JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY
·
2021
·
IF 8.067
Fengnian Zhang,Fuhao Cheng,Chufei Cheng,Meng Guo,Yufeng Liu,Yang Miao,Feng Gao,Xiaomin Wang
Abatract A series of compositionally complex fluorite oxides (CCFOs) were prepared by ball milling the mixture of ZrO 2 , HfO 2 , Y 2 O 3 , La 2 O 3 , and Pr 6 O 11 followed by conventional solid-state sintering. Both XRD and TG-DSC results demonstrated that single-phase (Zr 0.2 Hf 0.2 Pr 0.2 Y 0.2 La 0.2 )O 2-δ was formed at 1400 °C. Elements in bulk ceramic were uniformly distributed without evident accumulation according to SEM-EDS pictures. TEM results revealed that polycrystalline ceramic powder was assignable to cubic Fm-3m fluorite structure. The electrical conductivity ( σ ) was measured via EIS technology and activation energy ( E a ) of CCFOs was calculated in Arrhenius plots. In the temperature range of 300-750 °C, CCFOs preserved the same conduction mechanism and (Zr 0.1667 Hf 0.1667 Pr 0.1667 Y 0.25 La 0.25 )O 2-δ possessed higher σ and lower E a than other high entropy fluorite oxides which is related to the incorporation of Pr element or the connection of cation-V o complex.
研究领域:
材料科学
·
无机非金属材料
·
固体离子学
·
功能陶瓷
·
能源材料
✓ 已验证
DOI
高影响因子
Journal of Energy Chemistry
·
2022
·
IF 13.599
Xi Wang,Yong Wang,Yiyu Wu,Yunmiao Fan,Yang Tian
Li 6.4 La 3 Zr 1.4 Ta 0.6 O 12 (LLZTO) solid garnet-type electrolyte has been widely reported due to its outstanding safety and electrochemical stability. However, the inherent rigidity and brittleness of LLZTO lead to poor contact with anode/cathode and the operation failure of full cells. Herein, the dual-interlayers are constructed as the fast interfacial ion-migration channel by using Ti 3 C 2 T x (MXene, T x is –O, –OH, –F) with trace ionic liquid (IL), which promote the intimate contact between LLZTO and anode/cathode and suppress Li-dendrites growth. Notably, IL can wet the cathode to promote intimate interface contact and be decomposed into some inorganic compounds (such as Li 3 N, LiF, and Li 2 S x ), resulting in reduced interfacial resistance and fast Li-ion transportation. Consequently, in the prepared Li-symmetric cell, the interfacial resistance on the anode side plunges to 33.1 Ω cm −2 , and stably maintains over 1000 h without short circuit at 0.05 mA cm −2 . The full cell of Li|LiFePO 4 delivers a high initial capacity of 158.52 mA h g −1 and outstanding retention of 90.18% after 100 cycles at 60 °C and 0.2 C. Our work provides an efficient strategy to design dual-interlayers between LLZTO and anode/cathode for the interfacial modification to enhance the performance of solid garnet batteries.
研究领域:
材料科学
·
电化学
·
固态电池
·
界面工程
·
能源材料
✓ 已验证
DOI
高影响因子
JOURNAL OF POWER SOURCES
·
2020
·
IF 8.247
Donghao Wang,Yuqi Wu,Xuefan Zheng,Shijun Tang,Zhengliang Gong,Yong Yang
All-solid-state Li–S batteries (ASSLSBs) offer an opportunity to realize both high energy density , safety and reliability, via eliminating the polysulfides shuttle effect and flammable liquid electrolyte. However, the sluggish kinetics of S and Li 2 S solid conversion results in low discharge capacity at high active material loading, which is critical for ASSLSBs to implement the high energy density potential. Herein, nitrogen doped-carbon (NC) coated Li 2 S (Li 2 S@NC composite) is developed for ASSLSBs that highly improves electrochemical performance. A thin and uniform nitrogen doped-carbon layer is coated on Li 2 S via pyrolysis deposition approach to prepare Li 2 S@NC. The as obtained Li 2 S@NC composite exhibits greatly enhanced electrochemical performance with high reversible capacity, high coulombic efficiency of ~100%, good rate capability and cycling stability. Particularly, outstanding electrochemical performance with high capacity of 931 mAh g −1 can also be obtained at both high Li 2 S content (43%) and high areal Li 2 S loading (10.4 mg cm −2 ).
