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中国物理学会期刊

基于自组装有机层异质结的高灵敏近红外光电晶体管及其血氧检测应用

Highly Sensitive Near-Infrared Phototransistors Based on Self-Assembled Organic Layer Heterojunction for Blood Oxygen Detection

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  • 有机近红外光探测器在柔性可穿戴系统中展现出独特适配性,其中光电晶体管因内禀的光门控增益特性备受期待。然而,窄带隙给体中激子解离驱动力不足与有机半导体中激子扩散长度短的叠加效应,导致光生电荷产生与分离效率双低,光门控效应难以充分激活。因此,引入高效激子解离界面是突破近红外有机光电晶体管灵敏度瓶颈的必要途径。本文通过液面自组装转移法构筑了PDPPBTT/PC61BM层异质结,并基于底栅顶接触晶体管架构,系统探究了异质结界面在光生激子解离、电荷俘获及沟道电导调制中的关键作用。在该构型中,P型聚合物半导体PDPPBTT同时作为近红外光吸收层与空穴传输沟道,PC61BM作为电子受体层,二者之间形成的给受体异质结界面为光生激子的高效解离及电子-空穴的空间分离提供了强劲驱动力。材料表征与电学测试结果表明,光生电子可有效转移至PC61BM受体层及界面陷阱态中,形成长寿命空间分离电荷,进而诱导显著的光门控效应,持续调控PDPPBTT沟道内空穴浓度,实现光电流信号的高效放大。得益于上述界面协同增益机制,该器件在近红外光照下展现出优异的光探测性能:响应度最高达1.26×106 A·W-1,在暗电流散粒噪声限制下估算的比探测率达6.96×1015 Jones,响应上升和下降时间分别为0.26 s和0.21 s。进一步地,利用该器件成功实现了透射式光电容积脉搏波信号的采集,并基于双波长PPG信号对血氧饱和度进行了初步估算。上述结果充分表明,给受体层异质结界面调控是突破近红外有机光电晶体管探测性能瓶颈的有效策略,并为其在微弱生理信号检测中的实际应用提供了坚实的实验依据。

     

    Near-infrared organic photodetectors are highly attractive for flexible wearable systems, with organic phototransistors offering particular promise due to their intrinsic photogating gain that enables amplification of weak optical signals. However,the performance of such devices is often constrained by the limited driving force for exciton dissociation in narrow-bandgap donors and the short exciton diffusion length typical of organic semiconductors, both of which hinder efficient photocarrier generation and separation and subsequently suppress the photogating effect. To overcome this sensitivity bottleneck, the introduction of a well-designed excitondissociation interface is critical. In this work, we fabricate a PDPPBTT/PC61BM layer heterojunction via self-assembly transfer and integrate it into a bottom-gate, top-contact transistor architecture. We systematically investigate the role of this heterojunction interface in facilitating exciton dissociation, charge trapping, and modulation of channel conductance. The p-type polymer PDPPBTT serves a dual function as both the near-infrared absorber and the hole-transporting channel, while PC61BM acts as the electron-accepting layer. The resulting donor-acceptor interface provides a substantial driving force for exciton dissociation and enables efficient spatial separation of electrons and holes. Optical and electrical characterization reveal that photogenerated electrons are transferred to the PC61BM layer and interfacial trap states, forming longlived negative charges that are effectively separated from holes. These trapped charges induce a pronounced photogating effect, which continuously modulates the hole density in the PDPPBTT channel and significantly boosts the photocurrent. Under near-infrared illumination, the device exhibits a maximum responsivity of 1.26×106 A·W-1 and a specific detectivity of 6.96×1015 Jones, estimated under the dark-current shot-noise limit, with rise and fall times of 0.26 s and 0.21 s, respectively. Furthermore, the device is capable of recording transmissive photoplethysmographic (PPG) signals, allowingfor a preliminary estimation of blood oxygen saturation through dual-wavelength PPG measurements. Collectively, these findings demonstrate that engineering donor- acceptor layer heterojunctions offers an effective route to overcoming the performance limitations of near-infrared organic phototransistors and provides a solid experimental foundation for their application in detecting weak physiological optical signals.

     

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