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JOURNAL OF ALLOYS AND COMPOUNDS · 2019 · IF 4.175

3D graphene aerogel framework enwrapped LiFePO4 submicron-rods with improved lithium storage performance

Xiaohui Tian,Zhonghua Chen,Yanbin Zhu,Xiao Huang,Guan Wu,Yingke Zhou

The three-dimensional (3D) graphene aerogel (GA)-wrapped LiFePO 4 submicron-rod composite (LFP@GA) has been prepared successfully through a solvothermal method followed with rapid freeze-drying. Monodispersed LiFePO 4 submicron-rods are well-enwrapped with the graphene sheets and which further form a highly porous and conductive 3D structure, leading to the overall rapid electron transport of the composite electrode and affording many interwoven pores for fast supply of Li + and storage of electrolyte. Moreover, the combination of the rod-shaped LFP and porous 3D structure can effectively relieve the stress resulted from the structural change during the insertion/deinsertion of Li + . Owing to these particular structure and characteristics, the LFP@GA composite presents a high discharge capacity (162.7 mAh g −1 at 0.1 C), a remarkable rate capacity (119.9 mAh g −1 at 5 C) and an excellent long-term cycle stability after 1000 cycles at 1 C (86.5% capacity retention), which is potential for use in Li-ion batteries.

研究领域: 材料科学 · 电化学 · 纳米材料 · 能源存储 · 锂离子电池
✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2022 · IF 16.744

Interface defect chemistry enables dendrite-free lithium metal anodes

Tiansheng Mu,Hongfu Lu,Yang Ren,Xin Wan,Xing Xu,Siping Tan,Yulin Ma,Geping Yin

Lithium dendrite can cause battery failure and safety risks, which is a major obstacle for the commercial application of lithium metal anodes. Herein, an artificial protective layer with interface defects is proposed to promote the interfacial electrochemical kinetics and achieve the ultra-long electrochemical plating/stripping stability. Taking titanium oxide (TiO 2 ) as a research object, the interfacial oxygen-deficient TiO 2 coating (H-TiO 2 ) shows the faster lithium ion diffusion kinetics compared to the pristine TiO 2 layer and fresh lithium metal anode, and this interfacial defect chemistry can facilitate homogenous lithium ion flux and regulate lithium metal dendrite-free electrodeposition. Specifically, the H-TiO 2 protective layer endows lithium metal anodes ultra-long cycling stability up to 1990 h at 2.0 mA cm −2 with a low overpotential of 27.5 mV. Remarkably, the artificial H-TiO 2 coating improves the cycling stability (97.5 mAh g −1 after 350cycles) and rate performance (68.5 mAh g −1 at 4.0C) of full cells paired with LiFePO 4 cathode. More importantly, this work opens a door for regulating lithium metal reversible electrodeposition by interface defect chemistry.

研究领域: 材料科学 · 电化学 · 能源存储 · 纳米材料 · 表面化学 · 固态离子学
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CHEMICAL ENGINEERING JOURNAL · 2022 · IF 16.744

Rationally designing composite gel polymer electrolyte enables high sulfur utilization and stable lithium anode

Pengfei Xie,Ruyi Yang,Yingke Zhou,Bingyin Zhang,Xiaohui Tian

The lithium-sulfur battery is an attractive energy-storage device with low cost and high energy density. However, its development is still restricted by “shuttle effect”, lithium dendrite growth and safety problem. Herein, a novel PEO-PAN-LLZO composite gel polymer electrolyte (CGPE) was designed to overcome these issues. A porous composite membrane with excellent mechanical and interfacial properties was formed after casting dispersion of PAN, PEO, LLZO sheets, which can effectively absorb electrolyte, inhibit “shuttle effect” and protect lithium anode. A conductive acetylene black layer was coated on the membrane to further hinder the migration and enhance the redox kinetics of polysulfides. The CGPE based lithium-sulfur battery displays remarkably high specific capacities (1459 and 942 mAh/g at 0.1 and 1C respectively) and outstanding cycling performance (555 mAh/g at 1C after 500 cycles, average decay/cycle of 0.082%). The unique CGPE is promising for the practical application of high-performance lithium-sulfur battery.

