光激发
胶体金
分子
激发态
质子化
纳米颗粒
电离
分析物
化学
极化率
光化学
生物分子
离子
电子转移
电化学发光
化学物理
材料科学
纳米技术
有机化学
物理化学
电极
原子物理学
物理
作者
Wei Huang,Samuel Kin‐Man Lai,Kaiqing Liang,Keyuan Pu,Xin Wang,Yuping Chen,Kwan‐Ming Ng
标识
DOI:10.1021/acs.jpcc.3c01164
摘要
Gold nanoparticles (AuNPs) have been widely utilized as an effective substrate for triggering molecular ionization upon photoexcitation. However, its underlying mechanism(s) remains unclear. Here, by blocking heat transfer and electron transfer on photo-excited AuNPs with a thin layer of silica shell (i.e., Au@SiO2 NPs), the critical role of the enhanced E-field in ionizing nearby molecules was evidenced. The enhanced E-field of the Au core could enhance the protonation of amino acids (via short-range interaction) by polarizing the analyte molecules. In contrast, the polarizability of the Au core showed a more pronounced effect to enhance the metal cationization process (Na+ and K+ adduction via long-range interaction) by polarizing both the analyte molecules and metal ions and was successfully applied to the sensitive analysis of amino acids in human serum.
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