Abstract
Porous carbon with hierarchical pores has been produced from wet bamboo shoots via molten base carbonization and activation at 700 °C, with a short residence time of 1 hour, using two different reactor configurations. The produced carbon exhibited a notable specific surface area (SSA) of 1198.47 m2 g-1 from the vertical reactor (V-1) and a surface area of 1190.51 m2 g-1 from the horizontal reactor (H-1), approaching that of the commercial YP50F (1425.89 m2 g-1). The SSA of derived carbon material is linked to abundant micropores developed during in situ carbon activation at elevated temperatures facilitated by KOH and the interaction of biomass components at room temperature. Also, elemental analysis revealed increased oxygen and nitrogen content in V-1 (27.04 % and 2.74 %, respectively) compared to H-1 (25.88 % and 1.65%, respectively), and XPS analysis revealed different bond states for oxygen and nitrogen in V-1 compared to H-1. These differences in chemical composition were possibly influenced by reaction environments, compounds, and gases released during carbonisation, possibly affecting their behaviour towards eletrolytes. The urther testing of derived carbons in an electrochemical double-layer capacitor showed that V-1 exhibited the highest specific capacitance (164.75 F g-1) compared to H-1 (160.26 F g-1) in an organic electrolyte (1 M TEABF4/AN). This increased capacitance is attributed to its larger SSA, hierarchical hierachical pores, and increased oxygen and nitrogen content that enhances capacitance resulting from some reversible electro-adsorption processes that do not require electron transfer (pseudo-capacitive mechanism). Both H-1 and V-1 carbons exhibited better capacitance compared to YP50F (143.08 F g-1) and demonstrated cycling stability of 10,000 cycles with a capacity retention ability of 98 % at a specific current of 0.1 A g-1, demonstrating their potential as an alternative electrode material. These results highlight the potential for achieving hierarchical porous carbon from wet biomass via a process route that saves both time and energy towards biomass to carbon conversion.
