Document Type
Thesis
Date of Award
Spring 4-23-2025
Keywords
Quantum Dots, Shell, Perovskite, Photoluminescence, CsPbBr3, PbS, Stability, Passivation, PLQY
Degree Name
Chemistry (BA, BS)
Department
CHEMISTRY
First Advisor
Dr. Yiliang Luan
Second Advisor
Dr. Nikolay Dimitrov
Series
Science and Mathematics
Abstract
Halide perovskite quantum dots (HPQDs) have attracted considerable attention for optoelectronic applications due to their outstanding optical properties, including high photoluminescent quantum yield (PLQY), tunable band gap, high absorption coefficients, etc. However, their practical implementation is limited by poor stability under ambient conditions such as moisture, heat, and light. To overcome these challenges, surface passivation and shelling engineering have emerged as effective strategies to enhance HPQD stability by encapsulating their surface with a protective material. Conventional shelling techniques, however, often face limitations related to lattice mismatch and interfacial incompatibility. In this study, we report the successful synthesis of PbS@CsPbBr3 (shell@core) QDs via an in situ shelling process employing an activated sulfur precursor. This approach enables low-temperature shell growth which mitigates the thermal degradation of the CsPbBr3 QDs core. The resulting PbS@CsPbBr3 QDs exhibit enhanced PLQY and stability, while retaining their intrinsic spectral properties. Additionally, we systematically examined the influence of shelling stoichiometry and temperature on the structural and optical properties of the PbS@CsPbBr3 QDs. This work not only presents a robust strategy for stabilizing HPQDs but also offers valuable insights into the rational design of surface passivation methods.
Recommended Citation
Pitcher, Noah, "In Situ Synthesis of PbS Shell on CsPbBr3 QD for Enhanced Stability and Photoluminescence" (2025). Undergraduate Honors Theses. 50.
https://orb.binghamton.edu/undergrad_honors_theses/50