
NSF Org: |
CBET Division of Chemical, Bioengineering, Environmental, and Transport Systems |
Recipient: |
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Initial Amendment Date: | July 2, 2013 |
Latest Amendment Date: | July 2, 2013 |
Award Number: | 1333649 |
Award Instrument: | Standard Grant |
Program Manager: |
Carole Read
cread@nsf.gov (703)292-2418 CBET Division of Chemical, Bioengineering, Environmental, and Transport Systems ENG Directorate for Engineering |
Start Date: | September 1, 2013 |
End Date: | August 31, 2017 (Estimated) |
Total Intended Award Amount: | $214,757.00 |
Total Awarded Amount to Date: | $214,757.00 |
Funds Obligated to Date: |
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History of Investigator: |
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Recipient Sponsored Research Office: |
3141 CHESTNUT ST PHILADELPHIA PA US 19104-2875 (215)895-6342 |
Sponsor Congressional District: |
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Primary Place of Performance: |
3201 Arch St Philadelphia PA US 19104-2737 |
Primary Place of
Performance Congressional District: |
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Unique Entity Identifier (UEI): |
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Parent UEI: |
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NSF Program(s): | EchemS-Electrochemical Systems |
Primary Program Source: |
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Program Reference Code(s): |
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Program Element Code(s): |
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Award Agency Code: | 4900 |
Fund Agency Code: | 4900 |
Assistance Listing Number(s): | 47.041 |
ABSTRACT
PI: Baxter, Jason / Murray, Christopher
Proposal Number: 1333649 / 1335821
Institution: Drexel University / University of Pennsylvania
Title: Collaborative Research: Ultrafast Carrier Dynamics in Semiconductor Nanocrystal Solar Cells
Close-packed arrays of semiconductor nanocrystals (NCs), or quantum dots, are ideal systems for fundamental investigations of photo-induced charge and energy transfer in interacting quantum-confined materials. The materials, diameters, and arrangement of the NCs can be used to tune the inter-NC coupling to exploit both the properties of the individual NCs and the long-range effects of the solid. The emergent optical, electronic, and thermal properties of NC superlattices may lead to transformational improvements in applications including photovoltaics, photonics, and thermoelectrics.
The broad objectives of this proposal are (1) to understand ultrafast charge carrier generation, separation, recombination, and transport phenomena in semiconductor nanocrystal superlattices, and (2) to control these fundamental photophysical processes to improve solar cell performance. Specifically, we will investigate films of CdSe, CdTe, and Cu2ZnSnS4 (CZTS) NCs. CdSe and CdTe NCs are excellent model systems because their synthesis and optical properties are well-understood, enabling fundamental ultrafast studies of carrier dynamics in glassy arrays and ordered superlattices of a single monodisperse NC species, as well as binary NC superlattices. CZTS NCs provide an exciting new direction for high efficiency photovoltaics made from non-toxic, earth-abundant elements. The PIs will refine the synthesis of monodisperse CZTS NCs to enable meaningful ultrafast spectroscopic characterization.
This approach centers on time-resolved terahertz spectroscopy (TRTS) and femtosecond visible/infrared transient absorption (TA) to probe intraband and interband transitions, respectively. THz spectroscopy is an ideal, non-contact probe of electronic materials because the THz frequency regime (0.1 - 3 THz) brackets typical carrier scattering rates in semiconductors. THz spectroscopy is unique in its abilities to distinguish between excitons and free carriers and to measure their dynamics on sub-picosecond to nanosecond time scales, providing an excellent complement to our steady-state field effect transistor (FET) measurements. Pump-probe TRTS and TA are ideal techniques to investigate the dynamics of interfacial charge transfer, recombination, and inter-NC transport of photoexcited carriers on their natural time and energy scales.
This work will advance our understanding of the physical phenomena that govern ultrafast exciton and free carrier dynamics in NCs and NC superlattices. Specific studies will include: (1) Determining mechanisms of charge transport in NC superlattices, e.g. by extended states or by activated hopping; (2) Measuring dynamics of inter-NC coupling, interfacial charge transfer, and long-range charge transport in superlattices of a single monodisperse NC species; (3) Determining the dependence of dynamics and transport mechanisms on NC size, capping ligand, inter-NC spacing, and long range order; (4) Understanding charge separation and transport in binary NC superlattices; and (5) Incorporating good candidate materials into solar cells to demonstrate improvements in efficiency that result from carefully designed NC architectures. This work will address the challenge of maintaining quantum-confined NC photophysics while also enabling long range charge transport necessary for devices. PI Baxter?s expertise in ultrafast spectroscopy and solar cells and PI Murray?s expertise in synthesis of NCs and superlattices make the team well-equipped to carry out this work.
