文献检索

查找使用阿拉丁产品的科研文献

检索与阿拉丁产品相关的同行评审论文、DOI、PubMed 编号、期刊、作者、CAS 号及研究领域。

科研影响力快照

与阿拉丁产品相关的已发表科研成果

在搜索之前,这些指标可帮助访客快速了解产品关联科研的规模与质量。

346,364+ SCI 论文 与阿拉丁产品引用相关
2,295,288.15 总影响因子 匹配文献记录中影响因子的总和
81.20 最高期刊影响因子 匹配期刊中的最高 IF
6.63 平均期刊影响因子 匹配文献的平均 IF

参考指标 指标基于阿拉丁文献引用数据库及期刊影响因子记录。文献关联仅供科研参考,请以原始文献为准。

热门产品

视图 列表 网格

4 项

设置提升方向
LiODFB
Frontiers in Chemistry · 2019 · IF 3.782

Concentrated LiODFB Electrolyte for Lithium Metal Batteries

Yu Juan,Gao Na,Peng Jiaxin,Ma Nani,Liu Xiaoyan,Shen Chao,Xie Keyu,Fang Zhao

Nowadays, lithium (Li) metal batteries arouse widespread concerns due to its ultrahigh specific capacity (3,860 mAh g−1). However, the growth of Li dendrites has always limited their industrial development. In this paper, the use of concentrated electrolyte with lithium difluoro(oxalate)borate (LiODFB) salt in 1, 2-dimethoxyethane (DME) enables the good cycling of a Li metal anode at high Coulombic efficiency (up to 98.1%) without dendrite growth. Furthermore, a Li/Li cell can be cycled at 1 mA cm−2 for over 3,000 h. Besides, compared to conventional LiPF6-carbonate electrolyte, Li/LiFePO4 cells with 4 M LiODFB-DME exhibit superior electrochemical performances, especially at high temperature (65°C). These outstanding performances can be certified to the increased availability of Li+ concentration and the merits of LiODFB salt. We believe that the concentrated LiODFB electrolyte is help to enable practical applications for Li metal anode in rechargeable batteries.

CAS / MDL: 15365-14-7
研究领域: 材料科学 · 电化学
✓ 已验证 产品关联 DOI PubMed 高影响因子
查看原文 查看 PubMed
ACS Applied Energy Materials · 2021 · IF 6.024

Coral-like Li7La3Zr2O12-Filled PVDF-HFP/LiODFB Composite Electrolytes for Solid-State Batteries with Excellent Cycle Performance

Shengdong Tao,Jian Li,Lihua Wang,Weiguo Huang,Minchao Zhang,Zhexi Chi,Shuohan Wang,Yongzhi Chen,Lei Shang

Development of an active filler with a large specific surface area, fast ion conductivity phase, special shape, and high electrochemical stability is a critical issue for prominent performance composite solid-state electrolytes (CSEs) in solid-state lithium-ion batteries. Here, we report large specific surface area and coral-like cubic Li7La3Zr2O12 (LLZO) that was synthesized via a metal–organic framework (MOF) at a low calcination temperature (1000 °C). As active fillers, the coral-like cubic LLZO and lithium oxalyldifluroborate (LiODFB) uniformly distributed in a poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) matrix provide an interconnected Li-ion transport channel in CSE, which manifests outstanding properties such as a favorable electrochemical stability window (of 4.85 V vs Li/Li+), high ionic conductivity (1.65 × 10–4 S cm–1, 20 °C), and superior interface compatibility with lithium metal. The assembled LiFePO4/CSE/Li and LiCoO2/CSE/Li cells convey predominate performance and initial specific capacities of 135.0 and 135.9 mA h g–1 at 0.5 C, with capacity retention values of 83.51% after 500 cycles and 93.90% after 200 cycles. The coral-like LLZO with a large specific area reduces polymer crystallinity and provides a large phase interface in CSE through interaction of LLZO with LiODFB and PVDF-HFP. The results suggest that coral-like LLZO prepared by MOFs is a promising filler in CSEs for solid-state lithium-ion batteries.

