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@INPROCEEDINGS{Kwati:1017831,
author = {Kwati, Leonard and Staykov, Aleksandar and Wiff, Juan Paulo
and Meulenberg, Wilhelm and Matsumoto, Hiroshige},
title = {{C}atalytic {A}ctivity of {L}n{C}o 0.5 {N}i 0.5 {O} 3-Δ
({L}n = {L}a, {P}r, {N}d) '{P}ositrodes' on {C}eramic
{P}rotonic {E}lectrolytes},
issn = {2151-2043},
reportid = {FZJ-2023-04354},
year = {2023},
abstract = {Proton-conducting solid-oxide electrolyzers and fuel cells
represent viable, intermediate-temperature green energy
conversion and storage technologies. Interest in this class
of materials as electrolytes stems from their high ionic
conductivity and inherent advantages in the gas flow
configuration over traditional solid oxide cells in which
the electrolyte is an oxygen ion conductor. However, their
commercial viability has been hindered, in part, by the
development of corresponding single-phase electrode
components with mixed proton-electron conductivity and
effective catalytic activity toward oxygen reduction and
evolution reactions (ORR/OER). This paper investigates the
origin of catalytic activity in LnCo0.5Ni0.5O3-δ (Ln=La, Pr
and Nd) perovskites positrodes (positive electrode) by low
energy-ion scattering (LEIS) and DFT studies. LEIS results
reveal that La, Pr, and Pr cations dominate the outer atomic
layer, with profound implications for catalytic activity.
Whereas First principle calculations were performed using
the plane-wave DFT method and hybrid HSE06 functional
suggest, the catalytic activity and electronic properties
depend on the valence shell structure of the Ln-site cation
and their redox properties.},
month = {May},
date = {2023-05-28},
organization = {Electrochemical Society Meeting
Abstracts 243, Boston (USA), 28 May
2023 - 2 Jun 2023},
cin = {IEK-1},
ddc = {540},
cid = {I:(DE-Juel1)IEK-1-20101013},
pnm = {1232 - Power-based Fuels and Chemicals (POF4-123)},
pid = {G:(DE-HGF)POF4-1232},
typ = {PUB:(DE-HGF)1},
doi = {10.1149/MA2023-01402826mtgabs},
url = {https://juser.fz-juelich.de/record/1017831},
}