Loading…

Oxygen Evolution Reaction on Perovskites: A Multieffect Descriptor Study Combining Experimental and Theoretical Methods

The correlation between ex situ electronic conductivity, oxygen vacancy content, flat-band potential (E fb), and the oxygen evolution reaction (OER) activity for a wide range of perovskite compositions [La1–x Sr x CoO3−δ series (with x = 0, 0.2, 0.4, 0.6, 0.8), LaMO3−δ series (M = Cr, Mn, Fe, Co, Ni...

Full description

Saved in:
Bibliographic Details
Published in:ACS catalysis 2018-10, Vol.8 (10), p.9567-9578
Main Authors: Cheng, Xi, Fabbri, Emiliana, Yamashita, Yuya, Castelli, Ivano E, Kim, Baejung, Uchida, Makoto, Haumont, Raphael, Puente-Orench, Inés, Schmidt, Thomas J
Format: Article
Language:English
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:The correlation between ex situ electronic conductivity, oxygen vacancy content, flat-band potential (E fb), and the oxygen evolution reaction (OER) activity for a wide range of perovskite compositions [La1–x Sr x CoO3−δ series (with x = 0, 0.2, 0.4, 0.6, 0.8), LaMO3−δ series (M = Cr, Mn, Fe, Co, Ni), Ba0.5Sr0.5Co0.8Fe0.2O3−δ (BSCF), and PrBaCo2O6−δ (PBCO)] are investigated experimentally and theoretically. It is found that all of these parameters can affect the OER activity; however, none of them alone play a crucial role in determining the electrocatalytic activity. The correlation of one single physicochemical property with the OER activity always presents deviation points, indicating that a limitation does exist for such 2-dimensional correlations. Nevertheless, these deviations can be explained considering other physicochemical properties and their correlation with the OER activity. Hence, this work aims in simultaneously linking the OER activity with several physicochemical materials properties. The concept of the OER/multidescriptor relationship represents a significant advancement in the search and design of highly active oxygen evolution catalysts, in the quest for efficient anodes in water electrolyzers.
ISSN:2155-5435
2155-5435
DOI:10.1021/acscatal.8b02022