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Highly proton conductive membranes based on carboxylated cellulose nanofibres and their performance in proton exchange membrane fuel cells
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Centres, Wallenberg Wood Science Center.
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemical Engineering, Applied Electrochemistry.
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Centres, Wallenberg Wood Science Center.ORCID iD: 0000-0002-9663-7705
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemical Engineering, Applied Electrochemistry.ORCID iD: 0000-0001-9203-9313
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2019 (English)In: Journal of Materials Chemistry A, ISSN 2050-7488, E-ISSN 2050-7496, Vol. 7, no 43, p. 25032-25039Article in journal (Refereed) Published
Abstract [en]

The performance of thin carboxylated cellulose nanofiber-based (CNF) membranes as proton exchange membranes in fuel cells has been measured in situ as a function of CNF surface charge density (600 and 1550 μmol g−1), counterion (H+ or Na+), membrane thickness and fuel cell relative humidity (RH 55 to 95%). The structural evolution of the membranes as a function of RH, as measured by Small Angle X-ray Scattering, shows that water channels are formed only above 75% RH. The amount of absorbed water was shown to depend on the membrane surface charge and counter ions (H+ or Na+). The high affinity of CNF for water and the high aspect ratio of the nanofibers, together with a well-defined and homogenous membrane structure, ensures a proton conductivity exceeding 1 mS cm−1 at 30 °C between 65 and 95% RH. This is two orders of magnitude larger than previously reported values for cellulose materials and only one order of magnitude lower than Nafion 212. Moreover, the CNF membranes are characterized by a lower hydrogen crossover than Nafion, despite being ≈30% thinner. Thanks to their environmental compatibility and promising fuel cell performance the CNF membranes should be considered for new generation proton exchange membrane fuel cells.

Place, publisher, year, edition, pages
Royal Society of Chemistry, 2019. Vol. 7, no 43, p. 25032-25039
National Category
Chemical Engineering
Identifiers
URN: urn:nbn:se:kth:diva-263094DOI: 10.1039/C9TA04898GISI: 000496150500033Scopus ID: 2-s2.0-85074709979OAI: oai:DiVA.org:kth-263094DiVA, id: diva2:1366434
Note

QC 20191030

Available from: 2019-10-29 Created: 2019-10-29 Last updated: 2022-06-26Bibliographically approved
In thesis
1. Electrochemical properties of alternative polymer electrolytes in fuel cells
Open this publication in new window or tab >>Electrochemical properties of alternative polymer electrolytes in fuel cells
2019 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Fuel cells, using hydrogen as energy carrier, allow chemically‑stored energy to be utilized for many applications, including balancing the electrical grid and the propulsion of vehicles. To make the fuel cell technology more accessible and promote a sustainable energy society, this thesis focuses on alternative polymer electrolytes, as they can potentially lead to a lower cost and a more environmentally‑friendly fuel cell. The main subject is anion exchange membrane fuel cells (AEMFCs), for which the importance of gas diffusion electrode morphology and platinum electrode reactions are investigated. Properties of the membrane such as water flux during operation are evaluated. Furthermore, novel polymer electrolytes are studied: variations of poly(phenylene oxide)‑based membranes in AEMFCs; and cellulose‑based membranes in a proton exchange membrane fuel cell (PEMFC).

 

The AEMFC results show that the performance is dependent on the electrode morphology. Electrochemical experiments in a hydrogen/hydrogen cell combined with modelling show that the hydrogen oxidation reaction proceeds through the Tafel‑Volmer reaction pathway on platinum. Application of the model in a hydrogen/oxygen cell shows that the cathode has the slowest reaction rate. During operation, the water flux through the membrane is directed from the anode where water is produced to the cathode where it is consumed. This leads to an increase in water content at both electrodes, which implies that electrode flooding is more likely than dry‑out during operation. The effect of membrane thickness on water flux is shown to be larger than the effect of polymer structure for several different types of poly(phenylene oxide)‑based membranes. The comparison of these polymers also indicates that a high conductivity, for the relative humidity achieved in a fuel cell, promotes increased performance. Finally, the study of cellulose-based membranes in a PEMFC shows that cellulose as a renewable, natural polymer has promising properties, such as stable conductivity for relative humidities above 65 % and a low gas permeability.

Place, publisher, year, edition, pages
Stockholm: KTH Royal Institute of Technology, 2019. p. 59
Series
TRITA-CBH-FOU ; 2019:64
Keywords
fuel cell, anion exchange membrane, proton exchange membrane, electrode morphology, hydrogen oxidation reaction, water transport, poly(phenylene oxide), cellulose, bränslecell, anjonledande membran, protonledande membran, elektrodstruktur, vätgasoxidation, vattentransport, poly(fenylenoxid), cellulosa
National Category
Chemical Engineering
Research subject
Chemical Engineering
Identifiers
urn:nbn:se:kth:diva-263095 (URN)978-91-7873-365-1 (ISBN)
Public defence
2019-11-29, F3, Lindstedtsvägen 26, Stockholm, 10:00 (English)
Opponent
Supervisors
Available from: 2019-10-29 Created: 2019-10-29 Last updated: 2022-06-26Bibliographically approved

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Carlson, AnnikaYu, ShunLindbergh, GöranLindström, RakelSalazar-Alvarez, German

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Guccini, ValentinaCarlson, AnnikaYu, ShunLindbergh, GöranLindström, RakelSalazar-Alvarez, German
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