研究领域: 电化学储能 · 材料科学 · 纳米复合材料 · 能源化学 · 固态离子学 · 电池技术
✓ 已验证 DOI 高影响因子
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Nano Research · 2020 ·Vol. 13 ·期 9 ·2431-2437 · IF 8.183

Polymer matrix mediated solvation of LiNO3 in carbonate electrolytes for quasi-solid high-voltage lithium metal batteries

Wang Zijian,Yang Kai,Song Yongli,Lin Hai,Li Ke,Cui Yanhui,Yang Luyi,Pan Feng

Lithium (Li) metal is one of the most promising anodes for next-generation energy storage systems. However, the Li dendrite formation and unstable solid-electrolyte interface (SEI) have hindered its further application. Lithium nitrate (LiNO 3 ) is extensively used as an effective electrolyte additive in ether-based electrolytes to improve the stability of lithium metal. Nevertheless, it is rarely utilized in carbonate electrolytes due to its low solubility. Here, a novel gel polymer electrolyte (GPE) consisting of poly(vinylidene fluoride) (PVDF), poly(methyl methacrylate) (PMMA), poly(ethylene oxide) (PEO) with LiNO 3 additive is proposed to solve this issue. In this GPE, polyether-based PEO serves as a matrix for dissolving LiNO 3 which can be decomposed into a fast Li-ion conductor (Li 3 N) in conventional carbonate electrolytes to enhance the stability and Li + conductivity of the SEI film. As a result, dendrite formation is effectively suppressed, and a significantly improved average Coulombic efficiency (CE) of 97.2% in Li-Cu cell is achieved. By using this novel GPE coupled with Li anode and LiNi 0.5 Mn 0.3 Co 0.2 O 2 (NMC532), excellent capacity retention of 94.1% and high average CE of over 99.2% are obtained after 200 cycles at 0.5 C. This work presents fresh insight into practical modification strategies on high-voltage Li metal batteries.

研究领域: 电化学 · 材料科学 · 能源存储 · 高分子化学 · 界面化学 · 锂电池技术
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International Journal of Refrigeration · 2019 · IF 3.177

Performance comparison on different liquid desiccants in the liquid desiccant air-conditioning using electrodialysis regeneration: LiCl and LiBr aqueous solutions

Qing Cheng,Wang Pei

As different liquid desiccants show different dehumidification and operation characteristics, the comprehensive performance comparison between two liquid desiccants (LiCl and LiBr aqueous solutions) was conducted in this paper. The electronic conductivity of the LiBr aqueous solution was experimentally investigated and the electronic conductivity model of the LiBr solution was acquired. Compared with the LiCl solution, the LiBr solution has higher electronic conductivity within the concentration range of 20–40% and the temperature range of 20–60 °C, which means the ED regenerator using LiBr solution has lower electric resistance. The increase of the liquid desiccant concentration is beneficial to the moisture removal rate but harmful to the whole system COP and dehumidification efficiency, while the effect of the liquid desiccant temperature is opposite. Within the liquid desiccant temperature range of 20–30 °C, the whole system COP varies among 1 and 2.8 for the LiCl solution with the concentration of 38% at the exit of the ED regenerator, and it is among 2.5 and 5.8 for the LiBr solution with the concentration of 55% after regeneration. Using the LiCl solution can give the system the better dehumidification potential, while using LiBr solution can help the system to acquire the better whole performance and economy.

研究领域: 热能工程 · 暖通空调 · 化学工程 · 能源利用 · 环境控制技术
✓ 已验证 DOI 高影响因子
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NEW JOURNAL OF CHEMISTRY · 2024 ·Vol. 48 ·期 17 ·7911-7920 · IF 2.7

Large-scale synthesis of LiMn2O4 cathode materials via a rheology-assisted solid-phase method using citric acid

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
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JOURNAL OF POWER SOURCES · 2015 · IF 6.217

One-pot synthesis of carbon-coated nanosized LiTi2(PO4)3 as anode materials for aqueous lithium ion batteries

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
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APPLIED SURFACE SCIENCE · 2019 · IF 5.155

Surface-fluorinated Li4Ti5O12 nanowires/reduced graphene oxide composite as a high-rate anode material for Lithium ion batteries

