ELECTROCHIMICA ACTA
·
2014
·
IF 4.086
Minghao Sun,Haoxiang Zhong,Shuren Jiao,Hanqi Shao,Lingzhi Zhang
Carboxymethyl chitosan (C-CTS) was firstly reported as a water soluble binder for LiFePO 4 cathode in Li-ion batteries. The electrochemical performances of LiFePO 4 cathode with C-CTS binder was investigated and compared with the conventional water-soluble sodium carboxymethyl cellulose (CMC) and the commercial non-aqueous polyvinylidene difluoride (PVDF). LiFePO 4 cathode with C-CTS exhibited a comparable cycling performance, but better rate capability than that of CMC and PVDF, retaining 65% capacity of C/5 at 5 C rate as compared with 55.9% and 39.4% for CMC and PVDF, respectively. In addition, LiFePO 4 cathode with C-CTS exhibited excellent cycling performance at 60 °C, retaining 91.8%/62.1% capacity after 80 cycles at 1 C/10 C, respectively.
研究领域:
材料科学
·
电化学
·
能源存储
·
高分子化学
·
电池技术
✓ 已验证
DOI
高影响因子
ADVANCED MATERIALS
·
2012
·Vol. 24
·期 24
·3201-3204
·
IF 13.877
Shaohua Liu,Haiping Jia,Lu Han,Jiulin Wang,Pengfei Gao,Dongdong Xu,Jun Yang,Shunai Che
Graphical Hierarchical porous TiO 2 –B with thin nanosheets is successfully synthesized. TiO 2 –B polymorph ensures fast insertion of Li-ion due to its pseudocapacitive mechanism. The thin nanosheet walls with porous structure allow exposure to electrolytes for facile ionic transport and interfacial reaction. The joint advantages endow this material with high reversible capacity, excellent cycling performance, and superior rate capability.
研究领域:
材料科学
·
电化学
·
纳米科技
·
能源存储
·
无机非金属材料
·
电极材料
·
锂离子电池
✓ 已验证
DOI
高影响因子
ELECTROCHIMICA ACTA
·
2017
·
IF 4.798
Hedong Chen,Zhoulu Wang,Xianhua Hou,Lijun Fu,Shaofeng Wang,Xiaoqiao Hu,Haiqing Qin,Yuping Wu,Qiang Ru,Xiang Liu,Shejun Hu
Carbon-coated core-shell structure artificial graphite@plasma nano-silicon@carbon (AG@PNSi@C) composite, applying as lithium ion battery anode material , has been prepared via spray drying method. The plasma nano-silicon (<100 nm), which contained amorphous silicon , was synthesized by radio frequency induction plasma system with the high temperatures processing capability and high quench rates. The artificial graphite in the composite acts as the core which supports the particle and provides electroconductivity , while PNSi attached on the surface of the core, enhances the specific capacity of the composite. The as prepared composite shows superior performance as anode in lithium-ion batteries, regarding to the initial Coulombic efficiency and cycle life. The initial Coulombic efficiency of AG@PNSi@C electrode is 81.0% with a discharge capacity of 553 mAh g −1 and a recharge capacity of 448 mAh g −1 . During cycling, AG@PNSi@C exhibits excellent performance with a very low capacity fading that the discharge capacity maintains 498.2 mAh g −1 and 449.4 mAh g −1 after 250 cycles and 500 cycles. AG@PNSi@C also shows enhanced resistance against high current density . Besides the remarkable electrochemical performances , the facile and mass-producible synthesis process makes the AG@PNSi@C composite very promising for its application in lithium-ion batteries.
