螺旋面
手性(物理)
化学
纳米晶
对映选择合成
纳米技术
对映体
圆二色性
光热治疗
纳米棒
纳米结构
分子
纳米花
偶氮苯
晶体生长
化学物理
超分子化学
组合化学
马里蒂玛热带鱼
结晶学
作者
Ge Fang,Yu Tian,Haili Wei,Jingyi He,Xiaoxi Luan,Wenping Gao,Guangchao Zheng,Wing‐Leung Wong,Guobao Xu,Cunlan Guo,Fengxia Wu,Kwok-Yin Wong,Wenxin Niu
摘要
Helicoid gold (Au) nanocrystals exhibit pronounced chiroplasmonic responses arising from their three-dimensional chiral morphology and strong light–matter interactions. Achieving precise control over their chirality requires synthetic advances and a deeper understanding of the interplay among nanocrystal growth, structural chirality, and chiroptical activity. Here, we report a surfactant-layer engineering strategy that enables switching of growth pathways and reversal of chiroptical signals in helicoid Au nanocrystals by introducing aromatic additives, particularly 5-bromosalicylic acid (5-BSA), into a synthesis system using cysteine as chiral inducers. The incorporation of 5-BSA alters the growth pathway of helicoid Au nanocrystals, resulting in a transition in chiral morphology from C4-type pinwheel-like structures to C3-type propeller-like structures, accompanied by a reversal of the g-factor from −0.14 to +0.09. Mechanistic investigations reveal that 5-BSA modulates the surfactant interface, altering the relative growth rates along the ⟨100⟩ and ⟨111⟩ directions and deepening the concaveness of Au nanocrystals, which contributes to the reversal of chiroptical activity and the large g-factors. The strategy is generalizable to diverse aromatic molecules and chiral inducers, enabling the use of a single chiral inducer in one enantiomeric form to produce nanostructures with opposite signs of the chiroptical response. This work provides a flexible synthesis route for chiroplasmonic materials and deepens the mechanistic understanding linking enantioselective anisotropic growth and chiroptical responses.
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