Interplay of physical and textural properties in porous, nanostructured hard‑carbons as electrode materials for non-Faradic energy storage devices

Abstract

This work presents a systematic investigation on the non-Faradic energy storage ability of non-graphitizable, porosity engineered hard‑carbon nanostructures as electrode materials. The persistent challenge of inducing and tuning porosity in hard‑carbon nanostructures is overcome here, by utilizing dendritic fibrous nano silica (DFNS) as a sacrificial template for uniform and conformal deposition of carbon through thermal chemical vapor deposition, leading to the formation of porosity tuned, nanostructured hard‑carbon florets (NCF). This strategy enables precisely crafted six varieties of NCF with varying yet monodisperse dimensions (NCF 90, NCF 350, NCF 366, NCF 430, NCF 540 and NCF 600), SSA (494–719 m2/g) and textural features such as pore volume (0.67–1.24 cm3/g) and pore diameter (3.83–5.65 nm). In contrast to current understanding, NCF 366 with defect length of 16 nm, defect density of 2.65 × 1011 cm−2, micro- to mesoscale pore ratio of 0.16 and specific surface area of 535 m2/g achieves the highest energy density of 14.6 Wh/kg and power density 10.0 kW/kg, when compared to NCF 90 with higher SSA (719 m2/g) and pore volume (1.24 cm3/g). Thus, this work manifests the critical contributions of tuning the pore structures and optimizing the relative contributions from multi-scale pore structures to achieve high-performing energy storage devices.