Hyper-dendritic nanoporous zinc foam anodes

被引:155
作者
Chamoun, Mylad [1 ,2 ,5 ]
Hertzberg, Benjamin J. [2 ]
Gupta, Tanya [2 ]
Davies, Daniel [2 ]
Bhadra, Shoham [3 ]
Van Tassell, Barry [4 ]
Erdonmez, Can [1 ]
Steingart, Daniel A. [2 ]
机构
[1] Brookhaven Natl Lab, Sustainable Energy Technol Dept, Upton, NY 11973 USA
[2] Princeton Univ, Dept Mech & Aerosp Engn, Andlinger Ctr Energy & Environm, D428 EQuad, Princeton, NJ 08544 USA
[3] Princeton Univ, Andlinger Ctr Energy & Environm, Dept Elect Engn, Princeton, NJ 08544 USA
[4] CUNY, Dept Chem Engn, New York, NY 10021 USA
[5] Stockholm Univ, Dept Mat & Environm Chem, Arrhenius Lab, S-10691 Stockholm, Sweden
基金
美国国家科学基金会;
关键词
ALKALINE ELECTROLYTES; KINETIC-ANALYSIS; DEPOSITION; BEHAVIOR; MORPHOLOGY; BATTERY; ELECTRODEPOSITION; MECHANISM; EVOLUTION; CAPACITY;
D O I
10.1038/am.2015.32
中图分类号
T [工业技术];
学科分类号
120111 [工业工程];
摘要
The low cost, significant reduction potential and relative safety of the zinc electrode is a common hope for a reductant in secondary batteries, but it is limited mainly to primary implementation due to shape change. In this work, we exploit such shape change for the benefit of static electrodes through the electrodeposition of hyper-dendritic nanoporous zinc foam. Electrodeposition of zinc foam resulted in nanoparticles formed on secondary dendrites in a three-dimensional network with a particle size distribution of 54.1-96.0 nm. The nanoporous zinc foam contributed to highly oriented crystals, high surface area and more rapid kinetics in contrast to conventional zinc in alkaline mediums. The anode material presented had a utilization of similar to 88% at full depth-of-discharge (DOD) at various rates indicating a superb rate capability. The rechargeability of Zn-0/Zn2+ showed significant capacity retention over 100 cycles at a 40% DOD to ensure that the dendritic core structure was imperforated. The dendritic architecture was densified upon charge-discharge cycling and presented superior performance compared with bulk zinc electrodes.
引用
收藏
页码:e178 / e178
页数:8
相关论文
共 34 条
[1]
CONTROLLED CURRENT DEPOSITION OF ZINC FROM ALKALINE SOLUTION [J].
AROUETE, S ;
BLURTON, KF ;
OSWIN, HG .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1969, 116 (02) :166-&
[2]
THE BEHAVIOR OF ZINC ELECTRODE IN ALKALINE ELECTROLYTES .2. A KINETIC-ANALYSIS OF ANODIC-DISSOLUTION [J].
CACHET, C ;
SAIDANI, B ;
WIART, R .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1992, 139 (03) :644-654
[3]
THE BEHAVIOR OF ZINC ELECTRODE IN ALKALINE ELECTROLYTES .1. A KINETIC-ANALYSIS OF CATHODIC DEPOSITION [J].
CACHET, C ;
SAIDANI, B ;
WIART, R .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1991, 138 (03) :678-687
[4]
Surface treatment of zinc anodes to improve discharge capacity and suppress hydrogen gas evolution [J].
Cho, Yung-Da ;
Fey, George Ting-Kuo .
JOURNAL OF POWER SOURCES, 2008, 184 (02) :610-616
[5]
MECHANISM OF FORMATION OF ZINC DENDRITES [J].
DESPIC, AR ;
DIGGLE, J ;
BOCKRIS, JOM .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1968, 115 (05) :507-&
[6]
BEHAVIOR OF THE ZINC ELECTRODE IN ALKALINE-SOLUTIONS .2. REACTION ORDERS AT THE EQUILIBRIUM POTENTIAL [J].
DIRKSE, TP .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1979, 126 (04) :541-543
[7]
ANODIC BEHAVIOR OF ZINC IN AQUEOUS KOH SOLUTION .2. PASSIVATION EXPERIMENTS USING LINEAR SWEEP VOLTAMMETRY [J].
DIRKSE, TP ;
HAMPSON, NA .
ELECTROCHIMICA ACTA, 1972, 17 (03) :387-&
[8]
Ehrlich G.M., 2002, HDB BATTERIES
[9]
Falk S.U., 1969, ALKALINE STORAGE BAT
[10]
Real-time materials evolution visualized within intact cycling alkaline batteries [J].
Gallaway, Joshua W. ;
Erdonmez, Can K. ;
Zhong, Zhong ;
Croft, Mark ;
Sviridov, Lev A. ;
Sholklapper, Tal Z. ;
Turney, Damon E. ;
Banerjee, Sanjoy ;
Steingart, Daniel A. .
JOURNAL OF MATERIALS CHEMISTRY A, 2014, 2 (08) :2757-2764