Towards the Development and Fabrication of a Low-Cost Photovoltaic CellPhil Glover and Ian Braly
School of Chemical, Biological and Environmental Engineering, Oregon State University
Background:�A scalable source of sustainable energy is needed to meet increasing energy demands with minimal environmental impact.
�The cost of solar energy must be decreased 15-20 times before it will be competitive with current energy costs.1
�Cu2ZnSnS4 (CZTS) thin films offer a low-cost alternative as an absorber material for photovoltaics.
Methods:
Future Work:�Perform microreactor syntheses investigating the effect of
-Increased temperature-Varied reactant stoichiometry�10% efficient CZTS devices have been reported utilizing
Photovoltaic Cell Construction
�Sulfur and metal precursors prepared in separate ethylene glycol solutions.
�Precursors pumped into separate preheating coils.
�Tee mixes precursors at desired temperature for CZTS nanoparticle formation.
�Reaction conditions designed to investigate the effect of precursor concentration and stoichiometry on the size, composition, and band-gap of CZTS nanoparticles
Accomplishments:
�Designed microreactor for small scale continuous production of solar absorber layer.
�Developed and demonstrated effectiveness of air as segmentation fluid in continuous reaction.
�Synthesized CZTS with low temperature, low residence time reaction.
�Performed Design of Experiments to investigate effects of precursor concentration and stoichiometricratios.
�Produced nanoparticles with desired 1.5 eV band-gap.
Air Pump Reactant Pump
Sulfur precursor Metal precursors
Mixing tee Segmenting tee
CZTS ink
Segmenting Air
“Ink blobs”
170°C Glycerol Heating Bath
Microreactor Flow Diagram
Metal Precursor Solution:�CuCl�ZnCl2
Sulphur Precursor Solution:�Thioacetemide
Solvent:
Kesterite Unit Cell3
Project Focus
Results:
-Varied reactant stoichiometry
�Increase reactor coil length to increase residence time.
�Investigate bulk crystalline and optical properties of synthesized material.
�Construct a solar cell with CZTS continuously synthesized by the microreactor.
� Test photovoltaic device efficiency.
Acknowledgments:�Sharp Labs of America for financial support�Dr. Herman for lab access and resources�Brendan Flynn for XRD and project guidance�Dr. Harding for project supervision�Dr. Yi and Teresa Sawyer for SEM training�Wei Wang for UV-Vis training�Bill Donnithorne for project documentation
References:1. Basic Needs for Solar Energy Utilization. Department of Energy.
2005.2. Todorov et. Al. High-Efficiency Solar Cell with Earth-Abundant
Liquid-Processed Absorber. Advanced Energy Materials. 2010. 3. Fischereder et. Al. Investigation of Cu2ZnSnS4 Formation from
Metal Salts and Thioacetamide. Chem Mater. 2010.4. Chang, C.H. et. al. Synthesis and post-processing of
nanomaterials using microreaction technology. J Nanopart Res. 2008.
�10% efficient CZTS devices have been reported utilizing batch liquid processing techniques.2
�Current synthesis techniques are expensive and energy intensive.
-Multi-target sputtering-Hot-injection batch synthesis with harsh solvents-Vacuum techniques
�Continuous, uniform synthesis of nanoparticles is possible with microreactor technology.
�Microreactors utilize high surface area to volume ratios.4
-Reduces heat and mass transfer limitations-Allows two-phase segmented flow
Objectives:�Characterize CZTS particles from batch reactions to verify experimental parameters
�Develop microreactor process for continuous CZTS production using inexpensive, non-toxic solvents.
�Integrate continuously synthesized CZTS into photovoltaic cells.
�Report efficiency of photovoltaic cells with CZTS absorber layer.
�ZnCl2�SnCl4•H2O
Solvent:�Ethylene glycol
XRD Characterization
UV-Vis Spectra�The low concentration, adjusted stoichiometry run yielded the desired copper-poor, zinc rich composition.
�The high concentration run resulted lower incorporations of zinc. This indicates that the order of reaction of zinc is lower than that of the other metal reactants.
�Nanoparticles form and agglomerate in the microreactor in order to reduce surface energy during their growth. The “ideal” runs yielded a zinc-poor stoichiometry. �All samples match expected peak locations, confirming
the formation of particles with the desired lattice structure.
�Extrapolation from linear region of the high concentration sample shows desired 1.5 eV band-gap.
�Lack of a linear region in the other samples indicates the presence of multiple compounds.