Controlling the deposition of Pt nanoparticles within the surface region of Nafion
2011
Sode, A. | Ingle, N.J.C. | McCormick, M. | Bizzotto, D. | Gyenge, E. | Ye, S. | Knights, S. | Wilkinson, D.P.
The chemical reduction of Pt-complexes to generate Pt nanoparticles within the surface region of a Nafion membrane may provide an alternative route to producing more efficient and robust membrane electrode assemblies for fuel cells. Controlling the deposition to enable manipulation of the Pt loading and distribution is a necessary first step to allow full exploration of a Nafion–noble metal composite. We find that the hydration state of the Nafion has the most significant impact on constraining where Pt deposition happens in the Nafion membrane. When coupled with variations in the pH of the working solutions, the depth of the Pt deposition zone can be varied from a sharply defined 200nm on up to a 15μm. A suggested mechanism to explain these findings is provided, based on the use of NaBH₄ as reductant and Pt(NH₃)₄(NO₃)₂ as the source of Pt. We also present electrochemical and spatially resolved conductivity measurements that suggested the deposted Pt nanoparticles form an interconnected network with the Nafion.
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