Strategies to mitigate Pt dissolution in low Pt loading proton exchange membrane fuel cell: II. A gradient Pt loading design

2017 ◽  
Vol 247 ◽  
pp. 1169-1179 ◽  
Author(s):  
Haoran Yu ◽  
Andrea Baricci ◽  
Andrea Casalegno ◽  
Laure Guetaz ◽  
Leonard Bonville ◽  
...  
2017 ◽  
Vol 247 ◽  
pp. 1155-1168 ◽  
Author(s):  
Haoran Yu ◽  
Andrea Baricci ◽  
Andrea Bisello ◽  
Andrea Casalegno ◽  
Laure Guetaz ◽  
...  

2021 ◽  
Author(s):  
Minhua Shao ◽  
Fei Xiao ◽  
Qi Wang ◽  
Gui-Liang Xu ◽  
Xueping Qin ◽  
...  

Abstract Proton exchange membrane fuel cell converts hydrogen and oxygen into electricity with zero emission1. The high cost and low durability of Pt-based electrocatalysts for oxygen reduction reaction hinder its wide applications2,3. The development of non-precious metal electrocatalysts also reaches the bottleneck because of the low activity and durability4,5. Here we rationally design a hybrid electrocatalyst consisting of atomically dispersed Pt and Fe single atoms and intermetallic PtFe alloy nanoparticles. The Pt mass activity of the hybrid catalyst is 3.5 times higher than that of commercial Pt/C in a fuel cell. More importantly, the fuel cell with an ultra-low Pt loading in the cathode (0.015 mgPt cm-2) shows unprecedented durability, with 93.6% activity retention after 100,000 cycles and no noticeable current drop at 0.6 V for at least 206 h. These results highlight the importance of the synergistic effects among active sites in hybrid electrocatalysts and provide an alternative way to design more active and durable low-Pt electrocatalysts for electrochemical devices.


Energy ◽  
2010 ◽  
Vol 35 (9) ◽  
pp. 3941-3957 ◽  
Author(s):  
A. Esmaeilifar ◽  
S. Rowshanzamir ◽  
M.H. Eikani ◽  
E. Ghazanfari

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>


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