量子点
材料科学
光致发光
吸收(声学)
荧光
金属
近红外光谱
壳体(结构)
光电子学
纳米技术
芯(光纤)
胶体
红外线的
化学工程
光学
复合材料
物理
工程类
冶金
作者
Xin Tong,Xiang‐Tian Kong,Yufeng Zhou,Fabiola Navarro‐Pardo,Gurpreet Singh Selopal,Shuhui Sun,Alexander O. Govorov,Haiguang Zhao,Zhiming M. Wang,Federico Rosei
标识
DOI:10.1002/aenm.201701432
摘要
Abstract “Giant” core/shell quantum dots (g‐QDs) are a promising class of materials for future optoelectronic technologies due to their superior chemical‐ and photostability compared to bare QDs and core/thin shell QDs. However, inadequate light absorption in the visible and near‐infrared (NIR) region and frequent use of toxic heavy metals (e.g., Cd and Pb) are still major challenges for most g‐QDs (e.g., CdSe/CdS) synthesized to date. The synthesis of NIR, heavy metal‐free, Zn‐treated spherical CuInSe 2 /CuInS 2 g‐QDs is reported using the sequential cation exchange method. These g‐QDs exhibit tunable NIR optical absorption and photoluminescence (PL) properties. Transient fluorescence spectroscopy shows prolonged lifetime with increasing shell thickness, indicating the formation of quasi type‐II band alignment, which is further confirmed by simulations. As a proof‐of‐concept, as‐synthesized g‐QDs are used to sensitize TiO 2 as a photoanode in a photoelectrochemical (PEC) cell, demonstrating an efficient and stable PEC system. These results pave the way toward synthesizing NIR heavy metal‐free g‐QDs, which are very promising components of future optoelectronic technologies.
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