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Open AccessDOI: 10.1007/s40843-025-3916-3Original Research

Circularly Polarized Light Detection in Achiral Organic Semiconductors via Chiral Plasmonic Resonance

Tianjin University

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Circularly Polarized Light Detection in Achiral Organic Semiconductors via Chiral Plasmonic Resonance
Graphical Abstract / Figure
Published In
SCIENCE CHINA Materials
Published:January 15, 2026Edition:Vol. 69, Issue 7 • pp. 100-112Citation:CHANG Wenxuan et al. (2026), SCIENCE CHINA Materials
Impact Factor3.5 (Q2 Scopus)
Source Journal中国科学: 材料

Key Takeaways & Executive Findings

  • • • Achieved a dissymmetry factor (g) of 0.35 at 515 nm in achiral organic semiconductors, a value comparable to or exceeding many intrinsically chiral systems, enabling high-contrast CPL discrimination without complex chiral synthesis. • • Nearly tenfold responsivity enhancement via chiral plasmonic resonance and hot-carrier injection, directly improving signal-to-noise ratio and sensitivity in photodetection, critical for low-light imaging and communication. • • Utilized a self-assembled monolayer of L-phenylalanine–modified gold nanoparticles, a solution-processable method that eliminates costly lithographic patterning and chiral HPLC separation, reducing manufacturing complexity and cost. • • The hybrid architecture merges plasmonic chirality with organic semiconductor versatility, offering a scalable platform for on-chip chiroptoelectronic and polarization-imaging technologies, addressing the scalability bottleneck of current CPL detectors.

Abstract

Circularly polarized light (CPL) detection is critical to emerging technologies in optical communication, chiral sensing, and bio-inspired imaging. However, current devices rely on intrinsically chiral semiconductors that are synthetically complex and costly to scale. Here, we demonstrate robust CPL detection in achiral organic semiconductors by exploiting chiral plasmonic resonance (CPR). A self-assembled monolayer of L-phenylalanine–modified gold nanoparticles imparts optical chirality to adjacent semiconductors while enhancing photocurrent through plasmon-induced hot-carrier processes. The resulting hybrid devices exhibit nearly tenfold responsivity enhancement and a high dissymmetry factor of 0.35 at 515 nm. Mechanistic analysis reveals a field-driven, hot-carrier-assisted route to helicity sensitivity. This solution-processable approach merges plasmonic chirality with organic semiconductor versatility, providing a scalable platform for next-generation on-chip chiroptoelectronic and polarization-imaging technologies.

1. Introduction

Conventional circularly polarized light (CPL) detection relies on bulky optical assemblies—polarizers, wave plates—that are fundamentally incompatible with on-chip miniaturization. Intrinsic CPL photodetectors based on inorganic metastructures or 2D materials demand costly lithography and strict geometric precision. Hybrid perovskites, despite high performance, degrade under ambient conditions. Organic semiconductors offer molecular tunability and solution processability, but intrinsically chiral OSCs are rare, requiring multistep asymmetric syntheses and chiral HPLC separation, severely limiting scalability.

This work circumvents the synthetic bottleneck by employing chiral plasmonic resonance (CPR) to impart optical chirality to achiral organic semiconductors. A self-assembled monolayer of L-phenylalanine–modified gold nanoparticles provides the chiral response and enhances photocurrent via hot-carrier injection. This approach achieves a dissymmetry factor of 0.35 at 515 nm and a tenfold responsivity enhancement, all through a solution-processable route. It directly addresses the scalability and cost barriers of existing CPL detectors, offering a practical path toward integrated chiroptoelectronic devices.

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Cite This Research Paper
CHANG Wenxuan, ZHANG Siyuan, SHEN Xianfeng, ZHU Rongjiao, LI Rongjin, HU Wenping (2026). Circularly Polarized Light Detection in Achiral Organic Semiconductors via Chiral Plasmonic Resonance. SCIENCE CHINA Materials. https://doi.org/10.1007/s40843-025-3916-3
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Frequently Asked Questions

What is the operational stability of the hybrid device under continuous illumination and ambient conditions?

The paper does not specify long-term stability data, but the use of achiral organic semiconductors and gold nanoparticles suggests potential robustness. However, organic semiconductors can degrade under UV exposure and oxygen; encapsulation would likely be required for commercial deployment.

How does the dissymmetry factor of 0.35 compare to state-of-the-art intrinsically chiral organic photodetectors, and what are the trade-offs?

A g-factor of 0.35 is competitive with many intrinsically chiral systems, which often range from 0.1 to 0.5. The trade-off is that the chiral response is induced by the plasmonic layer, which may limit spectral tunability and require precise nanoparticle assembly. However, the solution-processable method offers scalability advantages.

What is the external quantum efficiency (EQE) or specific detectivity of the device?

The paper reports a 'nearly tenfold responsivity enhancement' but does not provide absolute responsivity or EQE values. For practical applications, these metrics are essential to benchmark against commercial photodetectors.

Can this approach be extended to other achiral organic semiconductors beyond the one studied?

The principle is general: any achiral semiconductor with suitable energy alignment to accept hot carriers from gold nanoparticles could be used. However, the efficiency of hot-carrier injection depends on the interface and band alignment, so material-specific optimization is required.

What is the fabrication yield and reproducibility of the self-assembled monolayer of L-phenylalanine-modified gold nanoparticles?

The paper does not provide yield statistics. Self-assembly processes can be sensitive to surface preparation and concentration, but solution processing typically offers high uniformity. Scale-up would require rigorous process control to ensure consistent monolayer coverage and chiral response.

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