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Mg(TFSI)2
ELECTROCHIMICA ACTA · 2018 · IF 5.116

A long cycle-life Na-Mg hybrid battery with a chlorine-free electrolyte based on Mg(TFSI)2

Jing Zeng,Zulai Cao,Yang Yang,Yunhui Wang,Yueying Peng,Yiyong Zhang,Jing Wang,Jinbao Zhao

The commercial applications of rechargeable magnesium batteries (RMBs) are hindered by the slow diffusion kinetic of Mg 2+ ions in cathode materials. To overcome this problem, we design a new Na-Mg hybrid battery with the NaTi 2 (PO 4 ) 3 @Carbon (NTP@C) nanoparticles as a cathode material, the Mg metal as an anode and the Mg(TFSI) 2  + NaBH 4 - triglyme/1,2-Dimethoxyethane (DME) as a hybrid electrolyte. For the first time, the Mg(TFSI) 2 is applied as a Mg 2+ ions source in the chlorine-free Na-Mg hybrid electrolyte with NaBH 4 as both Na + ions source and moisture scavenger. The NTP@C/Mg hybrid battery shows excellent electrochemical performance. The corresponding average capacity decay after 1000 cycles is only 0.004% and 0.008% per cycle at 2 C and 10 C, respectively. Even at 20 C, about 60 mAh g −1 can be obtained after 26000 cycles. The impressive capacity retention of 93.7% and 90.2% can be obtained at 5 and 10 C, respectively. The excellent electrochemical performance of the hybrid battery confirms the feasibility using Mg(TFSI) 2 in the chlorine-free hybrid electrolyte for long term cycle. The developed NTP@C/Mg hybrid battery possesses the advantages of excellent electrochemical performances, good safety and low cost, making it promising for the commercial applications, especially for the large-scale energy storages.

CAS / MDL: 16940-66-2
研究领域: 材料科学 · 电化学
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2025 · IF 9.7

An ultra-dilute Mg(TFSI)2 based electrolyte enabling reversible Mg metal anode

Caiyun Wang,Xingxing Wu,Yufan Xia,Xuan Zhang,Hongge Pan,Mi Yan,Yong Li,Yinzhu Jiang

Mg metal anodes experience significant passivation of harmful side reactions in conventional electrolyte consisting of magnesium bis(trifluoromethane sulfonyl)imide (Mg(TFSI) 2 ) in 1,2-dimethoxyethane (DME), which critically impedes the advancement of high-performance rechargeable magnesium batteries. Herein, an innovative electrolyte system comprising an ultra-dilute 0.02 M Mg(TFSI) 2 in DME with 4-chlorobutyl methyl ether (CME) as co-solvent is strategically devised. This unique formulation effectively suppresses the formation of TFSI − -derived passivation byproducts while simultaneously facilitating the establishment of protective Cl-rich interphase, thereby achieving exceptional reversibility in Mg plating/stripping processes. Remarkably, Mg electrodes demonstrate stable cycling performance with a minimal overpotential of 70 mV at 0.1 mA cm −2 in the optimized 0.02 M Mg(TFSI) 2 -DME/CME electrolyte. More impressively, the system maintains reversible electrochemical operation for 400 h even at 2 mA cm −2 . This work presents a novel electrolyte formulation for overcoming the limitations of Mg metal anode in conventional Mg(TFSI) 2 based electrolytes, offering new perspectives for the development of next-generation rechargeable magnesium batteries.

CAS / MDL: 10031-43-3 872-50-4
研究领域: 电化学 · 能源材料 · 电池技术
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CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

An artificial interphase enables the use of Mg(TFSI)2-based electrolytes in magnesium metal batteries

Rupeng Zhang,Can Cui,Ruinan Li,Yaqi Li,Chunyu Du,Yunzhi Gao,Hua Huo,Yulin Ma,Pengjian Zuo,Geping Yin

