uu.seUppsala University Publications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Surface Modified Nanocellulose Fibers Yield Conducting Polymer-Based Flexible Supercapacitors with Enhanced Capacitances
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - Ångström, Inorganic Chemistry.
Uppsala University, Disciplinary Domain of Science and Technology, Technology, Department of Engineering Sciences, Nanotechnology and Functional Materials.
Uppsala University, Disciplinary Domain of Science and Technology, Technology, Department of Engineering Sciences, Nanotechnology and Functional Materials.
Uppsala University, Disciplinary Domain of Science and Technology, Technology, Department of Engineering Sciences, Nanotechnology and Functional Materials.
Show others and affiliations
2015 (English)In: ACS Nano, ISSN 1936-0851, E-ISSN 1936-086X, Vol. 9, no 7, 7563-7571 p.Article in journal (Refereed) Published
Abstract [en]

We demonstrate that surface modified nanocellulose fibers (NCFs) can be used as substrates to synthesize supercapacitor electrodes with the highest full electrode-normalized gravimetric (127 F g(-1)) and volumetric (122 F cm(-3)) capacitances at high current densities (300 mA cm(-2) approximate to 33 A g(-1)) until date reported for conducting polymer-based electrodes with active mass loadings as high as 9 mg cm(-2). By introducing quaternary amine groups on the surface of NCFs prior to polypyrrole (PPy) polymerization, the macropore volume of the formed PPy-NCF composites can be minimized while maintaining the volume of the micro- and mesopores at the same level as when unmodified or carboxylate groups functionalized NCFs are employed as polymerization substrates. Symmetric, aqueous electrolyte-based, devices comprising these porosity-optimized electrodes exhibit device-specific volumetric energy and power densities of 3.1 mWh cm(-3) and 3 W cm(-3) respectively; which are among the highest values reported for conducting polymer electrodes in aqueous electrolytes. The functionality of the devices is verified by powering a red light-emitting diode with the device in different mechanically challenging states.

Place, publisher, year, edition, pages
2015. Vol. 9, no 7, 7563-7571 p.
Keyword [en]
energy storage devices, conducting polymers, modified nanocellulose, porosity optimization, capacitance
National Category
Chemical Sciences Nano Technology
Research subject
Engineering Science with specialization in Nanotechnology and Functional Materials
Identifiers
URN: urn:nbn:se:uu:diva-261306DOI: 10.1021/acsnano.5b02846ISI: 000358823200094PubMedID: 26083393OAI: oai:DiVA.org:uu-261306DiVA: diva2:851136
Funder
Swedish Foundation for Strategic Research , RMA-110012Carl Tryggers foundation
Available from: 2015-09-03 Created: 2015-09-01 Last updated: 2017-12-04
In thesis
1. On the electrochemical performance of energy storage devices composed of cellulose and conducting polymers
Open this publication in new window or tab >>On the electrochemical performance of energy storage devices composed of cellulose and conducting polymers
2016 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Applications that require electrical energy storage are becoming increasingly diverse. This development is caused by a number of factors, such as an increasing global energy demand, the advent of electric vehicles, the utilization of intermittent renewable energy sources, and advances in disposable and organic electronics. These applications will set different demands on their electrical energy storage and, thus, there will be no single technology used for all applications. For some applications the choice of energy storage materials will be extremely important. Conventional batteries and supercapacitors rely on the use of nonrenewable inorganic materials mined from depleting ores, hence, requiring large amounts of energy for their processing. Such materials also add a significant cost to the final product, making them less attractive for large scale applications. Conducting polymers, on the other hand, constitute a class of materials that can be used for organic matter based energy storage devices.

The aim of this thesis was to investigate the use of a composite consisting of the conducting polymer polypyrrole (PPy) and cellulose derived from Cladophora sp. algae for electrical energy storage. The polymer was coated onto the cellulose fibers by chemical polymerization resulting in a flexible material with high surface area. By using this composite as electrodes, electrochemical cells consisting of disposable and non-toxic materials can be assembled and used as energy storage devices. The resistances of these prototype cells were found to be dominated by the resistance of the current collectors and to scale with the thickness of the separator, and can hence be reduced by cell design. By addition of nanostructured PPy, the weight ratio of PPy in the composite could be increased, and the cell voltages could be enhanced by using a carbonized negative electrode. Composites of cellulose and poly(3,4-ethylenedioxythiophene) could also be synthesized and used as electrode materials. The porosities of the electrodes were controlled by mechanical compression of the composite or by coating of surface modified cellulose fibers with additional PPy. Finally, the self-discharge was studied extensively. It was found that oxygen was responsible for the oxidation of the negative electrode, while the rate of self-discharge of the positive electrode increases with increasing potential. Through measurements of the charge prior to and after self-discharge, as well as with an electrochemical quartz crystal microbalance, it was found that the self-discharge of the positive electrode was linked to an exchange of the counter ions by hydroxide ions. It is also demonstrated that the self-discharge rate of a symmetric PPy based device can be decreased dramatically by proper balancing of the electrode capacities and by reducing the oxygen concentration. The results of this work are expected to contribute towards future industrial implementation of electric energy storage devices based on organic materials.

Place, publisher, year, edition, pages
Uppsala: Acta Universitatis Upsaliensis, 2016. 64 p.
Series
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, ISSN 1651-6214 ; 1403
Keyword
polypyrrole, supercapacitors, self-discharge
National Category
Nano Technology
Research subject
Engineering Science with specialization in Nanotechnology and Functional Materials
Identifiers
urn:nbn:se:uu:diva-300917 (URN)978-91-554-9651-7 (ISBN)
External cooperation:
Public defence
2016-09-30, Å80121, Ångströmlaboratoriet, Lägerhyddsvägen 1, Uppsala, 13:15 (English)
Opponent
Supervisors
Available from: 2016-09-09 Created: 2016-08-16 Last updated: 2016-09-13

Open Access in DiVA

No full text

Other links

Publisher's full textPubMed

Authority records BETA

Wang, ZhaohuiCarlsson, Daniel O.Tammela, PetterHua, KaiZhang, PengNyholm, LeifStrömme, Maria

Search in DiVA

By author/editor
Wang, ZhaohuiCarlsson, Daniel O.Tammela, PetterHua, KaiZhang, PengNyholm, LeifStrömme, Maria
By organisation
Inorganic ChemistryNanotechnology and Functional Materials
In the same journal
ACS Nano
Chemical SciencesNano Technology

Search outside of DiVA

GoogleGoogle Scholar

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 1224 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf