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@ARTICLE{Gunkel:826338,
author = {Gunkel, F. and Hoffmann-Eifert, S. and Heinen, R. A. and
Christensen, D. V. and Chen, Y. Z. and Pryds, N. and Waser,
R. and Dittmann, R.},
title = {{T}hermodynamic {G}round {S}tates of {C}omplex {O}xide
{H}eterointerfaces},
journal = {ACS applied materials $\&$ interfaces},
volume = {9},
number = {1},
issn = {1944-8252},
address = {Washington, DC},
publisher = {Soc.},
reportid = {FZJ-2017-00566},
pages = {1086 - 1092},
year = {2017},
abstract = {The formation mechanism of 2-dimensional electron gases
(2DEGs) at heterointerfaces between nominally insulating
oxides is addressed with a thermodynamical approach. We
provide a comprehensive analysis of the thermodynamic ground
states of various 2DEG systems directly probed in high
temperature equilibrium conductivity measurements. We
unambiguously identify two distinct classes of oxide
heterostructures: For epitaxial perovskite/perovskite
heterointerfaces (LaAlO3/SrTiO3, NdGaO3/SrTiO3, and
(La,Sr)(Al,Ta)O3/SrTiO3), we find the 2DEG formation being
based on charge transfer into the interface, stabilized by
the electric field in the space charge region. In contrast,
for amorphous LaAlO3/SrTiO3 and epitaxial γ-Al2O3/SrTiO3
heterostructures, the 2DEG formation mainly relies on the
formation and accumulation of oxygen vacancies. This class
of 2DEG structures exhibits an unstable interface
reconstruction associated with a quenched nonequilibrium
state.},
cin = {PGI-7},
ddc = {540},
cid = {I:(DE-Juel1)PGI-7-20110106},
pnm = {521 - Controlling Electron Charge-Based Phenomena
(POF3-521)},
pid = {G:(DE-HGF)POF3-521},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000392037400124},
doi = {10.1021/acsami.6b12706},
url = {https://juser.fz-juelich.de/record/826338},
}