研究领域:
材料科学
·
电化学
·
能源存储
·
固态电池
·
纳米材料
✓ 已验证
DOI
高影响因子
POWDER TECHNOLOGY
·
2024
·
IF 4.5
Huifeng Xu,Pengfei Wang,Saiwei Luan,Lixia Cheng,Zhenxiao Fu,Xiuhua Cao,Lei Zhang,Shuhui Yu,Rong Sun
Conventionally, tetragonality in BaTiO 3 powder is attributed to grain size, disregarding the role of Ba/Ti ratio. However, our study reveals a significant impact of Ba/Ti ratio on tetragonality in BaTiO 3 . With an increase in Ba/Ti ratio from 0.990 to 1.010, particle size remains around 200 nm. Tetragonality initially rises from 1.006 to a maximum of 1.0092 at Ba/Ti = 1.000, then decreases to 1.005. Lower tetragonality is associated with Ba or Ti vacancies, using density functional theory (DFT), we analyzed the electron density and lattice distinction in BaTiO 3 powders. Both Ba and Ti vacancies affect lattice distortion, the Ti vacancies leading to more significant lattice expansion and lower tetragonality than Ba vacancies. Using this powder, we fabricated high-density BaTiO 3 ceramics and multi-layer ceramics capacitors (MLCCs) with X7R temperature stability (−55 to 125 °C, ±15% coefficient) and excellent reliability. This strategy has broad implications for tetragonal BaTiO 3 nanopowders and MLCCs development.
研究领域:
材料科学
·
无机非金属材料
·
电子陶瓷
·
固态化学
·
功能材料
✓ 已验证
DOI
高影响因子
Materials Science and Engineering B-Advanced Functional Solid-State Materials
·
2015
·
IF 2.169
Xinghao Lin,Yanming Zhao,Youzhong Dong,Quan Kuang,Zhiyong Liang,Danlin Yan,Xudong Liu
A metaphosphate NaFe(PO 3 ) 3 compound has been obtained by solid state method here. This title compound belongs to the orthorhombic structure with the space group of P 2 1 2 1 2 1 (No. 19) and lattice parameters of a = 14.3390(3) Å, b = 14.3374(2) Å, c = 14.3642(1) Å. Its structure can be described as made up of infinite (PO 3 ) 1− chains connected by FeO 6 octahedra, while the monovalent Na cations are located in the tunnels determined by the connection of PO 4 tetrahedrons and FeO 6 octahedrons. Besides, the morphology, vibrational spectra, magnetic and sodium deinsertion/insertion properties of NaFe(PO 3 ) 3 compound are also presented and discussed here for the first time, which can provide more information about the physicochemical properties of this metaphosphate compound.
研究领域:
无机化学
·
材料科学
·
固体化学
·
电化学
·
能源材料
✓ 已验证
DOI
高影响因子
BULLETIN OF MATERIALS SCIENCE
·
2016
·Vol. 39
·期 1
·187-193
·
IF 0.895
CAO RENPING,QIN ZHENGDONG,JIANG SHENHUA,LIANG AIHUI,LUO ZHIYANG,YU XIAOGUANG
A series of CaNb 2 O 6 : x Sm 3+ (0 ≤
x
≤ 10 mol%) and CaNb 2 O 6 : Sm 3+ , Na + /B 3+ phosphors were synthesized by the solid-state reaction method in air. Their crystal structures and luminescence properties were investigated and analysed, respectively. Host CaNb 2 O 6 emitted blue light with excitation 270 nm. CaNb 2 O 6 : x Sm 3+ phosphors showed a systematically varied hue from blue to white by changing Sm 3+ ion concentration from 0 to 10 mol% with excitation of 270 nm and their chromaticity coordinates were the regions from (0.1665, 0.1767) to (0.2484, 0.2260). Luminescence properties of CaNb 2 O 6 : Sm 3+ phosphor were tuned and improved significantly by codoping B 3+ or Na + ions. Energy transfer between Nb \(_{\mathbf {2}}\textit {O}_{\mathbf {6}}^{\boldsymbol {2-}}\) group and Sm 3+ ion was observed and analysed via luminescence properties. The luminous mechanism was explained by energy level scheme and energy transfer process in CaNb 2 O 6 : Sm 3+ phosphor. The strong excitation band peaking at ∼ 407 nm indicated that the CaNb 2 O 6 : Sm 3+ , Na + /B 3+ phosphor has a potential application in white light-emitting diodes based on near-UV LED chip.
