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Revisiting a (001)-oriented layered lead chloride templated by 1,2,4-triazolium: structural phase transitions, lattice dynamics and broadband photoluminescence.

Authors :
Mączka, Mirosław
Sobczak, Szymon
Ptak, Maciej
Smółka, Szymon
Fedoruk, Katarzyna
Dybała, Filip
Herman, Artur P.
Paraguassu, Waldeci
Zaręba, Jan K.
Kudrawiec, Robert
Sieradzki, Adam
Katrusiak, Andrzej
Source :
Dalton Transactions: An International Journal of Inorganic Chemistry; 4/28/2024, Vol. 53 Issue 16, p6906-6919, 14p
Publication Year :
2024

Abstract

This study revisits a (001)-oriented layered lead chloride templated by 1,2,4-triazolium, Tz<subscript>2</subscript>PbCl<subscript>4</subscript>, which recently has been an object of intense research but still suffers from gaps in characterization. Indeed, the divergent reports on the crystal structures of Tz<subscript>2</subscript>PbCl<subscript>4</subscript> at various temperatures, devoid of independent verification of chiral phases through second harmonic generation (SHG), have led to an unresolved debate regarding the existence of a low-temperature phase transition (PT) and the noncentrosymmetric nature of the low-temperature phase. Now, by combining differential scanning calorimetry, single-crystal X-ray diffraction, dielectric, as well as linear and nonlinear optical spectroscopies on Tz<subscript>2</subscript>PbCl<subscript>4</subscript>, we reveal a sequence of reversible PTs at T<subscript>1</subscript> = 361 K (phase I–II), T<subscript>2</subscript> = 339 K (phase II–III), and T<subscript>3</subscript> = 280 K (phase III–IV). No SHG activity could be registered for any of the four crystal phases, as checked by wide-temperature range SHG screening, supporting their centrosymmetry. The dipole relaxation processes indicate a decrease in activation energy with increasing temperature, from 0.60, 0.38, to 0.24 eV observed for phase IV (space group P2<subscript>1</subscript>/c), phase III (Pnma), and phase II (Cmcm), respectively. This change is interpreted as a result of the diminishing strength of H-bonds as the system transforms from phase IV to III and subsequently to II. The weaker H-bonds facilitate the reorientation of Tz<superscript>+</superscript> cations in the presence of an external electric field. The photoluminescence spectra of Tz<subscript>2</subscript>PbCl<subscript>4</subscript> reveal an intriguing interplay of narrow and broadband emission, linked respectively to free excitons and excitons trapped on defects. Notably, as the temperature decreases from 300 K to 16 K, both the emission bands exhibit distinctive blue and red shifts, indicative of increased in-plane octahedral distortion. This dynamic behaviour transforms the photoluminescence of Tz<subscript>2</subscript>PbCl<subscript>4</subscript> from greenish-blue at 300 K to yellowish-green at 13 K, enriching our understanding of 2D lead halide perovskites and highlighting the optoelectronic potential of Tz<subscript>2</subscript>PbCl<subscript>4</subscript>. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14779226
Volume :
53
Issue :
16
Database :
Complementary Index
Journal :
Dalton Transactions: An International Journal of Inorganic Chemistry
Publication Type :
Academic Journal
Accession number :
176784900
Full Text :
https://doi.org/10.1039/d4dt00406j