The ion transfer reaction of 2-benzoylpyridine-thiosemicarbazone (HL), which has antimicrobial and antifungal properties and anticancer activity, has been studied to determine its lipophilicity by cyclic voltammetry a...The ion transfer reaction of 2-benzoylpyridine-thiosemicarbazone (HL), which has antimicrobial and antifungal properties and anticancer activity, has been studied to determine its lipophilicity by cyclic voltammetry at the water/1,2-dichloroethane (1,2-DCE) interface. The physicochemical parameters such as standard partition coefficient (lgPI)andthestandardGibbsenergyoftransfer("G0tr,,wI "o)oftheprotonatedformoftheligandwere measured asa function of pH in aqueous phase. The protonated form of the ligand exhibited reversible or quasi-reversible voltammograms at the1,2-DCEintherangeofpH1-5.Theprotonationconstantsoftheligand,pKa1andpKa2,weredeterminedspectrophotometrically and were found to be 12.14 and 3.24, respectively. The standard Gibbs energy of transfer ("G0tr,,wN" o) and the partition coefficient of neutral species (lgPN) were also determined by the shake-flask method. The standard Gibbs energy of transfer of this compound across the water/1,2-DCE interface was evaluated as the quantitative measure of its lipophilicity. The difference between lgPI and lgPN was related to the degree of charge delocalization and was used to evaluate qualitatively the lipophilicity of the ligand.展开更多
The dependence of the ratio R1 for transfer ionization to single capture for Cq+, Nq+, Oq+, Neq+ ions on Ne target upon the electronic structure of the projectile is studied. For Aq+-Ne collisions the ratio R1 decreas...The dependence of the ratio R1 for transfer ionization to single capture for Cq+, Nq+, Oq+, Neq+ ions on Ne target upon the electronic structure of the projectile is studied. For Aq+-Ne collisions the ratio R1 decreases as the atomic number Z of the projectile increases for q=4,5,6,7 sequences which provides strong evidence for the increase of the binding energy of the target valence electron after single electron capture. The increase in binding energy depends both upon the atomic number of the projectile and the target atom.展开更多
The production mechanism of heavy neutronrich nuclei is investigated by using the multinucleon transfer reactions of ^(136;148)Xe+^(208)Pb and ^(238)U+^(208)Pb in the framework of a dinuclear system model. The evapora...The production mechanism of heavy neutronrich nuclei is investigated by using the multinucleon transfer reactions of ^(136;148)Xe+^(208)Pb and ^(238)U+^(208)Pb in the framework of a dinuclear system model. The evaporation residual cross sections of target-like fragments are studied with the reaction system ^(148)Xe+^(208)Pb at near barrier energies. The results show that the final isotopic production cross sections in the neutron-deficient side are very sensitive to incident energy while it is not sensitive in the neutron-rich side. Comparing the isotopic production cross sections for the reactions of ^(208)Pb bombarded with stable and radioactive projectiles, we find that neutron-rich radioactive beams can significantly increase the production cross sections of heavy neutron-rich nuclei.展开更多
In this paper a projectile ion-recoil ion coincidence technique is used to investigate the transfer ionization processes in collisions of 0.22-6.30 MeV Cq＋ ions and 0.25-6.35 MeV 0q＋ ions （q=1, 2, 3, 4） with the H...In this paper a projectile ion-recoil ion coincidence technique is used to investigate the transfer ionization processes in collisions of 0.22-6.30 MeV Cq＋ ions and 0.25-6.35 MeV 0q＋ ions （q=1, 2, 3, 4） with the He atom separately. The cross section ratio f of transfer ionization to single electron transfer is measured, and the dependence of f on both charge state q and energy E of the projectiles is investigated. The electron-structure and the mechanisms leading to transfer ionization affect the dependence of f on q and E. Our measurements, along with other data published previously, suggest a similar dependence of f on charge state and energy of projectile for partially stripped ions over a large energy range. The maximum value of f is approximately 0.17q^0.60; the energy corresponding to maximum f is about 160q^0.60 keV/u.展开更多
