{"title":"Low-Cost, Facile, and Scalable Manufacturing of Single-Molecule-Integrated Catalytic Electrodes","authors":"Shu-Guo Han, San-Mei Wang, Mengke Hu, Wenbo Wei, Chao Zhan, Dong-Dong Ma* and Qi-Long Zhu*, ","doi":"10.1021/acsnano.5c0004810.1021/acsnano.5c00048","DOIUrl":null,"url":null,"abstract":"<p >To surmount the shortcomings of powder-based catalysts and small electrode sizes, the development of meter-scale integrated electrode materials is essential for practical electrocatalytic applications, which requires fine control over the effective surface grafting of catalytic active sites on large-size electrodes as well as addressing the challenge of balancing cost-effective and large-scale manufacturing with highly active and stable operation. Herein, we report a low-cost, facile, and scalable method for directly constructing meter-scale single-molecule-integrated catalytic electrodes using commercially available, flexible, and size-tailored conductive carbon textiles (e.g., graphite felt) and well-defined planar conjugated molecules (e.g., metallophthalocyanines) via heterostacking steered cross-scale heterointerfacial assembly. This universal method unlocks the limitations of traditional approaches that involve integrating powder-based catalysts, conductive carbon particles, binders (e.g., Nafion), and supported electrodes (e.g., carbon paper) through multiple processing steps and typically result in centimeter-level electrodes. Meaningfully, our method enables precise control over the size, composition, microenvironment, and structure of the single-molecule-integrated catalytic electrodes to match various electrocatalytic environments. As a proof of concept, an electrode integrated with thiophene-gilded cobalt phthalocyanine demonstrates outstanding catalytic activity and stability for CO<sub>2</sub> electroconversion in alkaline, neutral, and acidic media under industrially relevant current densities, and even in flowing paired-electrolysis system. This study provides comprehensive scientific data and engineering guidance for the systematic design of scalable, binder-free catalytic electrodes, thereby promising to drive sustainable energy-efficient electrolysis on an industrial scene.</p>","PeriodicalId":21,"journal":{"name":"ACS Nano","volume":"19 11","pages":"11273–11283 11273–11283"},"PeriodicalIF":16.0000,"publicationDate":"2025-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Nano","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsnano.5c00048","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
To surmount the shortcomings of powder-based catalysts and small electrode sizes, the development of meter-scale integrated electrode materials is essential for practical electrocatalytic applications, which requires fine control over the effective surface grafting of catalytic active sites on large-size electrodes as well as addressing the challenge of balancing cost-effective and large-scale manufacturing with highly active and stable operation. Herein, we report a low-cost, facile, and scalable method for directly constructing meter-scale single-molecule-integrated catalytic electrodes using commercially available, flexible, and size-tailored conductive carbon textiles (e.g., graphite felt) and well-defined planar conjugated molecules (e.g., metallophthalocyanines) via heterostacking steered cross-scale heterointerfacial assembly. This universal method unlocks the limitations of traditional approaches that involve integrating powder-based catalysts, conductive carbon particles, binders (e.g., Nafion), and supported electrodes (e.g., carbon paper) through multiple processing steps and typically result in centimeter-level electrodes. Meaningfully, our method enables precise control over the size, composition, microenvironment, and structure of the single-molecule-integrated catalytic electrodes to match various electrocatalytic environments. As a proof of concept, an electrode integrated with thiophene-gilded cobalt phthalocyanine demonstrates outstanding catalytic activity and stability for CO2 electroconversion in alkaline, neutral, and acidic media under industrially relevant current densities, and even in flowing paired-electrolysis system. This study provides comprehensive scientific data and engineering guidance for the systematic design of scalable, binder-free catalytic electrodes, thereby promising to drive sustainable energy-efficient electrolysis on an industrial scene.
期刊介绍:
ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.