Nanocolumnar Germanium Thin Films as a High-Rate Sodium-Ion Battery Anode Material

被引:174
作者
Abel, Paul R. [1 ]
Lin, Yong-Mao [1 ]
de Souza, Tania [1 ]
Chou, Chia-Yun [4 ,5 ]
Gupta, Asha [4 ,5 ]
Goodenough, John B. [4 ,5 ]
Hwang, Gyeong S. [1 ]
Heller, Adam [1 ,3 ]
Mullins, C. Buddie [1 ,2 ,3 ,4 ,5 ]
机构
[1] Univ Texas Austin, McKetta Dept Chem Engn, Austin, TX 78712 USA
[2] Univ Texas Austin, Dept Chem & Biochem, Austin, TX 78712 USA
[3] Univ Texas Austin, Ctr Electrochem, Austin, TX 78712 USA
[4] Univ Texas Austin, Texas Mat Inst, Austin, TX 78712 USA
[5] Univ Texas Austin, Ctr Nano & Mol Sci, Austin, TX 78712 USA
关键词
REACTIVE BALLISTIC DEPOSITION; TOTAL-ENERGY CALCULATIONS; ELECTRODE MATERIAL; FLUOROETHYLENE CARBONATE; HIGH-CAPACITY; LITHIUM; SILICON; CATHODE; NANOCOMPOSITES; NA3V2(PO4)(3);
D O I
10.1021/jp407322k
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
Both nanocolumnar and dense germanium thin films, synthesized by evaporative deposition, were tested as a potential anode material for sodium-ion batteries. The reversible capacity of the nanocolumnar films was found to be 430 mAh/g, which is higher than the theoretical capacity of 369 mAh/g. The nanocolumnar films retained 88% of their initial capacity after 100 cycles at C/5, whereas the dense films began to deteriorate after similar to 15 cycles. Additionally, the nanocolumnar films were stable at charge/discharge rates up to 27C (10 A/g). The diffusion coefficient for sodium in germanium was estimated, from impedance analysis of the dense films, to be 13 CM 2 s(-1). Modeling of diffusion in the sodium- germanium system predicts that sodium diffusion in the near-surface layers of the material is significantly faster than in the bulk. These results show that small feature sizes are critical for rapid, reversible electrochemical sodiation of germanium.
引用
收藏
页码:18885 / 18890
页数:6
相关论文
共 53 条
[1]   Nanostructured Si(i-x)Gex for Tunable Thin Film Lithium-Ion Battery Anodes [J].
Abel, Paul R. ;
Chockla, Aaron M. ;
Lin, Yong-Mao ;
Holmberg, Vincent C. ;
Harris, Justin T. ;
Korgel, Brian A. ;
Heller, Adam ;
Mullins, C. Buddie .
ACS NANO, 2013, 7 (03) :2249-2257
[2]   Improving the Stability of Nanostructured Silicon Thin Film Lithium-Ion Battery Anodes through Their Controlled Oxidation [J].
Abel, Paul R. ;
Lin, Yong-Mao ;
Celio, Hugo ;
Heller, Adam ;
Mullins, C. Buddie .
ACS NANO, 2012, 6 (03) :2506-2516
[3]   Oblique evaporation and surface diffusion [J].
Abelmann, L ;
Lodder, C .
THIN SOLID FILMS, 1997, 305 (1-2) :1-21
[4]   Carbon black:: a promising electrode material for sodium-ion batteries [J].
Alcántara, R ;
Jiménez-Mateos, JM ;
Lavela, P ;
Tirado, JL .
ELECTROCHEMISTRY COMMUNICATIONS, 2001, 3 (11) :639-642
[5]   Sodium iron pyrophosphate: A novel 3.0 V iron-based cathode for sodium-ion batteries [J].
Barpanda, Prabeer ;
Ye, Tian ;
Nishimura, Shin-ichi ;
Chung, Sai-Cheong ;
Yamada, Yuki ;
Okubo, Masashi ;
Zhou, Haoshen ;
Yamada, Atsuo .
ELECTROCHEMISTRY COMMUNICATIONS, 2012, 24 :116-119
[6]   PROJECTOR AUGMENTED-WAVE METHOD [J].
BLOCHL, PE .
PHYSICAL REVIEW B, 1994, 50 (24) :17953-17979
[7]   Sodium Ion Insertion in Hollow Carbon Nanowires for Battery Applications [J].
Cao, Yuliang ;
Xiao, Lifen ;
Sushko, Maria L. ;
Wang, Wei ;
Schwenzer, Birgit ;
Xiao, Jie ;
Nie, Zimin ;
Saraf, Laxmikant V. ;
Yang, Zhengguo ;
Liu, Jun .
NANO LETTERS, 2012, 12 (07) :3783-3787
[8]   High capacity Li ion battery anodes using Ge nanowires [J].
Chan, Candace K. ;
Zhang, Xiao Feng ;
Cui, Yi .
NANO LETTERS, 2008, 8 (01) :307-309
[9]   Challenges for Na-ion Negative Electrodes [J].
Chevrier, V. L. ;
Ceder, G. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2011, 158 (09) :A1011-A1014
[10]   Solution-Grown Germanium Nanowire Anodes for Lithium-Ion Batteries [J].
Chockla, Aaron M. ;
Klavetter, Kyle C. ;
Mullins, C. Buddie ;
Korgel, Brian A. .
ACS APPLIED MATERIALS & INTERFACES, 2012, 4 (09) :4658-4664