Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Petter Tammela is active.

Publication


Featured researches published by Petter Tammela.


ACS Nano | 2015

Surface Modified Nanocellulose Fibers Yield Conducting Polymer-Based Flexible Supercapacitors with Enhanced Capacitances

Zhaohui Wang; Daniel O Carlsson; Petter Tammela; Kai Hua; Peng Zhang; Leif Nyholm; Maria Strømme

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) ≈ 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.


Journal of Materials Chemistry | 2014

High areal and volumetric capacity sustainable all-polymer paper-based supercapacitors

Zhaohui Wang; Petter Tammela; Peng Zhang; Maria Strømme; Leif Nyholm

All-polymer paper-based electrodes with a thickness up to hundreds of micrometers (e.g. 290 mu m), large active mass loadings (>20 mg cm(-2)) and relatively high densities (1.23 g cm(-3)) can be ...


Journal of Materials Chemistry | 2016

Solution-processed poly(3,4-ethylenedioxythiophene) nanocomposite paper electrodes for high-capacitance flexible supercapacitors

Zhaohui Wang; Petter Tammela; Jinxing Huo; Peng Zhang; Maria Strømme; Leif Nyholm

Although the development of nanostructured poly(3,4-ethylenedioxythiophene) (PEDOT) with large capacitance and high mechanical flexibility is crucial for the realization of high-performance superca ...


Nanoscale | 2014

Freestanding nanocellulose-composite fibre reinforced 3D polypyrrole electrodes for energy storage applications

Zhaohui Wang; Petter Tammela; Peng Zhang; Jinxing Huo; Fredric Ericson; Maria Strømme; Leif Nyholm

It is demonstrated that 3D nanostructured polypyrrole (3D PPy) nanocomposites can be reinforced with PPy covered nanocellulose (PPy@nanocellulose) fibres to yield freestanding, mechanically strong and porosity optimised electrodes with large surface areas. Such PPy@nanocellulose reinforced 3D PPy materials can be employed as free-standing paper-like electrodes in symmetric energy storage devices exhibiting cell capacitances of 46 F g(-1), corresponding to specific electrode capacitances of up to ∼185 F g(-1) based on the weight of the electrode, and 5.5 F cm(-2) at a current density of 2 mA cm(-2). After 3000 charge/discharge cycles at 30 mA cm(-2), the reinforced 3D PPy electrode material also showed a cell capacitance corresponding to 92% of that initially obtained. The present findings open up new possibilities for the fabrication of high performance, low-cost and environmentally friendly energy-storage devices based on nanostructured paper-like materials.


Bioelectrochemistry | 2015

Biosupercapacitors for powering oxygen sensing devices

Michal Kizling; Sylwia Dramińska; Krzysztof Stolarczyk; Petter Tammela; Zhaohui Wang; Leif Nyholm; Renata Bilewicz

A biofuel cell comprising electrodes based on supercapacitive materials - carbon nanotubes and nanocellulose/polypyrrole composite was utilized to power an oxygen biosensor. Laccase Trametes versicolor, immobilized on naphthylated multi walled carbon nanotubes, and fructose dehydrogenase, adsorbed on a porous polypyrrole matrix, were used as the cathode and anode bioelectrocatalysts, respectively. The nanomaterials employed as the supports for the enzymes increased the surface area of the electrodes and provide direct contact with the active sites of the enzymes. The anode modified with the conducting polymer layer exhibited significant pseudocapacitive properties providing superior performance also in the high energy mode, e.g., when switching on/off the powered device. Three air-fructose biofuel cells connected in a series converted chemical energy into electrical giving 2 mW power and open circuit potential of 2V. The biofuel cell system was tested under various externally applied resistances and used as a powering unit for a laboratory designed two-electrode minipotentiostat and a laccase based sensor for oxygen sensing. Best results in terms of long time measurement of oxygen levels were obtained in the pulse mode -45 s for measurement and 15 min for self-recharging of the powering unit.


RSC Advances | 2015

Asymmetric supercapacitors based on carbon nanofibre and polypyrrole/nanocellulose composite electrodes

Petter Tammela; Zhaohui Wang; Sara Frykstrand; Peng Zhang; Ida-Maria Sintorn; Leif Nyholm; Maria Strømme

Asymmetric, all-organic supercapacitors (containing an aqueous electrolyte), exhibiting a capacitance of 25 F g−1 (or 2.3 F cm−2) at a current density of 20 mA cm−2 and a maximum cell voltage of 1.6 V, are presented. The devices contain a composite consisting of polypyrrole covered Cladophora cellulose fibres (PPy–cellulose) as the positive electrode while a carbon nanofibre material, obtained by heat treatment of the same PPy–cellulose composite under nitrogen gas flow, serves as the negative electrode. Scanning and transmission electron microscopy combined with X-ray photoelectron spectroscopy data show that the heat treatment gives rise to a porous carbon nanofibre material, topologically almost identical to the original PPy–cellulose composite. The specific gravimetric capacitances of the carbon and the PPy–cellulose electrodes were found to be 59 and 146 F g−1, respectively, while the asymmetric supercapacitors exhibited a gravimetric energy density of 33 J g−1. The latter value is about two times higher than the energy densities obtainable for a symmetric PPy–cellulose device as a result of the larger cell voltage range accessible. The capacitance obtained for the asymmetric devices at a current density of 156 mA cm−2 was 11 F g−1 and cycling stability results further indicate that the capacity loss was about 23% during 1000 cycles employing a current density of 20 mA cm−2. The present results represent a significant step forward towards the realization of all-organic material based supercapacitors with aqueous electrolytes and commercially viable capacitances and energy densities.


Nanoscale | 2015

Nanocellulose coupled flexible polypyrrole@graphene oxide composite paper electrodes with high volumetric capacitance

Zhaohui Wang; Petter Tammela; Maria Strømme; Leif Nyholm


Journal of Materials Chemistry | 2014

Efficient high active mass paper-based energy-storage devices containing free-standing additive-less polypyrrole–nanocellulose electrodes

Zhaohui Wang; Petter Tammela; Peng Zhang; Maria Strømme; Leif Nyholm


Journal of Materials Chemistry | 2015

Flexible freestanding Cladophora nanocellulose paper based Si anodes for lithium-ion batteries

Zhaohui Wang; Chao Xu; Petter Tammela; Jinxing Huo; Maria Strømme; Kristina Edström; Torbjörn Gustafsson; Leif Nyholm


Advanced Energy Materials | 2017

Cellulose‐based Supercapacitors: Material and Performance Considerations

Zhaohui Wang; Petter Tammela; Maria Strømme; Leif Nyholm

Collaboration


Dive into the Petter Tammela's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge