Development of new alternative electrode materials is essential in order for the polymer electrolyte fuel cell (PEFC) to be able to reach a broad market. Today, high platinum loadings are required, especially on the cathode, to obtain sufficient activity for oxygen reduction. In addition, electrode degradation causes loss of catalyst surface area and requires high initial loadings to maintain the cell performance over time. There are problems related to Pt also on the anode side where poisoning of the catalyst, by e.g. CO, reduces the activity.

Approaches to improve the electrodes and reduce their costs are continuously evaluated and include alternative catalysts or supports as well as new structures and morphologies of the catalyst layer. Alternative catalysts, based on non-precious metals, Pt alloys/mixtures, and/or novel supports should preferably reduce the total amount of Pt, increase the activity, and be stable in the fuel cell environment. The support material can influence the activity by spill-over effects as well as changing the electronic structure of the catalyst. New support materials can improve the activity, utilization, and stability of the catalyst or of the support itself.

Tungsten oxide is a material which has been extensively investigated for a wide range of applications, mainly, due to its unique electrochromic properties but also for its electrocatalytic activities. The electrochromism allows tungsten oxide to intercalate/deintercalate ions (of e.g. H, Li, Na, K, Pb, Cd) into its structure in the formation of tungsten bronzes. The most widely studied form is the hydrogen tungsten bronze where protons are inserted in the oxide structure as HxWO3 and 0 < x < 1. The bronze formation mechanism has been the subject for numerous studies and it is suggested that the hydrogen atoms form hydroxyl bonds in the tungsten oxide.
SEM WO3 Electrode

The bronze formation is greatly affected by the water content, porosity, and also crystallinity, which in turn affect the catalytic properties of tungsten oxide. At the same time as protons can be incorporated in the WOx structure, they also have a significant mobility which means that WOx functions as a proton conductor under these conditions. Since the hydrogen tungsten bronze formation is dependent on the water content, large variation in conductivity has been reported when varying the relative humidity. Moreover, Pt supported on tungsten oxide has been shown to affect the bronze formation and both an increased intensity of the hydrogen intercalation/deintercalation peaks as well as a shift of the peak potential to higher potentials has been reported.

Tungsten oxide has been evaluated both as support and active catalyst in fuel cell anode as well as cathode electrodes. Sole tungsten oxide has displayed activity for hydrogen oxidation, which was attributed to high porosity and high surface area. Combined Pt and tungsten oxide based catalysts have been investigated for methanol/ethanol oxidation, CO oxidation, hydrogen oxidation as well as oxygen reduction. For methanol oxidation, the Pt on WOx system has shown improved efficiency over Pt catalyst due to both the spill-over of hydrogen from Pt to WOx but also the ability of WOx to provide oxygen atoms at low potentials and thereby avoiding CO-poisoning. Others have attributed the improved performance to an increased electrochemical active surface area (ECSA) of Pt on WOx.

Tungsten oxide is also relatively stable in acidic environment, which is a prerequisite for use in polymer electrolyte fuel cell applications. However, some dissolution of tungsten oxides has been reported. In a previous study, we examined the impact of different metal oxides on the stability and activity of platinum in thin model cathodes in a PEFC. Pt on WOx did exhibit an improved activity for oxygen reduction and possibly also an improved stability compared to Pt alone. Interesting features such as reduced platinum oxide formation and platinum catalyzed hydrogen tungsten bronze formation were also seen when Pt was deposited on WOx.

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