High voltage is necessary for high energy lithium-ion batteries but difficult to achieve because of the highly deteriorated cyclability of the batteries.A novel strategy is developed to extend cyclability of a high vo...High voltage is necessary for high energy lithium-ion batteries but difficult to achieve because of the highly deteriorated cyclability of the batteries.A novel strategy is developed to extend cyclability of a high voltage lithium-ion battery,LiNi_(0.5)Mn_(1.5)O_(4)/Graphite(LNMO/Graphite)cell,which emphasizes a rational design of an electrolyte additive that can effectively construct protective interphases on anode and cathode and highly eliminate the effect of hydrogen fluoride(HF).5-Trifluoromethylpyridine-trime thyl lithium borate(LTFMP-TMB),is synthesized,featuring with multi-functionalities.Its anion TFMPTMB-tends to be enriched on cathode and can be preferentially oxidized yielding TMB and radical TFMP-.Both TMB and radical TFMP can combine HF and thus eliminate the detrimental effect of HF on cathode,while the TMB dragged on cathode thus takes a preferential oxidation and constructs a protective cathode interphase.On the other hand,LTFMP-TMB is preferentially reduced on anode and constructs a protective anode interphase.Consequently,a small amount of LTFMP-TMB(0.2%)in 1.0 M LiPF6in EC/DEC/EMC(3/2/5,wt%)results in a highly improved cyclability of LNMO/Graphite cell,with the capacity retention enhanced from 52%to 80%after 150 cycles at 0.5 C between 3.5 and 4.8 V.The as-developed strategy provides a model of designing electrolyte additives for improving cyclability of high voltage batteries.展开更多
Compared with graphite,the lower sodiation potential and larger discharge capacity of hard carbon(HC)makes it the most promising anode material for sodium-ion battery.Utilizing ether-based electrolyte rather than conv...Compared with graphite,the lower sodiation potential and larger discharge capacity of hard carbon(HC)makes it the most promising anode material for sodium-ion battery.Utilizing ether-based electrolyte rather than conventional carbonate-based electrolyte,HC achieves superior electrochemical performance.Nevertheless,the mechanism by which ether-based electrolyte improves the properties of HC is still controversial,primarily focusing on whether it forms solid electrolyte interphase(SEI)film.In this work,according to the sodium storage mechanisms in HC at low voltage(<0.1 V),including Na^(+)-diglyme co-interaction into the carbon layer(SEI forbidden)and desolvated Na^(+)insertion in the irregular carbon holes(SEI required),the NaPF6concentration in ether-based electrolyte was regulated,so as to construct a discontinuous-SEI on the surface of the HC anode,which significantly enhances the electrochemical performances of HC.Specifically,with 0.2 M NaPF6ether-based electrolyte,HC deliverers a discharge capacity of 459.7 mA h g^(-1)at 0.1 C and stays at 357.2 mA h g^(-1)after 500 cycles at 1 C,which is substantially higher than that of higher/lower salt concentration electrolytes.展开更多
Lithium-metal battery based on Ni-rich cathode provides high energy density but presents poor cyclic stability due to the unstable electrode/electrolyte interfaces on both cathode and anode.In this work,we report a ne...Lithium-metal battery based on Ni-rich cathode provides high energy density but presents poor cyclic stability due to the unstable electrode/electrolyte interfaces on both cathode and anode.In this work,we report a new strategy to address this issue.It is found that the cyclic stability of Ni-rich/Li battery can be significantly improved by using succinic anhydride(SA) as an electrolyte additive.Specifically,the capacity retention of LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)(NCM811)/Li cell is improved from 14% to 83% after 200cycles at 1 C between 3.0 and 4.35 V by applying 5% SA.The underlying mechanism of SA contribution is understood by comparing the effects of malic anhydride(MA) and citraconic anhydride(CA), both of which share a similar molecular structure to SA but show different effects.On anode side,SA can but MA and CA cannot form a protective solid electrolyte interphase(SEI) on Li anode.On cathode side,three anhydrides can suppress the formation of hydrogen fluoride from electrolyte oxidation decomposition,but SA behaves best.Typically,MA shows adverse effects on the interface stability of Li anode and NCM811 cathode,which originates from its high acidity.Though the acidity of MA can be mitigated by substituting a methyl for one H atom at its C=C bond,the substituent CA cannot compete with SA in cyclic stability improvement of the cell,because the SEI resulting from CA is not as robust as that from SA,which is related to the binding energy of the SEI components.This understanding reveals the importance of the electrolyte acidity on the Ni-rich cathode and the robustness of the SEI on Li anode,which is helpful for rationally designing new electrolyte additives to further improve the cyclic stability of high-energydensity Ni-rich/Li batteries.展开更多
