Abstract

Near-infrared (NIR) circularly polarized light (CPL) photodetection is of great importance due to its broad application potential in bioimaging, wearable healthcare, optical communication, and advanced optoelectronic systems. In this study, a supramolecular chirality evolution strategy in chiral low-bandgap fused-ring conjugated molecules (LFCs) is presented for high-performance NIR CPL photodetection using Schottky barrier vertical organic field-effect transistors (SB-VOFETs). Halogen substitution combined with thermal annealing drives inversion and amplification of supramolecular chirality in enantiopure LFC thin films. F-substituted LFCs exhibit progressive domain growth and hierarchical ordering with increasing annealing temperature, whereas Cl-substituted LFCs show limited structural evolution above 150°C. These distinct crystallization behaviors directly correlate with chiroptical responses, with F-substituted LFCs achieving a maximum absorption dissymmetry factor (|gabs|) of ∼0.1. When integrated into SB-VOFETs, the optimized chiral films enable highly efficient NIR CPL photodetection, delivering a photocurrent dissymmetry factor (|gph|) of ∼0.1, a specific detectivity of 4.9 × 1011 Jones, an external quantum efficiency exceeding 900%, and a fast response time of ∼600 µs at 850 nm. These metrics represent the highest performance reported for NIR CPL. This study provides design guidelines for advancing high-performance chiral optoelectronic devices through the synergistic integration of atomic substitution, thermal annealing, and device architecture engineering.

Near-infrared (NIR) circularly polarized light (CPL) carries information that conventional light cannot, making it valuable for applications ranging from autonomous vehicle sensors and bioimaging to optical security and advanced communications. Detecting this light accurately, however, has remained difficult because the organic semiconductor films used in these devices often lose the molecular order needed to distinguish different polarization states.

A research team, led by Professor BongSoo Kim of the Department of Chemistry at UNIST and Professor Joon Hak Oh of Seoul National University has found a way to overcome that limitation. By controlling how chiral organic semiconductor molecules organize within thin films, the researchers significantly improved the films' ability to distinguish between left- and right-handed CPL. When incorporated into a photodetector, the optimized films delivered what the team reports as the highest performance yet achieved for NIR CPL detection.

Unlike conventional light detectors, CPL can distinguish between two different polarization states of light. This additional information can reveal not only an object's shape but also properties, such as its surface composition or molecular structure, making the technology valuable for sensing and imaging applications. 

The researchers achieved the improvement by applying a simple thermal annealing process to thin films made from fluorine-substituted chiral organic semiconductor molecules. Rather than remaining randomly arranged, the molecules reorganized into larger, more ordered crystal domains. This more ordered molecular arrangement strengthened the film's interaction with CPL.

As a result, the film's ability to selectively absorb CPL increased more than threefold after annealing at 250°C, with its absorption dissymmetry factor rising from approximately 0.03 to 0.1. Structural analysis confirmed that the annealed films adopted a highly ordered molecular arrangement closely resembling that of single crystals.

The researchers also discovered an unexpected effect. As the molecular packing reorganized, the film reversed the polarization it preferentially absorbed, demonstrating that heat treatment could control not only the strength but also the handedness of the material's optical response. By comparison, similar films containing chlorine instead of fluorine showed little structural change above 150°C and exhibited lower polarization selectivity after annealing.

To turn these improved optical properties into measurable electrical signals, the team integrated the optimized films into a vertical organic transistor. The device architecture efficiently collected and amplified charges generated by incoming light, allowing the detector to fully capitalize on the improved molecular organization.

The resulting photodetector achieved a photocurrent dissymmetry factor of 0.1 at a wavelength of 850 nanometers, demonstrating excellent discrimination between left- and right-handed CPL. It also recorded a specific detectivity of 4.9 × 10¹¹ Jones, an external quantum efficiency of up to 909%, and a response time of less than 600 microseconds—the highest performance reported to date for NIR CPL detectors.

“We found that simply controlling how the molecules organize within a thin film can dramatically improve how the materials respond to CPL,” the research team said. “We hope this strategy will help advance next-generation optical sensors and imaging technologies that rely on precise light detection.”

Their findings were published online in  Advanced Science on June 28, 2026. The research was supported by the National Research Foundation of Korea (NRF) and the Ministry of Science and ICT (MSIT).

Journal Reference

Jaeyong Ahn, Kwangmin Kim, Sangwook Lee,   et al ., “Thermally Driven Supramolecular Chirality Evolution in Low-Bandgap Fused-Ring Conjugated Molecules for High-Performance NIR Circularly Polarized Light Detection,”   Adv. Sci., (2026).