Leanne A Milburn, Evan I Wroe, Mairi Eyres, Joshua M Lawrence, Jenny Z Zhang
{"title":"Operando Microscopy of Photosynthetic Microbial Biohybrids Using Fluorescent Chemical Probes.","authors":"Leanne A Milburn, Evan I Wroe, Mairi Eyres, Joshua M Lawrence, Jenny Z Zhang","doi":"10.1021/acselectrochem.5c00517","DOIUrl":null,"url":null,"abstract":"<p><p>Photosynthetic biohybrids, often in the form of biophotoelectrochemical devices, aim to achieve solar-to-chemical conversion by pairing biotic and abiotic materials to leverage the beneficial attributes of both. Numerous works have highlighted the importance of a well-tuned bio-electrode interface for high biophotoelectrode performance. However, the dynamics of these interfaces in photosynthetic biohybrids are poorly understood, necessitating the development of new tools to disentangle the various (bio)-chemical processes occurring simultaneously. In this work, we construct an <i>operando</i> confocal microscopy platform to deeply analyze the dynamics in biofilm morphology, interfacial pH, and membrane potential. These methods assert that light availability is the main driver of microenvironment formation at the interface of a model <i>Synechocystis</i>-indium tin oxide bioelectrode. The potential of the electrode only induces a substantial impact outside of the potential range -0.32 to +0.48 V vs. Ag/AgCl at typical current densities. This toolkit provides a foundation for further elucidating interfacial dynamics and rational design of these systems and can be expanded to other bioelectrochemical constructs.</p>","PeriodicalId":520400,"journal":{"name":"ACS electrochemistry","volume":"2 4","pages":"964-973"},"PeriodicalIF":0.0000,"publicationDate":"2026-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13051432/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS electrochemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1021/acselectrochem.5c00517","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/4/2 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Photosynthetic biohybrids, often in the form of biophotoelectrochemical devices, aim to achieve solar-to-chemical conversion by pairing biotic and abiotic materials to leverage the beneficial attributes of both. Numerous works have highlighted the importance of a well-tuned bio-electrode interface for high biophotoelectrode performance. However, the dynamics of these interfaces in photosynthetic biohybrids are poorly understood, necessitating the development of new tools to disentangle the various (bio)-chemical processes occurring simultaneously. In this work, we construct an operando confocal microscopy platform to deeply analyze the dynamics in biofilm morphology, interfacial pH, and membrane potential. These methods assert that light availability is the main driver of microenvironment formation at the interface of a model Synechocystis-indium tin oxide bioelectrode. The potential of the electrode only induces a substantial impact outside of the potential range -0.32 to +0.48 V vs. Ag/AgCl at typical current densities. This toolkit provides a foundation for further elucidating interfacial dynamics and rational design of these systems and can be expanded to other bioelectrochemical constructs.
光合生物杂交,通常以生物光电化学装置的形式,旨在通过配对生物和非生物材料来利用两者的有益属性来实现太阳能到化学的转化。许多工作都强调了良好调谐的生物电极界面对于高生物光电极性能的重要性。然而,人们对光合作用生物杂交体中这些界面的动力学知之甚少,这就需要开发新的工具来解开同时发生的各种(生物)化学过程。在这项工作中,我们构建了一个operando共聚焦显微镜平台,深入分析生物膜形态、界面pH和膜电位的动态。这些方法断言,光的可用性是微环境形成的主要驱动力在一个模型聚囊藻-氧化铟锡生物电极的界面。在典型电流密度下,电极的电位仅在-0.32至+0.48 V vs. Ag/AgCl的电位范围之外产生实质性影响。该工具包为进一步阐明这些系统的界面动力学和合理设计提供了基础,并可以扩展到其他生物电化学结构。