Effect of type and stoichiometry of fuels on performance of polybenzimidazole-based proton exchange membrane fuel cells operating at the temperature range of 120-160 °C

Energy ◽  
2021 ◽  
pp. 121791
Author(s):  
Sung Kwan Ryu ◽  
Mohanraj Vinothkannan ◽  
Ae Rhan Kim ◽  
Dong Jin Yoo
2021 ◽  
Author(s):  
Hongying Tang ◽  
Kang Geng ◽  
Lei Wu ◽  
Junjie Liu ◽  
Zhiquan Chen ◽  
...  

Abstract Conventional proton exchange membrane fuel cells (PEMFCs) operate at a narrow temperature range, either under low temperature conditions (80‒90°C) using fully-humidified perfluorosulfonic acid (Nafion®) membranes or under non-humidified high temperature conditions (140‒180°C) using phosphoric acid (PA)-doped membranes to avoid water condensation-induced PA leaching. To allow wide operational flexibility over the full spectrum of temperature and humidity ranges, we present an innovative design strategy by using PA-doped intrinsically ultramicroporous membranes constructed from rigid and contorted high free volume polymers. The membranes with an average ultramicropore radius of 3.3 Å showed a significant siphoning effect as confirmed by the delocalization of PA in 31P NMR, thus allowing high retention of PA even under highly humidified conditions and presenting more than three orders of magnitude higher proton conductivity retention than conventional dense PA-doped polybenzimidazole membranes (PBI/PA). The resulting PEMFCs display impressive performance over a much broader temperature range from − 20 to 200°C and can accomplish over 100 start-up/shut-down cycles even at − 20°C. The broad operational flexibility rendered from the high PA-retention can ultimately simplify heat and water management and thereby reduce PEMFC costs.


2019 ◽  
Vol 7 (25) ◽  
pp. 15288-15301 ◽  
Author(s):  
Xiaoxiao Zhang ◽  
Xudong Fu ◽  
Shoukun Yang ◽  
Yuanfang Zhang ◽  
Rong Zhang ◽  
...  

An ionogel incorporated into poly(2,5-benzimidazole) membranes was designed for the applications of PEMFCs in a wide temperature range.


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>


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.


2020 ◽  
Vol 30 (6) ◽  
pp. 855-860
Author(s):  
Ruixiang Wang ◽  
Pengyang Zhang ◽  
Yucheng Wang ◽  
Yuesheng Wang ◽  
Karim Zaghib ◽  
...  

Energies ◽  
2021 ◽  
Vol 14 (10) ◽  
pp. 2975
Author(s):  
Zikhona Nondudule ◽  
Jessica Chamier ◽  
Mahabubur Chowdhury

To decrease the cost of fuel cell manufacturing, the amount of platinum (Pt) in the catalyst layer needs to be reduced. In this study, ionomer gradient membrane electrode assemblies (MEAs) were designed to reduce Pt loading without sacrificing performance and lifetime. A two-layer stratification of the cathode was achieved with varying ratios of 28 wt. % ionomer in the inner layer, on the membrane, and 24 wt. % on the outer layer, coated onto the inner layer. To study the MEA performance, the electrochemical surface area (ECSA), polarization curves, and electrochemical impedance spectroscopy (EIS) responses were evaluated under 20, 60, and 100% relative humidity (RH). The stratified MEA Pt loading was reduced by 12% while maintaining commercial equivalent performance. The optimal two-layer design was achieved when the Pt loading ratio between the layers was 1:6 (inner:outer layer). This MEA showed the highest ECSA and performance at 0.65 V with reduced mass transport losses. The integrity of stratified MEAs with lower Pt loading was evaluated with potential cycling and proved more durable than the monolayer MEA equivalent. The higher ionomer loading adjacent to the membrane and the bi-layer interface of the stratified catalyst layer (CL) increased moisture in the cathode CL, decreasing the degradation rate. Using ionomer stratification to decrease the Pt loading in an MEA yielded a better performance compared to the monolayer MEA design. This study, therefore, contributes to the development of more durable, cost-effective MEAs for low-temperature proton exchange membrane fuel cells.


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