Electro-Thermal Modeling of Large Format Lithium-Ion Pouch Cells: A Cell Temperature Dependent Linear Polarization Expression

2016 ◽  
Vol 163 (14) ◽  
pp. A3046-A3062 ◽  
Author(s):  
Alexander Rheinfeld ◽  
Stephan Kosch ◽  
Simon V. Erhard ◽  
Patrick J. Osswald ◽  
Bernhard Rieger ◽  
...  
2012 ◽  
Vol 160 (2) ◽  
pp. A212-A217 ◽  
Author(s):  
Nerea Nieto ◽  
Luis Díaz ◽  
Jon Gastelurrutia ◽  
Isabel Alava ◽  
Francisco Blanco ◽  
...  

Energies ◽  
2019 ◽  
Vol 12 (7) ◽  
pp. 1251 ◽  
Author(s):  
Daniel Worwood ◽  
James Marco ◽  
Quirin Kellner ◽  
Elham Hosseinzadeh ◽  
Ryan McGlen ◽  
...  

Cooling the surface of large format batteries with solid conductive plates, or fins, has an inherent advantage of reducing the number of liquid seals relative to some mini-channel cold plate designs, as liquid is not passed through the numerous individual plates directly. This may reduce the overall pack leakage risk which is of utmost importance due to safety concerns associated with the possibility of a cell short circuit and thermal runaway event. However, fin cooling comes at a cost of an increased thermal resistance which can lead to higher cell temperatures and a poorer temperature uniformity under aggressive heat generation conditions. In this paper, a novel graphite-based fin material with an in-plane thermal conductivity 5 times greater than aluminium with the same weight is presented for advanced battery cooling. The thermal performance of the fin is benchmarked against conventional copper and aluminium fins in an experimental programme cycling real 53 Ah pouch cells. The results from the extensive experimental testing indicate that the new fin can reduce both the peak measured temperature and surface temperature gradient by up to 8 °C and 5 °C respectively, when compared to aluminium fins under an aggressive electric vehicle duty-cycle.


2014 ◽  
Vol 147 ◽  
pp. 319-329 ◽  
Author(s):  
Ahmadou Samba ◽  
Noshin Omar ◽  
Hamid Gualous ◽  
Odile Capron ◽  
Peter Van den Bossche ◽  
...  

2018 ◽  
Vol 129 ◽  
pp. 218-230 ◽  
Author(s):  
Mehrdad Mastali ◽  
Evan Foreman ◽  
Ali Modjtahedi ◽  
Ehsan Samadani ◽  
Amir Amirfazli ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Shofu Matsuda ◽  
Yuuki Niitsuma ◽  
Yuta Yoshida ◽  
Minoru Umeda

AbstractGenerating electric power using CO2 as a reactant is challenging because the electroreduction of CO2 usually requires a large overpotential. Herein, we report the design and development of a polymer electrolyte fuel cell driven by feeding H2 and CO2 to the anode (Pt/C) and cathode (Pt0.8Ru0.2/C), respectively, based on their theoretical electrode potentials. Pt–Ru/C is a promising electrocatalysts for CO2 reduction at a low overpotential; consequently, CH4 is continuously produced through CO2 reduction with an enhanced faradaic efficiency (18.2%) and without an overpotential (at 0.20 V vs. RHE) was achieved when dilute CO2 is fed at a cell temperature of 40 °C. Significantly, the cell generated electric power (0.14 mW cm−2) while simultaneously yielding CH4 at 86.3 μmol g−1 h−1. These results show that a H2-CO2 fuel cell is a promising technology for promoting the carbon capture and utilization (CCU) strategy.


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