Abstract

The structures and electrochemical properties of a series of annealed AB 5, La 10.5Ce 4.3Pr 0.5Nd 1.4Ni 64.3− x Co 5.0Mn 4.6Al 6.0Cu 3.2Zr 0.2Fe x ( x = 0.0, 0.5, 1.0, and 1.5), metal hydride alloys were studied for improvement in the low-temperature performance of nickel/metal hydride batteries. As the Fe-content in the alloy increases, the following was observed: lattice constant a first increases and then decreases; lattice constant c and c/ a ratio increase; unit cell volume increases monotonically; the main AB 5 phase becomes hyper-stoichiometric containing no Zr and its Fe-content is close to the target composition; an additional AB 7 phase appears; maximum gaseous hydrogen storage, PCT plateau pressure, and hysteresis first increase and then decrease while the trend of reversible hydrogen storage is the opposite; enthalpy and entropy of hydride formation remain unchanged; electrochemical full capacity decreases while the high-rate dischargeability and surface reaction exchange current increase; and bulk hydrogen diffusion increases first and then decreases by very small amounts. The product of charge-transfer resistance and double-layer capacitance measured at −40 °C indicates an improvement in the surface catalysis with Fe-addition. In the sealed cell, the addition of Fe improves both the specific power and −10 °C low temperature performance, slightly reduces the charge retention, and first marginally improves and then deteriorates the cycle life performance.

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