803
Performance and Durability of an Alkaline Direct Methanol Fuel Cell Employing a Nitrogen Post-Doped PtRu/C Anode

Wednesday, May 14, 2014
Grand Foyer, Lobby Level (Hilton Orlando Bonnet Creek)
P. Joghee, S. Pylypenko (Colorado School of Mines), K. Wood (Department of Matellurgical & Materials Engineering, Colorado School of Mines, Golden, CO), G. Bender (National Renewable Energy laboratory, 1617 Cole Boulevard, Golden, CO 80401), and R. O'Hayre (Department of Matellurgical & Materials Engineering, Colorado School of Mines, Golden, CO)

 

 

         Alkaline direct methanol fuel cells (ADMFCs) are attractive due to the enhanced electro-kinetics and lower methanol crossover compared to acid-based DMFCs1. However, performance and long-term stability results to-date are insufficient for commercial application. Recently, we have demonstrated that acid based DMFC anodes employing nitrogen pre and post-doped PtRu/C catalytic materials provide markedly higher performance and stability when compared to standard (un-doped) state-of-the-art commercial PtRu/C catalysts2,3,4. In this work, a commercial PtRu/C catalyst that has been post-doped with nitrogen (PtRu/C-N) is evaluated for the anode of a single-cell ADMFC. In the post-doped approach, nitrogen is incorporated onto the commercial PtRu/C (HS-10000) catalyst by ion implantation technique.

           XPS analysis for the PtRu/C doped with nitrogen using high dosage ion implantation shows that 1-2 at.% nitrogen was incorporated into the material. The formation of lower-binding energy nitrogen species was particularly favored. Furthermore, the XPS and TEM results revealed that a fraction of PtRu particles reorganize to form small well-dispersed nanoparticles on the surface of the carbon. Fig.1 shows the methanol stripping voltammetry curves used to measure the electrochemical surface area (ECSA) for the PtRu/C-N and un-doped PtRu/C catalysts at 25¢ªC (scan rate 5mV sec-1). The PtRu/C-N exhibits higher ECSA (51.5 m2 g-1) as compared with the un-doped counterpart (35.4 m2 g-1).

              Fig. 2 compares the ADMFC (using a Tokuyama A-201 membrane) performances for anodes with PtRu/C-N (3mg cm-2) vs. un-doped PtRu/C (3mg cm-2) in 2M NaOH + 2M CH3OH at 80¢ªC. In both cases, 40wt.% Pt/C (2mg cm-2) catalyst was used in the cathode. The anode with PtRu/C-N exhibits improved performance, particularly, in the ohmic and mass transfer regions as compared to the un-doped PtRu/C anode. The improved performance of nitrogen post-doped catalyst can be at least partially attributed to the observed higher ECSA as noted above. The PtRu/C-N delivers maximum power densities of 140 and 110 mW cm-2 whereas the un-doped PtRu/C delivers maximum power densities of 117 and 100 mW cm-2using oxygen and air, respectively. The performance of PtRu/C-N based anode among the best ever reported for an ADMFC under similar catalyst loading and measurement conditions. A long-term durability test for the ADMFC with the anodes of PtRu/C-N and un-doped PtRu/C is underway to see the effect of nitrogen on the stability of PtRu.

References

  1. A. V. Tripkovic, K. D. Popovic, B. N. Grgur, B. Blizanac, P. N. Ross and M. Markovic, Electrochim. Acta, 47 (2002) 3707.
  2. A. R. Corpuz, T. S. Olson, P. Joghee, S. Pylypenko, A. A. Dameron, H. N. Dinh, K. J. O’Neill, K. E. Hurst, G. Bender, T. Gennett, B. S. Pivovar, R. M. Richards and R. P. O’Hayre, J. Power Sources, 217 (2012)142.
  3. J. Prabhuram, S. Pylypenko, T. S. Olson, A.  Dameron, A. Corpuz, K. Wood, K. O’Neill, K.  Hurst, G.  Bender, H. N. Dinh, T. Gennett, B. Pivovar and R. O’Hayre, J. Electrochem. Soc. 159 (11) (2012) F768-F778.
  4. A. Corpuz, K. N. Wood, S. Pylypenko, A. A. Dameron, J. Prabhuram, T. S. Olson, G. Bender, H. Dinh, T. Gennett, R. M. Richards and R. O’Hayre, J. Power Sources, 248 (2014) 296.

Acknowledgements

This work was supported by the Army Research Office under grant #W911NF-09-1-0528 and the U.S. Department of Energy EERE, Fuel Cell Technologies Program, under Contract No. DE-AC36-08-GO28308 with the National Renewable Energy Laboratory. The authors also acknowledge surface analysis and fuel cell testing facilities provided at NREL.