Due to the good safety and high energy density , rechargeable Mg-metal batteries (RMMBs) have been regarded as a potential competitor of Li-metal batteries (LMBs). However, the Mg(TFSI) 2 -based conventional electrolytes will cause large overpotential in reversible plating/stripping attributed to the high ion transport impedance of the electrolyte decomposition products. Here, an artificial interphase composed of amorphous (a-) MgCl 2 @polymer on the Mg-metal surface is prepared by in-situ chemical reaction of metallic Mg with H 3 PO 4 and SiCl 4 in sequence, and can effectively inhibit the electrolyte decomposition and facilitate Mg 2+ transport, which plays the role of solid electrolyte interface (SEI) on Mg anode. The Mg-Mg symmetrical cell with modified Mg electrode exhibits lower overpotential (~0.25 V) and interfacial impedance than bare Mg electrode in 0.5 M Mg(TFSI) 2 /DME electrolyte. The voltage hysteresis in the Mg-S and Mg-Mo 6 S 8 batteries with the modified Mg anode is greatly improved compared to bare Mg anode. This work provides a new idea for future applications of passivation-free Mg-metal anode technology in the MMBs based on conventional electrolytes.

研究领域: 材料科学 · 能源技术
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POLYMER · 2025 · IF 4.5

Fabrication and optical properties of transparent PMMA/BPEF blend films via reactive melt extrusion with catalysis of Mg(TFSI)2

Zhanpeng Xu,Kang Li,Huihui Xu,Tingzi Yan,Yongjin Li

This study utilized a straightforward one-step method, melt extrusion , to blend polymethyl methacrylate (PMMA) with 9,9-bis[4-(2-hydroxyethoxy)phenyl]fluorene (BPEF) to fabricate optically transparent polymer blends , utilizing Mg(TFSI) 2 as the catalyst for the ester exchange reaction. All polymer blends demonstrated excellent mechanical and optical properties , achieving high transparency (≥90 %) in the visible spectrum. Differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) results indicated that the blends formed a thermodynamically homogeneous system. Additionally, gel permeation chromatography (GPC) confirmed the occurrence of ester exchange reactions between PMMA and BPEF in both salted and unsalted blends. Very interestingly, without Mg(TFSI) 2 one hydroxyl group of BPEF is linked to PMMA side group through transesterification reaction, leading to a zero birefringence . Nonetheless, the inclusion of Mg(TFSI) 2 appears to facilitate the ester exchange reaction between both hydroxyl groups of BPEF and a single PMMA chain, which causes a cyclic ring structure. Such cyclic ring structure orients parallel to the planar plan, which then increases n // and also Δn.

CAS / MDL: 117344-32-8
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Small Methods · 2023 · IF 12.4

Building Organic–Inorganic Robust Interphases from Deep Eutectic Solution for Highly Stable Mg Metal Anode in Conventional Electrolyte

Xuejun Zhou,Guyue Li,Yifan Yu,Meng Lei,Keyi Chen,Chilin Li

Magnesium metal batteries (MMBs) currently face challenges suffering from severe Mg metal passivation and extremely high overpotential in conventional electrolytes. Herein, a strategy of using a low-cost deep eutectic solution (DES) is proposed to modify Mg anode with the monolithic and compact coating of a MgCl 2 -Al-MgCl 2 sandwich structure, enabling the stable and reversible Mg plating–stripping behavior. An organic/nanocrystal hybrid interphase is in-situ built through a facile Mg-Al displacement reaction between aluminum-chloro clusters and Mg in AlCl 3 /Et 3 NHCl solution, and it can effectively minimize the adverse interfacial passivation reaction and surface diffusion barrier, affording the high ion-conduction and electronic insulation. This DES-assisted method guarantees a highly reversible cycling of Mg metal anode (over 5000 h at 0.1 mA cm −2 and 400 h at 2.0 mAh cm −2 ) in Mg(TFSI) 2 /DME electrolyte with the improved interfacial kinetics and low overpotential. Even at a much higher current density of 1 mA cm −2 , the overpotential only undergoes a slight increase from 0.2 V (at 0.1 mA cm −2 ) to 0.23 V. The corresponding full cells with CuS and phenanthraquinone cathodes deliver satisfactory cyclic performance. The DES modification strategy provides a new solution to the design of robust and conductive solid electrolyte interphase for achieving high-voltage and durable MMBs.

研究领域: 材料科学 · 电化学 · 能源存储 · 电池技术
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