perovskites have been assessed as potential noble-metal-free OER electrocatalysts prepared by sol–gel method. All results demonstrate that Cu element in the B-site of perovskites had little effect on the OER performance, and LaNi<subscript>0.8</subscript>Fe<subscript>0.2</subscript>O<subscript>3– δ </subscript> is a potential alternative electrocatalyst for OER application. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17932920
Volume :
15
Issue :
6
Database :
Complementary Index
Journal :
NANO
Publication Type :
Academic Journal
Accession number :
144520617
Full Text :
https://doi.org/10.1142/S1793292020500770