Determining Factor on the Polarization Behavior of Magnesium Deposition for Magnesium Battery Anode

被引:37
作者
Tuerxun, Feilure [1 ]
Yamamoto, Kentaro [1 ]
Hattori, Masashi [1 ]
Mandai, Toshihiko [2 ,3 ]
Nakanishi, Koji [1 ,4 ]
Choudhary, Ashu [5 ]
Tateyama, Yoshitaka [2 ,3 ]
Sodeyama, Keitaro [2 ,3 ]
Nakao, Aiko [6 ]
Uchiyama, Tomoki [1 ]
Matsui, Masaki [7 ]
Tsuruta, Kazuki [8 ]
Tamenori, Yusuke [8 ]
Kanamura, Kiyoshi [9 ]
Uchimoto, Yoshiharu [1 ]
机构
[1] Kyoto Univ, Grad Sch Human & Environm Studies, Kyoto 6068316, Japan
[2] Natl Inst Mat Sci NIMS, Ctr Green Res Energy & Environm Mat, Tsukuba, Ibaraki 3050044, Japan
[3] Natl Inst Mat Sci NIMS, Int Ctr Mat Nanoarchitecton, Tsukuba, Ibaraki 3050044, Japan
[4] Hyogo Univ, Lab Adv Sci & Technol Ind, Kamigori, Hyogo 6781205, Japan
[5] NIMS, Res & Serv Div Mat Data & Integrated Syst, Tsukuba, Ibaraki 3050047, Japan
[6] RIKEN, Bioengn Lab, Wako, Saitama 3510198, Japan
[7] Kobe Univ, Dept Chem Sci & Engn, Kobe, Hyogo 6518501, Japan
[8] Japan Synchrotron Radiat Res Inst JASRI, Res & Utilizat Div, Sayo, Hyogo 6795198, Japan
[9] Tokyo Metropolitan Univ, Grad Sch Urban Environm Sci, Dept Appl Chem, Hachioji, Tokyo 1920397, Japan
基金
日本科学技术振兴机构;
关键词
magnesium rechargeable battery; magnesium deposition; anode/electrolyte interface; operando soft X-ray absorption spectroscopy; passivation layer; coordination structure; LIQUID-AMMONIA SOLUTIONS; ELECTROLYTE-SOLUTIONS; POLY(ETHYLENE OXIDE); RAMAN-SPECTROSCOPY; ALUMINUM-CHLORIDE; BOROHYDRIDE ION; STABILITY; TRIGLYME; METAL; DISSOLUTION;
D O I
10.1021/acsami.0c03696
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
To clarify the origin of the polarization of magnesium deposition/dissolution reactions, we combined electrochemical measurement, operando soft X-ray absorption spectroscopy (operando SXAS), Raman, and density functional theory (DFT) techniques to three different electrolytes: magnesium bis(trifluoromethanesulfonyl)amide (Mg(TFSA)(2))/triglyme, magnesium borohydride (Mg(BH4)(2))/tetrahydrofuran (THF), and Mg(TFSA)(2)/2-methyltetrahydrofuran (2-MeTHF). Cyclic voltammetry revealed that magnesium deposition/dissolution reactions occur in Mg(TFSA)(2)/triglyme and Mg(BH4)(2)/THF, while the reactions do not occur in Mg(TFSA)(2)/2-MeTHF. Raman spectroscopy shows that the [TFSA](-) in the Mg(TFSA)(2)/triglyme electrolyte largely does not coordinate to the magnesium ions, while all of the [TFSA](-) in Mg(TFSA)(2)/2-MeTHF and [BH4](-) in Mg(BH4)(2)/THF coordinate to the magnesium ions. In operando SXAS measurements, the intermediate, such as the Mg+ ion, was not observed at potentials above the magnesium deposition potential, and the local structure distortion around the magnesium ions increases in all of the electrolytes at the magnesium electrode|electrolyte interface during the cathodic polarization. Our DFT calculation and X-ray photoelectron spectroscopy results indicate that the [TFSA](-), strongly bound to the magnesium ion in the Mg(TFSA)(2)/2-MeTHF electrolyte, undergoes reduction decomposition easily, instead of deposition of magnesium metal, which makes the electrolyte inactive electrochemically. In the Mg(BH4)(2)/THF electrolyte, because the [BH4](-) coordinated to the magnesium ions is stable even under the potential of the magnesium deposition, the magnesium deposition is not inhibited by the decomposition of [BH4](-). Conversely, because [TFSA](-) is weakly bound to the magnesium ion in Mg(TFSA)(2)/triglyme, the reduction decomposition occurs relatively slowly, which allows the magnesium deposition in the electrolyte.
引用
收藏
页码:25775 / 25785
页数:11
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