Abstract

High-temperature polymer electrolyte fuel cells (HT-PEFCs) are a suitable technology for decentralized small scale electricity and heat production. HT-PEFCs do not require hydrogen infrastructure and are characterized by a simpler and therefore less expensive system compared to available fuel cell systems. In combination with a reformer unit, HT-PEFC systems offer an efficiency gain over conventional combustion of hydrocarbons, such as natural gas. In near future, HT-PEFCs will be even more effective and efficient when renewable biofuels and hydrogen are widespread available. We present an efficient HT-PEFC based combined heat and power (µ-CHP) system for the provision of electrical energy and hot water in single family households (see Table 1). Due to the optimized design and layout of the fuel cell based µ-CHP system and the respective manufacturing processes of the catalysts and the membrane electrode assemblies (MEA), the demand for cost effective and greenhouse gas efficient energy at customer level is addressed. Major efforts were devoted to the establishment of scalable catalyst deposition methods, which enable a loss-free utilization of precious metals. By using appropriate multimetallic catalyst systems at anode and cathode, the precious metal loading was reduced by approx. 20% in comparison to commercially available electrodes without compromising performance (see Figure 1) [1]. Furthermore, by introducing post-preparation treatments, the stability of the catalysts was enhanced over commercial Pt/C. The activity and stability of the catalyst systems were evaluated ex situ by means of cyclic voltammetry and accelerated stress tests using a rotating disk electrode (RDE) setup. Furthermore, the catalyst systems were characterized in situ by means of polarization curves, continuous operation, accelerated stress tests and electrochemical impedance spectroscopy measurements at single cell, stack and at system level (see Figure 1). Acknowledgment Financial support was provided by The Climate and Energy Fund of the Austrian Federal Government and The Austrian Research Promotion Agency (FFG) through the program Energieforschung (e!Mission). [1] A. Schenk, C. Grimmer, M. Perchthaler, S. Weinberger, B. Pichler, C. Heinzl, C. Scheu, F.-A. Mautner, B. Bitschnau, V. Hacker, Platinum–cobalt catalysts for the oxygen reduction reaction in high temperature proton exchange membrane fuel cells – Long term behavior under ex-situ and in-situ conditions, J. Power Sources. 266 (2014) 313–322. Figure 1

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