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Since the 1980s there has been a significant lowering of the platinum loading of polymer
electrolyte fuel cell electrodes from about 410 mg cm2(platinum black) to about 0.4 mg cm2 or
even less (carbon supported platinum), by the introduction of ionomer (liquid Nafion)
impregnated gas diffusion electrodes, extending the three-dimensional reaction zone. From the
1990s to the present studies have been carried out to decrease the loss of performance during
cell operation due both to the presence of liquid water causing flooding of the catalyst layer and
mass transport limitations and to the poisoning of platinum by the use of reformed fuels. This
review deals with the developments in electrode configuration going from dual layer to three layer
electrodes. The preparation methods, the characteristics and the optimal composition of both
diffusion and reactive layers of these electrodes are described. The improvement in the
performance of both CO tolerant anodes and cathodes with enhanced oxygen reduction by Pt
alloying is also discussed.
Electrochemical studies on low catalyst loading gas diffusion electrodes for polymer electrolyte fuel cells
are reported. The best performance is obtained with an electrode formed from 20 wt% Pt/C, 0.4 mg Pt
cm2 and 1.1 mg Nafion cm2 in the catalyst layer and 15% PTFE in a diffusion layer of 50 m thickness,
for both the cathode and the anode. However, it is also observed that the platinum requirement can be
diminished to values close to 0.2 mg Pt cm2 in the cathode and 0.1 mg pt cm2in the anode, without
appreciably affecting the good characteristics of the fuel cell response. The experimental fuel cell data were
analysed using theoretical models of the electrode structure and of the fuel cell system. It is seen that most
of the electrode systems present limiting currents and some also show linear diffusion components arising
from diffusion limitations in the gas channels and/or in the thin film of electrolyte covering the catalyst
particles.
Oxygen evolution from acid solutions has been investigated on two kinds of RuO2-based
electrodes; compact and cracked (porous) films. The kinetic study has been carried out by
means of potentiostatic curves. A method is suggested to estimate the surface
concentration of active sites. The reaction order with respect to active sites and the
activation energy have been determined. The mechanism is shown to differ on the two
kinds of film in relation to theS(site)-OH bond strength and the surface concentration of
intermediates. The behaviour of films on silica glass substrates is reported for the first
time.
The interfacial ohmic losses between the bipolar plate and the MEA can significantly reduce the
overall power output from a SPFC. For graphitic bipolar plate materials, these losses are
insignificant relative to stainless steel, where the existence of a passive film on the surface greatly
reduces electrical conductivity. In this paper we have evaluated different bipolar plate materials,
and present long-term fuel cell data for Poco graphite, titanium, 316 and 310 stainless steel. The
properties of the passive film on the surface of 316 and 310 stainless steel are markedly different.
Although both were adequately corrosion resistant in a fuel cell environment, 310 tended to
produce higher fuel cell performance and like 316, no degradation was observed after 1400 h
testing. Analysis of the passive film indicated that this increased performance was related to the
decreased thickness of the oxide film.
This review focuses on the use of inorganic oxide semiconductors for the photoassisted
generation of hydrogen from water. Representative studies spanning approximately three
decades are included in this review. The topics covered include a discussion of the types
of water photosplitting approaches, an ideal photoelectrolysis system, an examination of
why oxide semiconductors are attractive for this application, a review of both classical
and more recent studies on titanium dioxide, tungsten trioxide, and other binary metal
oxides, perovskites and other ternary oxides, tantalates and niobates, miscellaneous
multinary oxides, semiconductor alloys and mixed semiconductor composites, and twinphotosystem configurations for water splitting.
The electrochemical oxidation of phenol in the presence of NaCl for wastewater treatment was
studied at Ti/SnO2 and Ti/IrO2 anodes. The experimental results have shown that the presence of
NaCl catalyses the anodic oxidation of phenol only at Ti/IrO2 anodes due to the participation of
electro-generated ClO in the oxidation. Analysis of the oxidation products has shown that initially
organo-chlorinated compounds are formed in the electrolyte which are further oxidized to volatile
organics (CHCl3).
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An attempt was made to increase the ionic conductivity of novel, heterogeneous, anion-selective membranes by increasing the porosity of their surface
skin. This was based on the addition of a water-soluble compon...
Jaromr Hnt, Martin Paidar, Jan Schauer, Jan itka in Journal of Applied Electrochemistry (2012)
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Bifunctional electrodes for an integrated waterelectrolysis and hydrogen-oxygen fuel cell with a solid
polymer electrolyte
An alternative concept of an integrated water electrolysis/hydrogen-hydrogen fuel cell using metal electrocatalysts...2 a storage efficiency of 50% was
calculated; with the alternative concept of oxidation and r...
J. Ahn, R. Holze in Journal of Applied Electrochemistry (1992)
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LaNiO3 electrodes were prepared, in the form of thin films on platinum by the methods of spray pyrolysis and sequential coating of mixed metal nitrate
solutions followed by thermal decomposition. The films were a...
R. N. Singh, L. Bahadur, J. P. Pandey, S. P. Singh in Journal of Applied Electrochemistry (1994)