5 research outputs found
Solution-Processed 8‑Hydroquinolatolithium as Effective Cathode Interlayer for High-Performance Polymer Solar Cells
Solution-processed
8-hydroxyquinolinatolithium (s-Liq) was successfully applied as an
efficient cathode interlayer in bulk heterojunction polymer solar
cells (PSCs), giving rise to enhancement in device performance. The
ultraviolet photoelectron spectra results revealed that the presence
of s-Liq could lower work function of Al cathode, allowing for the
ohmic contacts with the fullerene acceptor for better electron extraction
and also a larger work function difference between the two electrodes,
which leads to an increase in open-circuit voltage (<i>V</i><sub>oc</sub>). Scanning Kelvin probe microscopy study on the surface
potential of active layers suggested that an interfacial dipole was
formed in the s-Liq interlayer between the active layer and the Al
cathode, which enhanced the intrinsic built-in potential in the device
for better charge transportation and extraction. Consequently, the <i>V</i><sub>oc</sub>, fill factor, and current density of the
device can be improved by the introduction of s-Liq interlayer, leading
to a power conversion efficiency (PCE) improvement. With PTB7 (or
PTB7-Th) as the donor and PC<sub>71</sub>BM as the acceptor, the s-Liq-based
PSC devices exhibited a PCE of 8.37% (or 9.04%), much higher than
those of devices with the evaporated Liq (7.62%) or commonly used
PFN (8.14%) as the cathode interlayer. Moreover, the s-Liq-based devices
showed good stability, maintaining 75% (in N<sub>2</sub>) and 45%
(in air) of the initial PCE after 7 days, respectively. These results
suggest the great potential of s-Liq as cathode interlayer material
for high-performance solar cells application
Robust Interfacial Exchange Bias and Metal–Insulator Transition Influenced by the LaNiO<sub>3</sub> Layer Thickness in La<sub>0.7</sub>Sr<sub>0.3</sub>MnO<sub>3</sub>/LaNiO<sub>3</sub> Superlattices
Artificial
heterostructures based on LaNiO<sub>3</sub> (LNO) have been widely
investigated with the aim to realize the insulating antiferromagnetic
state of LNO. In this work, we grew [(La<sub>0.7</sub>Sr<sub>0.3</sub>MnO<sub>3</sub>)<sub>5</sub>-(LaNiO<sub>3</sub>)<sub><i>n</i></sub>]<sub>12</sub> superlattices on (001)-oriented SrTiO<sub>3</sub> substrates by pulsed laser deposition and observed an unexpected
exchange bias effect in field-cooled hysteresis loops. Through X-ray
absorption spectroscopy and magnetic circular dichroism experiments,
we found that the charge transfer at the interfacial Mn and Ni ions
can induce a localized magnetic moment. A remarkable increase of exchange
bias field and a transition from metal to insulator were simultaneously
observed upon decreasing the thickness of the LNO layer, indicating
the antiferromagnetic insulator state in 2 unit cells LNO ultrathin
layers. The robust exchange bias of 745 Oe in the superlattice is
caused by an interfacial localized magnetic moment and an antiferromagnetic
state in the ultrathin LNO layer, pinning the ferromagnetic La<sub>0.7</sub>Sr<sub>0.3</sub>MnO<sub>3</sub> layers together. Our results
demonstrate that artificial interface engineering is a useful method
to realize novel magnetic and transport properties
Atomic-Scale Magnetism of Cr-Doped Bi<sub>2</sub>Se<sub>3</sub> Thin Film Topological Insulators
