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Batteries 2017, 3(3), 22; doi:10.3390/batteries3030022

Comparison of C14- and C15-Predomiated AB2 Metal Hydride Alloys for Electrochemical Applications

1
Department of Chemical Engineering and Materials Science, Wayne State University, Detroit, MI 48202, USA
2
BASF/Battery Materials—Ovonic, 2983 Waterview Drive, Rochester Hills, MI 48309, USA
3
Institute for Energy Technology, P.O. Box 40, NO-2027 Kjeller, Norway
4
Department of Physics, University of Science and Technology Beijing, Beijing 100083, China
5
Department of Materials Science and Engineering, Norwegian University of Science and Technology, NO-7491 Trondheim, Norway
*
Author to whom correspondence should be addressed.
Academic Editor: Catia Arbizzani
Received: 24 May 2017 / Revised: 7 July 2017 / Accepted: 11 July 2017 / Published: 28 July 2017
(This article belongs to the Special Issue Nickel Metal Hydride Batteries 2017)
View Full-Text   |   Download PDF [1886 KB, uploaded 28 July 2017]   |  

Abstract

Herein, we present a comparison of the electrochemical hydrogen-storage characteristics of two state-of-art Laves phase-based metal hydride alloys (Zr21.5Ti12.0V10.0Cr7.5Mn8.1Co8.0Ni32.2Sn0.3Al0.4 vs. Zr25.0Ti6.5V3.9Mn22.2Fe3.8Ni38.0La0.3) prepared by induction melting and hydrogen decrepitation. The relatively high contents of lighter transition metals (V and Cr) in the first composition results in an average electron density below the C14/C15 threshold ( e / a ~ 6.9 ) and produces a C14-predominated structure, while the average electron density of the second composition is above the C14/C15 threshold and results in a C15-predominated structure. From a combination of variations in composition, main phase structure, and degree of homogeneity, the C14-predominated alloy exhibits higher storage capacities (in both the gaseous phase and electrochemical environment), a slower activation, inferior high-rate discharge, and low-temperature performances, and a better cycle stability compared to the C15-predominated alloy. The superiority in high-rate dischargeability in the C15-predominated alloy is mainly due to its larger reactive surface area. Annealing of the C15-predominated alloy eliminates the ZrNi secondary phase completely and changes the composition of the La-containing secondary phase. While the former change sacrifices the synergetic effects, and degrades the hydrogen storage performance, the latter may contribute to the unchanged surface catalytic ability, even with a reduction in total volume of metallic nickel clusters embedded in the activated surface oxide layer. In general, the C14-predominated alloy is more suitable for high-capacity and long cycle life applications, and the C15-predominated alloy can be used in areas requiring easy activation, and better high-rate and low-temperature performances. View Full-Text
Keywords: metal hydride; nickel metal hydride battery; Laves phase alloy; electrochemistry; synergetic effect metal hydride; nickel metal hydride battery; Laves phase alloy; electrochemistry; synergetic effect
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MDPI and ACS Style

Young, K.-H.; Nei, J.; Wan, C.; Denys, R.V.; Yartys, V.A. Comparison of C14- and C15-Predomiated AB2 Metal Hydride Alloys for Electrochemical Applications. Batteries 2017, 3, 22.

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