A diamine-assisted
polymerization method is invented to synthesize
nano-LiMnPO4 coated with highly homogeneous polyamides.
The additive, p-phenylenediamine with a diamine and
an aromatic group, enters the whole reaction, effectively adsorbed
on the LiMnPO4. p-Phenylenediamine suppresses
the particle growth and maintains the reaction pH value that promotes
the formation of impurity-free LiMnPO4. When carbon is
prepared with sucrose, the LiMnPO4/C prepared with large
amounts of p-phenylenediamine exhibits a capacity
of 134 mAhg–1 at 0.1C. To further synthesize a more
homogeneous and conductive carbon, p-phenylenediamine
and acyl chloride are in situ polymerized to two types of polyamide,
aromatic (known as, aramid) and semialiphatic polyamide. The N-doped
carbon pyrolyzed from the polyamide allows a fast Li-ion migration
into the LiMnPO4. Lithium ions are favorable for being
adsorbed/desorbed on the N-doped carbon as compared with the nondoped
carbon. It is demonstrated that N is bonding with P and Mn on the
LiMnPO4 surface, decreasing the contact resistance of carbon.
Thus, LiMnPO4/N-doped C exhibits better cycling performance
and rate capability than the LiMnPO4/C prepared with sucrose.