CHEMICAL ENGINEERING JOURNAL
·
2021
·
IF 13.273
Yinwei Fu,Xiaofeng Lei,Huiming Yin,Xizheng Liu
Flexible lithium–air batteries (LABs) with a redox mediator (RM) in the electrolyte demonstrate enhanced round-trip efficiency. However, their cycle performance is unsatisfactory due to severe corrosion of the Li metal anode. Herein, we propose a two step gelatinization strategy to fabricate a gradient RMs (including LiI, TMPD, and DMPZ) gel electrolyte, in which the bare electrolyte gelatinization on the Li surface and then the electrolyte contained RMs sequentially gelled on the formed gel. The RMs mainly distributed at the surface and anchored at the cathode side. By suppressing the shuttle of RMs in the electrolyte and alleviating the passivation of the Li anode, the mid-charging potentials can reach 3.44 and 4.08 V at the 15th cycle with and without the LiI mediator, respectively. The energy efficiency is 63% even at the 150th cycle, whereas the corresponding energy efficiency are only 47% and 51% for the LABs with liquid and normal gel electrolytes, respectively. Moreover, the cycle life of the battery containing the gradient gel electrolyte is three times longer than that with the liquid electrolyte. The gel electrolyte further offers the flexibility of the device, and the laminated cells thus fabricated can readily operate under harsh bending conditions.
研究领域:
电化学
·
能源材料
·
纳米材料
·
界面化学
·
储能技术
·
先进电池
·
功能高分子
·
柔性电子
✓ 已验证
DOI
高影响因子
CERAMICS INTERNATIONAL
·
2021
·Vol. 47
·期 16
·22776-22785
·
IF 4.527
Kaidan Wu,Yefeng Feng,Jin Ke,Bingwen Yang,Zhiling Guo,Deping Xiong,Miao He
Graphite nanosheets coated by LiF/SnO 2 composites are designed to obtain a lithium ion anode material with excellent performance. LiF nanoparticles play a significant role in improving the electrochemical performance by inhibiting electrolyte decomposition and providing excess Li sources during cycling. The obtained LiF@SnO 2 @C electrode shows an outstanding capacity of 951.9 mAhg −1 at 0.2 Ag -1 after 370 cycles and excellent long cycling performance of 650.0 mAhg −1 at 1.0 Ag -1 after 930 cycles. First-principles calculations demonstrate that F-doped SnO 2 (−2211.8 eV) has a lower free energy compared to SnO 2 (−1937.4 eV), resulting in a robust composite architecture that gives rise to high cycling stability.
研究领域:
材料科学
·
电化学
·
纳米科技
·
能源存储
·
计算材料学
✓ 已验证
DOI
高影响因子
Small
·
2024
·Vol. 20
·期 24
·2308304
·
IF 13
Weiqun Li,Chucheng Luo,Jimin Fu,Juan Yang,Xiangyang Zhou,Jingjing Tang,B. Layla Mehdi
Lithium–ion batteries (LIBs) has been developed over the last three decades. Increased amount of silicon (Si) is added into graphite anode to increase the energy density of LIBs. However, the amount of Si is limited, due to its structural instability and poor electronic conductivity so a novel approach is needed to overcome these issues. In this work, the synthesized chromium silicide (CrSi 2 ) doped Si nanoparticle anode material achieves an initial capacity of 1729.3 mAh g −1 at 0.2C and retains 1085 mAh g −1 after 500 cycles. The new anode also shows fast charge capability due to the enhanced electronic conductivity provided by CrSi 2 dopant, delivering a capacity of 815.9 mAh g −1 at 1C after 1000 cycles with a capacity degradation rate of <0.05% per cycle. An in situ transmission electron microscopy is used to study the structural stability of the CrSi 2 -doped Si, indicating that the high control of CrSi 2 dopant prevents the fracture of Si during lithiation and results in long cycle life. Molecular dynamics simulation shows that CrSi 2 doping optimizes the crack propagation path and dissipates the fracture energy. In this work a comprehensive information is provided to study the function of metal ion doping in electrode materials.
