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用于尺寸和形状可控的砷化铟胶体量子点的硅氢硅烷还原剂。

Si-H Hydrosilane Reducing Agents for Size- and Shape-Controlled InAs Colloidal Quantum Dots.

作者信息

Skorotetcky Maxim S, Mir Wasim J, Sheikh Tariq, Yorov Khursand E, Saidzhonov Bedil M, Daws Sawsan, Zhou Renqian, Hedhili Mohamed N, Abulikemu Mutalifu, Mohammed Omar F, Bakr Osman M

机构信息

Center for Renewable Energy and Storage Technologies (CREST),  Division of Physical Science and Engineering, King Abdullah University of Science and Technology, Thuwal, 23955-6900, Kingdom of Saudi Arabia.

KAUST Core Labs, King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Kingdom of Saudi Arabia.

出版信息

Adv Mater. 2025 Jan;37(4):e2412105. doi: 10.1002/adma.202412105. Epub 2024 Dec 4.

Abstract

InAs colloidal quantum dots (CQDs) are a promising heavy-metal-free material for infrared optoelectronic devices. However, their synthesis is limited by their reagents: the acutely toxic and difficult to source tris(trimethylsilyl)arsine ((TMS)As), as well as the strong reducing agents (e.g., Super Hydride). A reducing agent is introduced based on hydrosilanes (Si-H) to address both challenges. A synthesis strategy with this agent is demonstrated, resulting in monodisperse InAs CQDs with a tunable first excitonic peak between 520 and 900 nm by hot injection, and between 900 and 1550 nm by continuous injection. Furthermore, by avoiding the use of carboxyl group-containing compounds, such as oleic acid or indium acetate, the synthesis minimizes surface oxidation during InAs CQDs formation. The synthesized InAs CQDs are of high optoelectronic quality, with a lower concentration of deep trap states, as evident by the remarkable characteristics of photodetectors fabricated from these CQDs: low dark current (≈150 nA cm), external quantum efficiency (32% at 900 nm), and a fast photoresponse time (≈4.4 µs). The elimination of (TMS)As in the synthesis overcomes a key practical barrier for exploiting and exploring the properties of large InAs CQDs in optoelectronic applications.

摘要

砷化铟胶体量子点(CQDs)是一种用于红外光电器件的很有前景的无重金属材料。然而,它们的合成受到试剂的限制:剧毒且难以获取的三(三甲基硅基)砷((TMS)As)以及强还原剂(如超级氢化物)。引入了一种基于硅烷(Si-H)的还原剂来应对这两个挑战。展示了一种使用这种试剂的合成策略,通过热注入得到了具有520至900纳米之间可调谐的第一激子峰的单分散砷化铟CQDs,通过连续注入则得到了900至1550纳米之间可调谐的第一激子峰。此外,通过避免使用含羧基的化合物,如油酸或醋酸铟,该合成方法在砷化铟CQDs形成过程中使表面氧化最小化。合成的砷化铟CQDs具有高的光电质量以及较低浓度的深陷阱态,由用这些CQDs制造的光电探测器的显著特性可以看出:低暗电流(≈150 nA cm)、外部量子效率(在900纳米处为32%)以及快速的光响应时间(≈4.4微秒)。合成过程中消除(TMS)As克服了在光电子应用中开发和探索大型砷化铟CQDs特性的一个关键实际障碍。

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