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Boosting the capacity of all-organic paper supercapacitors using wood derivatives
RISE - Research Institutes of Sweden (2017-2019), ICT, Acreo. Linköping University, Sweden.ORCID-id: 0000-0002-2904-7238
Linköping University, Sweden.
Linköping University, Sweden.
Linköping University, Sweden; Stellenbosch University, South Africa.
2018 (Engelska)Ingår i: Journal of Materials Chemistry A, ISSN 2050-7488, E-ISSN 2050-7496, Vol. 6, nr 1, s. 145-152Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Printed and flexible organic electronics is a steadily expanding field of research and applications. One of the most attractive features of this technology is the possibility of large area and high throughput production to form low-cost electronics on different flexible substrates. With an increasing demand for sustainable energy production, low-cost and large volume technologies to store high-quality energy become equally important. These devices should be environmentally friendly with respect to their entire life cycle. Supercapacitors and batteries based on paper hold great promise for such applications due to the low cost and abundance of cellulose and other forest-derived components. We report a thick-film paper-supercapacitor system based on cellulose nanofibrils, the mixed ion-electron conducting polymer PEDOT: PSS and sulfonated lignin. We demonstrate that the introduction of sulfonated lignin into the cellulose-conducting polymer system increases the specific capacitance from 110 to 230 F g(-1) and the areal capacitance from 160 mF cm(-2) to 1 F cm(-2). By introducing lignosulfonate also into the electrolyte solution, equilibrium, with respect to the concentration of the redox molecule, was established between the electrode and the electrolyte, thus allowing us to perform beyond 700 charge/discharge cycles with no observed decrease in performance.

Ort, förlag, år, upplaga, sidor
2018. Vol. 6, nr 1, s. 145-152
Nationell ämneskategori
Naturvetenskap
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URN: urn:nbn:se:ri:diva-33379DOI: 10.1039/c7ta06810gScopus ID: 2-s2.0-85038626009OAI: oai:DiVA.org:ri-33379DiVA, id: diva2:1187272
Tillgänglig från: 2018-03-02 Skapad: 2018-03-02 Senast uppdaterad: 2023-06-09Bibliografiskt granskad

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Edberg, Jesper

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