研究领域:
材料科学
·
电化学
·
纳米科技
·
能源存储
·
固体物理
·
计算材料学
✓ 已验证
DOI
高影响因子
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2015
·Vol. 27
·期 4
·3549-3556
·
IF 1.569
Wang Lu,Yang Zhouyong,Ni Xiuyuan
We prepare the mesoporous polythiophene–WO 3 film through in situ polymerization which is initiated by WO 3 , and fabricate the electrochromic device with the composite film. The influences of the electrolyte ions, film morphologies and counter electrode on the electrochromism of the devices are explored by UV–Vis transmittance spectra and cyclic voltammetry tests. With the aim to enhance the contrast optical transmittance, we develop the binary composite electrolytes of LiClO 4 and N(C 4 H 9 ) 4 ClO 4 solution which can promote intercalation/deintercalation process. Besides that, we use polyethylene oxide as pore-forming agent on the polythiophene–WO 3 films, so that it will be easier for electrolyte ions to diffuse in the porous film. A NiO layer also has a complementary effect on the cathodic coloration films and increases the contrast optical transmittance remarkably. Equipped with the binary electrolyte and the NiO layer as the counter electrode, the film device exhibits high performance with the contrast optical transmittance (ΔT) of 62 % and the coloration efficiency of 212.6 cm 2 /C.
研究领域:
材料科学
·
电化学
·
功能材料
·
纳米材料
·
能源材料
·
表面科学
✓ 已验证
DOI
高影响因子
Carbon Neutralization
·
2023
·Vol. 2
·期 6
·738-745
·
IF 0
Dabei Wu,Joseph Nzabahimana,Xianluo Hu
The development of organic lithium batteries (OLBs) offers a promising opportunity for the advancement of green and sustainable energy storage systems. However, organic cathode materials face challenges in terms of conductivity, electrochemical activity, and dissolution. Here, we address these limitations by introducing a sulfur-linked carbonyl compound called poly(dichlorobenzoquinone sulfide) (PDBS), which is polymerized in situ on reduced graphene oxide by a mixed solvent thermal method. The resulting carbonyl compound electrode materials exhibit favorable properties as organic cathode materials for OLBs. After 4000 cycles at a current density of 1000 mA g −1 , the carbonyl compound electrodes exhibit a discharge capacity of 102 mAh g −1 . This remarkable performance indicates excellent stability and long cycle life, which are crucial for practical applications. These results suggest that PDBS, a designable sulfur-linked carbonyl compound, holds great promise as an effective organic cathode material for OLBs. In addition, this work provides valuable insights into improving the electrochemical performance of organic cathode materials.
研究领域:
材料科学
·
电化学
·
能源存储
·
纳米复合材料
·
有机电极材料
✓ 已验证
DOI
SEPARATION AND PURIFICATION TECHNOLOGY
·
2022
·
IF 9.136
Kai Wang,Guangzhen Li,Yanhong Li,Yuan Chen,Ling Zhang,Zhiying Zhu,Zhiyong Xu,Wenbo Zhao
In the present work, a kind of amine alkyl siloxane N -butyl-N-((1,1,3-trimethyl-3,3-diphenyldisiloxaneyl)methyl)butan-1-amine (BTDMBA) was synthesized and used to capture SO 2 . Its thermal decomposition temperature is 160℃, which is comparable with that of Ionic liquids (ILs), but its viscosity is only 125 mPa∙s at 25℃ after the absorption of SO 2 , which is much lower than that of ILs. The reaction mechanism is that BTDMBA reacted with SO 2 to form charge transfer complex BTDMBA∙SO 2 . The reaction enthalpy and entropy change are −83.95 kJ/mol and −240.48 J·mol −1 ·K −1 , respectively, which are more negative than that of ILs. By comparing the enthalpy and entropy change of amine alkyl siloxane and absorbents reported in literatures, an unexpected entropy enthalpy compensation phenomenon was discovered and the isokinetic temperature was found to be 371 K. Based on this phenomenon and the optimization objective function, it was also found that with the decrease of entropy change, the optimal absorption and desorption temperature difference increased initially and decreased afterwards. The maximum of entropy changes is −201 J·mol −1 ·K −1 for absorbent to achieve recycle absorption capacity 0.79 mol/mol under the condition of absorption pressure 0.002 bar and desorption pressure 1 bar.