研究领域:
材料科学
·
无机化学
·
发光材料
·
固体物理
·
光电子学
✓ 已验证
DOI
高影响因子
Journal of Energy Chemistry
·
2022
·
IF 13.599
Jiang Wang,Gangtie Lei,Teng He,Hujun Cao,Ping Chen
One of the major obstacles to the application of potassium-ion batteries in large-scale energy storage is the lack of safe and effective electrolytes. KNH 2 , a new potassium-ion solid electrolyte has been developed in this study. Its ionic conductivity reaches 4.84 × 10 −5 S cm −1 at 150 °C and can reach 3.56 × 10 −4 S cm −1 after mechanochemical treatment. The result from electron paramagnetic resonance (EPR) measurement shows that the increment of ionic conductivity is dependent on the concentration of nitrogen defects in the KNH 2 electrolyte. To the best of our knowledge, this is the first report that adopts inorganic amide as an electrolyte for potassium-ion battery and initiates the search for a new amide-based solid electrolyte for an all-solid-state potassium-ion battery.
研究领域:
材料科学
·
电化学
·
能源存储
·
固态离子学
·
无机化学
✓ 已验证
DOI
高影响因子
Small
·
2021
·Vol. 18
·期 5
·2104508
·
IF 13.281
Jinzhu Wang,Jipeng Hao,Chaomin Duan,Xinchao Wang,Kai Wang,Cheng Ma
Solid-state fluoride-ion batteries (FIBs) circumvent multiple formidable bottlenecks of lithium-ion batteries, but their overall performance remains inferior due to the absence of appropriate solid electrolytes. Presently the conductivity of most solid electrolytes for FIBs is too low to enable room-temperature cycling, while the few sufficiently conductive ones only allow for very low discharge voltages because of the narrow electrochemical stability window (ESW). Here, high room-temperature conductivity and a decent ESW are simultaneously achieved by designing a solid electrolyte CsPb 0.9 K 0.1 F 2.9 . Its room-temperature conductivity is 1.23 × 10 −3 S cm −1 , comparable to the most conductive system reported so far (PbSnF 4 , 5.44 × 10 −4 –1.6 × 10 −3 S cm −1 ), but the ESW is several times broader. With these appealing characteristics simultaneously achieved in the solid electrolyte, a cell with much higher voltages than other room-temperature-operable solid-state FIBs in literature is successfully constructed, and stably cycled at 25 °C for 4581 h without considerable capacity fade.
研究领域:
材料科学
·
电化学
·
固态离子学
·
能源存储
·
无机功能材料
✓ 已验证
DOI
高影响因子
JOURNAL OF POWER SOURCES
·
2016
·
IF 6.333
Gang Peng,Xiayin Yao,Hongli Wan,Bingxin Huang,Jingyun Yin,Fei Ding,Xiaoxiong Xu
An insightful study on the fundamental lithium storage behavior of all-solid-state lithium battery with a structure of LiNi 0.8 Co 0.15 Al 0.05 O 2 (NCA)/Li 10 GeP 2 S 12 /Li-In is carried out in this work. The relationship between electrochemical performances and particle size, surface impurities and defects of the NCA positive material is systematically investigated. It is found that a ball-milling technique can decrease the particle size and remove surface impurities of the NCA cathode while also give rise to surface defects which could be recovered by a post-annealing process. The results indicate that the interfacial resistance between the NCA and Li 10 GeP 2 S 12 is obviously decreased during the ball-milling followed by a post-annealing. Consequently, the discharge capacity of NCA in the NCA/Li 10 GeP 2 S 12 /Li-In solid-state battery is significantly enhanced, which exhibits a discharge capacity of 146 mAh g −1 at 25 °C.
