Nanofibrillated Cellulose-Based Electrolyte and Electrode for Paper-Based Supercapacitors Show others and affiliations
2018 (English) In: ADVANCED SUSTAINABLE SYSTEMS, ISSN 2366-7486, Vol. 2, no 1, article id UNSP 1700121Article in journal (Refereed) Published
Abstract [en]
Solar photovoltaic technologies could fully deploy and impact the energy conversion systems in our society if mass-produced energy-storage solutions exist. A supercapacitor can regulate the fluctuations on the electrical grid on short time scales. Their mass-implementation requires the use of abundant materials, biological and organic synthetic materials are attractive because of atomic element abundancy and low-temperature synthetic processes. Nanofibrillated cellulose (NFC) coming from the forest industry is exploited as a three-dimensional template to control the transport of ions in an electrolyte-separator, with nanochannels filled of aqueous electrolyte. The nanochannels are defined by voids in the nanocomposite made of NFC and the proton transporting polymer polystyrene sulfonic acid PSSH. The ionic conductivity of NFC-PSSH composites (0.2 S cm(-1) at 100% relative humidity) exceeds sea water in a material that is solid, feel dry to the finger, but filled of nanodomains of water. A paper-based supercapacitor made of NFC-PSSH electrolyte-separator sandwiched between two paper-based electrodes is demonstrated. Although modest specific capacitance (81.3 F g(-1)), power density (2040 W kg(-1)) and energy density (1016 Wh kg(-1)), this is the first conceptual demonstration of a supercapacitor based on cellulose in each part of the device; which motivates the search for using paper manufacturing as mass-production of energy-storage devices.
Place, publisher, year, edition, pages WILEY-V C H VERLAG GMBH , 2018. Vol. 2, no 1, article id UNSP 1700121
Keywords [en]
composites; energy density; nanofibrillated cellulose (NFC); power density; supercapacitors
National Category
Energy Systems
Identifiers URN: urn:nbn:se:liu:diva-160844 DOI: 10.1002/adsu.201700121 ISI: 000427112400004 Scopus ID: 2-s2.0-85081058004 OAI: oai:DiVA.org:liu-160844 DiVA, id: diva2:1359920
2019-10-102019-10-102026-02-12