研究领域:
物理化学
·
环境化学
·
分离科学
·
能源材料
·
工业气体净化
·
绿色化工
✓ 已验证
DOI
高影响因子
JOURNAL OF CLUSTER SCIENCE
·
2017
·Vol. 28
·期 6
·3059-3066
·
IF 1.471
Liang Hua,Yang Zhen-Yuan,Yan Min-Hao,Xie Su-Yuan
The fullerenes that violate isolated pentagon rule (IPR) have unusual electronic properties resulting from their fused-pentagon structures. Numerous non-IPR fullerenes have now been captured by chlorination, affording opportunity to go insight into the properties involved in non-IPR fullerenes in the forms of chlorofullerenes (CFs). Here cyclic voltammetry (CV) is employed to probe the electrochemical properties of non-IPR #1809 C 60 Cl 8 in comparison with those of #271 C 50 Cl 10 . Differing from IPR-satisfying CFs such as C 60 Cl 8 and C 60 Cl 10 (referring to I
h -symmetric C 60 ), the two non-IPR CFs exhibit divergent electroactive polymerization characters. In addition, the electrocatalytic effect of ferrocene that is otherwise employed as internal reference has been shown in the CV process of CFs.
研究领域:
材料化学
·
物理化学
·
纳米材料
·
电化学
·
富勒烯化学
✓ 已验证
DOI
高影响因子
IONICS
·
2020
·Vol. 26
·期 9
·4239-4246
·
IF 2.394
Zhang Yi,Feng Wei,Zhen Yichao,Zhao Peiyao,Wang Xiaohui,Li Longtu
Li 7 La 3 Zr 2 O 12 (LLZO) with cubic phase structure is a kind of lithium-ion-conducting nanoparticles. According to the previous studies, incorporation of c-LLZO can improve electrochemical properties of PEO-based composite polymer electrolytes (CPEs). Therefore, in our study, we synthesized a kind of room-temperature-stable cubic phase LLZAO (Li 6.25 La 3 Zr 2 Al 0.25 O 12 ) nanofibers, and we aimed to confirm the optimal content of LLZAO nanofibers in PEO-based CPEs. With the incorporating 10 wt% LLZAO nanofibers, ionic conductivity of CPEs are 9.87×10 −5 S cm −1 at 30 °C and 8.66×10 −4 S cm −1 at 60 °C. The Li/CPE incorporating 10 wt% LLZAO nanofibers/Li symmetric cell exhibits little voltage fluctuation in 1000 cycles under a current density of 0.5 mA cm −2 , demonstrating better cycling stability with long cycle life. The LiFePO 4 /CPE incorporating 10 wt% LLZAO nanofibers/Li cell has a high initial discharge-specific capacity of 155.6 mAh g −1 under 0.1 C rate at 60 °C and remains 94.5% of capacity after 100 cycles. This cell also has great cycling performance under 0.2 C and 0.5 C rate, indicating good rate performance. Our work indicates that incorporation of LLZAO nanofibers enhances electrochemical properties and cycling stability of PEO-based all-solid-state lithium-ion batteries.
研究领域:
材料科学
·
电化学
·
能源存储
·
固态电池
·
高分子材料
·
纳米材料
·
电化学能量转换
✓ 已验证
DOI
高影响因子
JOURNAL OF POWER SOURCES
·
2024
·
IF 8.1
Zhengwu Wang,Yannan Zhang,Bao Zhang,Dong Yang,Kai Zhou,Yixue Huang,Fei Wang,Jianguo Duan,Xianshu Wang,Peng Dong,Yingjie Zhang
Spinel LiNi 0.5 Mn 1.5 O 4 (LNMO) has gained significant attention as a promising cathode material for lithium-ion batteries due to its high working voltage (>4.7 V) and energy density . However, challenges such as electrolyte decomposition-induced material interface erosion and transition metal dissolution under high operating voltage hinder its commercial use. In this study, a thin and uniform Sm 2 O 3 layer has been successfully deposited on the surface of LNMO using a wet chemical method . A comprehensive investigation of surface morphology , crystal structure, and electrochemical performance of the modified LNMO is conducted. The results demonstrate that the Sm 2 O 3 surface modification acts as a robust multifunctional protective layer, effectively shielding against hydrofluoric acid-induced chemical attack and enhancing the migration efficiency of lithium ions . Notably, the capacity retention rate of LNMO@Sm 2 O 3 (3 wt%) remains up to 88 % after 280 cycles, significantly surpassing the uncoated counterpart. The coated material exhibits a capacity of 114 mAh g −1 even under 10 C rate conditions. Moreover, the AC impedance values and manganese dissolution of the modified material in the organic electrolyte are considerably lower than those of the uncoated counterpart. Theoretical calculations strongly support the experimental findings, revealing higher Mn vacancy formation energy and density of states at the Fermi energy level for the Sm 2 O 3 -modified electrodes. This research contributes to the field of surface modification and paves the way for further enhancements in the electrochemical performance of other high-voltage manganese-based lithium-ion batteries (LIBs).
