Cs_(x)WO_(3)/TiO_(2) composites with full-spectrum catalytic activity were prepared by solvothermal reaction.The composites were characterized using X-ray diffraction(XRD)analysis,scanning electron microscopy(SEM),tra...Cs_(x)WO_(3)/TiO_(2) composites with full-spectrum catalytic activity were prepared by solvothermal reaction.The composites were characterized using X-ray diffraction(XRD)analysis,scanning electron microscopy(SEM),transmission electron microscopy(TEM),specific surface area testing,X-ray photoelectron spectroscopy(XPS),and UV-Vis diffuse reflectance spectra(UV-Vis DRS).Cs_(x)WO_(3) and TiO_(2) were uniformly bonded together in the compos-ites.The heterojunction structure was formed.The band gap was reduced from 2.75 to 2.65 eV.The photocatalytic property of Cs_(x)WO_(3)/TiO_(2)was demonstrated by the degradation rates of 20 mg·L^(-1) methylene blue dye,which were 99.7%,91.4%,and 70.7%under irradiation from a 300 W high-pressure mercury lamp,a 500 W xenon lamp,and a 400 W infrared lamp,respectively.After five cycles of photocatalytic degradation,the composite photocatalyst still showed a degradation efficiency of 87.6%.This indicates that Cs_(x)WO_(3)/TiO_(2) has good photocatalytic degradability and cyclic stability.The photocatalytic mechanism of Cs_(x)WO_(3)/TiO_(2)was investigated.The trapping experiments of the active species showed that the main active substances were the empty hole(h+)and hydroxyl radical(·OH).展开更多
The microstructure and texture of C/C composites with a resin-derived carbon, a rough laminar （RL） pyrocarbon and a smooth laminar pyrocarbon, before and after braking tests, were investigated by Raman spectroscopy....The microstructure and texture of C/C composites with a resin-derived carbon, a rough laminar （RL） pyrocarbon and a smooth laminar pyrocarbon, before and after braking tests, were investigated by Raman spectroscopy. The full width at half maximum （FWHM） of the D-band indicates the amount of defects in the in-plane lattice, while the G-to-D band intensity （peak area） ratios （lC/ID） is used to evaluate the degree of graphitization. The results show that the FWHM of D-band of sample with RL pyrocarbon changes greatly from 36 cm-1 to 168 cm 1 after braking tests, which indicates that a large number of lattice defects are produced on its wear surface. However, the graphitization degree of resin-derived carbon sample rises significantly, because the IC/1D increases from 0.427 to 0.928. Braking tests under normal loading conditions, involving high temperature and high pressure, produce a lot of lattice defects on the wear surface, and induce the graphitization of the surface. Sample with RL pyrocarbon having a low hardness is easy to deform, and has the most lattice defects on the wear surface after braking. While raw materials with resin-derived carbon have the lowest graphitization degree which rises greatly during braking.展开更多
The optimization of electrolytes and the material removal mechanisms for Cu electrochemical mechanical planarization(ECMP)at different pH values including 5-methyl-1H-benzotriazole(TTA),hydroxyethylidenediphosphoric a...The optimization of electrolytes and the material removal mechanisms for Cu electrochemical mechanical planarization(ECMP)at different pH values including 5-methyl-1H-benzotriazole(TTA),hydroxyethylidenediphosphoric acid(HEDP),and tribasic ammonium citrate(TAC)were investigated by electrochemical techniques,X-ray photoelectron spectrometer(XPS)analysis,nano-scratch tests,AFM measurements,and polishing of Cu-coated blanket wafers.The experimental results show that the planarization efficiency and the surface quality after ECMP obtained in alkali-based solutions are superior to that in acidic-based solutions,especially at pH=8.The optimal electrolyte compositions(mass fraction)are 6% HEDP,0.3% TTA and 3% TAC at pH=8.The main factor affecting the thickness of the oxide layer formed during ECMP process is the applied potential.The soft layer formation is a major mechanism for electrochemical enhanced mechanical abrasion.The surface topography evolution before and after electrochemical polishing(ECP)illustrates the mechanism of mechanical abrasion accelerating electrochemical dissolution,that is,the residual stress caused by the mechanical wear enhances the electrochemical dissolution rate.This understanding is beneficial for optimization of ECMP processes.展开更多
An iridium （Ⅲ） bis[（4,6-difluorophenyl）pyridinato-N, C^2][6-（6＇-（4＂-（ 5＂-phenyl- 1＂, 3＂, 4＂-oxadiazole-2＂-yl） phenoxy） hexyloxy picolinate） was synthesized and characterized by IH NMR and elementary ...An iridium （Ⅲ） bis[（4,6-difluorophenyl）pyridinato-N, C^2][6-（6＇-（4＂-（ 5＂-phenyl- 1＂, 3＂, 4＂-oxadiazole-2＂-yl） phenoxy） hexyloxy picolinate） was synthesized and characterized by IH NMR and elementary analysis in order to study the effect of ancillary ligand of the oxadiazole-based picolinic acid derivative on optophysical properties of its iridium complex, and further to obtain an iridium complex with highly-efficient blue emission. The thermal stability, UV absorption and photoluminescent properties of this iridium complex were investigated. Compared with iridium （Ⅲ） bis[（4,6-difluorophenyl）pyridinato-N, C^2]（picolinate） reported as a highly-efficient blue electroluminescent material, this iridium complex bearing an oxadiazole-based picolinic acid derivative presents higher thermal stability, more intense UV absorption at 291 nm and similar photoluminescent spectrum peaked at 469 nm. This indicates that tuning ancillary ligand of picolinic acid with an oxadiazole unit can improve the optophysical properties of its iridium complex.展开更多
