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The sulfolane-based liquid electrolyte with LiClO_(4)additive for the wide-temperature operating high nickel ternary cathode

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Nano Research 2023年第3期16卷 3855-3863页

作者： Yixin Zhu Shuang He Jiayi Ding Guangyu Zhao Fang Lian School of Materials Science and Engineering University of Science and Technology BeijingBeijing 100083China University of New South Wales PontypriddCF371DLUK

An adequate wide temperature electrolyte for high nickel ternary cathode is urgent to further develop high energy density batteries.Herein,a comprehensive double-salt local high-concentration sulfolane-based electrolyte(DLi)is proposed with specific sheath structure to build stable interface on the LiNi_(0.8)Co_(0.1)Mn_(0.1O2)(NCM811)cathode at wide operating temperature between−60 and 55℃.Lithium perchlorate(LiClO_(4))in combination with high concentration lithium bis-(trifluoromethanesulfonyl)imide(LiTFSI)strengthens the internal interaction between anion and cation in the solvation structure,increasing Li+transference number of the electrolyte to 0.61.Moreover,the structure and component characteristics of the passive interface layer on NCM811 are modulated,decreasing desolvation energy of Li+ions,benefiting Li+transport dynamics especially at low temperature,and also ensuring the interfacial stability at a wide operating temperature range.As a result,the cathode with DLi exhibits excellent high-temperature storage performance and high capacity retention of 80.5%in 100 cycles at 55℃.Meanwhile,the Li||NCM811 cells can deliver high discharge capacity of 160.1,136.1,and 110.3 mAh·g^(−1)under current density of 0.1 C at−20,−40,and−60℃,maintaining 84.5%,71.8%,and 58.2%of the discharge capacity at 30℃,respectively.Moreover,it enables NCM811 cathode to achieve a reversible capacity of 142.8 mAh·g^(−1)in 200 cycles at−20℃and 0.2 C.Our studies shed light on the molecular strategy of wide operational temperature electrolyte for high nickel ternary cathode.

关键词： liquid electrolyte high nickel ternary cathode wide temperature interface sheath structure

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Observation of high ionic conductivity of polyelectrolyte microgels in salt-free solutions

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Chinese Chemical Letters 2024年第4期35卷 255-259页

作者： Qiangwei Wang Huijiao Liu Mengjie Wang Haojie Zhang Jianda Xie Xuanwei Hu Shiming Zhou Weitai Wu State Key Laboratory for Physical Chemistry of Solid Surfaces Collaborative Innovation Center of Chemistry for Energy MaterialsThe Key Laboratory for Chemical Biology of Fujian Provinceand Department of ChemistryCollege of Chemistry and Chemical EngineeringXiamen UniversityXiamen 361005China School of Materials Science and Engineering Xiamen University of TechnologyXiamen 361024China Hefei National Laboratory for Physical Sciences at the Microscale University of Science and Technology of ChinaHefei 230026China School of Chemistry and Chemical Engineering Ningxia UniversityYinchuan 750021China

Here, we report an observation that illustrate the potential of polyelectrolyte microgels in salt-free solutions to display a high ionic conductivity. Laser light scattering and ionic conductivity tests on very dilute aqueous dispersions of the microgels indicate that both small size and swollen state of gel particles play vital roles, which should favor the counterions to freely penetrate and leave gel particles, and thus can contribute to the ion-conducting property. Upon discovering this on microgels that are composed of imidazolium-based poly(ionic liquid), we also illustrate the generality of the finding to single lithium-ion polyelectrolyte microgels that are of more technically relevant features for applications, for instance, as injectable liquid “microgel-in-solution” electrolytes of high conductivity(ca. 8.2 × 10^(-2)S/m at 25.0 ℃ for1.0 × 10^(-2)g/m L of microgels in a LiNO_(3)-free 1:1 v/v mixture of 1,2-dioxolane and dimethoxymethane) and high lithium-ion transference number(0.87) for use in the rechargeable lithium-sulfur battery.

