NanoPhotonics Centre, Cavendish Laboratory, Department of Physics, University of Cambridge, Cambridge CB30HE, U.K.
Department of Physics and Astronomy, University College London, London WC1E 6BT, U.K.
ACS Nano. 2022 Dec 27;16(12):21120-21128. doi: 10.1021/acsnano.2c09081. Epub 2022 Dec 5.
Conducting polymers are a key component for developing wearable organic electronics, but tracking their redox processes at the nanoscale to understand their doping mechanism remains challenging. Here we present an spectro-electrochemical technique to observe redox dynamics of conductive polymers in an extremely localized volume (<100 nm). Plasmonic nanoparticles encapsulated by thin shells of different conductive polymers provide actively tuned scattering color through switching their refractive index. Surface-enhanced Raman scattering in combination with cyclic voltammetry enables detailed studies of the redox/doping process. Our data intriguingly show that the doping mechanism varies with polymer conductivity: a disproportionation mechanism dominates in more conductive polymers, while sequential electron transfer prevails in less conductive polymers.
导电聚合物是开发可穿戴有机电子产品的关键组成部分,但在纳米尺度上跟踪它们的氧化还原过程以了解其掺杂机制仍然具有挑战性。在这里,我们提出了一种光谱电化学技术,用于观察极局部体积(<100nm)中导电聚合物的氧化还原动力学。由不同导电聚合物的薄壳包裹的等离子体纳米粒子通过切换其折射率提供主动调谐的散射颜色。表面增强拉曼散射与循环伏安法相结合,可对氧化还原/掺杂过程进行详细研究。我们的数据令人感兴趣地表明,掺杂机制随聚合物电导率的变化而变化:歧化机制在导电性更高的聚合物中占主导地位,而顺序电子转移在导电性较低的聚合物中占主导地位。