As a promising cathode material,Na_(3)V_(2)(PO_(4))_(2)F_(3)(NVPF)has attracted wide attention for sodium-ion batteries(SIBs)because of its high operating voltage and high structural stability.However,the low intrinsi...As a promising cathode material,Na_(3)V_(2)(PO_(4))_(2)F_(3)(NVPF)has attracted wide attention for sodium-ion batteries(SIBs)because of its high operating voltage and high structural stability.However,the low intrinsic electronic conductivity and insufficient Na ion mobility of NVPF limit its development.Herein,K-doping NVPF is prepared through a facile ball-milling combined calcination method.The effects of K-doping on the crystal structure,kinetic properties and electrochemical performance are investigated.The results demonstrate that the Na_(2.90)K_(0.10)V_(2)(PO_(4))_(3)F_(3)(K0.10-NVPF)exhibits a high capacity(120.8 mAh g^(-1) at 0.1 C),high rate capability(66 mAh g^(-1) at 30 C)and excellent cycling performance(a capacity retention of 97.5%at 1 C over 500 cycles).Also,the occupation site of K ions in the lattice,electronic band structure and Na-ion transport kinetic property in K-doped NVPF are investigated by density functional theory(DFT)calculations,which reveals that the K-doped NVPF exhibits improved electronic and ionic conductivities,and located K^(+) ions in the lattice to contribute to high reversible capacity,rate capability and cycling stability.Therefore,the K-doped NVPF serves as a promising cathode material for high-energy and high-power SIBs.展开更多
In this study,K+-doped γ-Ce2 S3 was successfully prepared via a gas-solid reaction method using CeO2,K2 CO3,and CS2 as raw materials.The effects of the suitable sulfide system and different molar ratios of K to Ce(nK...In this study,K+-doped γ-Ce2 S3 was successfully prepared via a gas-solid reaction method using CeO2,K2 CO3,and CS2 as raw materials.The effects of the suitable sulfide system and different molar ratios of K to Ce(nK/Ce=0-0.30) on the phase composition,crystal structure,chromaticity and thermal stability ofγ-Ce2 S3 were systematically investigated.Pure γ-Ce2 S3 was obtained by calcining the doped samples at840℃ for 150 min.After calcination at the same temperature the undoped K+samples exhibit a pure α-phase.Samples with a K/Ce molar ratio(nK/Ce) of 0.10-0.25 comprise only the γ-phase;and when nK/Ce exceeds 0.25,a new heterogeneous phase,KCeS2,emerges.For values of nK/Ce in the range of0-0.25,the γ-Ce2 S3 lattice parameters gradually increases with increasing K+ content.When nK/Ceexceedes 0.25,the lattice parameters remains unchanged.As nK/Ce increased,the synthesized color gradually changes from red to orange—red and finally,to yellow.The redness value a* reaches the maximum(L*=33.86,a*=36.68,b*=38.15) when nK/Ce=0.10,The nK/Ce=0.10 composition continues to exhibit the y-phase after heat treatment at 420℃ for 10 min in air.The K+doping fills the internal vacancies of γ-Ce2 S3 and formed a solid solution,which is beneficial for the stability of its lattice,thus improving the thermal stability of γ-Ce2 S3(from 350 to 420℃).展开更多
Dy3+/Eu3+ co-doped cubic lattice Na YF4 single crystal with high quality in the size of ~Φ1.0 cm×10.0 cm was grown by an improved Bridgman method using potassium fluoride(KF) as assistant flux. X-ray diffraction...Dy3+/Eu3+ co-doped cubic lattice Na YF4 single crystal with high quality in the size of ~Φ1.0 cm×10.0 cm was grown by an improved Bridgman method using potassium fluoride(KF) as assistant flux. X-ray diffraction(XRD), absorption spectra, excitation spectra and emission spectra are measured to investigate the phase and luminescent properties of the crystal. The effects of excitation wavelength and concentrations of Dy3+ and Eu3+ ions on the luminescent characteristics are analyzed. The Na YF4 single crystal with the doping molar concentrations of 1.205% Dy3+ and 0.366% Eu3+ exhibits an excellent white light emission with chromaticity coordinates of x=0.321, y=0.332. It indicates that the Dy3+/Eu3+ co-doped cubic lattice Na YF4 single crystal can be a potential luminescent material for the ultraviolet(UV) light excited white light emitting diode(w-LED).展开更多