研究领域:
材料科学
·
电化学
·
能源存储
·
固态离子学
·
电池技术
✓ 已验证
DOI
高影响因子
Journal of Materials Chemistry A
·
2020
·Vol. 9
·期 7
·3985-3994
·
IF 11.301
Ruidi Wang,Bei-Bei Xu,Jiachen Wang,Xue Lu Wang,Ye-Feng Yao
The relationship between the structural characteristics and photocatalytic reaction mechanisms of graphitic carbon nitride (g-C3N4) still remains unclarified at the molecular level, which severely hinders the further development of this field. The present study addresses this issue by employing an innovative strategy to investigate the relationship between the H-containing structures of g-C3N4 and its water splitting properties. The exchangeable and unexchangeable protons of the H-containing groups of g-C3N4 were differentiated by selective deuteration, providing a way to distinguish the hydrophilic and relatively non-hydrophilic H-containing groups of g-C3N4. A combination of advanced solid-state NMR approaches reveals that amino group defects (CN2(NHx)) on the C–N skeleton of the photocatalyst likely serve as hydrophilic active sites for facilitating the photocatalytic hydrogen evolution reaction. Accordingly, the newly synthesized g-C3N4 sample having a high concentration of CN2(NHx) by design demonstrates an enhanced H2 yield by a factor of 17 compared to that of pure g-C3N4.
研究领域:
材料化学
·
光催化
·
固体核磁共振
·
表面科学
·
能源材料
✓ 已验证
DOI
高影响因子
IONICS
·
2021
·Vol. 27
·期 8
·3339-3346
·
IF 2.817
Liu Huirong,Li Jianling,Feng Wei,Han Guimei
Commercial lithium-ion batteries have safety risks due to the use of electrolyte-containing flammable organic solvents. The development of all solid-state lithium ion batteries with solid electrolyte is a feasible technical way to improve the safety of batteries. In this work, PVDF-based composite solid-state electrolytes (CSEs) were prepared by coupling Li 6.4 La 3 Zr 1.4 Ta 0.6 O 12 (LLZTO) and polyvinylidene fluoride (PVDF). The electrochemical performance and interfacial compatibility between composite electrolyte and electrode were improved by the combination of appropriate amount of Li-ion-conducting particles and the insulating polymer. The corresponding solid-state battery of LiFePO 4 |PVDF-LLZTO-CSE| Li is fabricated and delivers initial discharge capacity of 162.4 mAh g -1 , and coulomb efficiency is approximately 98.5%. And the solid-state battery exhibits satisfactory rate capability and cycling stability at room temperature. This study suggests that a combination of the lithium garnet particles and insulating polymer is one of the promising methods to solve the problem of liquid electrolyte.
研究领域:
材料科学
·
电化学
·
能源存储
·
固态离子学
·
电池技术
✓ 已验证
DOI
高影响因子
IONICS
·
2018
·Vol. 25
·期 1
·241-251
·
IF 2.347
Wen Xinge,Dong Tao,Liu Ao,Zheng Shuohang,Chen Shimou,Han Yifan,Zhang Suojiang
As a polymer host, one polymeric ionic liquid poly(methyl methacrylate-1-vinyl-3-ethyl-imidazolium bis(trifluoromethylsulfonyl) imide) (abbr. P(MMA-co-VEImTFSI)) was successfully synthesized and characterized. Four poly(vinylidene fluoride-co-hexafluoropropylene) (abbr. PVDF-HFP)-based polymer electrolytes were prepared by blending 0, 5,15, and 25 wt% P(MMA-co-VEImTFSI). The electrochemical performances of the prepared electrolytes were studied carefully. The results revealed that increasing the polymeric ionic liquid content, the ionic conductivity of the polymer electrolytes could be enhanced and it obeyed the Arrhenius rule. The highest ionic conductivity of the polymer electrolytes was up to 2.09 × 10 −3 S cm −1 at room temperature. The polymer with 25 wt% polymeric ionic liquid showed an excellent electrochemical performance for supercapacitor electrolyte. After 2000 cycles, the retention of capacitance in P(MMA-co-VEImTFSI)-based polymer electrolyte was above 80%. It implied that the present P(MMA-co-VEImTFSI) polymeric ionic liquid was a decent component candidate in the high-performance polymer electrolytes.
研究领域:
材料科学
·
电化学
·
高分子化学
·
能源存储
·
功能材料
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）