4.6 Article

Origin of Intraband Optical Transitions in Ag2Se Colloidal Quantum Dots

期刊

JOURNAL OF PHYSICAL CHEMISTRY C
卷 125, 期 31, 页码 17556-17564

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.1c05371

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资金

  1. National Science Foundation (NSF) [ECCS-1809064]
  2. Department of Defense (DOD) Office of Naval Research [N00014-20-1-2231]
  3. MRI programs of the National Science Foundation [DMR-1420073, DMR-0923251]
  4. Imaging and Surface Science Facilities of Advanced Science Research Center at the Graduate Center of CUNY

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In the past 30 years, scientists have utilized quantum confinement to obtain size-tunable interband optical transitions in colloidal quantum dots and have explored intraband optical transitions in Ag2Se CQDs for potential applications in the infrared region. By synthesizing environmentally benign Ag2Se CQDs, researchers have demonstrated a crossover from interband to intraband optical absorption, providing insights into the size-dependent properties and factors influencing stable electron states and tunable intraband absorption in the mid-wave infrared region.
In the past 30 years, scientists have utilized quantum confinement to obtain size-tunable interband optical transitions in colloidal quantum dots (CQDs) and implemented them in various optoelectronic applications throughout the electromagnetic spectrum. The infrared (IR) region is particularly important with applications in telecommunications, night-time surveillance, and satellite imaging for agricultural water conservation. Nearly all progress with CQDs in the IR region has been achieved using interband transitions in Pb- and Hg-based heavy metal compounds with narrow band gaps. An alternative approach is to exploit intraband optical transitions originating from external- or self-dopants, which could expand the library of materials for IR-optoelectronic devices to include nontoxic materials. Herein, we present a simple two-precursor hot-injection (170 degrees C) synthesis of 2.6-6.5 nm diameter environmentally benign Ag2Se CQDs that exhibit a crossover from interband near-infrared (NIR) absorption to intraband mid-wave infrared (MWIR) absorption above a critical size of 5.1 nm. CQDs smaller than 5.1 nm are photoactive in the NIR, exhibiting multiple well-defined excitonic peaks and stable room-temperature emission in the NIR and short-wave infrared (SWIR) regions of the electromagnetic spectrum. Films cast from these CQDs and ligand-exchanged with ethanedithiol exhibit NIR photoconductivity. In contrast, CQDs larger than 5.1 nm exhibit MWIR absorbance. Compared to other synthetic methods that generate Ag2Se CQDs over a limited size range, our approach allows access to both ultrasmall and large Ag2Se CQDs, enabling a detailed study of the size-dependent interband to intraband optical transition. We compare the competing effects of quantum confinement, environmental Fermi level, and particle stoichiometry to provide guidelines for stable electron occupation of the 1S(e) state and obtain tunable intraband MWIR absorption.

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