ACS Applied Materials & Interfaces
·
2017
·
IF 7.504
Xiaoyu Jiang,Ziqi Zeng,Lifen Xiao,Xinping Ai,Hanxi Yang,Yuliang Cao
Development of intrinsically safe and long lifespan sodium-ion batteries (SIBs) is urgently needed for large-scale energy storage applications. However, most of the currently developed SIBs suffer from insufficient cycle life and potential unsafety. Herein, we construct an all-phosphate sodium-ion battery (AP-SIB) using a Na3V2(PO4)3 cathode, NaTi2(PO4)3 anode, and nonflammable trimethyl phosphate (TMP) electrolyte. The AP-SIB exhibits not only high safety, high rate performance, and ultralong cycle life but also zero-strain characteristics due to the inverse volume change of the phosphate cathode and anode during charge and discharge cycles, offering a safer and cycle-stable Na-ion technology for electric storage applications.
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PubMed
高影响因子
JOURNAL OF SOLID STATE ELECTROCHEMISTRY
·
2020
·Vol. 25
·期 2
·527-534
·
IF 2.646
Yan Binggong,Kang Lei,Kotobuki Masashi,He Linchun,Liu Bin,Jiang Kaiyong
We report effectiveness of dopants selected from group 13, such as B, Ga, and In, on the conductivity of Li 1.5 Al 0.5 Ge 1.5 (PO 4 ) 3 (LAGP) that is recognized as one of the promising solid electrolytes for next-generation solid-state lithium batteries. To minimize loss of versatile element, crystallization of LAGP using a microwave irradiation is introduced. Experimental results demonstrate that B enhances grain boundary conductivity, while Ga improves the bulk ionic conductivity. Co-doping of B and Ga leads to enhanced total ionic conductivity and remarkably reduced activation energy.
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ACS Applied Materials & Interfaces
·
2018
·
IF 8.097
Peng Wei,Yanxiang Liu,Zhihao Wang,Yangyang Huang,Yu Jin,Yi Liu,Shixiong Sun,Yuegang Qiu,Jian Peng,Yue Xu,Xueping Sun,Chun Fang,Jiantao Han,Yunhui Huang
NaTi2(PO4)3 (NTP) with a sodium superionic conductor three-dimensional (3D) framework is a promising anode material for sodium-ion batteries (SIBs) because of its suitable potential and stable structure. Although its 3D structure enables high Na-ion diffusivity, low electronic conductivity severely limits NTP’s practical application in SIBs. Herein, we report porous NTP/C nanofibers (NTP/C-NFs) obtained via an electrospinning method. The NTP/C-NFs exhibit a high reversible capacity (120 mA h g–1 at 0.2 C) and a long cycling stability (a capacity retention of ∼93% after 700 cycles at 2 C). Furthermore, sodium-ion full cells and hybrid sodium-ion capacitors have also been successfully assembled, both of which exhibit high-rate capabilities and remarkable cycling stabilities because of the high electronic/ionic conductivity and impressive structural stability of NTP/C-NFs. The results show that the nanoscale-tailored NTP/C-NFs could deliver new insights into the design of high-performing and highly stable anode materials for room-temperature SIBs.
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高影响因子
ACS Applied Materials & Interfaces
·
2024
·
IF 8.3
Changwei Luo,Guoqiang Zhao,Mengyang Zhang,Bin Wu,Qingsong Hua
NASICON-type Li1.3Al0.3Ti1.7(PO4)3 (LATP) is a widely used solid electrolyte in solid-state lithium batteries, owing to its excellent chemical stability against moisture and high total ionic conductivity. However, traditionally, densification of LATP has been achieved through a high-temperature sintering process (approximately 1000 °C) owing to its poor sinterability. Herein, we report a facile synthesis route to obtain highly sinterable LATP solid electrolyte using tetrabutyl titanate (C16H36O4Ti) as the titanium source and incorporating the traditional solid-state reaction method. The synthetic LATP powder mixed with a low ratio of LiTiPO5 exhibited a hybrid crystalline–amorphous phase structure, which facilitated grain fusion, promoted structural homogeneity, and facilitated structural densification under low-temperature sintering. The sintered LATP pellet, which exhibited an interconnected structure and indistinct grain boundaries, achieved a relative density of >90% and an ionic conductivity of 0.667 mS/cm at a sintering temperature of only 750 °C. Additionally, we systematically studied and demonstrated the synthesis reaction mechanism, sintering behavior, and ionic diffusion kinetics of LATP electrolytes. Our study paves the way for synthesizing highly sinterable LATP solid electrolytes using a simple, additive-free, and cost-effective method.
