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@ARTICLE{Cho:135194,
author = {Cho, Deok-Yong and Tappertzhofen, Stefan and Waser, R. and
Valov, Ilia},
title = {{B}ond nature of active metal ions in {S}i{O}2-based
electrochemical metallization memory cells},
journal = {Nanoscale},
volume = {5},
number = {5},
issn = {2040-3372},
address = {Cambridge},
publisher = {RSC Publ.},
reportid = {FZJ-2013-03159},
pages = {1781-1784},
year = {2013},
abstract = {Electrochemical metallization cells are candidates for the
next-generation non-volatile memory devices based on
resistive switching. Despite the intensive studies in recent
years a microscopic model of the processes in these
nanoscale electrochemical systems is still missing and the
physicochemical properties of the active metal ions have
been rarely reported. We examined the bonding
characteristics of Cuz+ and Ag+ ions in SiO2-based cells
using soft X-ray absorption spectroscopy. Whereas the
Ag/SiO2 interfaces showed no chemical interaction of Ag
ions, the Cu/SiO2 showed clear signatures of partial
oxidation into two ionic species of Cu2+ and Cu+. The
analyses on the orbital hybridization strength evidently
showed that the Cu2+–O2− bonds in SiO2 are much weaker
than the Cu+–O2− bonds, analogous to the case of bulk
CuO and Cu2O. This suggests that the Cu2+ ions should be
more mobile and with a dominating role in the process of
resistive switching.},
cin = {PGI-7 / JARA-FIT},
ddc = {600},
cid = {I:(DE-Juel1)PGI-7-20110106 / $I:(DE-82)080009_20140620$},
pnm = {421 - Frontiers of charge based Electronics (POF2-421)},
pid = {G:(DE-HGF)POF2-421},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000314931900007},
doi = {10.1039/c3nr34148h},
url = {https://juser.fz-juelich.de/record/135194},
}