文摘Cs_(x)WO_(3)/TiO_(2) composites with full-spectrum catalytic activity were prepared by solvothermal reaction.The composites were characterized using X-ray diffraction(XRD)analysis,scanning electron microscopy(SEM),transmission electron microscopy(TEM),specific surface area testing,X-ray photoelectron spectroscopy(XPS),and UV-Vis diffuse reflectance spectra(UV-Vis DRS).Cs_(x)WO_(3) and TiO_(2) were uniformly bonded together in the compos-ites.The heterojunction structure was formed.The band gap was reduced from 2.75 to 2.65 eV.The photocatalytic property of Cs_(x)WO_(3)/TiO_(2)was demonstrated by the degradation rates of 20 mg·L^(-1) methylene blue dye,which were 99.7%,91.4%,and 70.7%under irradiation from a 300 W high-pressure mercury lamp,a 500 W xenon lamp,and a 400 W infrared lamp,respectively.After five cycles of photocatalytic degradation,the composite photocatalyst still showed a degradation efficiency of 87.6%.This indicates that Cs_(x)WO_(3)/TiO_(2) has good photocatalytic degradability and cyclic stability.The photocatalytic mechanism of Cs_(x)WO_(3)/TiO_(2)was investigated.The trapping experiments of the active species showed that the main active substances were the empty hole(h+)and hydroxyl radical(·OH).
基金Project(2006CB600906) supported by the National Basic Research Program of China
文摘The microstructure and texture of C/C composites with a resin-derived carbon, a rough laminar （RL） pyrocarbon and a smooth laminar pyrocarbon, before and after braking tests, were investigated by Raman spectroscopy. The full width at half maximum （FWHM） of the D-band indicates the amount of defects in the in-plane lattice, while the G-to-D band intensity （peak area） ratios （lC/ID） is used to evaluate the degree of graphitization. The results show that the FWHM of D-band of sample with RL pyrocarbon changes greatly from 36 cm-1 to 168 cm 1 after braking tests, which indicates that a large number of lattice defects are produced on its wear surface. However, the graphitization degree of resin-derived carbon sample rises significantly, because the IC/1D increases from 0.427 to 0.928. Braking tests under normal loading conditions, involving high temperature and high pressure, produce a lot of lattice defects on the wear surface, and induce the graphitization of the surface. Sample with RL pyrocarbon having a low hardness is easy to deform, and has the most lattice defects on the wear surface after braking. While raw materials with resin-derived carbon have the lowest graphitization degree which rises greatly during braking.
基金Project(50975058)supported by the National Science Foundation of China
文摘The optimization of electrolytes and the material removal mechanisms for Cu electrochemical mechanical planarization(ECMP)at different pH values including 5-methyl-1H-benzotriazole(TTA),hydroxyethylidenediphosphoric acid(HEDP),and tribasic ammonium citrate(TAC)were investigated by electrochemical techniques,X-ray photoelectron spectrometer(XPS)analysis,nano-scratch tests,AFM measurements,and polishing of Cu-coated blanket wafers.The experimental results show that the planarization efficiency and the surface quality after ECMP obtained in alkali-based solutions are superior to that in acidic-based solutions,especially at pH=8.The optimal electrolyte compositions(mass fraction)are 6% HEDP,0.3% TTA and 3% TAC at pH=8.The main factor affecting the thickness of the oxide layer formed during ECMP process is the applied potential.The soft layer formation is a major mechanism for electrochemical enhanced mechanical abrasion.The surface topography evolution before and after electrochemical polishing(ECP)illustrates the mechanism of mechanical abrasion accelerating electrochemical dissolution,that is,the residual stress caused by the mechanical wear enhances the electrochemical dissolution rate.This understanding is beneficial for optimization of ECMP processes.
基金Projects(20772101,50473046) supported by the National Natural Science Foundation of ChinaProject(2007FJ3017) supported by the Hunan Provincial Science Foundation, ChinaProject(07C764) supported by the Science Foundation of the Education Department of Hunan Province,China
文摘An iridium （Ⅲ） bis[（4,6-difluorophenyl）pyridinato-N, C^2][6-（6＇-（4＂-（ 5＂-phenyl- 1＂, 3＂, 4＂-oxadiazole-2＂-yl） phenoxy） hexyloxy picolinate） was synthesized and characterized by IH NMR and elementary analysis in order to study the effect of ancillary ligand of the oxadiazole-based picolinic acid derivative on optophysical properties of its iridium complex, and further to obtain an iridium complex with highly-efficient blue emission. The thermal stability, UV absorption and photoluminescent properties of this iridium complex were investigated. Compared with iridium （Ⅲ） bis[（4,6-difluorophenyl）pyridinato-N, C^2]（picolinate） reported as a highly-efficient blue electroluminescent material, this iridium complex bearing an oxadiazole-based picolinic acid derivative presents higher thermal stability, more intense UV absorption at 291 nm and similar photoluminescent spectrum peaked at 469 nm. This indicates that tuning ancillary ligand of picolinic acid with an oxadiazole unit can improve the optophysical properties of its iridium complex.