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高影响因子
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2021
·Vol. 32
·期 5
·5821-5830
·
IF 2.478
Hu Peng,Deng Zhaoping,Wang Teshen,Li Zepeng,Ma Yanlin
In this study, a series of Eu 3+ -doped NaBaBi 2 (PO 4 ) 3 red phosphors were synthesized by high-temperature solid-phase reaction method, and the phase structure and photoluminescence properties of the samples were investigated in detail. All the diffraction peaks of the phosphors with various Eu 3+ concentrations are well matched with the NaBaBi 2 (PO 4 ) 3 standard phase, indicating that Eu 3+ ions have no effect on the host structure. Under the excitation of 391 nm wavelength, the emission spectra consisted of four characteristic emission peaks at 595, 617, 656 and 703 nm, respectively. The strongest emission peaking at 617 nm originates from the 5 D 0 → 7 F 2 electron transitions of Eu 3+ ions. The optimum concentration of Eu 3+ ions in NaBaBi 2 (PO 4 ) 3 :Eu 3+ is 9% concentration. The phosphor exhibits strong absorption capacity in the near-ultraviolet region. The Commission International de I’Eclairage chromaticity coordinates of the NaBaBi 2 (PO 4 ) 3 :Eu 3+ samples are located in the red region, indicating that the phosphors are suitable red component to applied in near-ultraviolet-based white light-emitting diodes.
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高影响因子
CERAMICS INTERNATIONAL
·
2024
·
IF 5.1
Shumin Duan,Zhenjun Qing,An Liu,Haiyan Li,Yan Xue
The single-phase, cubic-structured Ba 3 La(PO 4 ) 3 ceramics were synthesized using the traditional solid-state reaction method. The ceramic sintered at 1375 °C exhibited a relative density of 95.4 %, indicative of a dense microstructure and excellent sintering characteristics. Furthermore, they displayed remarkable microwave dielectric properties : ε r = 9.54, Q × f = 32820 GHz, and τ f = −43.1 ppm/°C. In addition, the relative density is positively correlated with ε r and Q × f of ceramics. According to the complex chemical bond theory, the ionicity of the Ba/La–O bond has a more significant impact on the ε r , while the lattice energy and bond energy of the P–O bond respectively dominate the Q × f and τ f values. Moreover, the results from Raman spectroscopy indicate that several prominent Raman bands are associated with the vibration of the P–O bond. These findings suggest that Ba 3 La(PO 4 ) 3 ceramics hold promise for applications in high-frequency microwave communication.
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Advanced Sustainable Systems
·
2023
·Vol. 9
·期 7
·2300233
·
IF 7.1
Sijie Yu,Yuwei Chen,Yangyang Huang,Huabin Sun,Yu Xie,Sihao Du,Wei Luo
NASICON (NAtrium Super Ionic CONductor)-structured Na 4 MnCr(PO 4 ) 3 has attracted attention as a promising cathode for sodium-ion batteries due to its high operating voltage and specific capacity contributed by multielectron reactions. Unfortunately, its intrinsic low electronic conductivity significantly hinders the release of specific capacity and rate capability, preventing its practical application. Herein, a carbon layer with dual conductive networks connected by chain-like Ketjen black (KB) is built on the surface of Na 4 MnCr(PO 4 ) 3 material. This novel Na 4 MnCr(PO 4 ) 3 /C@KB composite material exhibits improved rate capability of 61.2 mAh g −1 at 2 C compared to 19.5 mAh g −1 of Na 4 MnCr(PO 4 ) 3 /C and high reversible capacity of 88.0 mAh g −1 at 1 C with 73% capacity retention after 100 cycles. The enhanced electrochemical performance can be ascribed to an increase of electronic conductivity enabled by the dual conductive 3D network construction and an adequate infiltration of electrolyte by substantial pores existence in carbon layer. A promising dual conductive network design strategy is demonstrated here for improving the performance of NASICON-structured cathodes.
