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作 者:Cheng Ma Xiaodan Gou Zejing Xing Min-Xuan Wang Wenlei Zhu Qin Xu Dechen Jiang Jun-Jie Zhu
机构地区:[1]School of Chemistry and Chemical Engineering,Yangzhou University.Yangzhou 225002,P.R.China [2]State Key Laboratory of Analytical Chemistry for Life Science,State Key Laboratory of Pollution Control and Resource Reuse,School of Chemistry and Chemical Engineering,School of the Environment,Nanjing University,Nanjing 210023,P.R.China.
出 处:《Research》2024年第3期205-215,共11页研究(英文)
基 金:the National Natural Science Foundation of China(grant numbers 22374125,21834004,22174061,22076161,22176086,and 22025403);the Natural Science Foundation of Jiangsu Province(grant number BK20210189);the State Key Laboratory of Pollution Control and Resource Reuse(grant number PCRR-ZZ-202106);the Foundation of State Key Laboratory of Analytical Chemistry for Life Science(grant number SKLACLS2201);Yangzhou University Interdisciplinary Research Foundation for Chemistry Discipline of Targeted Support(grant number yzuxk202009);Fund for Jiangsu Distinguished Professor and Yangzhou University Start-up Fund,Lvyangjinfeng Talent Program of Yangzhou,Young academic leaders of Jiangsu Province(2018);Talent Support Program of Yangzhou University,and The Open Project Program of Jiangsu Key Laboratory of Zoonosis(no.R2013).
摘 要:Electrochemiluminescence (ECL) has established itself as an excellent transduction technique in biosensing and light-emitting device, while conventional ECL mechanism depending on spontaneous emission of luminophores lacks reversibility and tunable emission characters, limiting the universality of ECL technique in the fields of fundamental research and clinical applications. Here, we report the first observation of stimulated emission route in ECL and thus establish a reversible tuning ECL microscopy for single-cell imaging. This microscopy uses a focused red-shifted beam to transfer spontaneous ECL into stimulated ECL, which enables selective and reversible tuning of ECL emission from homogeneous solution, single particles, and single cells. After excluding other possible competitive routes, the stimulated ECL emission route is confirmed by a dual-objective system in which the suppressed spontaneous ECL is accompanied by the enhanced stimulated ECL. By incorporating a commercial donut-shaped beam, the sharpness of single-cell matrix adhesion is improved 2 to 3 times compared with the counterpart in confocal ECL mode. The successful establishment of this stimulated emission ECL will greatly advance the development of light-emitting device and super-resolution ECL microscopy.
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