Current,
there is an urgent demand for electrode materials with
superior electrochemical performances for the development of supercapacitors.
A nitrogen-doped carbon skeleton (NCS) assembled by carbon nanotubes
and graphene layers is designed and synthesized utilizing a layer-shaped
humate-based zeolitic imidazolate framework (ZIF) (HA-CoFe-ZIF) as
a template in this work. The synthesized NCS is mainly composed of
graphitized carbon with a few hydroxyl groups on its surface, synchronously
doped by 9.5 at % nitrogen in the state of pyridinic N and pyrrolic
N. The rich mesoporous structure entitles it to a high Brunauer–Emmett–Teller
(BET) specific surface area of 427 m2 g–1 and suitable BET average pore diameter of 3.14 nm. The NCS has a
high capacity of 324 F g–1 at 1 A g–1, good rate capability (capacitance retention of 71% from 5 to 100
A g–1), and excellent cycling stability (capacitance
retention of 96 and 87% after 5000 and 10 000 cycles, respectively).
The fabricated NCS//AC asymmetric supercapacitor also exhibits a high
capacity of 93 F g–1 at 1 A g–1, large energy density of 10.3 Wh kg–1 at 331 W
kg–1, and good cycling performance (capacitance
retention of 88% after 5000 cycles). Our elaborately designed NCS
materials exhibit multiple structural advantages including rich mesoporous
structure, various graphitic carbon, and high-dosage nitrogen doping,
resulting in high capacitance performances. This humate-based metal–organic
framework (MOF)-derived strategy provides a good idea for the synthesis
of high-performance carbon skeleton materials applied to energy storage.