Chemistry Seminar Series 291 (11/3/17)
November 3, 2017 - 3:00pm
Thomas E. Mallouk, Ph.D., Pennsylvania State University
Future solar energy conversion systems (both photovoltaic and fuel-producing solar cells)must be efficient, stable, and inexpensive in order to be competitive with fossil energy sources. In biological photosynthesis, the internal quantum efficiency for light-induced charge separation is near unity, and similarly high efficiencies can be achieved in photovoltaic cells based on dye sensitization of semiconductors. However it remains a challenge to adapt either kind of molecular photosystem to the efficient production of solar fuels.
By coupling the photosensitizers of dye cells to nanoparticulate or molecular oxygen evolution catalysts, we can now make solar cells that split water with visible light. We have recently developed a kinetic model that successfully reproduces the transient photocurrent behavior universally observed with dye-sensitized water splitting cells. Their poor efficiency and stability are a consequence of charge recombination at the dye-sensitizer interface, which in turn is related to the trapping of protons generated in the water oxidation reaction.
This problem of proton management at the anode of water splitting solar cells has led us to investigate system-level issues that arise with (photo)electrochemical fuel production near neutral pH. In buffer-based water splitting cells, losses from solution resistance and electrochemically generated pH gradients become substantial in cells that run continuously for periods of hours. This problem can however be addressed by using bipolar membranebased cells in which the cathode and anode operate at low and high pH, respectively. Bipolar membranes enable efficient water splitting and CO2 electrolysis, in principle using electrocatalysts that derive entirely from earth-abundant materials.
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