电化学发光
量子点
电致发光
光致发光
材料科学
光电子学
发光
纳米技术
量子产额
电化学
壳体(结构)
化学
荧光
电极
物理
光学
物理化学
复合材料
图层(电子)
作者
Zhiyuan Cao,Yufei Shu,Haiyan Qin,Bin Su,Xiaogang Peng
出处
期刊:ACS central science
[American Chemical Society]
日期:2020-06-01
卷期号:6 (7): 1129-1137
被引量:123
标识
DOI:10.1021/acscentsci.0c00484
摘要
Outstanding photoluminescence (PL) and electroluminescence properties of quantum dots (QDs) promise possibilities for them to meet challenging expectations of electrochemiluminescence (ECL), which at present relies on inefficient and spectral-irresolvable emitters based on transition-metal complexes (such as Ru(bpy)32+). However, ECL is reported to be extremely sensitive to the surface traps on the QDs likely because of the spatially and temporally separated electrochemical charge injections. Results here reveal that, by engineering the interior inorganic structure (CdSe/CdS/ZnS core/shell/shell structure) and inorganic–organic interface using new synthetic methods, the trap-insensitive QDs with near-unity PL quantum yield and monoexponential PL decay dynamics in water generated narrow band-edge ECL with efficiencies about six orders of magnitude higher than that of the standard Ru(bpy)32+. The band-edge and spectrally resolved ECL from CdSe/CdS/ZnS core/shell/shell QDs demonstrated a new readout scheme using electrochemical potential. Excellent ECL performance of QDs uncovered here offer opportunities to realize the full potential of ECL for biomedical detection and diagnosis.
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