High efficiency aqueous and hybrid lithium-air batteries enabled by Li1.5Al0.5Ge1.5(PO4)3 ceramic anode-protecting membranes

被引:53
作者
Safanama, Dorsasadat [1 ]
Adams, Stefan [1 ]
机构
[1] Natl Univ Singapore, Dept Mat Sci & Engn, Singapore, Singapore
基金
新加坡国家研究基金会;
关键词
NASICON-type ceramic; Anode-protecting membrane; Hybrid Li-air battery; Aqueous battery; Energy efficiency; 2e(-) oxygen reduction mechanism; CONDUCTING SOLID-ELECTROLYTE; GLASS-CERAMICS; SUPERIONIC CONDUCTIVITY; DOPED LI7LA3ZR2O12; IONIC-CONDUCTIVITY; LI+/H+ EXCHANGE; LI5LA3M2O12; M; WATER; STABILITY; PERFORMANCE;
D O I
10.1016/j.jpowsour.2016.11.076
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
Due to their extremely high specific energy, rechargeable Li-air batteries could meet the demand for large-scale storage systems to integrate renewable sources into the power grid. Li-air batteries with aqueous catholytes with high solubility of discharge products have a higher potential to reach their slightly lower theoretical limits in practical devices. In this work, we demonstrate aqueous and hybrid Li-air batteries with NASICON-type Li(1+x)A(x)Ge(2-x)(PO4)(3) ceramic as anode-protecting membrane. The LAGP ceramic pellets with room temperature conductivity >10(-4) S cm(-1) are synthesized by melt quenching and subsequently annealed based on our optimized heat treatment cycle. Hybrid Li-air batteries are assembled by sandwiching LAGP membranes between Li-anode chamber and catholyte solutions (of various pH values) with CNT/Pt as air-cathode. When the two electron reduction mechanism prevails, overpotentials below 0.2 V are achieved for currents up to 0.07 mA cm(-2) leading to energy efficiencies exceeding 98%. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:294 / 301
页数:8
相关论文
共 63 条
[1]   Ion transport and phase transition in Li7-xLa3(Zr2-xMx)O12 (M = Ta5+, Nb5+, x=0, 0.25) [J].
Adams, Stefan ;
Rao, Rayavarapu Prasada .
JOURNAL OF MATERIALS CHEMISTRY, 2012, 22 (04) :1426-1434
[2]  
[Anonymous], 2011, WORLD EN OUTL
[3]   HIGH LI+ CONDUCTING CERAMICS [J].
AONO, H ;
IMANAKA, N ;
ADACHI, G .
ACCOUNTS OF CHEMICAL RESEARCH, 1994, 27 (09) :265-270
[4]   A critical review on lithium-air battery electrolytes [J].
Balaish, Moran ;
Kraytsberg, Alexander ;
Ein-Eli, Yair .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2014, 16 (07) :2801-2822
[5]   Reaction mechanisms of Li0.30La0.57TiO3 powder with ambient air: H+/Li+ exchange with water and Li2CO3 formation [J].
Boulant, Anthony ;
Bardeau, Jean Francois ;
Jouanneaux, Alain ;
Emery, Joel ;
Buzare, Jean-Yves ;
Bohnke, Odile .
DALTON TRANSACTIONS, 2010, 39 (16) :3968-3975
[6]   IONIC-CONDUCTIVITY OF LISICON SOLID-SOLUTIONS, LI2+2XZN1-XGEO4 [J].
BRUCE, PG ;
WEST, AR .
JOURNAL OF SOLID STATE CHEMISTRY, 1982, 44 (03) :354-365
[7]   Selection of oxygen reduction catalysts for rechargeable lithium-air batteries-Metal or oxide? [J].
Cheng, H. ;
Scott, K. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2011, 108 (1-2) :140-151
[8]   Structure and ionic conductivity in lithium garnets [J].
Cussen, Edmund J. .
JOURNAL OF MATERIALS CHEMISTRY, 2010, 20 (25) :5167-5173
[9]   Fast Li+ ion conducting glass-ceramics in the system Li2O-Al2O3-GeO2-P2O5 [J].
Fu, J .
SOLID STATE IONICS, 1997, 104 (3-4) :191-194