The ratios of transfer ionization （TI） to single-electron capture （SC） cross sections have been measured for the collisions of partially stripped C^q＋ ions （q = 1-4） with He. The collision velocity ranges from ...The ratios of transfer ionization （TI） to single-electron capture （SC） cross sections have been measured for the collisions of partially stripped C^q＋ ions （q = 1-4） with He. The collision velocity ranges from 0.7 to 4.4 vo （vo is the Bohr velocity）. The projectile-ion and recoil-ion coincidence technique is used to separate the processes of TI and SC. The ratios reach the maximum when the velocity is about 3.7 vo. This can be explained qualitatively based on the two-step mechanism. The experimental results are also compared with the results calculated using the classical trajectory Monte Carlo （CTMC） method. The CTMC results are in agreement with the experimental data basically. The discrepancies in higher velocity region are interpreted by the effective charge effect.展开更多
The widely used energy transfer theory is a foundation of luminescence, in which the rates of Stokes and anti-Stokes processes have the same calculation formula. An improvement on the anti-Stokes energy transfer to ex...The widely used energy transfer theory is a foundation of luminescence, in which the rates of Stokes and anti-Stokes processes have the same calculation formula. An improvement on the anti-Stokes energy transfer to explain the fluorescence intensity reversal between the red and green fluorescence of Er（0.5）Yb（9.5）：FOV is reported in the present article. The range of the intensity reversal Z was measured to be 877. Dynamic processes for 16 levels were simulated. A coefficient, the improvement factor of the intensity ratio of Stokes to anti-Stokes processes in quantum Raman theory compared to classical Raman theory, is introduced to successfully describe the anti-Stokes energy transfer. A new method to calculate the distance between the rare earth ions, which is critical for the energy transfer calculation, is proposed. The validity of these important improvements is also proved by experiment.展开更多
Er2O3-doped bismuth silicate glasses are prepared by the conventional melt-quenching method, and the Er^3＋ ：^4 I13/2 → ^4I15/2 fluorescence properties are studied for different Er^3＋ concentrations. Infrared spect...Er2O3-doped bismuth silicate glasses are prepared by the conventional melt-quenching method, and the Er^3＋ ：^4 I13/2 → ^4I15/2 fluorescence properties are studied for different Er^3＋ concentrations. Infrared spectra are measured to estimate the exact content of OH- groups in the samples. Based on the electric dipole-dipole interaction theory, the interaction parameter CEr,Er for the migration rate of Er^3＋：^4 I13/2 → ^4I13/2 in proposed glasses is calculated.展开更多
The rate and cycling performances of the electrode materials are affected by many factors in a practical complicated electrode process. Learning about the limiting step in a practical electrochemical reaction is very ...The rate and cycling performances of the electrode materials are affected by many factors in a practical complicated electrode process. Learning about the limiting step in a practical electrochemical reaction is very important to effectively improve the electrochemical performances of the electrode materials. Li4Ti5O12, as a zero-strain material, has been considered as a promising anode material for long life Li-ion batteries. In this study, our results show that the Li4Ti5O12 pasted on Cu or graphite felt current collector exhibits unexpectedly higher rate performance than on A1 current collector. For Li4Ti5O12, the electron transfer between current collector and active material is the critical factor that affects its rate and cycling performances.展开更多
Li4Ti5012 (LTO) with rich R-TiO2 (17.06, 23.69, and 34.42 wt%), namely, R-TiO2@Li4Ti5O12 composites, were synthesized using the hydrothermal method and tetrabutyl titanate (TBT) as the precursor. Rietveld refinement o...Li4Ti5012 (LTO) with rich R-TiO2 (17.06, 23.69, and 34.42 wt%), namely, R-TiO2@Li4Ti5O12 composites, were synthesized using the hydrothermal method and tetrabutyl titanate (TBT) as the precursor. Rietveld refinement of X-ray diffraction (XRD) results show that the proportion of Li occupying 16d sites is extraordinary low and the lattice constants of LTO and R-TiO2 change with the ritanium dioxide content. EIS measurements showed that with in creasing R-TiO2 content, both its charge transfer impedance (Rct) and lithium ion diffusion coefficient (DLi) decreased. The changes of Rct and DLi caused by the increase of titanium dioxide content have synergic-antagonistic effects on the rate and cycle properties of Li4Ti5012. The rate performance is positively related to DLi, while the cycle property is negatively correlated with Rct, indicati ng that the rate performs nee is mainly related to DLi, while Rct more significantly affects the cycle performance. LTO-RT-17.06% exhibited excellent rate properties, especially under a high current density (5.0 C, 132.5 mAh/g) and LTO-RT-34.42% showed superior long-term cycle performance (0.012% capacity loss per cycle) compared to that of LTO-RT-17.06% and LTO-RT-23.69%.展开更多
