Cheng Qing , Kunhua Lin , Menglin Wang , Jia He , Rui Zhong , Kun Zhang , Kai Du , Yihan Wang , Qinjian Yin
{"title":"聚(3-己基噻吩)在室温下的铁磁性与分子量有关","authors":"Cheng Qing , Kunhua Lin , Menglin Wang , Jia He , Rui Zhong , Kun Zhang , Kai Du , Yihan Wang , Qinjian Yin","doi":"10.1016/j.polymer.2024.127765","DOIUrl":null,"url":null,"abstract":"<div><div>Poly (3-hexylthiophene) (P3HT) is one of the promising organic magnetic materials due to its abundant spin properties and excellent solution processing ability. However, the dependence relationship of its magnetic properties on its electronic structure and solid-state order in thin film is unclear. Herein, the effect of molecular weight (Mw) on the ferromagnetism at room temperature of P3HT films was investigated by a comparative study on P3HT with Mw ranging from 19 to 84 kDa. The interference of magnetic impurities was carefully excluded. Structural analyses were performed to investigate the aggregates morphology and molecular features of P3HT thin films with different Mw. Differences in P3HT film ferromagnetism were observed and attributed to variation of solid-state order in mixed solvent. The saturation magnetization (<em>M</em><sub>s</sub>) increases first and then decreases with the increase of Mw, reaching a maximum value of 38.8 emu g<sup>−1</sup> at 63 kDa, which was due to the largest molecular chain order and crystallinity of P3HT-63 kDa films. P3HT-84 kDa films had a higher proportion of disordered structural components and limited conjugation length, and yielding low crystallinity and magnetism (10.5 emu g<sup>−1</sup>).</div></div>","PeriodicalId":405,"journal":{"name":"Polymer","volume":"315 ","pages":"Article 127765"},"PeriodicalIF":4.1000,"publicationDate":"2024-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Molecular-weight dependence of ferromagnetism at room temperature of poly (3-hexylthiophene)\",\"authors\":\"Cheng Qing , Kunhua Lin , Menglin Wang , Jia He , Rui Zhong , Kun Zhang , Kai Du , Yihan Wang , Qinjian Yin\",\"doi\":\"10.1016/j.polymer.2024.127765\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Poly (3-hexylthiophene) (P3HT) is one of the promising organic magnetic materials due to its abundant spin properties and excellent solution processing ability. However, the dependence relationship of its magnetic properties on its electronic structure and solid-state order in thin film is unclear. Herein, the effect of molecular weight (Mw) on the ferromagnetism at room temperature of P3HT films was investigated by a comparative study on P3HT with Mw ranging from 19 to 84 kDa. The interference of magnetic impurities was carefully excluded. Structural analyses were performed to investigate the aggregates morphology and molecular features of P3HT thin films with different Mw. Differences in P3HT film ferromagnetism were observed and attributed to variation of solid-state order in mixed solvent. The saturation magnetization (<em>M</em><sub>s</sub>) increases first and then decreases with the increase of Mw, reaching a maximum value of 38.8 emu g<sup>−1</sup> at 63 kDa, which was due to the largest molecular chain order and crystallinity of P3HT-63 kDa films. P3HT-84 kDa films had a higher proportion of disordered structural components and limited conjugation length, and yielding low crystallinity and magnetism (10.5 emu g<sup>−1</sup>).</div></div>\",\"PeriodicalId\":405,\"journal\":{\"name\":\"Polymer\",\"volume\":\"315 \",\"pages\":\"Article 127765\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2024-11-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Polymer\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0032386124011017\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0032386124011017","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Molecular-weight dependence of ferromagnetism at room temperature of poly (3-hexylthiophene)
Poly (3-hexylthiophene) (P3HT) is one of the promising organic magnetic materials due to its abundant spin properties and excellent solution processing ability. However, the dependence relationship of its magnetic properties on its electronic structure and solid-state order in thin film is unclear. Herein, the effect of molecular weight (Mw) on the ferromagnetism at room temperature of P3HT films was investigated by a comparative study on P3HT with Mw ranging from 19 to 84 kDa. The interference of magnetic impurities was carefully excluded. Structural analyses were performed to investigate the aggregates morphology and molecular features of P3HT thin films with different Mw. Differences in P3HT film ferromagnetism were observed and attributed to variation of solid-state order in mixed solvent. The saturation magnetization (Ms) increases first and then decreases with the increase of Mw, reaching a maximum value of 38.8 emu g−1 at 63 kDa, which was due to the largest molecular chain order and crystallinity of P3HT-63 kDa films. P3HT-84 kDa films had a higher proportion of disordered structural components and limited conjugation length, and yielding low crystallinity and magnetism (10.5 emu g−1).
期刊介绍:
Polymer is an interdisciplinary journal dedicated to publishing innovative and significant advances in Polymer Physics, Chemistry and Technology. We welcome submissions on polymer hybrids, nanocomposites, characterisation and self-assembly. Polymer also publishes work on the technological application of polymers in energy and optoelectronics.
The main scope is covered but not limited to the following core areas:
Polymer Materials
Nanocomposites and hybrid nanomaterials
Polymer blends, films, fibres, networks and porous materials
Physical Characterization
Characterisation, modelling and simulation* of molecular and materials properties in bulk, solution, and thin films
Polymer Engineering
Advanced multiscale processing methods
Polymer Synthesis, Modification and Self-assembly
Including designer polymer architectures, mechanisms and kinetics, and supramolecular polymerization
Technological Applications
Polymers for energy generation and storage
Polymer membranes for separation technology
Polymers for opto- and microelectronics.