{"title":"自驱动光电探测器用液态水分子连接量子点","authors":"Zhihao Qian, Minhui Yang, Shisheng Lin","doi":"10.1002/adfm.202420182","DOIUrl":null,"url":null,"abstract":"<p>The interactions between solid quantum dots (QDs) are weak as the excitons in QDs are difficult to be dissolved into electrons and holes, which limits the performance of QDs based photodetector. Herein, through putting QDs inside the water, it is intriguingly found that excitons are dissolved into electrons and holes by the interaction between QDs and water molecules, which further contribute to the formation of long-range electron/hole transport channels within the water. At zero voltage bias, a transient photo-polarized current is repeatedly produced, the specific responsivity and detectivity of liquid-based photodetector with molybdenum disulfide (MoS<sub>2</sub>) QDs aqueous suspension can reach 188.1 mA W<sup>−1</sup> and 1.164 × 10<sup>10</sup> Jones with 820 nm illumination, respectively. The specific spectra of photodetectors can be promoted by selected QDs with different absorption peaks. Actually, the responsivity of liquid-based photodetector with cadmium selenide (CdSe) QDs exhibits the most significant enhancement effect at the peak of exciton absorption wavelength of QDs, as much more excitons in QDs can be dissolved into electrons and holes. It is anticipated that the ability to dissolve excitons in QDs and form conducting channels by dynamic construction of water molecules will bring possibilities for high-performance optoelectronic devices across a wide range of application scenarios.</p>","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"35 24","pages":""},"PeriodicalIF":19.9000,"publicationDate":"2025-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Liquid Water Molecular Connected Quantum Dots for Self-Driven Photodetector\",\"authors\":\"Zhihao Qian, Minhui Yang, Shisheng Lin\",\"doi\":\"10.1002/adfm.202420182\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The interactions between solid quantum dots (QDs) are weak as the excitons in QDs are difficult to be dissolved into electrons and holes, which limits the performance of QDs based photodetector. Herein, through putting QDs inside the water, it is intriguingly found that excitons are dissolved into electrons and holes by the interaction between QDs and water molecules, which further contribute to the formation of long-range electron/hole transport channels within the water. At zero voltage bias, a transient photo-polarized current is repeatedly produced, the specific responsivity and detectivity of liquid-based photodetector with molybdenum disulfide (MoS<sub>2</sub>) QDs aqueous suspension can reach 188.1 mA W<sup>−1</sup> and 1.164 × 10<sup>10</sup> Jones with 820 nm illumination, respectively. The specific spectra of photodetectors can be promoted by selected QDs with different absorption peaks. Actually, the responsivity of liquid-based photodetector with cadmium selenide (CdSe) QDs exhibits the most significant enhancement effect at the peak of exciton absorption wavelength of QDs, as much more excitons in QDs can be dissolved into electrons and holes. It is anticipated that the ability to dissolve excitons in QDs and form conducting channels by dynamic construction of water molecules will bring possibilities for high-performance optoelectronic devices across a wide range of application scenarios.</p>\",\"PeriodicalId\":112,\"journal\":{\"name\":\"Advanced Functional Materials\",\"volume\":\"35 24\",\"pages\":\"\"},\"PeriodicalIF\":19.9000,\"publicationDate\":\"2025-01-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Functional Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://advanced.onlinelibrary.wiley.com/doi/10.1002/adfm.202420182\",\"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}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://advanced.onlinelibrary.wiley.com/doi/10.1002/adfm.202420182","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
摘要
固体量子点之间的相互作用较弱,量子点中的激子难以溶解到电子和空穴中,这限制了量子点光电探测器的性能。本文通过将量子点放入水中,有趣地发现,量子点与水分子的相互作用使激子溶解为电子和空穴,这进一步促进了水中远程电子/空穴输运通道的形成。在零偏置电压下,反复产生瞬态光极化电流,在820 nm光照下,二硫化钼量子点水悬浮液基光电探测器的比响应率和探测率分别达到188.1 mA W−1和1.164 × 1010 Jones。选择具有不同吸收峰的量子点可以提高光电探测器的特异光谱。实际上,硒化镉(CdSe)量子点的液相光电探测器在量子点激子吸收波长的峰值处的响应性增强最为显著,因为量子点中有更多的激子可以溶解到电子和空穴中。预计通过水分子的动态构建来溶解量子点中的激子并形成导电通道的能力将为高性能光电器件在广泛的应用场景中带来可能性。
Liquid Water Molecular Connected Quantum Dots for Self-Driven Photodetector
The interactions between solid quantum dots (QDs) are weak as the excitons in QDs are difficult to be dissolved into electrons and holes, which limits the performance of QDs based photodetector. Herein, through putting QDs inside the water, it is intriguingly found that excitons are dissolved into electrons and holes by the interaction between QDs and water molecules, which further contribute to the formation of long-range electron/hole transport channels within the water. At zero voltage bias, a transient photo-polarized current is repeatedly produced, the specific responsivity and detectivity of liquid-based photodetector with molybdenum disulfide (MoS2) QDs aqueous suspension can reach 188.1 mA W−1 and 1.164 × 1010 Jones with 820 nm illumination, respectively. The specific spectra of photodetectors can be promoted by selected QDs with different absorption peaks. Actually, the responsivity of liquid-based photodetector with cadmium selenide (CdSe) QDs exhibits the most significant enhancement effect at the peak of exciton absorption wavelength of QDs, as much more excitons in QDs can be dissolved into electrons and holes. It is anticipated that the ability to dissolve excitons in QDs and form conducting channels by dynamic construction of water molecules will bring possibilities for high-performance optoelectronic devices across a wide range of application scenarios.
期刊介绍:
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