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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.
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页码:25775 / 25785
页数:11
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