Synthesis and Optical Properties of Ag–Ga–S Quantum Dots

• Published in: physica status solidi (b) 2022-10, Vol.259 (10), p.n/a
• Main Authors: Azhniuk, Yuriy, Lopushanska, Bohdana, Selyshchev, Oleksandr, Havryliuk, Yevhenii, Pogodin, Artem, Kokhan, Oleksandr, Ehm, Alexander, Lopushansky, Vasyl, Studenyak, Ihor, Zahn, Dietrich R.T.
• Format: Article
• Language: English
• Subjects: colloidal synthesis; optical absorption; photoluminescence; quantum dots; Raman spectroscopy; X-ray diffraction; X-ray photoemission spectroscopy
• ISSN: 0370-1972; 1521-3951
• DOI: 10.1002/pssb.202100349

Ag–Ga–S quantum dots (QDs) are obtained by colloidal synthesis in aqueous solutions with glutathione ligands at mild conditions. The QDs can be assigned to metastable orthorhombic, rhombohedral, or rocksalt‐type phases, assuming a significant internal pressure within crystallites, while the conventional tetragonal AgGaS2 phase is less likely formed. Similarly to these metastable phases, the QDs reveal a relatively narrow indirect bandgap contrary to the wide and direct bandgap of tetragonal AgGaS2. Size‐selected fractions of the colloidal solutions are separated by repeated centrifuging with addition of 2‐propanol. The QD size is evaluated from atomic force microscopy, while the crystallite size determined using the Scherrer formula is underestimated. X‐ray photoemission spectroscopy reveals that the QD composition changes from nearly stoichiometric for the fraction with the largest QDs toward Ag deficient and S rich for smaller QDs. The synthesized QDs are characterized by the absorption edge blueshift with decreasing QD size. A blueshift of the photoluminescence (PL) peak with decreasing QD size is observed as well as a nonmonotonous size dependence of the PL intensity. Raman spectra of the Ag–Ga–S QDs are discussed compared to those of bulk crystals and a strong contribution of surface phonons is revealed. Ag–Ga–S quantum dots are obtained by colloidal synthesis in aqueous solutions with glutathione at mild conditions. Optical absorption edge and photoluminescence maximum of the size‐selected quantum dots shift towards higher energies with decreasing quantum dot size. Experimentally measured Raman spectra of the Ag–Ga–S quantum dots reveal a strong contribution of surface phonons.