SnSb vs. Sn: improving the performance of Sn-based anodes for K-ion batteries by synergetic alloying with Sb

被引:53
作者
Gabaudan, Vincent [1 ,2 ]
Berthelot, Romain [1 ,2 ]
Sougrati, Moulay Tahar [1 ,2 ]
Lippens, Pierre-Emmanuel [1 ,2 ]
Monconduit, Laure [1 ,2 ]
Stievano, Lorenzo [1 ,2 ]
机构
[1] Univ Montpellier, CNRS, ICGM, UMR 5253, Montpellier, France
[2] CNRS, RS2E, Amiens, France
关键词
NEGATIVE ELECTRODE MATERIAL; PRUSSIAN WHITE ANALOGS; X-RAY-DIFFRACTION; POTASSIUM INTERCALATION; TIN; CAPACITY; MECHANISM; GRAPHITE; GRAPHENE; CATHODE;
D O I
10.1039/c9ta03760h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The electrochemical mechanism and performance of Sn-based electrodes are thoroughly studied in K-ion batteries. Low temperature ex situ(119)Sn Mossbauer spectroscopy combined with first principles calculations provides a clear description of the electrochemical mechanism, identifying the formation of poorly crystalline and/or nanosized KSn at the end of the potassiation of beta-Sn. During depotassiation, the formation of the intermediate phase K4Sn9 is established on the basis of DFT and Mossbauer spectroscopy. When tin is associated with antimony in SnSb, a different potassiation path is revealed for tin, with a huge impact on the overall performance. In fact, while the presence of antimony suppresses completely the decomposition of the electrolyte caused by tin particles, the new electrochemical potassiation/depotassiation mechanism drastically reduces the modifications in the local environment and the electrode morphology as evidenced by ex situ and post-mortem SEM analyses. Thanks to the positive impact of the association of tin with antimony, which reduces electrode degradation, a stable high specific capacity of more than 300 mA h g(-1) can be achieved for Sn-based negative electrodes in K-ion batteries.
引用
收藏
页码:15262 / 15270
页数:9
相关论文
共 53 条
[1]   SnSb electrodes for Li-ion batteries: the electrochemical mechanism and capacity fading origins elucidated by using operando techniques [J].
Antitomaso, Philippe ;
Fraisse, Bernard ;
Stievano, Lorenzo ;
Biscaglia, Stephane ;
Ayme-Perrot, David ;
Girard, Philippe ;
Sougrati, Moulay T. ;
Monconduit, Laure .
JOURNAL OF MATERIALS CHEMISTRY A, 2017, 5 (14) :6546-6555
[2]   The reaction mechanism of SnSb and Sb thin film anodes for Na-ion batteries studied by X-ray diffraction, 119Sn and 121Sb Mossbauer spectroscopies [J].
Baggetto, Loic ;
Hah, Hien-Yoong ;
Jumas, Jean-Claude ;
Johnson, Charles E. ;
Johnson, Jacqueline A. ;
Keum, Jong K. ;
Bridges, Craig A. ;
Veith, Gabriel M. .
JOURNAL OF POWER SOURCES, 2014, 267 :329-336
[3]   Anomalous, high-voltage irreversible capacity in tin electrodes for lithium batteries [J].
Beattie, SD ;
Hatchard, T ;
Bonakdarpour, A ;
Hewitt, KC ;
Dahn, JR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2003, 150 (06) :A701-A705
[4]  
Blaha P., 2001, WIEN2K AUGMENTED PLA
[5]   KVPO4F and KVOPO4 toward 4 volt-class potassium-ion batteries [J].
Chihara, Kuniko ;
Katogi, Akihiro ;
Kubota, Kei ;
Komaba, Shinichi .
CHEMICAL COMMUNICATIONS, 2017, 53 (37) :5208-5211
[6]   The Electrochemical Sodiation of Sb Investigated by Operando X-ray Absorption and Sb-121 Mossbauer Spectroscopy: What Does One Really Learn? [J].
Darwiche, Ali ;
Fehse, Marcus ;
Mahmoud, Abdelfattah ;
La Fontaine, Camille ;
Fraisse, Bernard ;
Hermann, Raphael P. ;
Doublet, Marie-Liesse ;
Monconduit, Laure ;
Sougrati, Moulay T. ;
Ben Yahia, Mouna ;
Stievano, Lorenzo .
BATTERIES-BASEL, 2018, 4 (02)
[7]   Facile synthesis and long cycle life of SnSb as negative electrode material for Na-ion batteries [J].
Darwiche, Ali ;
Sougrati, Moulay T. ;
Fraisse, Bernard ;
Stievano, Lorenzo ;
Monconduit, Laure .
ELECTROCHEMISTRY COMMUNICATIONS, 2013, 32 :18-21
[8]   Potassium Secondary Batteries [J].
Eftekhari, Ali ;
Jian, Zelang ;
Ji, Xiulei .
ACS APPLIED MATERIALS & INTERFACES, 2017, 9 (05) :4404-4419
[9]   Reversible Insertion of Sodium in Tin [J].
Ellis, L. D. ;
Hatchard, T. D. ;
Obrovac, M. N. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2012, 159 (11) :A1801-A1805
[10]  
Fassler TF, 1998, Z ANORG ALLG CHEM, V624, P561, DOI 10.1002/(SICI)1521-3749(199804)624:4<561::AID-ZAAC561>3.0.CO