Both the real part and imaginary part of complex permittivity approximately have a log-linear frequency dependency at low fre- quencies, especially at ultra-low frequencies under conditions of different moisture conce...Both the real part and imaginary part of complex permittivity approximately have a log-linear frequency dependency at low fre- quencies, especially at ultra-low frequencies under conditions of different moisture concentrations and temperatures, which is recognized as the low frequency dispersion (LFD). In order to explain this dispersion, a new mechanism of dielectric response of LFD of oil-paper insula- tion is proposed. A simplified one-dimensional mathematical model of concentration polarization carrier caused by slow migration is developed and solved, which indicates that ion mobility is closely related to the size of gap and the adsorption capacity of cellulose molecu- lar chains to ions. A stochastic statistical model of the carrier mobility induced LFD is also developed. Moreover, actual tests under 50 °C and 2% moisture content were put forward, as well as simulations with according current waveforms. The simulation results agreed well with the experimental data in that concentration polarization of carriers caused by slow migration is the probable cause of low frequency dispersion of dielectric response for oil-paper insulation diagnosis.展开更多
Lithium(Li) metal is widely considered as a promising anode for next-generation lithium metal batteries(LMBs) due to its high theoretical capacity and lowest electrochemical potential. However, the uncontrollable form...Lithium(Li) metal is widely considered as a promising anode for next-generation lithium metal batteries(LMBs) due to its high theoretical capacity and lowest electrochemical potential. However, the uncontrollable formation of Li dendrites has prevented its practical application. Herein, we propose a kind of multifunctional electrolyte additives(potassium perfluorinated sulfonates) from the multi-factor principle for electrolyte additive molecular design(EDMD) view to suppress the Li dendrite growth. The effects of these additives are revealed through experimental results, molecular dynamics simulations and firstprinciples calculations. Firstly, K^(+)can form an electrostatic shield on the surface of Li anode to prevent the growth of Li dendrites. Secondly, potassium perfluorinated sulfonates can improve the activity of electrolytes as co-conductive salts, and lower the electro-potential of Li nucleation. Thirdly, perfluorinated sulfonate anions not only can change the Li^(+)solvation sheath structure to decrease the desolvation energy barrier and increase the ion migration rate, but also can be partly decomposed to form the superior solid electrolyte interphase(SEI). Benefited from the synergistic effects, an outstanding cycle life over250 h at 1 m A cm^(-2) is achieved in symmetric Li||Li cells. In particular, potassium perfluorinated sulfonate additives(e.g., potassium perfluorohexyl sulfonate, denoted as K+PFHS) can also contribute to the formation of high-quality cathode electrolyte interphase(CEI). As a result, Li||LiNi_(0.6)Mn_(0.2)Co_(0.2)O_(2) full cells exhibit significantly enhanced cycling stability. This multi-factor principle for EDMD offers a unique insight on understanding the electrochemical behavior of ion-type electrolyte additives on both the Li metal anode and high-voltage cathode.展开更多
Ion mobility spectra for ten alcohols have been studied in an ion mobility spectrometry apparatus equipped with a corona discharge ionization source. Using protonated water cluster ions as the reactant ions and clean ...Ion mobility spectra for ten alcohols have been studied in an ion mobility spectrometry apparatus equipped with a corona discharge ionization source. Using protonated water cluster ions as the reactant ions and clean air as the drift gas, the alcohols exhibit different product ion characteristic peaks in their ion mobility spectra. The detection limit for these alcohols is at low concentration pmol/L level according to the concentration calibration by exponential dilution method. Based on the measured ion mobilities, several chemical physics parameters of the ion-molecular interaction at atmosphere were obtained, including the ionic collision cross sections, diffusion coefficients, collision rate constants, and the ionic radii under the hard-sphere model approximation.展开更多
采用上流有限元法定量分析了离子迁移率和离子复合率对±800 k V特高压直流输电线路地面合成场强和离子流密度的影响。结果表明,离子迁移率对地面合成场强影响不大,而地面离子流密度随着迁移率的增大呈线性变化;两者均随离子复合率...采用上流有限元法定量分析了离子迁移率和离子复合率对±800 k V特高压直流输电线路地面合成场强和离子流密度的影响。结果表明,离子迁移率对地面合成场强影响不大,而地面离子流密度随着迁移率的增大呈线性变化;两者均随离子复合率的增大而减小,且复合率对地面离子流密度计算的影响大于对地面合成场强的影响。展开更多
基金Project supported by National Nature Science Foundation of China （51107105）, Sichuan Science Fund for Young Scholars （2011JQ0009）.