Guorong Hu,Jilin Wu,Ke Du,Zhongdong Peng,Ming Jia,Hao Yang,Yanbing Cao

The surface-fluorinated Li 4 Ti 5 O 12 nanowires/reduced graphene oxide composite is synthesized through a hydrothermal procedure. Lithium ion transport is promoted by forming a special morphology of lithium titanate nanowires, meanwhile, electronic transmission is facilitated by surface fluorination and conductive network of graphene coating. These three kinds of synergistic effects greatly improve the rate performance of lithium titanate . The surface-fluorinated Li 4 Ti 5 O 12 nanowires/reduced graphene oxide composite exhibits high specific capacities (167.5 mAh g −1 at 1 C and even 132.6 mAh g −1 at 10 C) and good cyclic stability (95% capacity remain after 300 cycles at 5 C). The influences of surface fluorination and graphene coating on electrochemical performance of lithium titanate are investigated in detail in terms of reversible capacity, cyclability and rate capability. Its excellent electrochemical properties make it become possible to be a potential anode material for high-rate lithium-ion batteries applied in high power facilities.

研究领域: 材料科学 · 电化学 · 纳米科技 · 能源存储 · 锂离子电池
✓ 已验证 DOI 高影响因子
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Sustainable Energy & Fuels · 2021 ·Vol. 5 ·期 5 ·1538-1547 · IF 6.367

A facile preparation of PEO–LiClO4–fumed SiO2 composite solid-state electrolyte with improved electrochemical performance for lithium-metal batteries

Ruyan Lei,Yanping Yang,Chenjuan Yu,Yinsi Xu,Yuanzhuo Li,Jun Li

In order to improve the electrochemical performance and efficiently prepare a solid polymer electrolyte (SPE) for the lithium-metal battery (LMB), a fumed SiO2 (FS) with surface Si–OH group was used to fabricate FS-modified poly(ethylene oxide) (PEO)–LiClO4-based SPE by a facile preparation process. The influences of the FS content on the morphological properties, thermal properties, lithium salt dissociation, mechanical properties, and electrochemical properties of SPE were systematically analyzed. Results indicate that FS with the hydrophilic property was widely distributed throughout the amorphous phase of SPE, thus the crystallinity of SPE was reduced to 25.83% when the FS mass loading was 6.85 wt%. In addition, a greater dissociation degree of lithium salt was achieved after the addition of FS, and a higher ion conductivity of 3.03 × 10−4 S cm−1 and Li-ion migration number of 0.396 were recorded at 60 °C. The all-solid-state Li/SPE/Li coin cell showed excellent stable cyclability (380 h) and the LiFePO4 (LFP)/SPE/Li coin cell demonstrated good discharge specific capacity and coulomb efficiency of 96 mA h g−1 and 100.2%, respectively, after 100 cycles of galvanostatic charge–discharge operation under 0.5C at 60 °C. Thus, based on collective results, it is expected that SPE presented in this work is a promising electrolyte for next-generation high-energy all-solid-state LMB with enhanced safety.

研究领域: 材料科学 · 电化学 · 能源存储 · 高分子化学 · 固态离子学
✓ 已验证 DOI 高影响因子
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Small · 2022 ·Vol. 18 ·期 16 ·2107346 · IF 15.153

Interfacial Reviving of the Degraded LiNi0.8Co0.1Mn0.1O2 Cathode by LiPO3 Repair Strategy

Ze Feng,Shan Zhang,Xiaobing Huang,Yurong Ren,Dan Sun,Yougen Tang,Qunxuan Yan,Haiyan Wang

Nickel-rich cathode materials, owing to their high energy density and low cost, are considered to be one of the cathodes with the most potential in next-generation lithium-ion batteries. Unfortunately, this kind of cathode with highly active surface is easy to react with H 2 O and CO 2 when exposed to ambient air, resulting in the formation of lithium impurities and interfacial phase transition as well as deterioration of the electrochemical properties. In this work, the evolution mechanism of the structure and interface of LiNi 0.8 Co 0.1 Mn 0.1 O 2 during air-exposure is systematically investigated. Furthermore, a facile reviving strategy is proposed to restore the degraded LiNi 0.8 Co 0.1 Mn 0.1 O 2 by using LiPO 3 as the repair agent. The lithium impurities on the surface of the degraded sample can transform into the repair/coating layer, and part of the rock salt phase on the subsurface can revive to layered phase after repair heat treatment. As a result, the optimized cathode delivers an initial discharge capacity of 198.3 mAh g −1 at 0.1C and a capacity retention of 85.5% after 50 cycles. Although slightly lower than the bare sample (201 mAh g −1 and 88%), they are obviously higher than the exposed samples (166.5 mAh g −1 and 40.4%). The regenerated electrochemical properties should be attributed to the multifunctional repair layer that can efficiently reduce the surface lithium impurities, prevent the corrosion of electrolyte, and improve the interfacial Li + diffusion kinetics. This work can effectively reduce the waste of the degraded Ni-rich ternary materials and realize the transformation of “waste” into wealth.