Theoretical simulations about manipulating vector solitons with super-sech pulse shapes are conducted based on an optical fiber system.By changing the temporal pulses’parameters when the orthogonally polarized pulses...Theoretical simulations about manipulating vector solitons with super-sech pulse shapes are conducted based on an optical fiber system.By changing the temporal pulses’parameters when the orthogonally polarized pulses have the same or different input central wavelengths,the output modes in orthogonal directions will demonstrate different properties.When the input orthogonal modes have the same central wavelength,the“2+2”pseudo-high-order vector soliton can be generated when the time delay is changed.While under the condition of different central wavelengths,orthogonal pulses with multiple peaks accompanied with two wavelengths can be achieved through varying the projection angle,time delay or phase difference.Our simulations are helpful to the study of optical soliton dynamics in optical fiber systems.展开更多
We simulate the polarization manipulation of bright-dark vector bisolitons at 1-µm wavelength regime.Through changing the pulse parameters,different kinds of pulse shapes and optical spectra are generated in outp...We simulate the polarization manipulation of bright-dark vector bisolitons at 1-µm wavelength regime.Through changing the pulse parameters,different kinds of pulse shapes and optical spectra are generated in output orthogonal polarization directions.When the input vector bisoliton is polarization-locked with 1064 nm central wavelength,“1+1”fundamental dark-dark and“2+1”pseudo-high-order bright-dark group-velocity-locked vector solitons can be achieved through changing the projection angle.When the input vector bisoliton is group-velocity-locked with 1063 nm and 1065 nm central wavelengths,“2+1”and“2+2”pseudo-high-order bright-dark group-velocity-locked vector solitons,bright-dark group-velocity-locked vector solitons with chirp-like temporal oscillations are generated.Our simulation results can provide beneficial conduct for polarization manipulation of vector multi-solitons,and have promising applications in quantum information register,optical communications,nanophotonics,and all-optical switching.展开更多
基金supported by the National Natural Science Foundation of China(22179041)。
文摘High voltage is necessary for high energy lithium-ion batteries but difficult to achieve because of the highly deteriorated cyclability of the batteries.A novel strategy is developed to extend cyclability of a high voltage lithium-ion battery,LiNi_(0.5)Mn_(1.5)O_(4)/Graphite(LNMO/Graphite)cell,which emphasizes a rational design of an electrolyte additive that can effectively construct protective interphases on anode and cathode and highly eliminate the effect of hydrogen fluoride(HF).5-Trifluoromethylpyridine-trime thyl lithium borate(LTFMP-TMB),is synthesized,featuring with multi-functionalities.Its anion TFMPTMB-tends to be enriched on cathode and can be preferentially oxidized yielding TMB and radical TFMP-.Both TMB and radical TFMP can combine HF and thus eliminate the detrimental effect of HF on cathode,while the TMB dragged on cathode thus takes a preferential oxidation and constructs a protective cathode interphase.On the other hand,LTFMP-TMB is preferentially reduced on anode and constructs a protective anode interphase.Consequently,a small amount of LTFMP-TMB(0.2%)in 1.0 M LiPF6in EC/DEC/EMC(3/2/5,wt%)results in a highly improved cyclability of LNMO/Graphite cell,with the capacity retention enhanced from 52%to 80%after 150 cycles at 0.5 C between 3.5 and 4.8 V.The as-developed strategy provides a model of designing electrolyte additives for improving cyclability of high voltage batteries.
基金supported by the National Natural Science Foundation of China(No.21972049)。
文摘Compared with graphite,the lower sodiation potential and larger discharge capacity of hard carbon(HC)makes it the most promising anode material for sodium-ion battery.Utilizing ether-based electrolyte rather than conventional carbonate-based electrolyte,HC achieves superior electrochemical performance.Nevertheless,the mechanism by which ether-based electrolyte improves the properties of HC is still controversial,primarily focusing on whether it forms solid electrolyte interphase(SEI)film.In this work,according to the sodium storage mechanisms in HC at low voltage(<0.1 V),including Na^(+)-diglyme co-interaction into the carbon layer(SEI forbidden)and desolvated Na^(+)insertion in the irregular carbon holes(SEI required),the NaPF6concentration in ether-based electrolyte was regulated,so as to construct a discontinuous-SEI on the surface of the HC anode,which significantly enhances the electrochemical performances of HC.Specifically,with 0.2 M NaPF6ether-based electrolyte,HC deliverers a discharge capacity of 459.7 mA h g^(-1)at 0.1 C and stays at 357.2 mA h g^(-1)after 500 cycles at 1 C,which is substantially higher than that of higher/lower salt concentration electrolytes.
