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Tunable Plasmonic Quantum Light Source with Silver Nanoclusters on a Silver Surface
Cui Songbin,Kim Tae-Hwan,Ham Ungdon 한국물리학회 2020 THE JOURNAL OF THE KOREAN PHYSICAL SOCIETY Vol.77 No.2
Scanning tunneling luminescence (STL) can be used to investigate the optical properties of nanostructures with high spatial resolution beyond the diffraction limit of light. To get appropriate STL spectra, one needs to modify the tip repeatedly. However, such irreversible tip modification often leads to very unstable tips. Here, by using a scanning tunneling microscope (STM) tip, we demonstrate that STL spectra are tunable via silver nanocluster arrays fabricated directly on a silver surface. The silver nanoclusters are created by transferring silver atoms from the silver tip to the silver surface under STM. We found that the STL spectra were enhanced (suppressed) at higher (lower) energy on the clusters and that they showed opposite behaviors between the nanoclusters. Without relying on the irreversible tip shape modification, our findings indicate that we can tune the STL spectra simply by moving the STM tip over the nanoclusters. Our method can be used to provide a tunable light source for systematic nano-optical experiments and for nanoscale optical devices.
Unusual Diffusion Behavior of Copper-Hexadecafluoro-Phthalocyanine Molecules on Au(111)
Cui Songbin,Kim Tae-Hwan,Ham Ungdon 한국물리학회 2020 THE JOURNAL OF THE KOREAN PHYSICAL SOCIETY Vol.77 No.3
The unusual bias-voltage dependence of copper-hexadecafluoro-phthalocyanine (F16CuPc) molecules on Au(111) was investigated by using scanning tunneling microscopy/spectroscopy (STM/STS) at low temperatures. Depending on the bias polarity, the molecules seem to cover the whole surface of Au(111) at positive bias voltages while they are apparently invisible in STM images at negative bias voltages. Here, we experimentally demonstrate that the molecular diffusivity on Au(111) varies according to the applied electric field induced between the STM tip and the Au(111) surface rather than the intrinsic molecule-substrate interaction. Such results are corroborated by STS measurements indicating that attraction/repulsion of a molecule indeed occurs under an STM tip at positive/negative bias voltages during sweeps of the bias voltage. In addition, we found that the diffusive molecules are immobilized at a temperature of 8 K at both positive and negative bias voltages due to a lack of thermal energy for diffusion.
Jingcui Yu,Songbin Fu,Peng Liu,Xiaobo Cui,Yu Sui,Guohua Ji,Rongwei Guan,Donglin Sun,Wei Ji,Fangli Liu,An Liu,Yuzhen Zhao,Yang Yu,Yan Jin,Jing Bai,Jingshu Geng,Yingwei Xue,Jiping Qi,Ki-Young Lee 한국분자세포생물학회 2011 Molecules and cells Vol.32 No.1
Previously, we identified 3 overlapping regions showing loss of heterozygosity (LOH, R_1-R_3 from 11 to 30 cM) on chromosome 17 in 45 primary gastric cancers (GCs). The data indicated the presence of tumor suppressor genes (TSGs) on chromosome 17 involved in GC. Among the putative TSGs in these regions, HIC1 (in SR_1) and TOB1 (in SR_3) remain to be examined in GC. By immunohistochemistry (IHC), methylation-specific PCR (MSP) and western blot, we evaluated the expression and regulation status for HIC1 and TOB1 protein in GC. We narrowed down the deletion intervals on chromosome 17 and defined five smaller LOH subregions, SR_1-SR_5 (0.54 to 3.42 cM), in GC. We found that HIC1 had downregulated expression in 86% (91/106) and was methylated in 87% (26/30) of primary GCs. Of the primary GCs showing downregulation of HIC1 protein, 75% (18/24) had methylated HIC1 gene. TOB1 was either absent or expressed at reduced levels in 75% (73/97) of the GC samples. In addition, a general reduction was found in total and the ratio of unphosphorylated to phosphorylated TOB1 protein levels in the differentiated GC cell lines. Further analysis revealed significant simultaneous downregulation of both HIC1 and TOB1 protein in GC tissue microarray samples (67%, 52/78) and in primary GCs (65%, 11/17). These results indicate that silencing of HIC1 and TOB1 expression is a common occurrence in GC and may contribute to the development and progression of the disease.
