Biomass
carbon-coated and pseudocapacitance-assisted α-Fe2O3 has recently gained more attention for enhanced
lithium storage performance. Herein, we used a waste poplar branch
as a biotemplate and a carbon source to prepare graphitic-C-doped
mesoporous α-Fe2O3 (α-Fe2O3/C) through a simple immersion–carbonization–calcination
method. The influence of carbon content on both the microstructures
and electrochemical properties was also studied. The product calcined
in air at 400 °C (Fe2O3/C400) presents a hierarchically tubular structure with cross-linkage
of 18% graphitic-C and α-Fe2O3 nanoparticles
with an average size of ∼28 nm. Meanwhile, the Fe2O3/C400 nanomaterial exhibits a large surface
area of 114 m2 g–1 and mesopore size
distribution centered at 2 nm. As lithium-ion battery anode material,
such a unique hierarchical structure presents a certain pseudocapacitance
behavior, thus improving its lithium storage performance. Electrochemical
measurements show that the Fe2O3/C400 nanomaterial exhibits higher specific capacity and better rate performance.
Especially, it can retain a capacity of 885 mA h g–1 at 1 A g–1 after cycling 1400 times, indicating
good capacity retention and long-cycling stability. The good electrochemical
performance mainly originates from the synergism of the unique microstructure
of the Fe2O3/C400 nanomaterial, suitable
doping of graphitic-C, and certain pseudocapacitance behavior. Thus,
the low-cost bifunctional biotemplate strategy can provide a useful
experience for the massive synthesis of pseudocapacitance-assisted
high-performance anodes.