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多种方法提高全有机电子光致发光传感器性能:同时监测氧和 pH 值。

Multiple approaches for enhancing all-organic electronics photoluminescent sensors: simultaneous oxygen and pH monitoring.

机构信息

Ames Laboratory-USDOE and Department of Physics and Astronomy, Iowa State University, Ames, IA 50011, United States.

出版信息

Anal Chim Acta. 2013 May 17;778:70-8. doi: 10.1016/j.aca.2013.03.042. Epub 2013 Mar 26.

Abstract

Key issues in using organic light emitting diodes (OLEDs) as excitation sources in structurally integrated photoluminescence (PL)-based sensors are the low forward light outcoupling, the OLEDs' broad electroluminescence (EL) bands, and the long-lived remnant EL that follows an EL pulse. The outcoupling issue limits the detection sensitivity (S) as only ~20% of the light generated within standard OLEDs can be forward outcoupled and used for sensor probe excitation. The EL broad band interferes with the analyte-sensitive PL, leading to a background that reduces S and dynamic range. In particular, these issues hinder designing compact sensors, potentially miniaturizable, that are devoid of optical filters and couplers. We address these shortcomings by introducing easy-to-employ multiple approaches for outcoupling improvement, PL enhancement, and background EL reduction leading to novel, compact all-organic device architectures demonstrated for simultaneous monitoring of oxygen and pH. The sensor comprises simply-fabricated, directionally-emitting, narrower-band, multicolor microcavity OLED excitation and small molecule- and polymer-based organic photodetectors (OPDs) with a more selective spectral response. Additionally, S and PL intensity for oxygen are enhanced by using polystyrene (PS):polyethylene glycol (PEG) blends as the sensing film matrix. By utilizing higher molecular weight PS, the ratio τ0/τ100 (PL decay time τ at 0% O2/τ at 100% O2) that is often used to express S increases ×1.9 to 20.7 relative to the lower molecular weight PS, where this ratio is 11.0. This increase reduces to ×1.7 when the PEG is added (τ0/τ100=18.2), but the latter results in an increase ×2.7 in the PL intensity. The sensor's response time is <10s in all cases. The microporous structure of these blended films, with PEG decorating PS pores, serves a dual purpose. It results in light scattering that reduces the EL that is waveguided in the substrate of the OLEDs and consequently enhances light outcoupling from the OLEDs by ~60%, and it increases the PL directed toward the OPD. The multiple functional structures of multicolor microcavity OLED pixels/microporous scattering films/OPDs enable generation of enhanced individually addressable sensor arrays, devoid of interfering issues, for O2 and pH as well as for other analytes and biochemical parameters.

摘要

在结构集成的光致发光(PL)传感器中使用有机发光二极管(OLED)作为激发源的关键问题是正向光外耦合率低、OLED 宽的电致发光(EL)带以及紧随 EL 脉冲的长寿命残余 EL。外耦合问题限制了检测灵敏度(S),因为只有标准 OLED 内产生的约 20%的光可以正向外耦合并用于传感器探头激发。EL 宽带会干扰对分析物敏感的 PL,导致背景降低 S 和动态范围。特别是,这些问题阻碍了设计紧凑的传感器,这些传感器潜在地是可小型化的,且没有光学滤波器和耦合器。我们通过引入易于采用的多种方法来改善外耦合、增强 PL 和降低背景 EL,从而解决了这些问题,这些方法为同时监测氧和 pH 提供了新颖、紧凑的全有机器件结构。该传感器由简单制造的、定向发射的、更窄带的多色微腔 OLED 激发和基于小分子和聚合物的有机光电探测器(OPD)组成,具有更具选择性的光谱响应。此外,通过使用聚苯乙烯(PS):聚乙二醇(PEG)混合物作为传感膜基质,增强了氧的 S 和 PL 强度。通过使用更高分子量的 PS,通常用于表示 S 的 PL 衰减时间 τ在 0% O2/τ在 100% O2 的比值 τ0/τ100 增加了×1.9 至 20.7 倍,相对于低分子量 PS,当添加 PEG 时,该比值减小至×1.7(τ0/τ100=18.2),但后者会使 PL 强度增加×2.7。在所有情况下,传感器的响应时间都<10s。这些混合膜的微孔结构,PEG 修饰 PS 孔,具有双重作用。它导致光散射,减少在 OLED 衬底中导波的 EL,从而使 OLED 的光外耦合增强约 60%,并增加指向 OPD 的 PL。多色微腔 OLED 像素/微孔散射膜/OPD 的多功能结构可以产生增强的、可单独寻址的传感器阵列,不存在干扰问题,可用于 O2 和 pH 以及其他分析物和生化参数。

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