11 research outputs found
Electric-Field Control of Spin–Orbit Torques in WS<sub>2</sub>/Permalloy Bilayers
Transition
metal dichalcogenides (TMDs) have drawn great attention owing to their
potential for electronic, optoelectronic, and spintronic applications.
In TMDs/ferromagnetic bilayers, an efficient spin current can be generated
by the TMDs to manipulate the magnetic moments in the ferromagnetic
layer. In this work, we report on the electric-field modulation of
spin–orbit torques (SOTs) in WS<sub>2</sub>/NiFe bilayers by
the spin-torque ferromagnetic resonance technique. It is found that
the radio frequency current can induce a spin accumulation at the
WS<sub>2</sub>/NiFe interface because of the interfacial Rashba–Edelstein
effect. As a consequence, the SOT ratio between the field-like and
antidamping-like torques can be effectively controlled by applying
the back-gate voltage in WS<sub>2</sub>/NiFe bilayers. These results
provide a strategy for controlling the SOT by using semiconducting
TMDs
Sulfur-Doped Black Phosphorus Field-Effect Transistors with Enhanced Stability
Black phosphorus
(BP) has drawn great attention owing to its tunable band gap depending
on thickness, high mobility, and large <i>I</i><sub>on</sub>/<i>I</i><sub>off</sub> ratio, which makes BP attractive
for using in future two-dimensional electronic and optoelectronic
devices. However, its instability under ambient conditions poses challenge
to the research and limits its practical applications. In this work,
we present a feasible approach to suppress the degradation of BP by
sulfur (S) doping. The fabricated S-doped BP few-layer field-effect
transistors (FETs) show more stable transistor performance under ambient
conditions. After exposing to air for 21 days, the charge-carrier
mobility of a representative S-doped BP FETs device decreases from
607 to 470 cm<sup>2</sup> V<sup>–1</sup> s<sup>–1</sup> (remained as high as 77.4%) under ambient conditions and a large <i>I</i><sub>on</sub>/<i>I</i><sub>off</sub> ratio of
∼10<sup>3</sup> is still retained. The atomic force microscopy
analysis, including surface morphology, thickness, and roughness,
also indicates the lower degradation rate of S-doped BP compared to
BP. First-principles calculations show that the dopant S atom energetically
prefers to chemisorb on the BP surface in a dangling form and the
enhanced stability of S-doped BP can be ascribed to the downshift
of the conduction band minimum of BP below the redox potential of
O<sub>2</sub>/O<sub>2</sub><sup>–</sup>. Our work suggests
that S doping is an effective way to enhance the stability of black
phosphorus
Microphotographs (×200) of a representative TNBC case.
<p>A: Hematoxylin-eosin staining. B–D: Immunohistochemical detection for ER, PR and HER-2, respectively. This case is negative for ER, PR and HER-2 (triple negative).</p
Chemoresistance-related miRNAs of the 11 selected miRNAs.
<p>Chemoresistance-related miRNAs of the 11 selected miRNAs.</p
Up-regulation of miR-130a-3p or miR-451a significantly changed MDA-MB-231 cells sensitivity to doxorubicin.
<p>A: Expression levels of miR-130a-3p or miR-451a were evaluated in different cell lines by qRT-PCR (** <i>P</i><0.01; *** <i>P</i><0.001, compared to MCF 10A). B: During doxorubicin treatment, miR-130a-3p or miR-451a were significantly down-regulated in MDA-MB-231 cells, respectively (*** <i>P</i><0.001, compared to vehicle control). C–D: Cells viability and cells apoptotic rate were analyzed by the cell counting kit-8 assay and flow cytometry, respectively (### <i>P</i><0.001, compared to vehicle control; * <i>P</i><0.05, ** <i>P</i><0.01, compared to Doxo group). All the results were obtained from three independent experiments. Doxo, doxorubicin.</p
qRT-PCR validation of miRNAs microarray results in TNBCs.
<p>Relative expression of miRNAs in TNBCs compared with their adjacent normal tissues by qRT-PCR. miR-10b-5p, miR-451a, miR-125b-5p, miR-31-5p, miR-195-5p, miR-130a-3p were down-regulated in cancer samples, whereas miR-155-5p, miR-21-3p, miR-181a-5p, miR-181b-5p and miR-183-5p were up-regulated. Dots, normalized ratio of miRNA expression values (TNBC/adjacent normal tissues).</p
miRNA differential expression in TNBC versus normal breast tissues.
<p>Hierarchical clustering of the 41 miRNAs with a significantly different expression. Rows, individual miRNAs; columns, individual tissue samples. Pseudocolors represent transcript levels above, equal to, and below the mean (red, black, and green, respectively). The scale represents the intensity of miRNA expression (log2 scale ranges between −9 and 5).</p
Additional file 1: Table S1.
Primers for coding sequences of ETV1 and miR-17-5p. (DOC 25 kb
Additional file 2: Table S2.
qRT-PCR primer sequences used in this study. (DOC 26 kb
Additional file 3: Figure S1.
Immunohistochemical staining of ETV1 in two representative TNBC tissues. a, c, Negative control of ETV1. b, d, Positive expression of ETV1. Among the 105 cases of TNBC, 79 cases were ETV1-positive and 26 were ETV1-negative according to the immunoreactivity score described in the text. Scale bar, 10 μm. (TIFF 22543 kb