Interfacial charge transfer is the key kinetic process dictating the operation of lithium-ion battery. Redox-mediated charge propagations of the electronic （e- and h＋ ） and ionic species （Li＋） at the electrode-e...Interfacial charge transfer is the key kinetic process dictating the operation of lithium-ion battery. Redox-mediated charge propagations of the electronic （e- and h＋ ） and ionic species （Li＋） at the electrode-electrolyte interface have recently gained increasing attention for better exploitation of battery materials. This article briefly summarises the energetic and kinetic aspects of lithium-ion batteries, and reviews the recent progress on various redox-assisted Li＋ storage approaches. From molecular wiring to polymer wiring and from redox targeting to redox flow lithium battery, the role of redox mediators and the way of the redox species functioning in lithium-ion batteries are discussed.展开更多
The properties of one-photon absorption（OPA）, emission and two-photon absorption（TPA） of a di-2-picolylaminebased zinc ion sensor are investigated by employing the density functional theory in combination with res...The properties of one-photon absorption（OPA）, emission and two-photon absorption（TPA） of a di-2-picolylaminebased zinc ion sensor are investigated by employing the density functional theory in combination with response functions.The responsive mechanism is explored. It is found that the calculated OPA and TPA properties are quite consistent with experimental data. Because the intra-molecular charge transfer（ICT） increases upon zinc ion binding, the TPA intensity is enhanced dramatically. According to the model sensor, we design a series of zinc ion probes which differ by conjugation center, acceptor and donor moieties. The properties of OPA, emission and TPA of the designed molecules are calculated at the same computational level. Our results demonstrate that the OPA and emission wavelengths of the designed probes have large red-shifts after zinc ions have been bound. Comparing with the model sensor, the TPA intensities of the designed probes are enhanced significantly and the absorption positions are red-shifted to longer wavelength range. Furthermore, the TPA intensity can be improved greatly upon zinc ion binding due to the increased ICT mechanism. These compounds are potential excellent candidates for two-photon fluorescent zinc ion probes.展开更多
Charge transfer cross sections for Kr^q＋ with Ne are calculated quantitatively by using modified classical over barrier model in order to clarify energy dependence of charge transfer cross sections in low energy regi...Charge transfer cross sections for Kr^q＋ with Ne are calculated quantitatively by using modified classical over barrier model in order to clarify energy dependence of charge transfer cross sections in low energy region. Essential of this model is taking the induced dipole potential into consideration. As a result, this calculation can reproduce systematic energy dependence of experimental results. This suggests that the bending trajectory of the projectile due to an induced dipole potential should be considered to describe pictures of collisions at low energy regime below 1 keV/u.展开更多
The collision dynamics and fragmentation process of molecule by highly charged ion impact for single electron capture processes at the low energies below 1 keV/u were studied. The collision energy dependence of the re...The collision dynamics and fragmentation process of molecule by highly charged ion impact for single electron capture processes at the low energies below 1 keV/u were studied. The collision energy dependence of the recoil momentum was obtained experimentally and compared it with those calculated by a theoretical model using a deflection function with polarization potential. A fairly good agreement between the measured and calculated results was reached. This suggests that the polarization potential plays a crucial role in the low-energy region.展开更多
Low-energy ion beam implantation （10 - 200 keV） has been proved to have a wide range of biological effects and is broadly used in the breeding of crops and micro-organisms.To understand its mechanisms better and fac...Low-energy ion beam implantation （10 - 200 keV） has been proved to have a wide range of biological effects and is broadly used in the breeding of crops and micro-organisms.To understand its mechanisms better and facilitate its applications, the developments in the bioeffects of low energy ion beam implantation in the past twenty years are summarized in this paper.展开更多