研究领域: 材料科学 · 电化学
✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF ELECTROANALYTICAL CHEMISTRY · 2017 · IF 3.012

Enhanced performance of the electrolytes based on sulfolane and lithium difluoro(oxalate)borate with enhanced interfacial stability for LiNi0.5Mn1.5O4 cathode

Hongming Zhou,Demin Xiao,Chengjie Yin,Zhaohui Yang,Kaiwen Xiao,Jian Li

The electrolytes based on lithium difluoro(oxalate)borate (LiODFB) and sulfolane (SL) including LiODFB-ethylene carbonate (EC)/dimethyl carbonate (DMC) and LiPF 6 -EC/DMC as the references have been studied on electrochemical performance and interfacial stability in Li/LiNi 0.5 Mn 1.5 O 4 cells. LiODFB-containing electrolytes show outstanding electrochemical stability within 5.5   V due to the passivation phenomenon on the cathodes, while LiPF 6 -containing electrolytes undergo continuous decomposition beyond 4.5   V. The initial charge/discharge profiles and cyclic voltammetry (CV) curves prove that the cell with LiODFB-SL/DMC(2:1 by vol.) electrolyte has lower degree of polarization and better reversibility. The cathode with LiODFB-SL/DMC(2:1 by vol.) electrolyte displays the best cycling performance and the cathode with LiPF 6 -EC/DMC(1:1 by vol.) electrolyte displays the worst cycling performance. AC impedance shows that the cell cycling with LiODFB-SL/DMC(2:1 by vol.) electrolyte has much smaller resistance of charge transfer on cathode/electrolyte interface than the cell cycling with LiODFB-EC/DMC(1:1 by vol.) electrolyte. The characterization of the cathode surfaces indicates that a more homogeneous and compact passivation layer forms on the cathode cycling with LiODFB-SL/DMC(2:1 by vol.) electrolyte to greatly improve the interfacial stability for the reason that SL motivates the passivation reaction of LiODFB and itself participates the formation of the passivation layers. Therefore, LiODFB-SL/DMC(2:1 by vol.) is a promising electrolyte for LiNi 0.5 Mn 1.5 O 4 cathode.

研究领域: 材料科学 · 电化学
✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF ALLOYS AND COMPOUNDS · 2021 · IF 5.316

Insight into wide temperature electrolyte based on lithiumdifluoro(oxalate)borate for high voltage lithium-ion batteries

Hongxia Chen,Bin Liu,Ya Wang,Hao Guan,Hongming Zhou

Spinel LiNi 0.5 Mn 1.5 O 4 (LNMO) cathode with high voltage plateau at around 4.7 V (vs. Li/Li + ) has attracted great attention. However, the lack of suitable electrolyte hinders its application. Although lithium difluoro(oxalate)borate (LiODFB)-based electrolyte has been proved to be suitable for high voltage electrolyte, traditional LiODFB-based electrolyte has poor low and high temperature performance. Therefore, we confirm that lithium difluorophosphate (LiPO 2 F 2 , LiDFP) as LiODFB-based electrolyte additive and dimethyl sulfite (DMS) as co-solvent significantly improve electrochemical performance of LNMO/Graphite full batteries at low and high temperature. Various physical and electrochemical techniques are used to investigate the effect of four electrolytes. The effect on cathode is mainly attributed to priority oxidation decomposition of LiDFP. The formed interface film can inhibit the dissolution of Mn 2+ , thereby improving the high temperature electrochemical performance. The effect on anode is that the interface film formed by LiODFB prevents continuous reduction of solvents and additive. The enhanced low temperature performance is due to the significantly increased ionic conductivity of DMS-containing electrolytes at low temperature. Besides, the formed of the cathode electrolyte interphase (CEI) membrane with low impedance by LiDFP can improve the kinetics of cathode/electrolyte interface, therefore enhancing the low and high temperature performance of LNMO/Graphite full cells.

研究领域: 材料科学 · 电化学
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
已复制

文献关联基于可获得的产品、CAS、DOI 及引用记录。收录不代表作者或出版方对阿拉丁产品的背书,请以原始文献为准。