基金financially funded by the Regional Innovation and Development Joint Fund,National Natural Science Foundation of China(No.U20A20249)National Key Research Program of China(No.2016YFB0901500)。
文摘As a promising cathode material,Na_(3)V_(2)(PO_(4))_(2)F_(3)(NVPF)has attracted wide attention for sodium-ion batteries(SIBs)because of its high operating voltage and high structural stability.However,the low intrinsic electronic conductivity and insufficient Na ion mobility of NVPF limit its development.Herein,K-doping NVPF is prepared through a facile ball-milling combined calcination method.The effects of K-doping on the crystal structure,kinetic properties and electrochemical performance are investigated.The results demonstrate that the Na_(2.90)K_(0.10)V_(2)(PO_(4))_(3)F_(3)(K0.10-NVPF)exhibits a high capacity(120.8 mAh g^(-1) at 0.1 C),high rate capability(66 mAh g^(-1) at 30 C)and excellent cycling performance(a capacity retention of 97.5%at 1 C over 500 cycles).Also,the occupation site of K ions in the lattice,electronic band structure and Na-ion transport kinetic property in K-doped NVPF are investigated by density functional theory(DFT)calculations,which reveals that the K-doped NVPF exhibits improved electronic and ionic conductivities,and located K^(+) ions in the lattice to contribute to high reversible capacity,rate capability and cycling stability.Therefore,the K-doped NVPF serves as a promising cathode material for high-energy and high-power SIBs.
基金Project supported by National Natural Science Foundation of China (51462010)Natural Science Foundation of Jiangxi Province(20161BAB206132,20171ACB20022)The Innovation fund of Jingdezhen Ceramic Institute (JYC-201803)。
文摘In this study,K+-doped γ-Ce2 S3 was successfully prepared via a gas-solid reaction method using CeO2,K2 CO3,and CS2 as raw materials.The effects of the suitable sulfide system and different molar ratios of K to Ce(nK/Ce=0-0.30) on the phase composition,crystal structure,chromaticity and thermal stability ofγ-Ce2 S3 were systematically investigated.Pure γ-Ce2 S3 was obtained by calcining the doped samples at840℃ for 150 min.After calcination at the same temperature the undoped K+samples exhibit a pure α-phase.Samples with a K/Ce molar ratio(nK/Ce) of 0.10-0.25 comprise only the γ-phase;and when nK/Ce exceeds 0.25,a new heterogeneous phase,KCeS2,emerges.For values of nK/Ce in the range of0-0.25,the γ-Ce2 S3 lattice parameters gradually increases with increasing K+ content.When nK/Ceexceedes 0.25,the lattice parameters remains unchanged.As nK/Ce increased,the synthesized color gradually changes from red to orange—red and finally,to yellow.The redness value a* reaches the maximum(L*=33.86,a*=36.68,b*=38.15) when nK/Ce=0.10,The nK/Ce=0.10 composition continues to exhibit the y-phase after heat treatment at 420℃ for 10 min in air.The K+doping fills the internal vacancies of γ-Ce2 S3 and formed a solid solution,which is beneficial for the stability of its lattice,thus improving the thermal stability of γ-Ce2 S3(from 350 to 420℃).
基金supported by the National Natural Science Foundation of China(Nos.51472125 and 51272109)the K.C.Wong Magna Fund in Ningbo University
文摘Dy3+/Eu3+ co-doped cubic lattice Na YF4 single crystal with high quality in the size of ~Φ1.0 cm×10.0 cm was grown by an improved Bridgman method using potassium fluoride(KF) as assistant flux. X-ray diffraction(XRD), absorption spectra, excitation spectra and emission spectra are measured to investigate the phase and luminescent properties of the crystal. The effects of excitation wavelength and concentrations of Dy3+ and Eu3+ ions on the luminescent characteristics are analyzed. The Na YF4 single crystal with the doping molar concentrations of 1.205% Dy3+ and 0.366% Eu3+ exhibits an excellent white light emission with chromaticity coordinates of x=0.321, y=0.332. It indicates that the Dy3+/Eu3+ co-doped cubic lattice Na YF4 single crystal can be a potential luminescent material for the ultraviolet(UV) light excited white light emitting diode(w-LED).