The ionization process in the collisions of He^2＋ with C^q＋ （q = 0-5） is investigated by using the continuum-distorted-wave eikonal-initial-state approximation. Double-differential cross sections for 1s and 2s sub...The ionization process in the collisions of He^2＋ with C^q＋ （q = 0-5） is investigated by using the continuum-distorted-wave eikonal-initial-state approximation. Double-differential cross sections for 1s and 2s sub-shells are obtained at the electron-ejected angle θ = 0° with the projectile energy ranging from 30keV/u to 10MeV/u. Variation of ionization mechanisms with q in C^q＋ is studied, and the dependences on the projectile energies and target sub-shells are also discussed. It is found that in the whole energy range, the absolute values of soft collision （SC） and binary encounter （BE） peaks decrease with increasing q. For the lower incident energies, the electron capture to the projectile continuum （ECC） peak decrease with increasing q as well as SC and BE peaks. For the higher incident energies （〉 1 MeV/u）, the absolute value of ECC peak increases with increasing q, so that the crossings of cross sections appear for C^q＋ with different q. This can be explained by the matching of velocities between the projectile and the electron initially bound to the target.展开更多
A preliminary design for a heavy ion driver inertial fusion（HIDIF） target is presented. The effect of target material and dimensions on transfer efficiency and symmetrical irradiation in the hohlraum are investigate...A preliminary design for a heavy ion driver inertial fusion（HIDIF） target is presented. The effect of target material and dimensions on transfer efficiency and symmetrical irradiation in the hohlraum are investigated.The analysis led to the evaluation of optimal target materials and dimensions to achieve a positive power balance of an ICF power plant.The results show that the best choice is a high Z material for cavity wall materials and a low Z material for the capsule ablator.It is concluded that for achieving the highest transfer efficiency and best symmetrization we need an area ratio between 5≤A2/A1≤9.展开更多
The mass transfer of thiophene through pervaporation（PV） membranes could be facilitated by certain transitional metal ions like Ag+, Mn2+, and Cr3+ thanks to their p complexation with thiophene. In this study, Ag+, ...The mass transfer of thiophene through pervaporation（PV） membranes could be facilitated by certain transitional metal ions like Ag+, Mn2+, and Cr3+ thanks to their p complexation with thiophene. In this study, Ag+, Mn2+, and Cr3+ ions were loaded onto the polyether block amide（PEBAX）/PAN composite membranes and were tested on the performance for separation of thiophene/n-heptane mixture. Pervaporation test results showed that the pervaporative separation index increased significantly to 73.1%, 75.5%, and 97.2% at 30 oC for the Ag+-, Mn2+-, Cr3+-loaded PEBAX membranes, respectively,as compared to the pristine PEBAX/PAN composite membrane.展开更多
基金the Scientific Research Projects (BAP) of Selcuk University, Turkey (2003/151).
文摘The ion transfer reaction of 2-benzoylpyridine-thiosemicarbazone (HL), which has antimicrobial and antifungal properties and anticancer activity, has been studied to determine its lipophilicity by cyclic voltammetry at the water/1,2-dichloroethane (1,2-DCE) interface. The physicochemical parameters such as standard partition coefficient (lgPI)andthestandardGibbsenergyoftransfer("G0tr,,wI "o)oftheprotonatedformoftheligandwere measured asa function of pH in aqueous phase. The protonated form of the ligand exhibited reversible or quasi-reversible voltammograms at the1,2-DCEintherangeofpH1-5.Theprotonationconstantsoftheligand,pKa1andpKa2,weredeterminedspectrophotometrically and were found to be 12.14 and 3.24, respectively. The standard Gibbs energy of transfer ("G0tr,,wN" o) and the partition coefficient of neutral species (lgPN) were also determined by the shake-flask method. The standard Gibbs energy of transfer of this compound across the water/1,2-DCE interface was evaluated as the quantitative measure of its lipophilicity. The difference between lgPI and lgPN was related to the degree of charge delocalization and was used to evaluate qualitatively the lipophilicity of the ligand.
文摘The dependence of the ratio R1 for transfer ionization to single capture for Cq+, Nq+, Oq+, Neq+ ions on Ne target upon the electronic structure of the projectile is studied. For Aq+-Ne collisions the ratio R1 decreases as the atomic number Z of the projectile increases for q=4,5,6,7 sequences which provides strong evidence for the increase of the binding energy of the target valence electron after single electron capture. The increase in binding energy depends both upon the atomic number of the projectile and the target atom.
