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Membraneless, room-temperature, direct borohydride/cerium fuel cell with power density of over 0.25 W/cm2
Authors:Da Mota Nicolas  Finkelstein David A  Kirtland Joseph D  Rodriguez Claudia A  Stroock Abraham D  Abruña Héctor D
Affiliation:Department of Chemistry and Chemical Biology, Baker Laboratory, Olin Hall, Cornell University, Ithaca, New York 14853, USA.
Abstract:The widespread adoption and deployment of fuel cells as an alternative energy technology have been hampered by a number of formidable technical challenges, including the cost and long-term stability of electrocatalyst and membrane materials. We present a microfluidic fuel cell that overcomes many of these obstacles while achieving power densities in excess of 250 mW/cm(2). The poisoning and sluggish reaction rate associated with CO-contaminated H(2) and methanol, respectively, are averted by employing the promising, high-energy density fuel borohydride. The high-overpotential reaction of oxygen gas at the cathode is supplanted by the high-voltage reduction of cerium ammonium nitrate. Expensive, ineffective membrane materials are replaced with laminar flow and a nonselective, porous convection barrier to separate the fuel and oxidant streams. The result is a Nafion-free, room-temperature fuel cell that has the highest power density per unit mass of Pt catalyst employed for a non-H(2) fuel cell, and exceeds the power density of a typical H(2) fuel cell by 50%.
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