Polymer electrolyte membrane (PEM) electrolysis of H2O2 from O2 and H2O with continuous on-line spectrophotometric product detection: Load flexibility studies

2021 ◽  
Vol 896 ◽  
pp. 115465
Author(s):  
Jessica Hübner ◽  
Benjamin Paul ◽  
Aleksandra Wawrzyniak ◽  
Peter Strasser
2020 ◽  
Author(s):  
Daniel John Seale Sandbeck ◽  
Niklas Mørch Secher ◽  
Masanori Inaba ◽  
Jonathan Quinson ◽  
Jakob Ejler Sørensen ◽  
...  

Cost and lifetime currently hinder widespread commercialization of polymer electrolyte<br>membrane fuel cells (PEMFCs). Reduced electrode Pt loadings lower costs; however, the impact<br>of metal loading (on the support) and its relation to degradation (lifetime) remain unclear. The<br>limited research on these parameters stems from synthetic difficulties and lack of in situ<br>analytics. This study addresses these challenges by synthesizing 2D and 3D Pt/C model catalyst<br>systems via two precise routes and systematically varying the loading. Pt dissolution was<br>monitored using on-line inductively coupled plasma mass spectrometry (on-line-ICP-MS), while<br>X-ray spectroscopy techniques were applied to establish the oxidation states of Pt in correlation<br>with metal loading. Dissolution trends emerge which can be explained by three particle<br>proximity dependent mechanisms: (1) shifts in the Nernst dissolution potential, (2) redeposition,<br>and (3) alteration of Pt oxidation states. These results identify engineering limitations, which<br>should be considered by researchers in fuel cell development and related fields. <br>


2008 ◽  
Vol 10 (7) ◽  
pp. 1048-1051 ◽  
Author(s):  
Hyung-Suk Oh ◽  
Jong-Gil Oh ◽  
Seungjoo Haam ◽  
Kundu Arunabha ◽  
Bumwook Roh ◽  
...  

2020 ◽  
Author(s):  
Daniel John Seale Sandbeck ◽  
Niklas Mørch Secher ◽  
Masanori Inaba ◽  
Jonathan Quinson ◽  
Jakob Ejler Sørensen ◽  
...  

Cost and lifetime currently hinder widespread commercialization of polymer electrolyte<br>membrane fuel cells (PEMFCs). Reduced electrode Pt loadings lower costs; however, the impact<br>of metal loading (on the support) and its relation to degradation (lifetime) remain unclear. The<br>limited research on these parameters stems from synthetic difficulties and lack of in situ<br>analytics. This study addresses these challenges by synthesizing 2D and 3D Pt/C model catalyst<br>systems via two precise routes and systematically varying the loading. Pt dissolution was<br>monitored using on-line inductively coupled plasma mass spectrometry (on-line-ICP-MS), while<br>X-ray spectroscopy techniques were applied to establish the oxidation states of Pt in correlation<br>with metal loading. Dissolution trends emerge which can be explained by three particle<br>proximity dependent mechanisms: (1) shifts in the Nernst dissolution potential, (2) redeposition,<br>and (3) alteration of Pt oxidation states. These results identify engineering limitations, which<br>should be considered by researchers in fuel cell development and related fields. <br>


2010 ◽  
Vol 195 (15) ◽  
pp. 4622-4627 ◽  
Author(s):  
Tommy T.H. Cheng ◽  
Nengyou Jia ◽  
Vesna Colbow ◽  
Silvia Wessel ◽  
Monica Dutta

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