The demand for versatile and sustainable energy materials
is on
the rise, given the importance of developing novel clean technologies
for transition to a net zero economy. Here, we present the synthesis,
characterization, and application of lignin-derived ordered mesoporous
carbons with various pore sizes (from 5 to approximately 50 nm) as
anodes in sodium-ion batteries. We have varied the pore size using
self-synthesized PEO
n
-
b
-PHA
m
block copolymers with different
PEO and PHA chain lengths, applying the “soft templating”
approach to introduce isolated spherical pores of 20 to 50 nm in diameters.
The pore structure was evaluated by transmission electron microscopy
(TEM), nitrogen physisorption, and small-angle X-ray scattering (SAXS).
We report the microstructure analysis of such mesoporous lignin-based
carbons using Raman spectroscopy and wide-angle X-ray scattering (WAXS).
In comparison with nontemplated carbon and carbons templated employing
commercial Pluronic F-127 and PIB
50
-
b
-PEO
45
, which created accessible channels and spherical pores up
to approximately 10 nm in diameter, the carbon microstructure analysis
revealed that templating with all applied polymers significantly impedes
graphitization upon thermal treatment. Furthermore, the gained knowledge
of similar carbon microstructures regardless of the type of template
allowed the investigation of the influence of different pore morphologies
in carbon applied as an anode material in sodium-ion batteries, supporting
the previous theories in the literature that closed pores are beneficial
for sodium storage while providing insights into the importance of
pore size.