化学
电化学发光
生物传感器
水溶液
电子转移
纳米技术
限制
组合化学
水介质
羧酸盐
半胱氨酸
电化学
自组装
化学稳定性
线性范围
微电极
分子
金属
小分子
电极
检出限
价(化学)
作者
Jidong Ge,H. Zhang,Xufeng Chen,Haoyuan Song,Tao Zhou,Jie Guan,Yue Cao,Chang-Jie Mao,Jun-Jie Zhu,Yang Zhou,Y. Andrew Wang
标识
DOI:10.1021/acs.analchem.5c06196
摘要
Magic-sized semiconductor clusters (MSCs) synthesized in organic solvents typically exhibit poor compatibility with aqueous media, which hampers electron transfer and leads to weak electrochemiluminescence (ECL), thereby limiting their biological and environmental applications. Here we report that cation-induced assembly confers aqueous stability on Cd15Se12 MSCs and simultaneously boosts their ECL efficiency. Using cysteine (Cys) as a stabilizing ligand, we prepared water-dispersible Cd15Se12-Cys MSCs and introduced multivalent metal cations (Mn+=Zn2+, Cd2+, K+, Na+, Al3+) to electrostatically bind the surface carboxylate groups, thereby driving spontaneous intercluster assembly. The assembled Cd15Se12-Cys-Mn+ MSCs exhibited a 10-fold enhancement in ECL intensity compared to unassembled counterparts, along with excellent signal stability over 1000 s of continuous operation. Mechanistic studies revealed that the cation valence critically dictates the assembly mode and ECL efficiency. Notably, Zn2+-modified assemblies functioned as highly efficient ECL emitters in a biosensing platform, enabling sensitive lactate detection in sweat with a broad linear range (0.01-50 mM). This work establishes cation-induced assembly as a general strategy to achieve aqueous-stable MSCs with enhanced ECL performance, opening new opportunities for their application in biosensing and environmental monitoring.
科研通智能强力驱动
Strongly Powered by AbleSci AI