Enhanced water transport in AEMs based on poly(styrene–ethylene–butylene–styrene) triblock copolymer for high fuel cell performance

2019 ◽  
Vol 10 (15) ◽  
pp. 1894-1903 ◽  
Author(s):  
Xueqiang Gao ◽  
Hongmei Yu ◽  
Bowen Qin ◽  
Jia Jia ◽  
Jinkai Hao ◽  
...  

Anion exchange membrane fuel cells (AEMFCs) have received a considerable amount of attention in the past decades as a lower cost alternative to proton exchange membrane fuel cells (PEMFCs).

2019 ◽  
Author(s):  
Valentina Guccini ◽  
Annika Carlson ◽  
Shun Yu ◽  
Göran Lindbergh ◽  
Rakel Wreland Lindström ◽  
...  

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<sup>-1</sup>), counterion (H<sup>+</sup>or Na<sup>+</sup>), 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 (Na<sup>+</sup>or H<sup>+</sup>). 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<sup>-1</sup>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.<br>


Author(s):  
Torsten Berning

Abstract A numerical analysis of an air-cooled proton exchange membrane fuel cell (PEMFC) has been conducted. The model utilizes the Eulerian multi-phase approach to predict the occurrence and transport of liquid water inside the cell. It is assumed that all the waste heat must be carried out of the fuel cell with the excess air which leads to a strong temperature increase of the air stream. The results suggest that the performance of these fuel cells is limited by membrane overheating which is ultimately caused by the limited heat transfer to the laminar air stream. A proposed remedy is the placement of a turbulence grid before such a fuel cell stack to enhance the heat transfer and increase the fuel cell performance.


Author(s):  
Cullen R. Buie ◽  
Jonathan D. Posner ◽  
Tibor Fabian ◽  
Suk-Won Cha ◽  
Fritz B. Prinz ◽  
...  

We have developed proton exchange membrane fuel cells (PEMFC’s) with integrated planar electroosmotic pumping structures that actively remove liquid water from cathode flow channels. Recent experimental and numerical investigations on PEMFC’s emphasize water management as a critical factor in the design of robust, high efficiency fuel cells. Although various passive water management strategies have been proposed, water is still typically removed by pumping air into cathode channels at flow rates significantly larger than those required by fuel cell stoichiometry. This method of water removal is thermodynamically unfavorable and constrains cathode flow channel design. EO pumps can relieve cathode design barriers and simplify water management in fuel cells. EO pumps have no moving parts, scale across a wide range of operation, and result in low parasitic power. We demonstrate and quantify the efficacy of EO water pumping using a single-pass fuel cell test channel. Our results show that removing water from the cathode using integrated EO pumping structures improves fuel cell performance and stability. These pumps enable operation with air flow rates of just two to three times stoichiometric requirements.


2017 ◽  
Vol 19 (11) ◽  
pp. 7751-7759 ◽  
Author(s):  
Manu Gautam ◽  
Mruthyunjayachari Chattanahalli Devendrachari ◽  
Ravikumar Thimmappa ◽  
Alagar Raja Kottaichamy ◽  
Shahid Pottachola Shafi ◽  
...  

Polarity governed amplification of fuel cell performance in graphene oxide-based proton exchange membrane fuel cells.


2019 ◽  
Author(s):  
Valentina Guccini ◽  
Annika Carlson ◽  
Shun Yu ◽  
Göran Lindbergh ◽  
Rakel Wreland Lindström ◽  
...  

<p>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<sup>-1</sup>), counterion (H<sup>+</sup>or Na<sup>+</sup>), 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 (Na<sup>+</sup>or H<sup>+</sup>). 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<sup>-1</sup>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.</p>


2019 ◽  
Author(s):  
Valentina Guccini ◽  
Annika Carlson ◽  
Shun Yu ◽  
Göran Lindbergh ◽  
Rakel Wreland Lindström ◽  
...  

<p>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<sup>-1</sup>), counterion (H<sup>+</sup>or Na<sup>+</sup>), 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 (Na<sup>+</sup>or H<sup>+</sup>). 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<sup>-1</sup>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.</p>


Author(s):  
Y. Zhou ◽  
G. Lin ◽  
A. J. Shih ◽  
S. J. Hu

Proton exchange membrane (PEM) fuel cells are favored in many applications due to their simplicity and relatively high power density. However, there has been a lack of understandings of the fundamental mechanisms of assembly and manufacturing induced phenomena and their influence on performance and durability. This paper presents a comprehensive analysis of assembly pressure induced phenomena in PEM fuel cells using multi-physics based modeling. A finite-element-based structural and mass-transfer model was developed by integrating mechanical deformation, mass transfer resistance, and electrical contact resistance to study the effects of assembly pressure and the fuel cell overall performance. Contact resistance, inhomogeneous deformation of membrane and GDL, electrochemical analysis were simulated. The fuel cell performance was predicted and an optimal assembly pressure was identified through this multi-physics model. Results show that PEM fuel cell performance first increases gradually to a maximum and then decreases with further assembly pressure increase. The influence of temperature and humidity on cell performance was also investigated.


2017 ◽  
Vol 10 (1) ◽  
pp. 96-105 ◽  
Author(s):  
Mohammed Jourdani ◽  
Hamid Mounir ◽  
Abdellatif El Marjani

Background: During last few years, the proton exchange membrane fuel cells (PEMFCs) underwent a huge development. Method: The different contributions to the design, the material of all components and the efficiencies are analyzed. Result: Many technical advances are introduced to increase the PEMFC fuel cell efficiency and lifetime for transportation, stationary and portable utilization. Conclusion: By the last years, the total cost of this system is decreasing. However, the remaining challenges that need to be overcome mean that it will be several years before full commercialization can take place.This paper gives an overview of the recent advancements in the development of Proton Exchange Membrane Fuel cells and remaining challenges of PEMFC.


2015 ◽  
Vol 3 (16) ◽  
pp. 8847-8854 ◽  
Author(s):  
Zhibin Guo ◽  
Ruijie Xiu ◽  
Shanfu Lu ◽  
Xin Xu ◽  
Shichun Yang ◽  
...  

A novel submicro-pore containing proton exchange membrane is designed and fabricated for application in high-temperature fuel cells.


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