Abstract

Binary and ternary (with the addition of Mn) TiFe-based intermetallic compound powders were fabricated by high energy ball milling, and their electrochemical behavior as negative electrodes was investigated in 6M-KOH. X-ray diffraction exhibited the single phase of nanostructured binary and ternary TiFe-based crystallites after 20 h of milling followed the amorphous phase formation. Addition of Mn increased peak broadening and in turn decreased the nanocrystallite size of TiFe. Electrode properties of 20, 40, 60, and 70 h binary milled products showed that the discharge capacity of the 60 h one offered a maximum discharge capacity of ~169 mAhg−1. Although substitution of Mn for Ti (Ti1−xFeMnx, x = 0.1, 0.2) caused a decrease in initial discharge capacity, the periodic stability increased compared to the binary TiFe and ternary TiFe1-xMnx (x = 0.1, 0.2). The ternary Ti0.9FeMn0.1 electrode maintained ~53% of its initial discharge capacity after five cycles of charge–discharge; this was just 28% in the case of binary TiFe electrode.

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