Electrolyte-Induced Band Bending and Barrier Tuning to Enhance Photodetection in Inkjet-Printed Organic–Inorganic Heterojunctions

IF 7.8 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
ACS Applied Materials & Interfaces Pub Date : 2026-10-21 Epub Date: 2026-10-07 DOI:10.1021/acsami.6c12401
Manvendra Singh, Mohammed Hadhi Pazhaya Puthanveettil, Subho Dasgupta
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引用次数: 0

Abstract

Hybrid organic–inorganic heterojunctions have attracted considerable interest in optoelectronic applications, as they combine the excellent electronic transport of inorganic semiconductors with the ease of processing and tunability of organic conductors. While the performance of such heterojunctions is strongly governed by their built-in electric field and interfacial band alignment, strategies for actively tuning these parameters in printed bulk heterojunctions have remained largely unexplored. In this regard, here we show an inkjet-printed bulk heterojunction diode with semiconducting amorphous indium gallium oxide (a-IGO) and conducting poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS), whose interfacial barrier can be dynamically modulated by a solvent (dimethyl sulfoxide, DMSO) or a composite solid polymer electrolyte (CSPE). Systematic studies of pristine, DMSO-treated, and CSPE-treated devices reveal that DMSO enhances charge transport in PEDOT:PSS, while mobile ions of CSPE penetrate the polymer matrix and accumulate at the heterojunction interface. Capacitance–voltage measurements show that ionic screening increases the built-in potential from 0.36 to 0.70 eV by inducing additional band bending within a-IGO. Consequently, the off-current decreases by more than two orders of magnitude, accompanied by a substantial enhancement in rectification ratio. The strengthened junction field promotes efficient separation of photogenerated carriers under ultraviolet illumination, increasing the photosensitivity from 103 to beyond 106 while achieving a responsivity of 80 A/W, a specific detectivity of 0.25 × 1012 Jones, and an external quantum efficiency of 27200%. This elevated built-in potential further enables zero-biased ultraviolet photodetection with a photosensitivity of ∼104 and a responsivity of 45 mA/W. Furthermore, a three-terminal electrolyte-gated device can demonstrate ion-induced modulation of the interfacial barrier, enabling a transition from rectifying to near-Ohmic behavior and thereby realizing a tuneable diode. This electrolyte-assisted ionic-modulation strategy enables reconfigurable hybrid heterojunctions for next-generation, energy-efficient sensing and multifunctional optoelectronic applications.

电解质诱导能带弯曲和势垒调谐增强喷墨印刷有机-无机异质结的光探测
有机-无机杂化异质结结合了无机半导体优异的电子输运特性和有机导体的易加工性和可调性,在光电应用领域引起了人们极大的兴趣。虽然这种异质结的性能受到其内置电场和界面带对齐的强烈影响,但在印刷体异质结中主动调整这些参数的策略在很大程度上仍未被探索。在这方面,我们展示了一种具有半导体非晶氧化铟镓(a- igo)和导电聚(3,4-乙烯二氧噻吩):聚苯乙烯磺酸盐(PEDOT:PSS)的喷墨印刷体异质结二极管,其界面势垒可以被溶剂(二甲基亚砜,DMSO)或复合固体聚合物电解质(CSPE)动态调制。对原始装置、DMSO处理装置和CSPE处理装置的系统研究表明,DMSO增强了PEDOT:PSS中的电荷输运,而CSPE的移动离子穿透聚合物基体并在异质结界面积聚。电容电压测量表明,离子筛选通过诱导a-IGO内额外的带弯曲,将内置电位从0.36增加到0.70 eV。因此,关闭电流减少了两个数量级以上,伴随着整流比的大幅提高。增强的结场促进了光生载流子在紫外线照射下的有效分离,光敏度从103提高到106以上,响应度达到80 a /W,比探测率为0.25 × 1012 Jones,外量子效率为27200%。这种升高的内置电位进一步实现了零偏紫外光检测,光敏性为~ 104,响应率为45 mA/W。此外,三端电解质门控器件可以演示离子诱导的界面势垒调制,从而实现从整流到近欧姆行为的过渡,从而实现可调谐二极管。这种电解质辅助离子调制策略为下一代节能传感和多功能光电应用提供了可重构的混合异质结。
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来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
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