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DTSTART;TZID=America/Los_Angeles:20251106T120000
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DTSTAMP:20260613T102336
CREATED:20251031T170505Z
LAST-MODIFIED:20251031T170505Z
UID:41119-1762430400-1762434000@www.chemistry.ucla.edu
SUMMARY:Chem 218 Student Exit Talk: Diego Garcia Vidales
DESCRIPTION:Conjugated polymers are electronic materials that combine semiconductor-like behavior with mechanical flexibility\, solution processability\, and chemical tunability. However\, their intrinsically low carrier density and heterogeneous microstructure pose challenges for efficient charge transport. To mitigate the low carrier density\, we incorporate carriers via chemical doping into semiconducting polymer thin films. This talk investigates how chemical doping and polymer morphology jointly dictate charge transport across molecular\, mesoscale\, and macroscopic length scales\, with implications for electronic and thermoelectric applications. We characterize the doped films using techniques such as four-point probe conductivity\, Seebeck coefficient measurements\, Hall effect measurements\, X-ray scattering\, and spectroscopy. We first study how the hygroscopicity of the counterions in doped polymer thin films can significantly influence electronic transport by enabling water uptake. We show that absorbed moisture introduces trap states and suppresses carrier mobility\, underscoring the need to consider environmental stability and dopant chemistry when chemically doping polymer devices. Second\, we dope the same polymer with four molecular dopants and find that the choice of dopant affects not only carrier generation but also structural ordering\, crystallite connectivity\, and Coulomb trapping\, leading to distinct charge-transport pathways and thermoelectric performance. Importantly\, we show that electrical conduction can be enhanced without sacrificing Seebeck coefficient either by mitigating Coulomb interactions or by activating charge transport through previously amorphous regions. Finally\, we isolate the role of the polymer microstructure by tuning the polymer crystallinity by controlling regioregularity. We find that higher intrinsic crystallinity promotes greater polaron delocalization and faster local transport\, and that dopant- induced crystallization in amorphous regions can enhance mesoscale connectivity. The combination of high local order and doping-enabled long-range connectivity is essential for maximizing mobility and thermoelectric performance. Overall\, this work establishes structure–doping–transport relationships in doped conjugated polymers and highlights design principles for next-generation polymer conductors: choose dopants that both minimize trapping and enable structural reinforcement\, and engineer polymer microstructure to balance local order and mesoscale connectivity.
URL:https://www.chemistry.ucla.edu/events/chem-218-student-exit-talk-diego-garcia-vidales/
LOCATION:Collaboratory Yoo Seminar & Conference Hall YH4222 
CATEGORIES:Chem 218 Student Exit Seminar,Physical
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DTSTART;TZID=America/Los_Angeles:20251106T160000
DTEND;TZID=America/Los_Angeles:20251106T170000
DTSTAMP:20260613T102336
CREATED:20250924T230612Z
LAST-MODIFIED:20251008T200047Z
UID:40686-1762444800-1762448400@www.chemistry.ucla.edu
SUMMARY:Houk-Jung Organic Colloquium 247 - Prof. Colleen Scott
DESCRIPTION:
URL:https://www.chemistry.ucla.edu/events/houk-jung-organic-colloquium-247-prof-colleen-scott/
LOCATION:Collaboratory Yoo Seminar & Conference Hall YH4222 
CATEGORIES:Organic Colloquium
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