研究领域:
材料科学
·
电化学
·
能源存储
·
纳米材料
·
电池技术
✓ 已验证
DOI
高影响因子
NEW JOURNAL OF CHEMISTRY
·
2024
·Vol. 48
·期 17
·7911-7920
·
IF 2.7
Pengchao Liang,Yuanchao Li,Xiangzhen Xiao,Shumin Fan,Jingjing Ma,Jingjie Liu,Yongqiang Dong,Yuhang Zong,Guangri Xu,Li Yang
Although they possess a high working voltage and environmental compatibility, and are low in cost with abundant resources, the poor cycling performance and rapid capacity attenuation of LiMn2O4 cathodes at high temperature restrict their extensive application. In this study, LiMn2O4 materials are synthesized by a simple rheology-assisted solid-phase method using citric acid as an additive. The citric acid improves the uniformity of the mixed raw materials, resulting in a reduction in particle agglomeration. Consequently, the synthesized LiMn2O4 shows an initial capacity of 117.4 mA h g−1 with a capacity retention of 79.50% at 2C after 300 cycles and 54.78% of the initial discharge capacity at 20C. This work provides a strategy for modifying multicomponent transition metal oxides for advanced lithium-ion batteries.
研究领域:
材料科学
·
电化学
·
能源存储
·
无机固体化学
·
电池技术
✓ 已验证
DOI
高影响因子
JOURNAL OF POWER SOURCES
·
2015
·
IF 6.217
Zhantao Liu,Xusong Qin,Hui Xu,Guohua Chen
In this study, a one-pot sintering process incorporating sol–gel preparation route and in-situ carbon coating was proposed for the synthesis of carbon-coated nanosized LiTi 2 (PO 4 ) 3 . Experimental results show that the prepared LiTi 2 (PO 4 ) 3 particles are of high crystallinity and well-coated by turbostratic carbon. Attributed to nanosized particles and enhanced conductivity provided by turbostratic carbon coating, the carbon-coated LiTi 2 (PO 4 ) 3 showed high rate performance and good cycling life in aqueous electrolyte. Particularly, the carbon-coated LiTi 2 (PO 4 ) 3 exhibited initial specific capacities of 103 and 89 mAh g −1 , and retained 80.6% and 97% of the initial capacities after 120 cycles at 1C and 10C in aqueous electrolyte, respectively. The high rate performance and good cycling life of carbon-coated LiTi 2 (PO 4 ) 3 in aqueous electrolyte reveal its potential as negative electrode in aqueous lithium-ion batteries for electric vehicles and industrial-scale energy storage systems .
研究领域:
材料科学
·
电化学
·
能源存储
·
纳米技术
·
无机化学
✓ 已验证
DOI
高影响因子
CERAMICS INTERNATIONAL
·
2021
·Vol. 48
·期 3
·3081-3095
·
IF 4.527
Mingchao Wang,Zhaoli Chen,Jingxuan Liu,Zhaojie Feng,Jingfang Zhang,Wenzheng Zhai,Haijun Zhang
To meet the high demand for ceramic/superalloy composite structural components in various fields, an advanced high-temperature adhesion technique was firstly developed by preparing a novel inorganic/organic hybrid adhesive suitable for ZrO 2 and TC4 . Chemical bonding started to work at ∼600°C, and became the crucial bonding mechanism at elevated temperatures. The formation of ZrSiO 4 and Ti 5 Si 3 at the interfaces of two substrates not only increased the interfacial connection strength , but also formed two gradient layers with a size of ∼2 μm to effectively alleviate the difference of composition and performance between the adhesive and substrates. In the temperature range of 500–900°C, the matching degree of CTE among ZrO 2 , adhesive and TC4 is higher, and the maximum difference does not exceed 3×10 -6 K -1 . Meanwhile, the formation of a composite structure containing various ceramics (ZrO 2 , SiC and ZrB 2 ) and intermetallics (Ni–Si, Al–Ni), and the improvement of structural compactness of adhesive from 500 to 900°C greatly improved the bonding strength to the maximum value of 31.4 MPa at 900°C. Also, the adhesive pretreated at 900°C showed good thermal cycling resistance, and the strength was still higher than 15 MPa after 50 cycles. For cured adhesive, when used directly in an extreme environment, it can provide bonding strength not less than 5 MPa in the whole temperature range, indicating that the adhesive possessed potential emergency repair convenience. This work significantly broadened the application of high-temperature-resistant adhesion technology in the connection of dissimilar ceramics and alloys.
