Quantum Confined Colloidal Copper-Chalcogenide Based Hetero-Nanorods
Celso de Mello Donega a
a Utrecht University, Condensed Matter and Interfaces, Debye Institute for nanomaterials science, Netherlands
Materials for Sustainable Development Conference (MATSUS)
Proceedings of MATSUS23 & Sustainable Technology Forum València (STECH23) (MATSUS23)
#NCFun23 - Fundamental Processes in Nanocrystals and 2D Materials
VALÈNCIA, Spain, 2023 March 6th - 10th
Organizers: Valerio Pinchetti and Shalini Singh
Invited Speaker, Celso de Mello Donega, presentation 044
DOI: https://doi.org/10.29363/nanoge.matsus.2023.044
Publication date: 22nd December 2022

Colloidal semiconductor heteronanocrystals (HNCs) exhibit unique optoelectronic properties that are inaccessible to single-component NCs, making them promising materials for a wide range of applications. The optoelectronic properties of HNCs are determined not only by the bandgap and band alignment of its constituent materials but also by their morphology and heteroarchitecture.1 Applications requiring efficient charge separation (e.g., photovoltaics and photocatalysis) and polarized emission greatly benefit from anisotropic morphologies, such as heteronanorods. Most of the work on heteronanorods has focused on Cd-chalcogenide-based HNCs. However, given the toxicity of Cd, the potential of these materials for large scale applications is limited.

Copper-chalcogenide based NCs have attracted increasing attention as promising alternatives for Cd- and Pb-chalcogenide NCs due to their low toxicity, large absorption cross-sections across a broad spectral range, composition-dependent band gaps in the 1 to 2.5 eV range, and photoluminescence tunability, spanning a spectral window that extends from the UV to the NIR depending on the NC size and composition.2,3

Several synthetic strategies have been used in the quest for high-quality colloidal copper chalcogenide based HNCs. The most promising ones are based on the multistage approach, which allows the combination of different synthesis techniques (e.g., cation exchange4,5 or seeded growth6-9) in a sequential manner in order to achieve the targeted preparation of colloidal HNCs. In this talk, I will discuss a selection of recent examples, chosen to illustrate specific synthesis strategies: CuInSe2/CuInS2 dot core/rod shell heteronanorods,4 Cu1.8S-based multicomponent axially segmented heteronanorods,5 CuInS2/ZnS dot core/rod shell heteronanorods,6 and Janus-type Cu2‒xS/CuInS2 and Cu2−xS/ZnS heteronanorods.8,9 I will show that by combining the design principles of post-synthetic heteroepitaxial seeded growth and nanoscale cation exchange into multistage synthesis strategies one can potentially gain access to a plethora of Cu-chalcogenide-based multicomponent heteronanorods with diameters in the quantum confinement regime.

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