Plasmonic Enhanced Nonlinear Absorption of Tris(2-aminoethyl)amine (TREN) Functional Ag, Pt, and Pd Nanoparticle-GQDs Complexes and Their Evaluation as Potential Bioimaging Applications.

阅读:17
作者:Unlu Bekir Asilcan, Kirit Esen, Celik Dogantan, Yildiz Elif Akhuseyin, Karatay Ahmet, Boyacioglu Bahadir, Ünver Hüseyin, Yilmazer Açelya, Yıldız Mustafa, Elmali Ayhan
Tris (2-aminoethyl)amine (TREN) functionalized N-doped graphene quantum dots (N-GQDs) and their Ag, Pd, and Pt nanocomposites were synthesized via a green one-step method and comprehensively characterized using FT-IR, UV-vis, TEM, and EDX. Spectroscopic analysis revealed π-π* transitions of C═C bonds (245-250 nm) and n-π* transitions of C═O and C═N bonds (334-350 nm), elucidating the materials' optical properties. Photoluminescence studies revealed excitation wavelength-dependent emissions, indicating the presence of edge defect levels. Femtosecond transient absorption spectroscopy revealed a shortened excited-state lifetime upon incorporation of a metal atom into TREN-GQDs. Nonlinear absorption was explored by using the open-aperture Z-scan method, revealing enhanced performance upon incorporation of plasmonic nanoparticles. Ag-incorporated samples exhibited the highest NLA response due to plasmon-enhanced two-photon absorption. Notably, Pt-incorporated N-GQDs showed improved NLA and good biocompatibility with the intracellular fluorescence response, positioning them as promising candidates for bioimaging applications. Density functional theory (DFT) calculations, including gas-phase optimizations and aqueous simulations, confirmed alignment with experimental results, highlighting the enhanced stability and reactivity of nanocomposites. These findings highlight the potential of these materials in various applications, such as optical limiting, imaging, photovoltaics, and sensing applications.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。