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BEGIN:VEVENT
DTSTART:20250113T193000Z
DTEND:20250113T203000Z
LOCATION:Clearihue (CLE) A127
SUMMARY:Chemistry Seminar - Brandi Cossairt
UID:20250113T193000Z-89554@events.uvic.ca
DTSTAMP:20240829T165504Z
URL:https://events.uvic.ca/chemistry/event/89554-chemistry-seminar-brandi
 -cossairt
CATEGORIES:Free,Lectures & seminars
LAST-MODIFIED:20241224T191221Z
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X-LIVEWHALE-TYPE:events
X-LIVEWHALE-ID:89554
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 t/80/crop/1/src_region/0\,25\,402\,428/7404_Brandi_Cossairt.rev.172497554
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X-LIVEWHALE-IMAGE-CAPTION:Brandi Cossairt
X-LIVEWHALE-SUMMARY:<p>\n  <strong><em>Discovering New Ways to Make and M
 odify Quantum Dots: Pushing the Frontiers of Precision Structure and Func
 tion</em></strong><br />\n  <br />\n  <a href="https://chem.washington.ed
 u/people/brandi-m-cossairt">Brandi Cossairt</a>\, Lloyd E. and Florence M
 . West Endowed Professor\, Department of Chemistry\, University of Washin
 gton<br />\n  <br />\n</p>\n<p>\n  Abstract: We are interested in develop
 ing colloidal nanocrystals for applications in classical and quantum ligh
 t technologies. Our approach leverages the extraordinary properties of na
 noscale systems and applies foundational design principles from molecular
  inorganic chemistry. In this talk\, we will examine strategies to overco
 me challenges in atomically precise synthesis and single particle placeme
 nt by exploiting the extremes of nanocrystal size. First\, the formation 
 of kinetically persistent cluster molecules as intermediates in the nucle
 ation of colloidal nanocrystals makes these materials of great interest f
 or determining and controlling mechanisms of crystal growth. These cluste
 rs are also high-fidelity models for understanding the structure\, bondin
 g\, and reactivity of larger nanocrystals\, which are characterized by en
 semble heterogeneity. The interconnection between structurally distinct m
 embers of these families\, as well as their interconversion and conversio
 n to larger nanocrystals\, will be discussed. Next\, producing scalable q
 uantum photonics platforms using colloidal QDs as single-photon emitters 
 is an outstanding challenge in quantum information science. We will explo
 re two methods to exploit QD size to facilitate the deterministic positio
 ning of single QDs into large arrays while maintaining their photostabili
 ty and single-photon emission properties. Specifically\, SiO2 and CdS she
 lling result in an increase in the QD physical size to allow precise posi
 tioning into ordered arrays using high-fidelity template-assisted self-as
 sembly and electrohydrodynamic inkjet printing. We show that single "colo
 ssal" QDs before and after assembly exhibit antibunching behavior at room
  temperature and can be deterministically positioned on photonic cavities
 .\n</p>
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