基金supported by the National Natural Science Foundation of China under Grants Nos.11635003,11025524 and 11161130520the National Basic Research Program of China under Grant No.2010CB832903+1 种基金the European Commission’s 7th Framework Programme(Fp7-PEOPLE-2010-IRSES)under Grant Agreement Project No.269131the Project funded by China Postdoctoral Science Foundation(Grant No.2016M600956)
文摘The production mechanism of heavy neutronrich nuclei is investigated by using the multinucleon transfer reactions of ^(136;148)Xe+^(208)Pb and ^(238)U+^(208)Pb in the framework of a dinuclear system model. The evaporation residual cross sections of target-like fragments are studied with the reaction system ^(148)Xe+^(208)Pb at near barrier energies. The results show that the final isotopic production cross sections in the neutron-deficient side are very sensitive to incident energy while it is not sensitive in the neutron-rich side. Comparing the isotopic production cross sections for the reactions of ^(208)Pb bombarded with stable and radioactive projectiles, we find that neutron-rich radioactive beams can significantly increase the production cross sections of heavy neutron-rich nuclei.
文摘In this paper a projectile ion-recoil ion coincidence technique is used to investigate the transfer ionization processes in collisions of 0.22-6.30 MeV Cq＋ ions and 0.25-6.35 MeV 0q＋ ions （q=1, 2, 3, 4） with the He atom separately. The cross section ratio f of transfer ionization to single electron transfer is measured, and the dependence of f on both charge state q and energy E of the projectiles is investigated. The electron-structure and the mechanisms leading to transfer ionization affect the dependence of f on q and E. Our measurements, along with other data published previously, suggest a similar dependence of f on charge state and energy of projectile for partially stripped ions over a large energy range. The maximum value of f is approximately 0.17q^0.60; the energy corresponding to maximum f is about 160q^0.60 keV/u.
文摘The ratios of transfer ionization （TI） to single-electron capture （SC） cross sections have been measured for the collisions of partially stripped C^q＋ ions （q = 1-4） with He. The collision velocity ranges from 0.7 to 4.4 vo （vo is the Bohr velocity）. The projectile-ion and recoil-ion coincidence technique is used to separate the processes of TI and SC. The ratios reach the maximum when the velocity is about 3.7 vo. This can be explained qualitatively based on the two-step mechanism. The experimental results are also compared with the results calculated using the classical trajectory Monte Carlo （CTMC） method. The CTMC results are in agreement with the experimental data basically. The discrepancies in higher velocity region are interpreted by the effective charge effect.
基金Project supported by the National Natural Science Foundation of China (Grant No 10674019)
文摘The widely used energy transfer theory is a foundation of luminescence, in which the rates of Stokes and anti-Stokes processes have the same calculation formula. An improvement on the anti-Stokes energy transfer to explain the fluorescence intensity reversal between the red and green fluorescence of Er（0.5）Yb（9.5）：FOV is reported in the present article. The range of the intensity reversal Z was measured to be 877. Dynamic processes for 16 levels were simulated. A coefficient, the improvement factor of the intensity ratio of Stokes to anti-Stokes processes in quantum Raman theory compared to classical Raman theory, is introduced to successfully describe the anti-Stokes energy transfer. A new method to calculate the distance between the rare earth ions, which is critical for the energy transfer calculation, is proposed. The validity of these important improvements is also proved by experiment.
基金Supported by the Science and Technology Department of Zhejiang Province under Grant No 2006C21082, the Natural Science Foundation of Zhejiang Province under Grant No 601011.
文摘Er2O3-doped bismuth silicate glasses are prepared by the conventional melt-quenching method, and the Er^3＋ ：^4 I13/2 → ^4I15/2 fluorescence properties are studied for different Er^3＋ concentrations. Infrared spectra are measured to estimate the exact content of OH- groups in the samples. Based on the electric dipole-dipole interaction theory, the interaction parameter CEr,Er for the migration rate of Er^3＋：^4 I13/2 → ^4I13/2 in proposed glasses is calculated.
