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Eliza Wieman

Publications and source records attributed to Eliza Wieman.

2 recordsLinked to original sources

Tracking thermal transport in colloidal quantum dot films using in-situ time-resolved X-ray diffraction

Colloidal quantum dots (QDs) and their thin-films are increasingly used in electronic and photonic devices replacing traditional bulk semiconductors. However, thermal properties of the QDs are comparatively underexplored relative to device development efforts. This study shows the use of time-resolved X-ray diffraction as a contact-free method to probe the thermal response of QDs in device-like environments, providing in-situ insights for future thermal management strategies. Through the extraction of Debye-Waller Factors on a sub-nanosecond timescale, we use time-resolved X-ray diffraction to directly capture the heating and cooling of core/shell CdSe/CdS QDs following pulsed optical excitation. In a QD thin-film that actively provides optical gain, the thermal conductivity is found to be as low as 0.55 $\mathrm{W\,m^{-1}\,K^{-1}}$, because of the poor heat flow within close-packed QD solids. For QDs dispersed in liquids, interfacial thermal conductance is found to dominate the thermal relaxation with a conductance on the order of 15 $\mathrm{MW\,m^{-2}\,K^{-1}}$.

cond-mat.mes-hall

Ultrafast symmetry control in photoexcited quantum dots

Symmetry control is essential for realizing unconventional properties, such as ferroelectricity, nonlinear optical responses, and complex topological order, thus it holds promise for the design of emerging quantum and photonic systems. Nevertheless, fast and reversible control of symmetry in materials remains a challenge, especially for nanoscale systems. Here, we unveil reversible symmetry changes in colloidal lead chalcogenide quantum dots on picosecond timescales. Using a combination of ultrafast electron diffraction and total X-ray scattering, in conjunction with atomic-scale structural modeling and first-principles calculations, we reveal that symmetry-broken lead sulfide quantum dots restore to a centrosymmetric phase upon photoexcitation. The symmetry restoration is driven by photoexcited electronic carriers, which suppress lead off-centering for about 100 ps. Furthermore, the change in symmetry is closely correlated with the electronic properties as shown by transient optical measurements. Overall, this study elucidates reversible symmetry changes in colloidal quantum dots, and more broadly defines a new methodology to optically control symmetry in nanoscale systems on ultrafast timescales.

cond-mat.mes-hall