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Carbide-derived carbon by room temperature chemical etching of MAX phase for supercapacitor application

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dc.contributor.author Varghese, S M
dc.contributor.author Sarath Kumar, S R
dc.contributor.author Rakhi, R B
dc.date.accessioned 2024-03-21T15:17:37Z
dc.date.available 2024-03-21T15:17:37Z
dc.date.issued 2024-01-08
dc.identifier.citation Applied Physics Letters; 124(2):023905 en_US
dc.identifier.uri https://pubs.aip.org/aip/apl/article/124/2/023905/2933107/Carbide-derived-carbon-by-room-temperature
dc.identifier.uri http://localhost:8080/xmlui/handle/123456789/4798
dc.description.abstract Porous carbons have attracted substantial interest within the realm of energy storage applications. However, their traditional production methods often involve the use of elevated temperatures. In this study, we introduce a simple technique to transform titanium silicon carbide (Ti3SiC2) MAX phases into porous carbons, known as carbide-derived carbons (CDCs), at room temperature by selective etching of the metal atoms (Ti and Si). We investigate how temperature affects the activation of CDCs so formed with potassium hydroxide to enhance their electrochemical properties. Our results unveil the remarkable potential of CDCs activated at 700 °C, demonstrating superior electrochemical performance with a specific capacitance of 198 F g−1 at a scan rate of 20 mV s−1 in a three-electrode configuration. The symmetric supercapacitor based on CDC-700 maintains a respectable specific capacitance of 98 F g−1 at 1 A g−1 and an energy density of 13.7 Wh kg−1 at a power density of 1 kW kg−1. This cost-effective approach offers a pathway for large-scale CDC production, with excellent specific supercapacitor characteristics, promising advancements in energy storage technology. en_US
dc.language.iso en en_US
dc.publisher AIP en_US
dc.title Carbide-derived carbon by room temperature chemical etching of MAX phase for supercapacitor application en_US
dc.type Article en_US


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  • 2024
    Research articles authored by NIIST researchers published in 2024

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