TY - JOUR
T1 - A Direct Alcohol Fuel Cell Driven by an Outer Sphere Positive Electrode
AU - Bhat, Zahid Manzoor
AU - Thimmappa, Ravikumar
AU - Devendrachari, Mruthunjayachari Chattanahalli
AU - Shafi, Shahid Pottachola
AU - Aralekallu, Shambulinga
AU - Kottaichamy, Alagar Raja
AU - Gautam, Manu
AU - Thotiyl, Musthafa Ottakam
N1 - Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/8/3
Y1 - 2017/8/3
N2 - Molecular oxygen, the conventional electron acceptor in fuel cells poses challenges specific to direct alcohol fuel cells (DAFCs). Due to the coupling of alcohol dehydrogenation with the scission of oxygen on the positive electrode during the alcohol crossover, the benchmark Pt-based air cathode experiences severe competition and depolarization losses. The necessity of heavy precious metal loading with domains for alcohol tolerance in the state of the art DAFC cathode is a direct consequence of this. Although efforts are dedicated to selectively cleave oxygen, the root of the problem being the inner sphere nature of either half-cell chemistry is often overlooked. Using an outer sphere electron acceptor that does not form a bond with the cathode during redox energy transformation, we effectively decoupled the interfacial chemistry from parasitic chemistry leading to a DAFC driven by alcohol passive carbon nanoparticles, with performance metrics ∼8 times higher than Pt-based DAFC-O2.
AB - Molecular oxygen, the conventional electron acceptor in fuel cells poses challenges specific to direct alcohol fuel cells (DAFCs). Due to the coupling of alcohol dehydrogenation with the scission of oxygen on the positive electrode during the alcohol crossover, the benchmark Pt-based air cathode experiences severe competition and depolarization losses. The necessity of heavy precious metal loading with domains for alcohol tolerance in the state of the art DAFC cathode is a direct consequence of this. Although efforts are dedicated to selectively cleave oxygen, the root of the problem being the inner sphere nature of either half-cell chemistry is often overlooked. Using an outer sphere electron acceptor that does not form a bond with the cathode during redox energy transformation, we effectively decoupled the interfacial chemistry from parasitic chemistry leading to a DAFC driven by alcohol passive carbon nanoparticles, with performance metrics ∼8 times higher than Pt-based DAFC-O2.
UR - http://www.scopus.com/inward/record.url?scp=85026813542&partnerID=8YFLogxK
U2 - 10.1021/acs.jpclett.7b01418
DO - 10.1021/acs.jpclett.7b01418
M3 - Article
C2 - 28686441
AN - SCOPUS:85026813542
SN - 1948-7185
VL - 8
SP - 3523
EP - 3529
JO - Journal of Physical Chemistry Letters
JF - Journal of Physical Chemistry Letters
IS - 15
ER -