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Reactivity Toward Ag+: A General Strategy to Generate a New Emissive Center from NIR-Emitting Gold Nanoparticles
The Journal of Physical Chemistry Letters ( IF 4.8 ) Pub Date : 2018-01-19 00:00:00 , DOI: 10.1021/acs.jpclett.7b03295
Yaping Wang 1 , Lulu Liu 1 , Lingshan Gong 1 , Ying Chen 1 , Jinbin Liu 1
Affiliation  

We report a facile strategy for the transformation of single NIR-emitting AuNPs to dual-NIR-emitting bimetallic [email protected] based on the robust reactivity toward Ag(I) ions under mild conditions. The reactivities toward Ag(I) ions were found to be significantly different between visible- and NIR-emitting glutathione (GSH)-coated AuNPs: the high GSH surface coverage on the 610 nm-emitting AuNPs resulted in a reversible interaction due to enough surface steric hindrance to resist Ag(I) ions from interaction with the Au(0) core, whereas the low GSH surface coverage on the 810 nm-emitting AuNPs led to both antigalvanic reaction and Ag(I)-carboxylate shell formation on the surface of the AuNPs, which were responsible for the formation of a new emissive center at 705 nm. This strategy was also demonstrated to exhibit excellent generalization toward various NIR-emitting AuNPs with surface chemistries containing carboxyl groups, opening a new pathway of tailoring the optical properties of metallic NPs through surface reactivity.

中文翻译:

对Ag +的反应性:从发射NIR的金纳米粒子产生新的发射中心的一般策略

我们报告了一个温和的条件下,基于对Ag(I)离子的稳固反应性,将单个发射NIR的AuNPs转换为发射双NIR的双金属[电子邮件保护]的简便策略。发现涂覆可见光和NIR的谷胱甘肽(GSH)的AuNPs对Ag(I)离子的反应性显着不同:由于表面足够多,发射610 nm的AuNPs的GSH表面覆盖率高,导致可逆的相互作用阻止Ag(I)离子与Au(0)核相互作用的空间位阻,而发射810 nm的AuNPs的低GSH表面覆盖率导致抗电反应和Ag(I)-羧酸盐壳形成AuNPs负责在705 nm处形成新的发射中心。
更新日期:2018-01-19
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