钙钛矿(结构)
光致发光
极性(国际关系)
材料科学
光催化
极地的
溶剂
纳米技术
纳米结构
量子点
解吸
化学工程
吸收(声学)
乙腈
奥斯特瓦尔德成熟
化学物理
光化学
化学
吸附
物理
光电子学
物理化学
有机化学
催化作用
复合材料
细胞
生物化学
工程类
天文
作者
Jeffrey T. DuBose,Andrew G. Christy,Jishnudas Chakkamalayath,Prashant V. Kamat
出处
期刊:ACS materials letters
[American Chemical Society]
日期:2021-12-06
卷期号:4 (1): 93-101
被引量:25
标识
DOI:10.1021/acsmaterialslett.1c00663
摘要
Perovskite nanoplatelets have potential use in optoelectronic and photocatalytic applications because of the enhanced quantum confinement they experience. However, often ignored is the effect of solvent polarity on the stability of these nanoplatelets. When perovskite nanoplatelets are exposed to small amounts (<1 vol %) of mildly polar solvents such as acetonitrile, the particles rapidly grow to larger nanostructures. Their quantum confinement is lost as they grow from uniform 2.6 nm thick particles to large nanostructures ∼85 nm in size. This ripening brings characteristic red-shifts in the absorption and photoluminescence of the particles as they transform. Using methyl acetate as a model polar solvent, we succeeded in establishing factors that control ligand desorption and lowering of the activation energy for ripening. These results highlight the challenges in using these quantum-confined nanoplatelets in applications such as photocatalysis, where polar solvents and/or intermediates may be unavoidable.
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