研究领域: 材料科学 · 电化学 · 能源存储 · 电池技术 · 界面工程
✓ 已验证 DOI 高影响因子
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Small · 2018 ·Vol. 14 ·期 31 ·1801420 · IF 9.598

Effective Suppression of Lithium Dendrite Growth Using a Flexible Single-Ion Conducting Polymer Electrolyte

Kuirong Deng,Jiaxiang Qin,Shuanjin Wang,Shan Ren,Dongmei Han,Min Xiao,Yuezhong Meng

A novel single-ion conducting polymer electrolyte (SIPE) membrane with high lithium-ion transference number, good mechanical strength, and excellent ionic conductivity is designed and synthesized by facile coupling of lithium bis(allylmalonato) borate (LiBAMB), pentaerythritol tetrakis (2-mercaptoacetate) (PETMP) and 3,6-dioxa-1,8-octanedithiol (DODT) in an electrospun poly(vinylidienefluoride) (PVDF) supporting membrane via a one-step photoinitiated in situ thiol–ene click reaction. The structure-optimized LiBAMB-PETMP-DODT (LPD)@PVDF SIPE shows an outstanding ionic conductivity of 1.32 × 10 −3 S cm −1 at 25 °C, together with a high lithium-ion transference number of 0.92 and wide electrochemical window up to 6.0 V. The SIPE exhibits high tensile strength of 7.2 MPa and elongation at break of 269%. Due to these superior performances, the SIPE can suppress lithium dendrite growth, which is confirmed by galvanostatic Li plating/stripping cycling test and analysis of morphology of Li metal electrode surface after cycling test. Li|LPD@PVDF|Li symmetric cell maintains an extremely stable and low overpotential without short circuiting over the 1050 h cycle. The Li|LPD@PVDF|LiFePO 4 cell shows excellent rate capacity and outstanding cycle performance compared to cells based on a conventional liquid electrolyte (LE) with Celgard separator. The facile approach of the SIPE provides an effective and promising electrolyte for safe, long-life, and high-rate lithium metal batteries.

研究领域: 材料科学 · 电化学 · 能源存储 · 高分子化学 · 电池技术
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Energy Technology · 2018 ·Vol. 6 ·期 11 ·2139-2145 · IF 3.175

Suppressing the Voltage Decay and Enhancing the Electrochemical Performance of Li1.2Mn0.54Co0.13Ni0.13O2 by Multifunctional Nb2O5 Coating

Wei Pan,Wenjie Peng,Guochun Yan,Huajun Guo,Zhixing Wang,Xinhai Li,Weihua Gui,Jiexi Wang,Ning Chen

This study focuses on suppressing the voltage decay and improving the electrochemical performance of Li-rich and manganese-based (LRM) material by Nb 2 O 5 coating, which is realized by an effective soft-chemical route using a mixture of ethanol and water as co-solvent. After Nb 2 O 5 coating, the resulted material demonstrates superior electrochemical performance as cathode material for LIBs. Particularly, it shows an excellent capacity retention of 98 % after 200 cycles at 1 C (1 C=250 mA g −1 ). Voltage decay within cycling is also obviously suppressed by Nb 2 O 5 coating. Moreover, it exhibits superior rate capacities, delivering 189 and 152 mAh g −1 at high current densities of 2 and 5 C, respectively. The improved electrochemical performance of Nb 2 O 5 coated sample can be attributed to that Nb 2 O 5 can suppress the phase transformation and voltage decay by acting as not only a fast ion conductor to accelerate the lithium ion diffusion at the cathode/electrolyte interface, but also an inert protective layer to reduce the direct contact between the cathode and electrolyte.

研究领域: 材料科学 · 电化学 · 能源存储 · 无机非金属材料 · 固态离子学
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