{"title":"Temperature-Induced Morphology Control of Fe-Polydopamine Coordination Complexes and Their Derivatives for Energy Storage Applications.","authors":"Incheol Heo,Min Seok Kang,Jaeseong Kim,Chanyoung Lee,Hee Soo Kim,Dong-Ha Lim,Won Cheol Yoo","doi":"10.1021/acs.nanolett.5c03768","DOIUrl":null,"url":null,"abstract":"Controlling the morphology of organic-inorganic complexes at the nanometer scale is crucial for electrochemical applications. We present a novel method for controlling Fe-polydopamine (Fe-PD) coordination complexes into rod, urchin, and hollow structures at high (80-90 °C), medium (40-60 °C), and low (0-10 °C) synthesis temperatures, respectively. Morphological evolution was driven by the balance between oriented and random polymerization pathways, with hollow structures formed through random growth followed by selective inner-core etching. H- and U-Fe-PDs were converted to H- and U-Fe@C composites after carbonization. H-Fe@C exhibited superior performance in lithium-metal anodes, achieving stable cycling for over 2500 h with exceptional overpotentials as low as 7.4 mV and 76% capacity retention after 1000 cycles, significantly outperforming U-Fe@C due to enhanced mass transport through the thin carbon shell (∼50 nm). This temperature-controlled strategy provides a versatile approach for designing morphology-driven materials for advanced energy storage.","PeriodicalId":53,"journal":{"name":"Nano Letters","volume":"76 1","pages":""},"PeriodicalIF":9.1000,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nano Letters","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acs.nanolett.5c03768","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
Controlling the morphology of organic-inorganic complexes at the nanometer scale is crucial for electrochemical applications. We present a novel method for controlling Fe-polydopamine (Fe-PD) coordination complexes into rod, urchin, and hollow structures at high (80-90 °C), medium (40-60 °C), and low (0-10 °C) synthesis temperatures, respectively. Morphological evolution was driven by the balance between oriented and random polymerization pathways, with hollow structures formed through random growth followed by selective inner-core etching. H- and U-Fe-PDs were converted to H- and U-Fe@C composites after carbonization. H-Fe@C exhibited superior performance in lithium-metal anodes, achieving stable cycling for over 2500 h with exceptional overpotentials as low as 7.4 mV and 76% capacity retention after 1000 cycles, significantly outperforming U-Fe@C due to enhanced mass transport through the thin carbon shell (∼50 nm). This temperature-controlled strategy provides a versatile approach for designing morphology-driven materials for advanced energy storage.
期刊介绍:
Nano Letters serves as a dynamic platform for promptly disseminating original results in fundamental, applied, and emerging research across all facets of nanoscience and nanotechnology. A pivotal criterion for inclusion within Nano Letters is the convergence of at least two different areas or disciplines, ensuring a rich interdisciplinary scope. The journal is dedicated to fostering exploration in diverse areas, including:
- Experimental and theoretical findings on physical, chemical, and biological phenomena at the nanoscale
- Synthesis, characterization, and processing of organic, inorganic, polymer, and hybrid nanomaterials through physical, chemical, and biological methodologies
- Modeling and simulation of synthetic, assembly, and interaction processes
- Realization of integrated nanostructures and nano-engineered devices exhibiting advanced performance
- Applications of nanoscale materials in living and environmental systems
Nano Letters is committed to advancing and showcasing groundbreaking research that intersects various domains, fostering innovation and collaboration in the ever-evolving field of nanoscience and nanotechnology.