A study is made of the deterioration mechanism of a Laves phase alloy elect
rode without addition of Ni powder by means of electrochemical impedance sp
ectra (EIS) X-ray diffraction (XRD), inductively coupled plasma (TCP) and X
-ray photoelectron spectroscopy (XPS). The XRD analysis shows that after cy
cling, the alloy bulk still has the capability to store hydrogen. The deter
ioration mechanism is considered to be mainly a surface process. In particu
lar, particle pulverization (increased specific surface area and reduced th
e particle size) is the main reason for electrode deterioration. Dissolutio
n of V and Mn increases gradually during cycling. On the other hand, partic
le pulverization increases further the dissolution fates of V and Mn, which
are proportional to the specific surface area due to the generation of a n
ew, fresh surface. In addition, it is demonstrated by XPS that the depth of
oxide layers of Zr and Mn increases with cycling and results in an increas
e in the reaction impedance and a decrease in the surface electronic conduc
tivity. Therefore, a change in the structure of the particle surface layer,
due to particle pulverization and dissolution of V and Mn, contributes to
the deterioration of the Laves phase electrode. (C) 1999 Elsevier Science S
.A. All rights reserved.