Abstract
The transition to sustainable energy technologies calls for supercapacitors that are not only efficient but also environmentally responsible. In this work, a step towards solving this challenge is taken by applying a low-temperature NaOH activation strategy to alder-wood-derived carbon. Such process generates an amorphous carbon matrix with thinly-layered sheets of graphene-like domains, facilitating efficient ion-electron transport, as revealed through comprehensive material characterizations. Various carbon structures were obtained by adjusting the alkali-to-carbon ratio and activation temperature wherein the most effective is 3:1 ratio at 600 °C (AWC 3-600). Its combined 2393 m2 g−1 surface area and 85.4% microporosity provides a pore architecture that works exceptionally well with aqueous electrolytes. When integrated into printed supercapacitors, it achieves ≈307 F g−1 in NaCl and ≈291 F g−1 in KxHyPO4. Even after 10,000 charge–discharge cycles, the devices retain 95% of their original capacitance, demonstrating long-term stability. The results of this study highlights the strong interactions between the electrolyte and pore structure, where NaCl benefits from the microporous AWC 3-600while KxHyPO4 performs better on the mesoporous structure obtained with an activation process of 4:1 ratio at 700 °C (AWC 4-700). This study shows that low-temperature NaOH activation offers an effective way to engineer biomass-derived carbons with tunable electrochemical behavior.
| Original language | English |
|---|---|
| Article number | e202500540 |
| Journal | Small Science |
| Volume | 6 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - Feb 2026 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- activated wood carbon
- energy density
- energy storage
- graphitization
- printed supercapacitors
- reduced graphene oxide
- specific capacitance
OECD Field of Science
- 2.4 Chemical Engineering
- 2.5 Materials Engineering
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