Development of Small Fish Robots Powered by Small and Ultra-Light Passive-Type Polymer Electrolyte Fuel Cells

2010 ◽  
Vol 22 (2) ◽  
pp. 150-157 ◽  
Author(s):  
Yogo Takada ◽  
◽  
Ryosuke Araki ◽  
Yukinobu Nakanishi ◽  
Motohiro Nonogaki ◽  
...  

Small fish robots, the size of a killifish – 5 cm long – are potentially in finding disaster victims in flooded areas, because of their ability to navigate narrow confines. Powering such robots, however, becomes a question, since the easiest answer – rechargeable batteries – has low energy density. The “Power Tube” we developed is a small and ultra-light passive-type polymer electrolyte fuel cell. Based on this fuel cell technology, we fabricated a 110 mm fish robot combining a drive, consisting of a DC motor and link, with a Power Tube having a hydrogen generator. We also fabricated an energy-efficient submersible fish robot with neodymium magnets and coil actuators, that methanol-fueled Power Tubes powered with a voltage booster.

2019 ◽  
Vol 21 (24) ◽  
pp. 13126-13134 ◽  
Author(s):  
J. Halter ◽  
T. Gloor ◽  
B. Amoroso ◽  
T. J. Schmidt ◽  
F. N. Büchi

The influence of phosphoric acid temperature and concentration on the wetting behavior of porous high temperature polymer electrolyte fuel cell materials is investigated.


Author(s):  
Yun Wang ◽  
Xiaoguang Yang

This paper seeks to develop 3D dynamic models for polymer electrolyte fuel cells (PEFCs) and hydrogen tanks, respectively. The dynamic model of PEFCs consists of multiple layers of a single PEFC and couples the various dynamic mechanisms in fuel cells, such as electrochemical double-layer discharging/charging, species transport, heat transfer, and membrane water uptake. The one of hydrogen tanks includes a 3D description of the hydride kinetics coupled with mass/heat transport in the hydrogen tank. Transient of fuel cell during step change in current is simulated. Dynamic responses of the cell voltage and heat generation rate are discussed. Hydrogen absorption process in the tank is considered. Temperature, reaction rate and heat rejection in the fuel tank are presented. Efforts are also made to discuss the coupling of these two systems in practice and associated issues.


2005 ◽  
Vol 2005.6 (0) ◽  
pp. 95-96
Author(s):  
Yogo TAKADA ◽  
Toshiaki TAMACHI ◽  
Toshinaga ISHII ◽  
Hiroyuki IMANISHI ◽  
Tomoyuki WAKISAKA

Author(s):  
Yun Wang

3D dynamic models are developed for polymer electrolyte fuel cells (PEFCs) and hydrogen tanks, respectively. In the fuel cell model, we consider the major transport and electrochemical processes within the key components of a single PEFC that govern fuel cell transient including the electrochemical double-layer behavior, mass/heat transport, liquid water dynamics, and membrane water uptake. As to modeling hydrogen tanks, we consider a LaNi5-based system and develop a general formula that describes hydrogen absorption/desorption. The model couples the hydride reaction kinetics and mass/heat transport. The dynamic characteristics of the PEFC and hydrogen tank, together with the possible coupling of the two systems, are discussed.


RSC Advances ◽  
2016 ◽  
Vol 6 (110) ◽  
pp. 108158-108163 ◽  
Author(s):  
Zehui Yang ◽  
Xinxin Yu ◽  
Yunfeng Zhang ◽  
Guodong Xu

Reducing platinum (Pt) usage in the polymer electrolyte fuel cells (PEFCs) has become one of the main issues in the global commercialization of PEFCs.


1996 ◽  
Author(s):  
V A Paganin ◽  
E A Ticianelli ◽  
E R Gonzalez

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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