基金supported by the "Hundred Talent Project" of the Chinese Academy of Sciencesthe National High Technology Research and Development Program of China(Grant No.2009AA033101)+3 种基金the National Basic Research Program of China(Grant Nos.2007CB936500 and 2010CB833102)the National Natural Science Foundation of China(Grant No.50972164)the Science and Technology Planning Project of Guangdong Province,China(Grant No.2010A090602001)the Knowledge Innovation Program of the Chinese Academy of Sciences(Grant No.KJCX2-YW-W26)
文摘The rate and cycling performances of the electrode materials are affected by many factors in a practical complicated electrode process. Learning about the limiting step in a practical electrochemical reaction is very important to effectively improve the electrochemical performances of the electrode materials. Li4Ti5O12, as a zero-strain material, has been considered as a promising anode material for long life Li-ion batteries. In this study, our results show that the Li4Ti5O12 pasted on Cu or graphite felt current collector exhibits unexpectedly higher rate performance than on A1 current collector. For Li4Ti5O12, the electron transfer between current collector and active material is the critical factor that affects its rate and cycling performances.
基金financially supported by the National Natural Science Foundation of China(No.51641206)Shandong Natural Science Foundation Project(No.ZR2015EM013)+1 种基金Special Funds for Independent Innovation and Transformation of Achievements in Shandong Province(No.2014CGZH0911)National Key R&D Program of China(No.2016YFB0100508)
文摘Li4Ti5012 (LTO) with rich R-TiO2 (17.06, 23.69, and 34.42 wt%), namely, R-TiO2@Li4Ti5O12 composites, were synthesized using the hydrothermal method and tetrabutyl titanate (TBT) as the precursor. Rietveld refinement of X-ray diffraction (XRD) results show that the proportion of Li occupying 16d sites is extraordinary low and the lattice constants of LTO and R-TiO2 change with the ritanium dioxide content. EIS measurements showed that with in creasing R-TiO2 content, both its charge transfer impedance (Rct) and lithium ion diffusion coefficient (DLi) decreased. The changes of Rct and DLi caused by the increase of titanium dioxide content have synergic-antagonistic effects on the rate and cycle properties of Li4Ti5012. The rate performance is positively related to DLi, while the cycle property is negatively correlated with Rct, indicati ng that the rate performs nee is mainly related to DLi, while Rct more significantly affects the cycle performance. LTO-RT-17.06% exhibited excellent rate properties, especially under a high current density (5.0 C, 132.5 mAh/g) and LTO-RT-34.42% showed superior long-term cycle performance (0.012% capacity loss per cycle) compared to that of LTO-RT-17.06% and LTO-RT-23.69%.
基金supported by the National Research Foundation,Prime Minister’s Office,Singapore under its Competitive Research Program(CRP Award No.NRFCRP8-2011-04)
文摘Interfacial charge transfer is the key kinetic process dictating the operation of lithium-ion battery. Redox-mediated charge propagations of the electronic （e- and h＋ ） and ionic species （Li＋） at the electrode-electrolyte interface have recently gained increasing attention for better exploitation of battery materials. This article briefly summarises the energetic and kinetic aspects of lithium-ion batteries, and reviews the recent progress on various redox-assisted Li＋ storage approaches. From molecular wiring to polymer wiring and from redox targeting to redox flow lithium battery, the role of redox mediators and the way of the redox species functioning in lithium-ion batteries are discussed.
基金Project supported by the Shandong Provincial Natural Science Foundation,China(Grant No.ZR2014AM026)the National Natural Science Foundation of China(Grant Nos.11374195 and 11404193)the Taishan Scholar Project of Shandong Province,China
文摘The properties of one-photon absorption（OPA）, emission and two-photon absorption（TPA） of a di-2-picolylaminebased zinc ion sensor are investigated by employing the density functional theory in combination with response functions.The responsive mechanism is explored. It is found that the calculated OPA and TPA properties are quite consistent with experimental data. Because the intra-molecular charge transfer（ICT） increases upon zinc ion binding, the TPA intensity is enhanced dramatically. According to the model sensor, we design a series of zinc ion probes which differ by conjugation center, acceptor and donor moieties. The properties of OPA, emission and TPA of the designed molecules are calculated at the same computational level. Our results demonstrate that the OPA and emission wavelengths of the designed probes have large red-shifts after zinc ions have been bound. Comparing with the model sensor, the TPA intensities of the designed probes are enhanced significantly and the absorption positions are red-shifted to longer wavelength range. Furthermore, the TPA intensity can be improved greatly upon zinc ion binding due to the increased ICT mechanism. These compounds are potential excellent candidates for two-photon fluorescent zinc ion probes.