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高影响因子
Energy Material Advances
·
2023
·
IF 12.9
Zhongyue Wang,Cheng Tang,Zhi Wang,Qing Zhang,Peng Lv,Kehan Yu,Jiajin Zheng,Wei Wei
Developing high-energy cathode for sodium ion batteries (SIBs) that enables 3-electron reaction is the most effective way to reduce high cost and solve range anxiety and safety hazards. Here, a novel NASICON-type Na 4 MnCr(PO 4 ) 3 (NMCP) is synthesized as a high-energy cathode for SIBs. The as-prepared 6.4 wt% carbon-coated NMCP (NMCP@C) cathode annealed at 700 °C delivers a discharge capacity of 107.3 mA h g −1 @0.1C, high rate capability up to 15C, and well capacity retention of 69.3% after 500 cycles at 5C within 1.4 ~ 4.3 V. Meanwhile, it also provides an exciting reversible capacity of 164.3 mA h g −1 @0.1C within 1.4 ~ 4.6 V and an ultrahigh energy density of 523.6 Wh kg −1 . Moreover, high sodium ion diffusion coefficients ( D Na+ , 10 −12 ~ 10 −9 cm 2 s −1 ) demonstrate the superior electrode process kinetics, and both solid solution and 2-phase reactions are involved in the sodium ion extraction/insertion process through ex situ x-ray diffraction analyses. Na 3.3 La 0.3 Zr 1.7 Si 2 PO 12 with 3 wt% Na 2 B 4 O 7 additive (NLZSP(NBO3)) ceramic electrolyte is utilized to assemble NMCP@C//NLZSP(NBO3)//Na solid-state sodium metal batteries for the first time, which reveals an initial discharge capacity of 99.1 mA h g −1 (1.4 ~ 4.3 V) and 121.7 mA h g −1 (1.4 ~ 4.6 V) at 0.1C and an excellent cycling performance (capacity retention of 75.8%/72.6% after 100 cycles at 0.2C) at 30 °C. All these confirm that NMCP@C is a high-energy cathode with great practical potential for all-solid-state SIBs.
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高影响因子
CHEMICAL PHYSICS LETTERS
·
2022
·
IF 2.719
Zixiang Guo,Xue Qin,Yulong Xie,Chanrong Lei,Tianyu Wei,Yuzhe Zhang
Nanoparticle LiTi 2 (PO 4 ) 3 was prepared by solvothermal and calcination methods. LiTi 2 (PO 4 ) 3 -xh(x = 5, 7, 9, 13) was successfully synthesized under different calcination times in nitrogen atmosphere, and LiTi 2 (PO 4 ) 3 –7h showed excellent rate and electrochemical performance. It delivered discharge capacities of 141.2, 119.9, 109.8, 98.2, 87.3, and 76.7 mAh·g −1 at rates of 0.5, 1, 2, 5, 10, and 20C, respectively. In particular, its initial discharge capacity can reach 123.3 mAh·g −1 at the high rate of 10C. Hence, these superior properties demonstrate that LiTi 2 (PO 4 ) 3 –7h has great application advantages as a cathode for lithium-ion batteries.
