6 research outputs found
Tailoring the Doping Mechanisms at Oxide Interfaces in Nanoscale
Here,
we demonstrate the nanoscale manipulations of two types of charge
transfer to the LaAlO<sub>3</sub>/SrTiO<sub>3</sub> interfaces: one
from surface adsorbates and another from oxygen vacancies inside LaAlO<sub>3</sub> films. This method can be used to produce multiple insulating
and metallic interface states with distinct carrier properties that
are highly stable in air. By reconfiguring the patterning and comparing
interface structures formed from different doping sources, effects
of extrinsic and intrinsic material characters on the transport properties
can be distinguished. In particular, a multisubband to single-subband
transition controlled by the structural phases in SrTiO<sub>3</sub> was revealed. In addition, the transient behaviors of nanostructures
also provided a unique opportunity to study the nanoscale diffusions
of adsorbates and oxygen vacancies in oxide heterostructures. Knowledge
of such dynamic processes is important for nanodevice implementations
ElectronāLattice Coupling in Correlated Materials of Low Electron Occupancy
In
correlated materials including transition metal oxides, electronic
properties and functionalities are modulated and enriched by couplings
between the electron and lattice degrees of freedom. These couplings
are controlled by external parameters such as chemical doping, pressure,
magnetic and electric fields, and light irradiation. However, the
electronālattice coupling relies on orbital characters, i.e.,
symmetry and occupancy, of t<sub>2g</sub> and e<sub>g</sub> orbitals,
so that a large electronālattice coupling is limited to e<sub>g</sub> electron system, whereas t<sub>2g</sub> electron system exhibits
an inherently weak coupling. Here, we design and demonstrate a strongly
enhanced electronālattice coupling in electron-doped SrTiO<sub>3</sub>, that is, the t<sub>2g</sub> electron system. In ultrathin
films of electron-doped SrTiO<sub>3</sub> [i.e., (La<sub>0.25</sub>Sr<sub>0.75</sub>)ĀTiO<sub>3</sub>], we reveal the strong electronālatticeāorbital
coupling, which is manifested by extremely increased tetragonality
and the corresponding metal-to-insulator transition. Our findings
open the way of an active tuning of the chargeālatticeāorbital
coupling to obtain new functionalities relevant to emerging nanoelectronic
devices
Tailoring LaAlO<sub>3</sub>/SrTiO<sub>3</sub> Interface Metallicity by Oxygen Surface Adsorbates
We
report an oxygen surface adsorbates induced metalāinsulator
transition at the LaAlO<sub>3</sub>/SrTiO<sub>3</sub> interfaces.
The observed effects were attributed to the terminations of surface
Al sites and the resultant electron-accepting surface states. By controlling
the local oxygen adsorptions, we successfully demonstrated the nondestructive
patterning of the interface two-dimensional electron gas (2DEG). The
obtained 2DEG structures are stable in air and also robust against
general solvent treatments. This study provides new insights into
the metalāinsulator transition mechanism at the complex oxide
interfaces and also a highly efficient technique for tailoring the
interface properties
PTRF/Cavinā1 is Essential for Multidrug Resistance in Cancer Cells
Since detergent-resistant lipid rafts play important
roles in multidrug
resistance (MDR), their comprehensive proteomics could provide new
insights to understand the underlying molecular mechanism of MDR in
cancer cells. In the present work, lipid rafts were isolated from
MCF-7 and adriamycin-resistant MCF-7/ADR cells and their proteomes
were analyzed by label-free quantitative proteomics. Polymerase I
and transcript release factor (PTRF)/cavin-1 was measured to be upregulated
along with multidrug-resistant P-glycoprotein, caveolin-1, and serum
deprivation protein response/cavin-2 in the lipid rafts of MCF-7/ADR
cells. PTRF knockdown led to reduction in the amount of lipid rafts
on the surface of MCF7/ADR cells as determined by cellular staining
with lipid raft-specific dyes such as S-laurdan2 and FITC-conjugated
cholera toxin B. PTRF knockdown also reduced MDR in MCF-7/ADR cells.
These data indicate that PTRF is necessary for MDR in cancer cells
via the fortification of lipid rafts
PTRF/Cavinā1 is Essential for Multidrug Resistance in Cancer Cells
Since detergent-resistant lipid rafts play important
roles in multidrug
resistance (MDR), their comprehensive proteomics could provide new
insights to understand the underlying molecular mechanism of MDR in
cancer cells. In the present work, lipid rafts were isolated from
MCF-7 and adriamycin-resistant MCF-7/ADR cells and their proteomes
were analyzed by label-free quantitative proteomics. Polymerase I
and transcript release factor (PTRF)/cavin-1 was measured to be upregulated
along with multidrug-resistant P-glycoprotein, caveolin-1, and serum
deprivation protein response/cavin-2 in the lipid rafts of MCF-7/ADR
cells. PTRF knockdown led to reduction in the amount of lipid rafts
on the surface of MCF7/ADR cells as determined by cellular staining
with lipid raft-specific dyes such as S-laurdan2 and FITC-conjugated
cholera toxin B. PTRF knockdown also reduced MDR in MCF-7/ADR cells.
These data indicate that PTRF is necessary for MDR in cancer cells
via the fortification of lipid rafts
Imprint Control of BaTiO<sub>3</sub> Thin Films via Chemically Induced Surface Polarization Pinning
Surface-adsorbed polar molecules
can significantly alter the ferroelectric properties of oxide thin
films. Thus, fundamental understanding and controlling the effect
of surface adsorbates are crucial for the implementation of ferroelectric
thin film devices, such as ferroelectric tunnel junctions. Herein,
we report an imprint control of BaTiO<sub>3</sub> (BTO) thin films
by chemically induced surface polarization pinning in the top few
atomic layers of the water-exposed BTO films. Our studies based on
synchrotron X-ray scattering and coherent Bragg rod analysis demonstrate
that the chemically induced surface polarization is not switchable
but reduces the polarization imprint and improves the bistability
of ferroelectric phase in BTO tunnel junctions. We conclude that the
chemical treatment of ferroelectric thin films with polar molecules
may serve as a simple yet powerful strategy to enhance functional
properties of ferroelectric tunnel junctions for their practical applications