Pressure-modulated intermolecular charge transfer in a cocrystal to achieve tunable luminescence.

Spectrochim Acta A Mol Biomol Spectrosc

Key Laboratory of Quantum Materials Under Extreme Conditions in Shandong Province, School of Physical Science and Information Technology, Liaocheng University, Liaocheng 252000, China. Electronic address:

Published: January 2026


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Cocrystal engineering offers the opportunity to achieve noncovalent synthesis of functional molecules with tunable luminescent features. In this study, Pe-4F2CN co-crystal was fabricated by using perylene (Pe) and tetrafluoroterephthalonitrile (4F2CN) through charge-transfer (CT)-induced assembly. The co-crystal exhibits two distinct emission bands and pronounced piezochromic properties, achieving the tunable luminescence from yellow to red upon compression. By the analysis of crystal structure and high-pressure IR spectroscopy combined with theoretical calculations, it revealed that the enhanced π-π and C-H···N interactions would regulate the charge-transfer process, thereby leading to the redshifts in photoluminescence (PL) and decreased emission intensity. This research not only demonstrates a novel approach to achieving tunable luminescence through pressure modulation, but also deepens the understanding of the relationship between intermolecular interactions and photophysical properties, which provides further guidance for the design of piezochromic materials.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.saa.2025.126718DOI Listing

Publication Analysis

Top Keywords

tunable luminescence
12
achieving tunable
8
pressure-modulated intermolecular
4
intermolecular charge
4
charge transfer
4
transfer cocrystal
4
cocrystal achieve
4
tunable
4
achieve tunable
4
luminescence cocrystal
4

Similar Publications

Circularly polarized luminescence (CPL) has emerged as a critical technology for anticounterfeiting and optical display applications due to its unique chiroptical properties. We report a multicolor CPL-emitting elastomeric film (P37/PSK@SiO-PDMS) that synergistically combines chiral helical polyacetylene (P37) and a surface-engineered perovskite (PSK@SiO) through hydrogen-bond-directed assembly. Confinement within the PDMS matrix drives P37 to self-assemble into a chiral supramolecular structure through hydrogen bonding, inducing a chiroptical inversion.

View Article and Find Full Text PDF

Covalent organic frameworks (COFs) have been emerging as versatile reticular materials due to their tunable structures and functionalities, enabled by precise molecular engineering at the atomic level. While the integration of multiple components into COFs has substantially expanded their structural complexity, the strategic engineering of diverse functionalities within a single framework the random distribution of linkers with varying lengths remains largely unexplored. Here, we report a series of highly crystalline mixed-length multivariate COFs synthesized using azobenzene and bipyridine as linkers, where tuning the ratio of linkers and incorporating palladium effectively modulates the balance between near-infrared (NIR) light absorption and catalytic sites for NIR-generation of hydrogen peroxide (HO).

View Article and Find Full Text PDF

The formation of heterostructure interfaces from quantum dots (or nanocrystals) and lower-dimensional (2D or quasi-2D) materials enables interfacial and optoelectronic property tuning. However, this strategy has not been sufficiently characterized, for example, the application of cesium halide nanocrystals to quasi-2D perovskite structures is underexplored, and the mechanisms of the resulting structural modifications and specific nanocrystal roles are not fully understood. Herein, the effects of postsynthetically surface-modifying quasi-2D perovskite films with CsX ( = Cl, Br, I) nanocrystals are examined to bridge this gap.

View Article and Find Full Text PDF

Ultralow-Cost Lacunary Metal-Oxo Framework Enables Efficient and Stable Organic Solar Cells.

Angew Chem Int Ed Engl

September 2025

Department of Material Science & Engineering, City University of Hong Kong, Kowloon, 999077, Hong Kong P.R. China.

Organic solar cells (OSCs) with p-i-n architecture usually exhibit decent efficiency due to the easily tunable energy levels of organic interfacial layers (ILs). However, their operational lifetime is limited by the morphological instability of organic ILs especially the electron-transporting layer (ETL) that shows strong self-aggregation tendency. Besides, organic ETLs are confronted with significant challenges including large batch-to-batch variations and high costs.

View Article and Find Full Text PDF

Helically ordered chiral super spaces enable optical chirality in hybrid organic-inorganic perovskite crystals.

J Colloid Interface Sci

September 2025

Department of Advanced Materials Engineering for Information & Electronics, Kyung Hee University, Gyeonggi-do 17104, Republic of Korea. Electronic address:

We present a supramolecular templating strategy for inducing chirality in hybrid perovskites via confined crystallization within chiral super spaces-nanoconfined, helically ordered cavities formed by the self-assembly of achiral bent-core molecules with chiral additives. Upon removal of the additives, the resulting porous films retain permanent chirality. Quasi-2D hybrid organic-inorganic perovskites crystallized within these templates exhibit distinct chiroptical activity, including mirror-image circular dichroism and circularly polarized light emitting (CPLE), with CPLE dissymmetry factors reaching up to 1.

View Article and Find Full Text PDF