量子点
分散性
配体(生物化学)
胶体
纳米晶
钝化
硝酸
纳米技术
化学
材料科学
相(物质)
反应性(心理学)
化学工程
无机化学
物理化学
有机化学
受体
病理
工程类
替代医学
医学
生物化学
图层(电子)
作者
Jea Woong Jo,Jongmin Choi,F. Pelayo Garcı́a de Arquer,Ali Seifitokaldani,Bin Sun,Young-Hoon Kim,Hyungju Ahn,James Fan,Rafael Quintero‐Bermudez,Junghwan Kim,Min‐Jae Choi,Se‐Woong Baek,Andrew H. Proppe,Grant Walters,Dae‐Hyun Nam,Shana O. Kelley,Sjoerd Hoogland,Oleksandr Voznyy,Edward H. Sargent
出处
期刊:Nano Letters
[American Chemical Society]
日期:2018-06-18
卷期号:18 (7): 4417-4423
被引量:57
标识
DOI:10.1021/acs.nanolett.8b01470
摘要
Colloidal quantum dots (CQDs) are promising solution-processed infrared-absorbing materials for optoelectronics. In these applications, it is crucial to replace the electrically insulating ligands used in synthesis to form strongly coupled quantum dot solids. Recently, solution-phase ligand-exchange strategies have been reported that minimize the density of defects and the polydispersity of CQDs; however, we find herein that the new ligands exhibit insufficient chemical reactivity to remove original oleic acid ligands completely. This leads to low CQD packing and correspondingly low electronic performance. Here we report an acid-assisted solution-phase ligand-exchange strategy that, by enabling efficient removal of the original ligands, enables the synthesis of densified CQD arrays. Our use of hydroiodic acid simultaneously facilitates high CQD packing via proton donation and CQD passivation through iodine. We demonstrate highly packed CQD films with a 2.5 times increased carrier mobility compared with prior exchanges. The resulting devices achieve the highest infrared photon-to-electron conversion efficiencies (>50%) reported in the spectral range of 0.8 to 1.1 eV.
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