文摘Both the real part and imaginary part of complex permittivity approximately have a log-linear frequency dependency at low fre- quencies, especially at ultra-low frequencies under conditions of different moisture concentrations and temperatures, which is recognized as the low frequency dispersion (LFD). In order to explain this dispersion, a new mechanism of dielectric response of LFD of oil-paper insula- tion is proposed. A simplified one-dimensional mathematical model of concentration polarization carrier caused by slow migration is developed and solved, which indicates that ion mobility is closely related to the size of gap and the adsorption capacity of cellulose molecu- lar chains to ions. A stochastic statistical model of the carrier mobility induced LFD is also developed. Moreover, actual tests under 50 °C and 2% moisture content were put forward, as well as simulations with according current waveforms. The simulation results agreed well with the experimental data in that concentration polarization of carriers caused by slow migration is the probable cause of low frequency dispersion of dielectric response for oil-paper insulation diagnosis.
基金supported by the National Natural Science Foundation of China (11675051)the China Postdoctoral Science Foundation (2020M672477)the Key Research and Development Program of Hunan Province,China (2018GK2031)。
文摘Lithium(Li) metal is widely considered as a promising anode for next-generation lithium metal batteries(LMBs) due to its high theoretical capacity and lowest electrochemical potential. However, the uncontrollable formation of Li dendrites has prevented its practical application. Herein, we propose a kind of multifunctional electrolyte additives(potassium perfluorinated sulfonates) from the multi-factor principle for electrolyte additive molecular design(EDMD) view to suppress the Li dendrite growth. The effects of these additives are revealed through experimental results, molecular dynamics simulations and firstprinciples calculations. Firstly, K^(+)can form an electrostatic shield on the surface of Li anode to prevent the growth of Li dendrites. Secondly, potassium perfluorinated sulfonates can improve the activity of electrolytes as co-conductive salts, and lower the electro-potential of Li nucleation. Thirdly, perfluorinated sulfonate anions not only can change the Li^(+)solvation sheath structure to decrease the desolvation energy barrier and increase the ion migration rate, but also can be partly decomposed to form the superior solid electrolyte interphase(SEI). Benefited from the synergistic effects, an outstanding cycle life over250 h at 1 m A cm^(-2) is achieved in symmetric Li||Li cells. In particular, potassium perfluorinated sulfonate additives(e.g., potassium perfluorohexyl sulfonate, denoted as K+PFHS) can also contribute to the formation of high-quality cathode electrolyte interphase(CEI). As a result, Li||LiNi_(0.6)Mn_(0.2)Co_(0.2)O_(2) full cells exhibit significantly enhanced cycling stability. This multi-factor principle for EDMD offers a unique insight on understanding the electrochemical behavior of ion-type electrolyte additives on both the Li metal anode and high-voltage cathode.
基金V. ACKNOWLEDGMENTS This work was support by the National Natural Science Foundation of China （No.20577049, No.20707025, and No.20907054）, the Chinese-Slovak Scientific and Technological Cooperation Project （No.4-03）, the Excellent Youth Foundation of Anhui Province Scientific Committee （No.06045098）, the Hefei Institutes of Physical Science, Chinese Academy of Science are gratefully acknowledged, and the Slovak Research and Development Agency, projects （No.LPP-0143-06 and No.SK- CN-029-07）.
文摘Ion mobility spectra for ten alcohols have been studied in an ion mobility spectrometry apparatus equipped with a corona discharge ionization source. Using protonated water cluster ions as the reactant ions and clean air as the drift gas, the alcohols exhibit different product ion characteristic peaks in their ion mobility spectra. The detection limit for these alcohols is at low concentration pmol/L level according to the concentration calibration by exponential dilution method. Based on the measured ion mobilities, several chemical physics parameters of the ion-molecular interaction at atmosphere were obtained, including the ionic collision cross sections, diffusion coefficients, collision rate constants, and the ionic radii under the hard-sphere model approximation.
