Compound having condensed polycyclic structure, organic thin film for light-receiving device, and light-receiving device

A compound with a fused polycyclic structure addresses the challenges of miniaturization, resolution, and light utilization in image sensors by enhancing charge transport and thermal stability in organic thin films, resulting in improved dark current characteristics and conversion efficiency.

JP2025040963APending Publication Date: 2025-03-25HODOGAYA CHEMICAL CO LTD
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Patent Information

Application Number
JP2024154975
Authority / Receiving Office
JP · JP
Patent Type
Applications
Current Assignee / Owner
Priority Date
2023-09-12
Filing Date
2024-09-09
Publication Date
2025-03-25

AI Technical Summary

Technical Problem

Existing image sensors face challenges in miniaturization, resolution, and light utilization due to the use of inorganic materials and prism-based systems, while organic materials offer potential but require improvements in charge transport, thermal stability, and dark current characteristics.

Method used

A compound with a fused polycyclic structure, represented by a specific general formula, is developed, which forms an organic thin film with excellent heat resistance, charge transport properties, and dark current characteristics, suitable for use as an electron blocking layer in photoreceptors.

Benefits of technology

The compound and its organic thin film significantly improve the dark current characteristics and conversion efficiency of photoreceptors, making them suitable for high-performance image sensors and optical sensors.

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Abstract

To provide a compound useful as a charge-blocking material for a light-receiving device, and a light-receiving device having excellent charge transport properties, heat resistance, and the like by using an organic thin film containing the compound.SOLUTION: The present invention provides a compound having a condensed polycyclic structure represented by the following formula (1), wherein A represents a single bond, a substituted or unsubstituted aromatic hydrocarbon group or the like, and Ar1 and Ar2 each represent a substituted or unsubstituted aromatic hydrocarbon group or the like.SELECTED DRAWING: None
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