School of Chemical and Biomedical Engineering, Nanyang Technological University , 70 Nanyang Drive, Singapore 637457.
J Am Chem Soc. 2014 May 14;136(19):6838-41. doi: 10.1021/ja502024d. Epub 2014 Apr 29.
We report a new strategy to synthesize core-shell metal nanoparticles with an interior, Raman tag-encoded nanogap by taking advantage of nanoparticle-templated self-assembly of amphiphilic block copolymers and localized metal precursor reduction by redox-active polymer brushes. Of particular interest for surface-enhanced Raman scattering (SERS) is that the nanogap size can be tailored flexibly, with the sub-2 nm nanogap leading to the highest SERS enhancement. Our results have further demonstrated that surface functionalization of the nanogapped Au nanoparticles with aptamer targeting ligands allows for specific recognition and ultrasensitive detection of cancer cells. The general applicability of this new synthetic strategy, coupled with recent advances in controlled wet-chemical synthesis of functional nanocrystals, opens new avenues to multifunctional core-shell nanoparticles with integrated optical, electronic, and magnetic properties.
我们报告了一种新的策略,通过利用纳米粒子模板自组装两亲性嵌段共聚物和氧化还原活性聚合物刷局部还原金属前体,合成具有内部拉曼标记编码纳米间隙的核壳金属纳米粒子。对于表面增强拉曼散射(SERS)特别感兴趣的是,纳米间隙的尺寸可以灵活地调整,亚 2nm 的纳米间隙导致最高的 SERS 增强。我们的结果还进一步表明,用适配体靶向配体对纳米间隙金纳米粒子进行表面功能化,可以实现对癌细胞的特异性识别和超灵敏检测。这种新的合成策略的通用性,加上最近在功能纳米晶体的可控湿化学合成方面的进展,为具有集成光学、电子和磁性特性的多功能核壳纳米粒子开辟了新的途径。