Biomass-derived heteroatom-doped
carbons have been considered to
be excellent lithium ion battery (LIB) anode materials. Herein, ultrathin
g-C
3
N
4
nanosheets anchored on N,P-codoped biomass-derived
carbon (N,P@C) were successfully fabricated by carbonization in an
argon atmosphere. The structural characteristics of the resultant
N,P@C were elucidated by SEM, TEM, FTIR, XRD, XPS, Raman, and BET
surface area measurements. The results show that N,P@C has a high
specific surface area (
S
BET
= 675.4 cm
3
/g), a mesoporous-dominant pore (average pore size of 6.898
nm), and a high level of defects (
I
D
/
I
G
= 1.02). The hierarchical porous structural
properties are responsible for the efficient electrochemical performance
of N,P@C as an anode material, which exhibits an outstanding reversible
specific capacity of 1264.3 mAh/g at 100 mA/g, an elegant rate capability
of 261 mAh/g at 10 A, and a satisfactory cycling stability of 1463.8
mAh/g at 1 A after 500 cycles. Because of the special structure and
synergistic contributions from N and P heteroatoms, the resultant
N,P@C endows LIBs with electrochemical performance superior to those
of most of carbon-based anode materials derived from biomass in the
literature. The findings in this present work pave a novel avenue
toward lignin volarization to produce anode material for use in high-performance
LIBs.