关键词： Polyelectrolhyte Stimuli-responsive Single-ion conducting liquid electrolyte Lithium metal battery

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Towards safe lithium-sulfur batteries from liquid-state electrolyte to solid-state electrolyte

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Frontiers of Materials Science 2023年第1期17卷 15-50页

作者： Zhiyuan Pang Hongzhou Zhang Lu Wang Dawei Song Xixi Shi Yue Ma Linglong Kong Lianqi Zhang Tianjin Key Laboratory for Photoelectric Materials and Devices School of Materials Science and EngineeringTianjin University of TechnologyTianjin 300384China College of Chemistry and Materials Science Shandong Agricultural UniversityTaian 271018China State Forestry and Grassland Administration Key Laboratory of Silviculture in Downstream Areas of the Yellow River School of ForestryShandong Agricultural UniversityTaian 271018China

Lithium-sulfur(Li-S)battery has been considered as one of the most promising future batteries owing to the high theoretical energy density(2600 W-h-kg-1)and the usage of the inexpensive active materials(elemental sulfur).The recent progress in fundamental research and engineering of the Li-S battery,involved in electrode,electrolyte,membrane,binder,and current collector,has greatly promoted the performance of Li s batteries from the laboratory level to the approaching practical level.However,the safety concerns still deserve attention in the following application stage.This review focuses on the development of the electrolyte for Li S batteries from liquid state to solid state.Some problems and the corresponding solutions are emphasized,such as the soluble lithium polysulfides migration,ionic conductivity of electrolyte,the interface contact between electrolyte and electrode,and the reaction kinetics.Moreover,future perspectives of the safe and high-performance Li S batteries arealso introduced.

关键词： lithium-sulfur battery liquid electrolyte polymer electrolyte solid-state electrolyte battery safety

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Hierarchical porous carbon derived from one-step self-activation of zinc gluconate for symmetric supercapacitors with high energy density

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Frontiers of Chemical Science and Engineering 2023年第4期17卷 387-394页

作者： Junlei Xiao Hua Zhang Yifan Wang Chunmei Zhang Shuijian He Shaohua Jiang Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources International Innovation Center for Forest Chemicals and MaterialsCollege of Materials Science and EngineeringNanjing Forestry UniversityNanjing 210037China College of Chemistry and Chemical Engineering Jiangxi Normal UniversityNanchang 330022China Institute of Materials Science and Devices School of Materials Science and EngineeringSuzhou University of Science and TechnologySuzhou 215009China

Porous carbons with high specific area surfaces are promising electrode materials for supercapacitors.However,their production usually involves complex,time-consuming,and corrosive processes.Hence,a straightforward and effective strategy is presented for producing highly porous carbons via a self-activation procedure utilizing zinc gluconate as the precursor.The volatile nature of zinc at high temperatures gives the carbons a large specific surface area and an abundance of mesopores,which avoids the use of additional activators and templates.Consequently,the obtained porous carbon electrode delivers a satisfactory specific capacitance and outstanding cycling durability of 90.9%after 50000 cycles at 10 A·g^(-1).The symmetric supercapacitors assembled by the optimal electrodes exhibit an acceptable rate capability and a distinguished cycling stability in both aqueous and ionic liquid electrolytes.Accordingly,capacitance retention rates of 77.8%and 85.7%are achieved after 50000 cycles in aqueous alkaline electrolyte and 10000 cycles in ionic liquid electrolyte.Moreover,the symmetric supercapacitors deliver high energy/power densities of 49.8 W·h·kg^(-1)/2477.8 W·kg^(-1) in the Et4NBF4 electrolyte,outperforming the majority of previously reported porous carbon-based symmetric supercapacitors in ionic liquid electrolytes.

关键词： self-activation zinc organic salts abundant mesopores symmetric supercapacitor liquid electrolyte

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