文摘Charge transfer cross sections for Kr^q＋ with Ne are calculated quantitatively by using modified classical over barrier model in order to clarify energy dependence of charge transfer cross sections in low energy region. Essential of this model is taking the induced dipole potential into consideration. As a result, this calculation can reproduce systematic energy dependence of experimental results. This suggests that the bending trajectory of the projectile due to an induced dipole potential should be considered to describe pictures of collisions at low energy regime below 1 keV/u.
基金supported in part by a Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan
文摘The collision dynamics and fragmentation process of molecule by highly charged ion impact for single electron capture processes at the low energies below 1 keV/u were studied. The collision energy dependence of the recoil momentum was obtained experimentally and compared it with those calculated by a theoretical model using a deflection function with polarization potential. A fairly good agreement between the measured and calculated results was reached. This suggests that the polarization potential plays a crucial role in the low-energy region.
文摘Low-energy ion beam implantation （10 - 200 keV） has been proved to have a wide range of biological effects and is broadly used in the breeding of crops and micro-organisms.To understand its mechanisms better and facilitate its applications, the developments in the bioeffects of low energy ion beam implantation in the past twenty years are summarized in this paper.
基金Supported by the National Natural Science Foundation of China under Grant Nos 10574018 and 10574020, the Science and Technology Foundation of Chinese Academy of Engineering Physics and National High-Tech ICF Committee in China.
文摘The ionization process in the collisions of He^2＋ with C^q＋ （q = 0-5） is investigated by using the continuum-distorted-wave eikonal-initial-state approximation. Double-differential cross sections for 1s and 2s sub-shells are obtained at the electron-ejected angle θ = 0° with the projectile energy ranging from 30keV/u to 10MeV/u. Variation of ionization mechanisms with q in C^q＋ is studied, and the dependences on the projectile energies and target sub-shells are also discussed. It is found that in the whole energy range, the absolute values of soft collision （SC） and binary encounter （BE） peaks decrease with increasing q. For the lower incident energies, the electron capture to the projectile continuum （ECC） peak decrease with increasing q as well as SC and BE peaks. For the higher incident energies （〉 1 MeV/u）, the absolute value of ECC peak increases with increasing q, so that the crossings of cross sections appear for C^q＋ with different q. This can be explained by the matching of velocities between the projectile and the electron initially bound to the target.
文摘A preliminary design for a heavy ion driver inertial fusion（HIDIF） target is presented. The effect of target material and dimensions on transfer efficiency and symmetrical irradiation in the hohlraum are investigated.The analysis led to the evaluation of optimal target materials and dimensions to achieve a positive power balance of an ICF power plant.The results show that the best choice is a high Z material for cavity wall materials and a low Z material for the capsule ablator.It is concluded that for achieving the highest transfer efficiency and best symmetrization we need an area ratio between 5≤A2/A1≤9.
基金The financial support from the Dean Project of Guangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology (2013Z009)the Guangxi Natural Science Fund (2014jjAA20079)the Guangdong Province of Quality and Technical Supervision Bureau (2018ZZ01) is greatly appreciated
文摘The mass transfer of thiophene through pervaporation（PV） membranes could be facilitated by certain transitional metal ions like Ag+, Mn2+, and Cr3+ thanks to their p complexation with thiophene. In this study, Ag+, Mn2+, and Cr3+ ions were loaded onto the polyether block amide（PEBAX）/PAN composite membranes and were tested on the performance for separation of thiophene/n-heptane mixture. Pervaporation test results showed that the pervaporative separation index increased significantly to 73.1%, 75.5%, and 97.2% at 30 oC for the Ag+-, Mn2+-, Cr3+-loaded PEBAX membranes, respectively,as compared to the pristine PEBAX/PAN composite membrane.
