Photocatalysis generally involves
three processes: (i) generation of electrons and holes by photoexcitation;
(ii) migration of the photogenerated charge carriers to the surface
and subsequent reduction/oxidization of the adsorbed reactants directly
by electrons/holes or by reactive oxygen species (ROS); and (iii)
recombination of the photogenerated electron-hole pairs. Desired
photocatalysts are expected to promote Process (i) and (ii) in the
meanwhile to suppress Process (iii). We attempt to gain fundamental
understanding of the effects of the chemical composition, electronic
structure, crystal structure and morphology of nanocrystals on the
three processes in photocatalysis. We are developing new materials
and/or optimize the shape and surface structure of nanocrystals
to improve the efficiency of photocatalysis and photoelectrochemical
processes.
We
are developing photocatalysts and photoelectrochemical cells
for solar energy utilization and environmental remediation.
Currently, the primary energy source is supplied by fossil fuels.
It is essential to increase the energy conversion/utilization
efficiency and to reduce the pollutant emission of power generation.
Photocatalysts and photoelectrochemical cells are emerging as
a potential CO2 capture technologies. Photocatalytic conversion
of CO2 not only removes CO2 from effluent gases but it also
converts CO2 into marketable commodity such as methane, methanol,
and formaldehyde. In addition, photoelectrochemical cells are
used to produce H2 from coal. By harnessing solar energy, the
H2 generation process is less energy-consuming than the conventional
methods. Also, H2 generation by photoelectrochemical cells will
significantly reduce the release of pollutants to the ecological
system. We are exploring to
mitigate or remove the environmental pollutants such as heavy
metals, small molecule toxins and pathogens by utilizing photocatalysts
and photoelectrochemical cells. |
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Conventional solid oxide fuel cells (SOFCs) use yttria-stabilized
zirconia (YSZ) electrolyte. However, its conductivity characteristics
require an operating temperature of over 900°C. Reduction of
the operating temperature of SOFCs to <800°C is one of the
main goals of current SOFC research programs. The challenge is that
the electrochemical reaction becomes considerably slower as temperature
is reduced. Due to the high activation energy of the oxygen reduction
reaction, whose polarization resistance increases rapidly with decreasing
temperature, the cathode requires particular attention when the
operating temperature is reduced. The cathode performance depends
on the electronic/ionic conductivity of the electrode, gas transport
through electrode porosity, and the electrocatalytic activity at
the three-phase boundary (TPB) areas among the gas, the electrolyte
and the cathodes. We strive to improve the cathode performance by
developing new materials and/or optimization of electrode architecture/microstructure.
In addition, we are investigating the effects of trace impurities
on the performance of SOFC anodes that are operated in coal-derived
syngas. We are identifying the elements that have the most detrimental
effects. We seek to establish the fundamental mechanism of the interaction
of impurities with the anode by electrochemical studies and microstructural
analysis. The knowledge obtained will lead to maximization of the
power density of SOFC and improvement of the reliability of SOFC
anode operated in the syngas environment. This work is part of the
DOE-funded project of “Direct Utilization of Coal Syngas in
High Temperature Fuel Cells” that is implemented by an interdisciplinary
research team of WVU.
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