检索结果-南通市图书馆

Modulating the Electrolyte Inner Solvation Structure via Low Polarity Co-solvent for Low-Temperature Aqueous Zinc-Ion Batteries

引用

Energy & Environmental Materials 2024年第5期7卷 108-117页

作者： Yongchao Kang Feng Zhang Houzhen Li wangran wei Huitong Dong Hao Chen Yuanhua Sang Hong Liu Shuhua Wang State Key Laboratory of Crystal Materials Shandong University Institute for Advanced Interdisciplinary Research (i AIR) University of Jinan

Aqueous zinc-ion batteries are regarded as the promising candidates for large-scale energy storage systems owing to low cost and high safety;however, their applications are restricted by their poor low-temperature performance. Herein, a low-temperature electrolyte for low-temperature aqueous zinc-ion batteries is designed by introducing low-polarity diglyme into an aqueous solution of Zn（ClO4）2. The diglyme disrupts the hydrogenbonding network of water and lowers the freezing point of the electrolyte to-105℃. The designed electrolyte achieves ionic conductivity up to16.18 mS cm-1at-45℃. The diglyme and ClO4-reconfigure the solvated structure of Zn2+, which is more favorable for the desolvation of Zn2+at low temperatures. In addition, the diglyme effectively suppresses the dendrites,hydrogen evolution reaction, and by-products of the zinc anode, improving the cycle stability of the battery. At-20℃, a Zn‖Zn symmetrical cell is cycled for 5200 h at 1 mA cm-2and 1 mA h cm-2, and a Zn‖polyaniline battery achieves an ultra-long cycle life of 10 000 times. This study sheds light on the future design of electrolytes with high ionic conductivity and easy desolvation at low temperatures for rechargeable batteries.

关键词： aqueous zinc-ion batteries high performance inner solvation structure low polarity co-solvent low-temperature electrolyte

来源：

同方期刊数据库评论

在线全文

同方期刊数据库

学校读者我要写书评

暂无评论

Branch-Chain-Rich Diisopropyl Ether with Steric Hindrance Facilitates Stable Cycling of Lithium Batteries at-20℃

引用

Nano-Micro Letters 2024年第10期16卷 121-135页

作者： Houzhen Li Yongchao Kang wangran wei Chuncheng Yan Xinrui Ma Hao Chen Yuanhua Sang Hong Liu Shuhua Wang State Key Laboratory of Crystal Materials Shandong UniversityJinan 250100People's Republic of China

Li metal batteries(LMBs)offer signifi-cant potential as high energy density alternatives;nev-ertheless,their performance is hindered by the slow desolvation process of electrolytes,particularly at low temperatures(LT),leading to low coulombic efficiency and limited cycle ***,it is essential to opti-mize the solvation structure thereby achieving a rapid desolvation process in LMBs at ***,we introduce branch chain-rich diisopropyl ether(DIPE)into a 2.5 M Li bis(fluorosulfonyl)imide dipropyl ether(DPE)elec-trolyte as a co-solvent for high-performance LMBs at-20℃.The incorporation of DIPE not only enhances the disorder within the electrolyte,but also induces a steric hindrance effect form DIPE’s branch chain,excluding other solvent molecules from Li+solvation *** of these factors contribute to the weak interactions between Li^(+)and solvent molecules,effectively reducing the desolvation energy of the ***,Li(50μm)||LFP(mass loading~10 mg cm^(-2))cells in DPE/DIPE based electrolyte demonstrate stable performance over 650 cycles at-20℃,delivering 87.2 mAh g^(-1),and over 255 cycles at 25℃ with 124.8 mAh g^(-1).DIPE broadens the electrolyte design from molecular structure considera-tions,offering a promising avenue for highly stable LMBs at LT.

关键词： Solvation structure Li metal battery Low temperature Steric hindrance Disorder

来源：

维普期刊数据库

同方期刊数据库评论

在线全文

学校读者我要写书评

暂无评论

欢迎您,

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

在线全文

在线全文

请选择保存的检索档案：

请选择收藏分类：

通借通还

欢迎您,

建议与咨询 留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

在线全文

在线全文

请选择保存的检索档案： 新增检索档案 确定 取消

请选择收藏分类： 新增自定义分类 确定 取消

通借通还

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

请选择保存的检索档案：

请选择收藏分类：