Magnetic doping is the most common method for breaking time-reversal-symmetry surface states of topological insulators (TIs) to realize novel physical phenomena and to create beneficial technological applications. Here we present a study of the magnetic coupling of a prototype magnetic TI, that is, Cr-doped Bi<sub>2</sub>Se<sub>3</sub>, in its ultrathin limit which is expected to give rise to quantum anomalous Hall (QAH) effect. The high quality Bi<sub>2–<i>x</i></sub>Cr<sub><i>x</i></sub>Se<sub>3</sub> epitaxial thin film was prepared using molecular beam epitaxy (MBE), characterized with scanning transimission electron microscopy (STEM), electrical magnetotransport, and X-ray magnetic circularly dichroism (XMCD) techniques, and the results were simulated using density functional theory (DFT) with spin–orbit coupling (SOC). We observed a sizable spin moment <i>m</i><sub>spin</sub> = (2.05 ± 0.20) μ<sub>B</sub>/Cr and a small and negative orbital moment <i>m</i><sub>orb</sub> = (−0.05 ± 0.02) μ<sub>B</sub>/Cr of the Bi<sub>1.94</sub>Cr<sub>0.06</sub>Se<sub>3</sub> thin film at 2.5 K. A remarkable fraction of the (Cr<sub>Bi</sub>–Cr<sub>I</sub>)<sup>3+</sup> antiferromagnetic dimer in the Bi<sub>2–<i>x</i></sub>Cr<sub><i>x</i></sub>Se<sub>3</sub> for 0.02 < <i>x</i> < 0.40 was obtained using <i>first-principles</i> simulations, which was neglected in previous studies. The spontaneous coexistence of ferro- and antiferromagnetic Cr defects in Bi<sub>2–<i>x</i></sub>Cr<sub><i>x</i></sub>Se<sub>3</sub> explains our experimental observations and those based on conventional magnetometry which universally report magnetic moments significantly lower than 3 μ<sub>B</sub>/Cr predicted by Hund’s rule
Enhancing the Spin–Orbit Coupling in Fe<sub>3</sub>O<sub>4</sub> Epitaxial Thin Films by Interface Engineering
By analyzing the in-plane angular
dependence of ferromagnetic resonance linewidth, we show that the
Gilbert damping constant in ultrathin Fe<sub>3</sub>O<sub>4</sub> epitaxial
films on GaAs substrate can be enhanced by thickness reduction and
oxygen vacancies in the interface. At the same time, the uniaxial
magnetic anisotropy due to the interface effect becomes significant.
Using the element-specific technique of X-ray magnetic circular dichroism,
we find that the orbital-to-spin moment ratio increases with decreasing
film thickness, in full agreement with the increase in the Gilbert
damping obtained for these ultrathin single-crystal films. Combined
with the first-principle calculations, the results suggest that the
bonding with Fe and Ga or As ions and the ionic distortion near the
interface, as well as the FeO defects and oxygen vacancies, may increase
the spin–orbit coupling in ultrathin Fe<sub>3</sub>O<sub>4</sub> epitaxial films and in turn provide an enhanced damping
Enhancing Magnetic Ordering in Cr-Doped Bi<sub>2</sub>Se<sub>3</sub> Using High‑<i>T</i><sub>C</sub> Ferrimagnetic Insulator
We
report a study of enhancing the magnetic ordering in a model magnetically
doped topological insulator (TI), Bi<sub>2–<i>x</i></sub>Cr<sub><i>x</i></sub>Se<sub>3</sub>, via the proximity
effect using a high-<i>T</i><sub>C</sub> ferrimagnetic insulator
Y<sub>3</sub>Fe<sub>5</sub>O<sub>12</sub>. The FMI provides the TI
with a source of exchange interaction yet without removing the nontrivial
surface state. By performing the elemental specific X-ray magnetic
circular dichroism (XMCD) measurements, we have unequivocally observed
an enhanced <i>T</i><sub>C</sub> of 50 K in this magnetically
doped TI/FMI heterostructure. We have also found a larger (6.6 nm
at 30 K) but faster decreasing (by 80% from 30 to 50 K) penetration
depth compared to that of diluted ferromagnetic semiconductors (DMSs),
which could indicate a novel mechanism for the interaction between
FMIs and the nontrivial TIs surface