研究领域:
材料科学
·
复合材料
·
界面工程
·
高温功能材料
·
连接技术
✓ 已验证
DOI
高影响因子
Journal of Energy Chemistry
·
2021
·
IF 9.676
Pengfei Zhou,Jing Zhang,Zhennan Che,Zuhao Quan,Ju Duan,Xiaozhong Wu,Junying Weng,Jinping Zhao,Jin Zhou
P2-Na 0.67 Ni 0.33 Mn 0.67 O 2 is considered as a promising cathode material for sodium-ion battery (SIBs) because of its high capacity and discharge potential. However, its practical use is limited by Na + /vacancy ordering and P2-O2 phase transition. Herein, a Ti 4+ /F − co-doping strategy is developed to address these issues. The optimal P2-Na 0.67 Ni 0.33 Mn 0.37 Ti 0.3 O 1.9 F 0.1 exhibits much enhanced sodium storage performance in the high voltage range of 2.0–4.4 V, including a cycling stability of 77.2% over 300 cycles at a rate of 2 C and a high-rate capability of 87.7 mAh g −1 at 6 C. Moreover, the P2-Na 0.67 Ni 0.33 Mn 0.37 Ti 0.3 O 1.9 F 0.1 delivers reversible capacities of 82.7 and 128.1 mAh g −1 at −10 and 50 °C at a rate of 2 C, respectively. The capacity retentions over 200 cycles at −10 °C is 94.2%, implying more opportunity for practical application. In-situ X-ray diffraction analysis reveals that both P2-O2 phase transitions and Na + /vacancy ordering is suppressed by Ti 4+ /F − co-doping, which resulting in fast Na + diffusion and stable phase structure. The hard carbon//P2-Na 0.67 Ni 0.33 Mn 0.37 Ti 0.3 O 1.9 F 0.1 full cell exhibits a high energy density of 310.2 Wh kg −1 and remarkable cyclability with 82.1% retention after 300 cycles at 1 C in the voltage range of 1.5–4.2 V. These results demonstrate that the co-doping Ti 4+ /F − is a promising strategy to improve the electrochemical properties of P2-Na 0.67 Ni 0.33 Mn 0.67 O 2 , providing a facile tactic to develop high performance cathode materials for SIBs.
研究领域:
材料科学
·
电化学
·
能源存储
·
无机化学
·
固态化学
·
电池技术
✓ 已验证
DOI
高影响因子
SOLID STATE IONICS
·
2016
·
IF 2.38
Shanshan Mo,Penghao Lu,Fei Ding,Zhibin Xu,Jiaquan Liu,Xingjiang Liu,Qiang Xu
Sulfide glasses with a high lithium-ion conductivity are promising solid electrolyte for all-solid-state lithium-ion batteries. In this study, 95(0.7Li 2 S–0.3P 2 S 5 )–5Li 3 PO 4 glass electrolyte is prepared by mixing 70Li 2 S-30P 2 S 5 (mol%) glass and Li 3 PO 4 crystal using mechanical milling technique. The effects on the structures and electrochemical properties of the obtained ternary sulfide glass were examined. The ternary sulfide glass shows a good electrochemical stability, which may exhibit a wide electrochemical window up to 10 V (vs. Li/Li + ). Furthermore, the 95(0.7Li 2 S-0.3P 2 S 5 )-5Li 3 PO 4 glass electrolyte displays an electrical conductivity of 2.513 × 10 − 3 S cm − 1 at 100 °C. The all-solid-state lithium-ion cell assembled with 95(0.7Li 2 S-0.3P 2 S 5 )-5Li 3 PO 4 glass electrolyte shows a favourable cyclability, which can reveal a discharge capacity of 144 mAh g − 1 at 0.05 °C and a discharge capacity of 63.9 mAh g − 1 at 0.1C after the 50th cycle at 100 °C, respectively.
研究领域:
材料科学
·
电化学
·
能源存储
·
固态离子学
·
锂电池技术
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）