{"title":"具有界面锚定生长层的超薄银电极用于柔性有机发光器件","authors":"Shihao Zhu , Yuehua Chen , Xuechun Wu , Jiahao Xu , Renhong Wang , Xinwen Zhang","doi":"10.1016/j.synthmet.2025.117955","DOIUrl":null,"url":null,"abstract":"<div><div>Ultrathin Ag electrodes with the low sheet resistance and high optical transmittance are the candidates for applications in flexible optoelectronic devices. However, the fabrication of ultrathin Ag electrodes with excellent optoelectrical properties and mechanical stability is challenging due to the fact that the ultrathin Ag layer obeys the Volmer-Weber growth mode when the Ag layer is too thin (<10 nm). In this paper, serine (Ser)-mediated anchoring the growth of ultrathin Ag films was proposed by the chemical bonding interactions between the group of -OH in Ser and Ag atoms. The composite transparent electrode of polyethylene terephthalate (PET)/Ser/Ag (7 nm)/MoO<sub>3</sub> (20 nm) possesses a low sheet resistance of ∼8.5 Ω/sq, a high optical transmittance of ∼87.2 % at 550 nm and the robust mechanical stability of 100,000 bending cycles at a bending radius of 5 mm. The excellent performance can be attributed to the formation of Ag-O bonds during the growth procedure of Ag films, resulting in the uniform growth of Ag films and outstanding adhesion to substrates. Flexible organic light-emitting devices were constructed based on the composite transparent electrodes, achieving a maximum luminance of ∼14070 cd/m<sup>2</sup> and a maximum current efficiency of ∼7.5 cd/A.</div></div>","PeriodicalId":22245,"journal":{"name":"Synthetic Metals","volume":"315 ","pages":"Article 117955"},"PeriodicalIF":4.6000,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ultrathin Ag electrodes with an interfacial anchoring growth layer for flexible organic light-emitting devices\",\"authors\":\"Shihao Zhu , Yuehua Chen , Xuechun Wu , Jiahao Xu , Renhong Wang , Xinwen Zhang\",\"doi\":\"10.1016/j.synthmet.2025.117955\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Ultrathin Ag electrodes with the low sheet resistance and high optical transmittance are the candidates for applications in flexible optoelectronic devices. However, the fabrication of ultrathin Ag electrodes with excellent optoelectrical properties and mechanical stability is challenging due to the fact that the ultrathin Ag layer obeys the Volmer-Weber growth mode when the Ag layer is too thin (<10 nm). In this paper, serine (Ser)-mediated anchoring the growth of ultrathin Ag films was proposed by the chemical bonding interactions between the group of -OH in Ser and Ag atoms. The composite transparent electrode of polyethylene terephthalate (PET)/Ser/Ag (7 nm)/MoO<sub>3</sub> (20 nm) possesses a low sheet resistance of ∼8.5 Ω/sq, a high optical transmittance of ∼87.2 % at 550 nm and the robust mechanical stability of 100,000 bending cycles at a bending radius of 5 mm. The excellent performance can be attributed to the formation of Ag-O bonds during the growth procedure of Ag films, resulting in the uniform growth of Ag films and outstanding adhesion to substrates. Flexible organic light-emitting devices were constructed based on the composite transparent electrodes, achieving a maximum luminance of ∼14070 cd/m<sup>2</sup> and a maximum current efficiency of ∼7.5 cd/A.</div></div>\",\"PeriodicalId\":22245,\"journal\":{\"name\":\"Synthetic Metals\",\"volume\":\"315 \",\"pages\":\"Article 117955\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2025-09-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Synthetic Metals\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0379677925001316\",\"RegionNum\":3,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Synthetic Metals","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0379677925001316","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Ultrathin Ag electrodes with an interfacial anchoring growth layer for flexible organic light-emitting devices
Ultrathin Ag electrodes with the low sheet resistance and high optical transmittance are the candidates for applications in flexible optoelectronic devices. However, the fabrication of ultrathin Ag electrodes with excellent optoelectrical properties and mechanical stability is challenging due to the fact that the ultrathin Ag layer obeys the Volmer-Weber growth mode when the Ag layer is too thin (<10 nm). In this paper, serine (Ser)-mediated anchoring the growth of ultrathin Ag films was proposed by the chemical bonding interactions between the group of -OH in Ser and Ag atoms. The composite transparent electrode of polyethylene terephthalate (PET)/Ser/Ag (7 nm)/MoO3 (20 nm) possesses a low sheet resistance of ∼8.5 Ω/sq, a high optical transmittance of ∼87.2 % at 550 nm and the robust mechanical stability of 100,000 bending cycles at a bending radius of 5 mm. The excellent performance can be attributed to the formation of Ag-O bonds during the growth procedure of Ag films, resulting in the uniform growth of Ag films and outstanding adhesion to substrates. Flexible organic light-emitting devices were constructed based on the composite transparent electrodes, achieving a maximum luminance of ∼14070 cd/m2 and a maximum current efficiency of ∼7.5 cd/A.
期刊介绍:
This journal is an international medium for the rapid publication of original research papers, short communications and subject reviews dealing with research on and applications of electronic polymers and electronic molecular materials including novel carbon architectures. These functional materials have the properties of metals, semiconductors or magnets and are distinguishable from elemental and alloy/binary metals, semiconductors and magnets.