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Updated: May 21, 2026

Preparation of Biomass-based Mesoporous Carbon with Higher Nitrogen-/Oxygen-chelating Adsorption for Cu(II) Through Microwave Pre-Pyrolysis
Published on: February 12, 2019
Synergistic effects of nitrogen doping in waste-fruit peel-derived activated carbons for supercapacitors and water
Vianney Kitenge1,2, Ndeye Fatou Diop1, Souleyman Thior1
1Department of Physics, SARChI Chair in Nanomaterials for Energy Storage and Water Purification Applications, University of Pretoria Pretoria 0002 South Africa Vianney.kitenge@up.ac.za Ncholu.manyala@up.ac.za.
Abstract:
Developing sustainable carbon materials from agricultural waste offers promising solutions to both energy-storage and water-treatment challenges. This study reports the synthesis of a nitrogen-doped Tondolo-derived activated carbon (N-TAC), an underexplored African wetland sedge whose fibrous morphology directs pore architecture. Rather than conventional dry mixing, K2CO3 and urea were co-dissolved and intimately blended with the finely reduced Tondolo precursor. This reagent-level homogeneity enabled a single pyrolysis at 700 °C in which carbonisation, chemical activation, and nitrogen doping proceeded concurrently. The N-TAC Near-surface nitrogen functionalities (pyridinic, pyrrolic, and graphitic) proved decisive in enhancing both electrochemical and adsorptive performance. Three-electrode characterization in 1 M NaNO3 revealed coexisting EDLC and pseudocapacitive mechanisms, with a low ESR of 2.05 Ω and relaxation time constant of 0.87 s confirming rapid ion diffusion kinetics. Trasatti deconvolution and Dunn's method reveal that pyridinic and pyrrolic sites selectively amplify pseudocapacitive contributions (63-71%) in the positive potential window, a window-dependent asymmetry not previously reported for neutral-electrolyte biomass carbons. The assembled symmetric device delivered 12.1 Wh kg-1 with 94% capacitance retention after 10 000 cycles. For water remediation, N-TAC achieved 99.9% methylene blue removal at 50 ppm with an adsorption capacity of 557.6 mg g-1, governed by chemisorption via electrostatic and π-π interactions, best described by pseudo-second-order kinetics (R 2 = 0.97) and the Temkin isotherm (R 2 = 0.958). These results position N-TAC as a competitive sustainable material at the water-energy nexus, with future perspectives including binder-free electrode fabrication, electrochemical degradation coupling, and regenerable architectures for long-term sustainability.