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高影响因子
OPTIK
·
2021
·
IF 2.443
Jimin Ding,Pengfei Zhu,Ziqing Li,Zhenyan Wang,Li Ai,Jianfu Zhao,Fapeng Yu,Xiulan Duan,Huaidong Jiang
K 2 TiYb(PO 4 ) 3 microcrystals with langbeinite structure have been prepared for the first time by solid state reaction. Pure K 2 TiYb(PO 4 ) 3 sample with size of 10–20 µm was obtained when the calcination temperature was 1000 °C. The microstructure and performance of the microcrystals are studied by using X-ray photoelectron spectra (XPS), FTIR and Raman spectra , UV-Vis diffuse reflectance spectra, and upconversion photoluminescence spectra. The electronic structure analysis by XPS shows that K 2 TiYb(PO 4 ) 3 has the stronger Ti-O ionic band and weaker P-O covalent band than KTiOPO 4 . The absorption peaks at 911 and 975 nm are assigned to the transition of Yb 3+ from 2 F 7/2 (0) to 2 F 5/2 (2′) and 2 F 5/2 (0′) levels, respectively. Under the excitation of 980 nm laser, K 2 TiYb(PO 4 ) 3 produces polychromatic luminescence: strong blue emission at 480 nm and weak red emission at 653 nm, and the corresponding lifetimes are 268.6 and 275.1 μs, respectively. The strong blue emission is assigned to the cooperative luminescence between Yb 3+ -Yb 3+ pairs, and the red emission is related to defects in the samples. All the CIE color coordinates for the langbeinite-type compounds are located in the blue region, which shows their great potential as blue upconversion photoluminescence materials.
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高影响因子
SOLID STATE IONICS
·
2024
·
IF 3
Ke Huang,Mingyang Duan,Xiaojuan Lu,Feng Zhang
As a new type of clean and efficient energy storage device, lithium-ion batteries have been widely used in electronic products, electric vehicles, and other fields, and the accompanying safety issues are of increasing concern. Therefore, solid-state lithium-ion conductors have become a current research hotspot. This paper used graphene oxide material to design and prepare Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 solid electrolytes by the co-precipitation method and performed some relevant characterizations. The results showed that the addition of graphene oxide optimized the electrolyte structure improved the density of the powder, promoted grain growth, improved the transport path of lithium ions, and thus increased the total ionic conductivity . The optimal doping ratio was 0.5 wt%, and the total ionic conductivity reached the maximum of 2.42 × 10 −4 S/cm. Compared to pure Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 , the ionic conductivity increased by 154% after using the graphene oxide . It is believed that larger grains, fewer grain boundaries, and denser microstructure resulted in a less distorted migration pathway for lithium ions. Under the influence of graphene oxide , Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 exhibited better air stability than pure Li 1.3 Al 0.3 Ti 1.7 (PO 4 ) 3 electrolyte. The electrolyte prepared in this study showed great application potential in all-solid-state batteries.
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高影响因子
MATERIALS CHEMISTRY AND PHYSICS
·
2024
·
IF 4.3
Yang Qu,Hongrui Jin,Li Lu,Yumei Wang,Kotobuki Mashashi,Binggong Yan
In all-solid-state batteries , the rigid point contact between the solid electrolyte and electrode results in poor cell interface wettability and generates large interfacial impedance, which hinders the application of solid-state batteries. To enhance ionic conductivity and interfacial wettability of NASICON-structured solid-state electrolyte Li 1.5 Al 0.5 Ge 1.5 (PO 4 ) 3 (LAGP), microporous LAGP with a hexagonal surface pattern is prepared using femtosecond laser followed by filling an ionic liquid electrolyte to form a solid-liquid composite electrolyte (HPL&IL). The effect of surface textures on the electrolyte-electrode interface is investigated. Experimental results demonstrate that cycling stability for Li|HPL&IL|Li cells can reach up to 350 h at a constant current density of 0.05 mA cm −2 at room temperature, and hexagonal surface textures promote uniform interfacial film formation while increasing contact area between electrode and electrolyte, providing more space for charge transfer at the interface.
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