Huagen Xiao,Songbin Liu,Yuan Huang 전력전자학회 2023 JOURNAL OF POWER ELECTRONICS Vol.23 No.3
Aiming at the problem of the grid connected and off grid switching control of grid connected inverters, an ac bus-voltage control method based on load impedance characteristics is proposed for single-phase photovoltaic grid-connected inverters with batteries in this paper. The proposed control method includes a detection algorithm for the load impedance angle and an AC bus-voltage control algorithm. Thus, grid-connected inverters can output active and reactive current in proportion to the load impedance characteristics without a special reactive power calculation module to support the AC bus voltage. At the same time, the proposed control method can avoid the switching action of the control algorithm when the grid-connected inverter is switched from grid-connected mode to island mode. Finally, simulation and experimental results verify the effectiveness of the proposed method.
TSPAN12 Precedes Tumor Proliferation by Cell Cycle Control in Ovarian Cancer
Ji, Guohua,Liang, Hongbin,Wang, Falin,Wang, Nan,Fu, Songbin,Cui, Xiaobo Korean Society for Molecular and Cellular Biology 2019 Molecules and cells Vol.42 No.7
TSPAN12, a member of the tetraspanin family, has been highly connected with the pathogenesis of cancer. Its biological function, however, especially in ovarian cancer (OC), has not been well elucidated. In this study, The Cancer Genome Atlas (TCGA) dataset analysis revealed that upregulation of TSPAN12 gene expression was significantly correlated with patient survival, suggesting that TSPAN12 might be a potential prognostic marker for OC. Further exploration showed that TSPAN12 overexpression accelerated proliferation and colony formation of OVCAR3 and SKOV3 OC cells. Knockdown of TSPAN12 expression in A2780 and SKOV3 cells decreased both proliferation and colony formation. Western blot analysis showed that several cyclins and cyclin-dependent kinases (CDK) (e.g., Cyclin A2, Cyclin D1, Cyclin E2, CDK2, and CDK4) were significantly involved in the regulation of cell cycle downstream of TSPAN12. Moreover, TSPAN12 accelerated mitotic progression by controlling cell cycle. Thus, our data demonstrated that TSPAN12 could be a novel molecular target for the treatment of OC.
TSPAN12 Precedes Tumor Proliferation by Cell Cycle Control in Ovarian Cancer
Guohua Ji,Hongbin Liang,Falin Wang,Nan Wang,Songbin Fu,Xiaobo Cui 한국분자세포생물학회 2019 Molecules and cells Vol.42 No.7
TSPAN12, a member of the tetraspanin family, has been highly connected with the pathogenesis of cancer. Its biological function, however, especially in ovarian cancer (OC), has not been well elucidated. In this study, The Cancer Genome Atlas (TCGA) dataset analysis revealed that upregulation of TSPAN12 gene expression was significantly correlated with patient survival, suggesting that TSPAN12 might be a potential prognostic marker for OC. Further exploration showed that TSPAN12 overexpression accelerated proliferation and colony formation of OVCAR3 and SKOV3 OC cells. Knockdown of TSPAN12 expression in A2780 and SKOV3 cells decreased both proliferation and colony formation. Western blot analysis showed that several cyclins and cyclin-dependent kinases (CDK) (e.g., Cyclin A2, Cyclin D1, Cyclin E2, CDK2, and CDK4) were significantly involved in the regulation of cell cycle downstream of TSPAN12. Moreover, TSPAN12 accelerated mitotic progression by controlling cell cycle. Thus, our data demonstrated that TSPAN12 could be a novel molecular target for the treatment of OC.