The understanding of fundamental photophysical processes such as interfacial charge transfer, recombination, and inter-NC transport in NC superlattices developed here can be applied to create high-efficiency NC solar cells. Availability of efficient, low-cost, clean, and sustainable solar cells made from earth-abundant, non-toxic materials would transform the US energy portfolio. This project will result in the education and training of two Ph.D. students and multiple undergraduates. Additionally, PI Baxter is developing new courses on "Fundamentals of Solar Cells" and lab-based "Nanomanufacturing for Energy Applications" for students from both universities. Outreach will extend to K-12 students by the PIs? continued participation in NanoDay@Penn, Philly Materials Day at Drexel, and mentoring local high school teachers through NSF RET and university programs. These programs are particularly beneficial for underrepresented groups since they target students and teachers from the School District of Philadelphia, whose student body is over 80% minorities.
PUBLICATIONS PRODUCED AS A RESULT OF THIS RESEARCH
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PROJECT OUTCOMES REPORT
Disclaimer
This Project Outcomes Report for the General Public is displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed in this Report are those of the PI and do not necessarily reflect the views of the National Science Foundation; NSF has not approved or endorsed its content.
Professors Jason Baxter at Drexel University and Christopher Murray at the University of Pennsylvania recently completed research for their collaborative award CBET-1333649/1335821, studying ultrafast carrier dynamics in semiconductor nanocrystal assemblies. Semiconductor nanocrystals, or quantum dots, typically have diameters of 1-10 nm; and their optical and electronic properties depend on size as well as composition. In order for nanocrystals to be employed in functional devices such as solar cells, transistors, and displays, they must be deposited to form thin films. Additionally, the bulky organic ligands required to synthesize stable suspensions of colloidal nanocrystals must be replaced with shorter capping groups that enable electronic coupling between neighboring nanocrystals in the film. With complementary expertise in nanocrystal synthesis and assembly and in ultrafast spectroscopy, the team has made important advances in understanding how photoexcited carrier dynamics depend on surface treatments in nanocrystal films.
The team investigated long range charge transport in films of monodisperse PbSe nanocrystals and demonstrated that both charge carrier mobility and photoexcited carrier lifetime depend strongly on the choice of capping ligand for nanocrystal films. This result provided insight into ligand selection for nanocrystal devices and addressed the long-standing question of why some ligands enable good transistors but poor solar cells, while other ligands show the inverse behavior. The team also investigated interfacial carrier transfer in binary nanocrystal superlattices, wherein nanocrystal of two different sizes assemble into an organized structure. Such structures had previously been assembled from nanocrystals capped with synthesis ligands, but those structures lacked electronic functionality. The team demonstrated an approach for ligand exchange at a liquid-air interface that enables strong electronic coupling between nanocrystals while maintaining the long range order of the lattice. Carrier transfer between nanocrystals can then proceed on picosecond (trillionth of a second) time scales. In related work, the team also elucidated the dependence of carrier dynamics on nanocrystal size, crystal phase, and ligand length for oxide and chalcogenide-sensitized oxide nanocrystal assemblies with potential applications in photovoltaics and photocatalysis. Collectively, this project has provided new fundamental understanding of nanocrystal assemblies and their associated carrier dynamics that could help to enable future optoelectronic devices.
Detailed research results have been disseminated to the research community and are also accessible to the general public. This grant resulted in 10 publications in peer-reviewed journals. Research was also presented at more than 10 national and international conferences.
This grant provided partial support for education and training of 6 PhD students. Two of these went on to prestigious Director’s Postdoctoral Fellowships at US national laboratories (Argonne, NREL), one works in industry on development of manufacturing tools for the semiconductor industry, and the others are completing their thesis work. Additionally, 1 undergraduate student participated in this project, and she is currently a student in an MS program at Imperial College London on Sustainable Energy Futures.
Last Modified: 11/30/2017
Modified by: Jason B Baxter
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