Silicon
oxide (SiO
x
) has outstanding
capacity and stable lithium-ion uptake/removal electrochemistry as
a lithium-ion anode material; however, its practical massive commercialization
is encumbered by unavoidable challenges, such as dynamic volume changes
during cycling and inherently inferior ionic conductivities. Recent
literature has offered a consensus that binders play a critical role
in affecting the electrochemical performance of Si-based electrodes.
Herein, we report an aqueous binder, γ-polyglutamic acid cross-linked
by epichlorohydrin (PGA–ECH), that guarantees enhanced properties
for SiO
x
anodes to implement long-term
cycling stability. The abundant amide, carboxyl, and hydroxyl groups
in the binder structure form strong interactions with the SiO
x
surface, which contribute strong interfacial
adhesion. The robust covalent interactions and strong supramolecular
interactions in the binder ensure mechanical strength and elasticity.
Additionally, the interactions between lithium ions and oxygen (nitrogen)
atoms of carboxylate (peptide) bonds, which serve as a Lewis base,
facilitate the diffusion of lithium ions. A SiO
x
anode using this PGA–ECH binder exhibits an impressive
initial discharge capacity of 1962 mA h g–1 and
maintains a high capacity of 900 mA h g–1 after
500 cycles at 500 mA g–1. Meanwhile, the assembled
SiO
x
||LiNi0.6Co0.2MnO0.2 full cell shows a reversible capacity of 155 mA
g–1 and displays 73% capacity retention after 100
cycles.