Probing electrical double layer via triboelectric charge transfer

摩擦电效应 材料科学 纳米技术 开尔文探针力显微镜 导电体 化学物理 静电学 电荷(物理) 纳米发生器 接触带电 静电感应 基质(水族馆) 表征(材料科学) 神经形态工程学 光电子学 分子动力学 电解质 拉曼光谱 纳米尺度 纳米机电系统 工作(物理) 电荷 电介质 双层(生物学) 空间电荷 离子 数码产品 记忆电阻器 离子键合 纳米孔 生物电子学
作者
Wei Yu,Xiang Li,Yu Gu,Lian Ding,Xiang Gao,Zhongqiang Zhang,Carita Kvarnström,Johan Bobacka,Ari Ivaska,Zhong‐Qun Tian,Zhong Lin Wang,Di Wei
出处
期刊:Nature Communications [Nature Portfolio]
卷期号:17 (1): 402-402 被引量:6
标识
DOI:10.1038/s41467-025-67094-9
摘要

The nanoscale electrical double layer (EDL) governs macroscopic phenomena such as ion adsorption and reaction kinetics, serving as a fundamental determinant in diverse applications ranging from sensing, and catalysis, to energy storage. While classical EDL models primarily describe conductive interfaces, most naturally occurring EDLs form at non-conductive surfaces in liquid environment, where characterization remains fundamentally challenging due to the constraints of conventional techniques. Here, we present a triboelectric nanogenerator (TENG)-based triboelectric charge transfer probe that utilizes the intrinsic solid-liquid contact electrification (CE) process to operando monitor the formation and evolution of the EDL at non-conductive interfaces. This bias-free and electrode-independent approach enables direct probing of interfacial charge dynamics fundamentally inaccessible to conventional electrochemical approaches constrained by conductive substrate dependencies and external potential requirements. This method also reveals distinct EDL behaviors, particularly in electrolytes with asymmetric ion sizes at concentrations exceeding 10-1 M and at non-conductive interfaces. Its fundamental mechanism and measurement precision were rigorously validated via atomic force microscopy, Kelvin probe force microscopy, surface-enhanced Raman spectroscopy, and molecular dynamics simulations, establishing a robust analytical platform and theoretical basis for EDL studies. This work introduces a CE-based methodology for direct triboelectric charge characterization on dielectric surfaces, overcoming conventional conductive substrate limitations. By integrating classical EDL theory with triboelectric frameworks, we establish models resolving interfacial charge dynamics across diverse solid-liquid interfaces, including high ionic strength regimes. It confirms material-agnostic applicability. This paradigm simultaneously advances fundamental EDL mechanisms and enables programmable charge manipulation for next-generation iontronic power, sensing, and neuromorphic devices. A triboelectric nanogenerator-based probe monitors the formation and evolution of the electrical double layer at nonconductive interfaces via solid-liquid contact electrification.
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