研究领域:
材料科学
·
电化学
·
能源存储
·
无机化学
·
纳米技术
·
表面工程
·
锂电池
✓ 已验证
DOI
高影响因子
TRANSACTIONS OF NONFERROUS METALS SOCIETY OF CHINA
·
2025
·Vol. 35
·期 7
·2341-2353
·
IF 4.7
Han-zhou LIU,Yan-chen LIU,Sheng-hao JING,Ya-qi HU,Zong-liang ZHANG,Si-liang LIU,Yang LIU,Zhi ZHUANG,Fan-qun LI,Fang-yang LIU
A dual-halide solid electrolyte, Li 3 YCl 3 Br 3 , was synthesized using a wet-chemistry route instead of the conventional mechanical ball-milling route. Li 3 YCl 3 B r3 exhibits an ion conductivity of 2.08 mS/cm and an electro- chemical stability window of 3.8 V. Additionally, an all-solid-state lithium-ion battery using Li 3 YCl 3 Br 3 and LiNi 0.83 Co 0.11 Mn 0.06 O 2 (NCM811) as the cathode material achieves a capacity retention of 93% after 200 cycles at 0.3 C and maintains a specific capacity of 115 mA·h/g during 2 C cycling. This exceptional performance is attributed to the high oxidative stability of Li 3 YCl 3 Br 3 and the in-situ formation of Y 2 O 3 inert protective layer on the NCM811 surface under high voltage. Consequently, the study demonstrates the feasibility of a simple, cost-effective wet-chemistry route for synthesizing multi-component halides, highlighting its potential for large-scale production of halide solid electrolytes for practical applications.
研究领域:
材料科学
·
电化学
·
固态离子学
·
能源存储
·
电池技术
·
无机非金属材料
·
纳米材料应用
✓ 已验证
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2015
·
IF 2.999
Jingwei Gu,Ying Zeng,Xiaofang Feng,Ximin Wu,Chunmei Zeng,Mingqi Li
Nanosilicon@nonstoichiometric silicon oxide where nanosilicon is embedded in SiO x matrix (abbreviated as nano-Si@SiOx), is a very attractive material structure to suppress the volume effect of silicon in Lithium-ion batteries. In this work, we demonstrate that the combination of electrolysis and peeling technique produce nano-Si@SiOx from bulk SiO 2 . X-ray diffraction (XRD), X-ray photoelectron spectra (XPS), scanning electron microscope (SEM) and high resolution transmission electron microscope (HRTEM) are employed to characterize the prepared materials. The average O/Si atomic ratio of the synthesized nano-Si@SiOx is about 0.91. The nano-Si@SiOx/graphite composite prepared using it as the precursor exhibits a stable discharge capacity of about 1560 mAh g −1 (calculated on the total mass of the composite) with good cyclic stability and rate capability. This work provides a new routine to prepare nano-Si@SiOx composite.
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
Small
·
2024
·Vol. 20
·期 31
·2310912
·
IF 13
Xunzhi Miao,Jianhe Hong,Shuo Huang,Liye Ding,Fang Wang,Min Liu,Quanquan Zhang,Hongyun Jin
All-solid-state lithium batteries (ASSLBs) are highly promising as next-generation energy storage devices owing to their potential for great safety and high energy density. This work demonstrates that composite solid polymer electrolyte with vertically-aligned card-house structure can simultaneously improve the high rate and long-term cycling performance of ASSLBs. The vertical alignment of laponite nanosheets creates fast and uniform Li + ion transport channels at the nanosheets/polymer interphase, resulting in high ionic conductivity of 8.9 × 10 −4 S cm −1 and Li + transference number of 0.32 at 60 °C, as well as uniformly distributed solid electrolyte interphase. Such electrolyte is characterized by high mechanical strength, low flammability, excellent structural stability and stable ion transport channels. In addition, the ASSLB cell with the electrolyte and LiFePO 4 cathode delivers a high discharge specific capacity of 124.8 mAh g −1 , which accounts for 85.6% of its initial capacity after 500 cycles at 1C. The reasonable design through structural control strategy by interconnecting the vertically-aligned nanosheets open a way to fabricate high performance composite solid polymer electrolytes.
研究领域:
材料科学
·
电化学
·
能源存储
·
高分子科学
·
纳米材料
·
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）