A pH-responsive assembly based on upconversion nanocrystals and ultrasmall nickel nanoparticles

被引:10
|
作者
Xu, Xia [1 ,2 ]
Long, Yan [1 ,2 ]
Lei, Pengpeng [1 ,2 ]
Dong, Lile [1 ,3 ]
Du, Kaimin [1 ,3 ]
Feng, Jing [1 ]
Zhang, Hongjie [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, 5625 Renmin St, Changchun 130022, Jilin, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Univ Sci & Technol China, Hefei 230026, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
OPTICAL-PROPERTIES; DRUG; NANOMATERIALS; NANOCARRIERS; LUMINESCENCE; SPECTROSCOPY; EXCITATIONS; NANOSHEETS;
D O I
10.1039/c7tc02665j
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We report a hybrid assembly based on NaYF4: Yb3+, Er3+/Tm3+@NaYF4 (core@shell) upconversion nanocrystals and ultrasmall Ni nanoparticles (abbreviated as core@shell@Ni) for rapid response towards pH in different PBS solutions. In this approach, Ni nanoparticles located on the surface of the core@shell upconversion nanocrystal serve as an efficient quencher for upconversion luminescence (UCL). A series of dynamic processes of the S-4(3/2) -> I-4(15/2) transition of Er3+ in Er3+-doped core@shell@Ni have been presented in order to discuss the energy transfer mechanisms between UCNPs and Ni nanoparticles. The upconversion luminescence can be recovered by incubating the core@shell@Ni assembly with pH 5.0 PBS that oxidizes Ni to Ni2+, while the UCL could be still quenched when the hybrid assembly was incubated with pH 7.4 PBS. However, the core@shell@Co assembly's response toward pH is not distinguished due to the rapid recovery of emission intensity both in pH 5.0 and 7.4 PBS. The ability of the core@shell@Ni assembly to distinguish different pH values may be a fine platform for the real-time optical monitoring of chemical reactions and many important physiological processes associated with pH.
引用
收藏
页码:9666 / 9672
页数:7
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