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With the rapid increment of the electric vehicle market, silicon has attracted tremendous attention as a promising anode material for lithium-ion batteries (LIB) due to its tenfold higher gravimetrical energy density compared with a traditional graphite anode. To eliminate the well-known poor cycle life issue originated from the large volume expansion of the silicon-based electrode, the development of novel polymeric binder is essential. Herein, we synthesized a novel silane-treated polyacrylonitrile (Si-PAN) as an anode binder using facile azide-nitrile click reaction. Incorporation of silane to the cyclized-PAN structure enhances affinity between the electrode components and a current collector because it has organic and inorganic moiety simultaneously in polymeric backbone. This work implements a Si-alloy (Si70Ni20Cu10) based electrode with improved capacity retention through the optimization of silane amount and thermal treatment condition. Namely, the electrode composing Si-treated PAN-2.0 binder and Si-alloy, after being thermally treated at 450 °C shows stable discharge capacity of 760 mA h g−1 upon 50 cycles, resulting in 46% capacity retention improvement against pristine PAN binder (at 450 °C). New binder demonstrates a great potential to improve the electrochemical properties of next-generation electrode materials for energy storage systems.

A Mg67Ni23Pd10 amorphous alloy was synthesized by rapid solidification and its electrode properties were examined. The discharge capacities increased with increasing cycle number and reached as high as 550 and 529 mAh/g at the discharge current densities of 10 and 20 mA/g, respectively. The plateau pressure of electrochemically derived P–C isotherm was about 10−5 MPa.

Mg–Ni–M (M=Ca, La or Pd) ternary alloys were synthesized by the melt-spinning technique. All as-solidified alloys possessed an amorphous single phase by the additional effect of the third element, though it was difficult to obtain an amorphous Mg 67 Ni 33 binary alloy by melt-spinning. We examined the thermal stability and electrochemical cyclic life property of the ternary amorphous alloys. The crystallization temperature of the amorphous alloys increases with increasing M content. All the alloys except Mg 67 Ni 28 Pd 5 examined in the present study maintain the amorphous structure even after hydrogen absorption at 373 K for Mg–Ni–Ca and Mg–Ni–Pd and at 423 K for Mg–Ni–La. The crystallization temperature increases by absorbing hydrogen, indicating that the alloys are thermally stabilized by hydrogen absorption. In the electrochemical cyclic life measurements up to five cycles, the Mg–Ni–Pd amorphous alloys exhibit high discharge capacities ranging from 100 to 400 mA h/g as well as small cyclic life degradation tendency, though the Mg–Ni–Ca and Mg–Ni–La amorphous alloys possess small discharge capacities of 10–100 mA h/g with significant cyclic life degradation. It is thus concluded that the good cyclic life property of the amorphous hydrogen storage alloys can be obtained by application of the melt-spinning technique to Mg-based alloys with appropriate alloy compositions.