Improving the Electrochemical Energy Storage Capacity of the Renewable Carbon Derived from Industrial Tea Waste

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Tarih

29.06.2022

Yazarlar

Karamustafa, Ayşenur
Sözer, Sözer
Merve Buldu-Akturk
Emre Erdem
Akgül, Gökçen
Oskay, Kürşat Oğuz

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info:eu-repo/semantics/closedAccess

Özet

Energy storage is gaining a vital role since the usage of portable electric/electronic devices and vehicles have been growing. Capacitors, called as electrochemical double layer capacitors or supercapacitors, find application on wide scale devices from mobile vehicles to huge electric vehicles with high energy and power densities, fast charge and discharge properties. Hence, energy is stored at the electrode–electrolyte interface, the electrode material forms the heart of this energy storage system. When the decreasing reserves of fossil resources and their environmental damages are considered, renewable 3-dimentional carbon could be a solution in the capacitor as carbon electrodes. Biomass-derived renewable carbon is cost-effective, abundant, sustainable, safety and environmentally friendly material. In this work, renewable carbon material was derived from industrial tea waste and three methods of graphitization, activation and heteroatom doping were implemented alltogether to develop the energy storage capacity of material. The structural ordering, surface area growth and capacitive contribution promoted the energy storage capacity to 25 F/g and high power density to 2.6 kW/kg of biowaste derived carbon

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tea waste, refined-renewable carbon, energy storage, supercapacitor

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Q4

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Ayşenur Karamustafaa, Sözer Sözera , Kürşad Oğuz Oskayb , Merve Buldu-Akturkc, Emre Erdemc , and Gökçen Akgüla, * a Department of Energy Systems Engineering, Engineering Faculty, Recep Tayyip Erdogan University, Rize, 53100 Turkey b Department of Metallurgy, Engineering Faculty, Cumhuriyet University, Sivas, 58140 Turkey c Department of Materials Science and Nano Engineering, Sabancı University, Istanbul, 34956 Turkey *e-mail: gokcen.akgul@erdogan.edu.tr Received September 14, 2021; revised January 10, 2022; accepted January 29, 2022