基金supported by the National Natural Science Foundation of China(Grant No.21872058)。
文摘Lithium-metal battery based on Ni-rich cathode provides high energy density but presents poor cyclic stability due to the unstable electrode/electrolyte interfaces on both cathode and anode.In this work,we report a new strategy to address this issue.It is found that the cyclic stability of Ni-rich/Li battery can be significantly improved by using succinic anhydride(SA) as an electrolyte additive.Specifically,the capacity retention of LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)(NCM811)/Li cell is improved from 14% to 83% after 200cycles at 1 C between 3.0 and 4.35 V by applying 5% SA.The underlying mechanism of SA contribution is understood by comparing the effects of malic anhydride(MA) and citraconic anhydride(CA), both of which share a similar molecular structure to SA but show different effects.On anode side,SA can but MA and CA cannot form a protective solid electrolyte interphase(SEI) on Li anode.On cathode side,three anhydrides can suppress the formation of hydrogen fluoride from electrolyte oxidation decomposition,but SA behaves best.Typically,MA shows adverse effects on the interface stability of Li anode and NCM811 cathode,which originates from its high acidity.Though the acidity of MA can be mitigated by substituting a methyl for one H atom at its C=C bond,the substituent CA cannot compete with SA in cyclic stability improvement of the cell,because the SEI resulting from CA is not as robust as that from SA,which is related to the binding energy of the SEI components.This understanding reveals the importance of the electrolyte acidity on the Ni-rich cathode and the robustness of the SEI on Li anode,which is helpful for rationally designing new electrolyte additives to further improve the cyclic stability of high-energydensity Ni-rich/Li batteries.
基金Project supported by the National Key Research and Development Program of China(Grant No.2018YFB0504500)the National Natural Science Foundation of China(Grant Nos.62105208,51972317,and 61875052)+2 种基金Shanghai Sailing Program(Grant No.20YF1447500)Special Project for Industrialization of High-tech Science and Technology between Jilin Province and the Chinese Academy of Sciences(Grant No.2021SYHZ0029)Natural Science Foundation of Shanghai(Grant No.22ZR1470700)。
文摘Theoretical simulations about manipulating vector solitons with super-sech pulse shapes are conducted based on an optical fiber system.By changing the temporal pulses’parameters when the orthogonally polarized pulses have the same or different input central wavelengths,the output modes in orthogonal directions will demonstrate different properties.When the input orthogonal modes have the same central wavelength,the“2+2”pseudo-high-order vector soliton can be generated when the time delay is changed.While under the condition of different central wavelengths,orthogonal pulses with multiple peaks accompanied with two wavelengths can be achieved through varying the projection angle,time delay or phase difference.Our simulations are helpful to the study of optical soliton dynamics in optical fiber systems.
基金Project supported by National Key Research and Development Program of China(Grant No.2018YFB0504500)the National Natural Science Foundation of China(Grant No.51672177)Shanghai Sailing Program(Grant No.20YF1447500).
文摘We simulate the polarization manipulation of bright-dark vector bisolitons at 1-µm wavelength regime.Through changing the pulse parameters,different kinds of pulse shapes and optical spectra are generated in output orthogonal polarization directions.When the input vector bisoliton is polarization-locked with 1064 nm central wavelength,“1+1”fundamental dark-dark and“2+1”pseudo-high-order bright-dark group-velocity-locked vector solitons can be achieved through changing the projection angle.When the input vector bisoliton is group-velocity-locked with 1063 nm and 1065 nm central wavelengths,“2+1”and“2+2”pseudo-high-order bright-dark group-velocity-locked vector solitons,bright-dark group-velocity-locked vector solitons with chirp-like temporal oscillations are generated.Our simulation results can provide beneficial conduct for polarization manipulation of vector multi-solitons,and have promising applications in quantum information register,optical communications,nanophotonics,and all-optical switching.
