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Ligands Induced the Growth of Colloidal AgInS2 Nanoparticles with Tuned Structure and Photoluminescence Property
Inorganic Chemistry ( IF 4.3 ) Pub Date : 2024-12-12 , DOI: 10.1021/acs.inorgchem.4c04037
Yongliang Zhang, Chenqian Hou, Ruixue Qin, Chao Wang, Shenda Huang, Cheng Chang, Jing Cai, Jia Li, Shuzhe Niu

Understanding the growth mechanism of AgInS2 nanoparticles could benefit the designed growth of I–III–VI2 nanomaterials and their applications in photonics, optoelectronics, etc. Herein, using tris(dibutyldithiocarbamate) indium(III) [In((C4H9)2NCS2)3] ([InR3]) and dibutyldithiocarbamate silver(I) [Ag((C4H9)2NCS2)] ([AgR]) precursors, AgInS2-based nanoparticles with different structures have been synthesized in a controlled manner through a one-pot approach via different growth mechanisms in 1-dodecanethiol (DDT) and oleylamine (OLA), respectively. The DDT and OLA could participate in the decomposition of precursors; thus, the [AgR]/DDT, [InR3]/DDT, [AgR]/OLA, and [InR3]/OLA were used herein to describe the decomposition steps. In DDT, the decomposition activity of [AgR]/DDT was much higher than that of [InR3]/DDT; thus, the sequential decomposition of [AgR]/DDT and [InR3]/DDT led to the formation of the Ag2S nanoparticles intermediate first, which then reacted with [InR3]/DDT to form metastable o-AgInS2 nanoparticles via the cation exchange and alloy process, and finally evolved into o-AgInS2@InSx core@shell nanoparticles, while in OLA, the decomposition activity of [AgR]/OLA was slightly higher than that of [InR3]/OLA. Thus, the quasi-co-decomposition of [AgR]/OLA and [InR3]/OLA led to the formation of Ag-rich Ag–In–S amorphous nanoparticles intermediate first and then quickly evolved into stable t-AgInS2/InSx nanoparticles. In addition, the photoluminescence quantum yield (PLQY) of t-AgInS2/InSx nanoparticles was higher than that of o-AgInS2@InSx nanoparticles.

中文翻译:


配体诱导胶体 AgInS2 纳米颗粒的生长,具有调谐结构和光致发光特性



了解 AgInS2 纳米颗粒的生长机制有助于 I-III-VI2 纳米材料的设计生长及其在光子学、光电子学等领域的应用。在此,使用三(二丁基二硫代氨基甲酸酯)铟(III) [In(C4H92NCS23] ([InR3])和二丁基二硫代氨基甲酸酯银(I) [Ag((C4H92NCS2)] ([AgR])前驱体,通过一锅法通过1-十二硫醇(DDT)和油胺(OLA)中的不同生长机制以受控方式合成了具有不同结构的AgInS2基纳米颗粒, 分别。DDT 和 OLA 可以参与前驱体的分解;因此,本文使用 [AgR]/DDT、[InR3]/DDT、[AgR]/OLA 和 [InR3]/OLA 来描述分解步骤。在 DDT 中,[AgR]/DDT 的分解活性远高于 [InR3]/DDT;因此,[AgR]/DDT 和 [InR3]/DDT 的连续分解首先导致 Ag2S 纳米颗粒中间体的形成,然后与 [InR3]/DDT 反应,通过阳离子交换和合金过程形成亚稳态的 o-AgInS 2 纳米颗粒,最后演变成 o-AgInS2@InSx core@shell纳米颗粒中,而在 OLA 中,[AgR]/OLA 的分解活性略高于 [InR3]/OLA。因此,[AgR]/OLA 和 [InR3]/OLA 的准共分解首先导致富含 Ag 的 Ag-In-S 无定形纳米颗粒的形成,然后迅速演变成稳定的 t-AgInS2/InS x 纳米颗粒。 此外,t-AgInS2/InSx 纳米颗粒的光致发光量子产率 (PLQY) 高于 o-AgInS 2@InSx 纳米颗粒。
更新日期:2024-12-13
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