Morphologically controlled synthesis of colloidal upconversion nanophosphors and their shape-directed self-assembly

被引:387
作者
Ye, Xingchen [1 ]
Collins, Joshua E. [2 ]
Kang, Yijin [1 ]
Chen, Jun [3 ]
Chen, Daniel T. N. [4 ]
Yodh, Arjun G. [4 ]
Murray, Christopher B. [1 ,3 ]
机构
[1] Univ Penn, Dept Chem, Philadelphia, PA 19104 USA
[2] Intelligent Mat Solut Inc, Princeton, NJ 08540 USA
[3] Univ Penn, Dept Mat Sci & Engn, Philadelphia, PA 19104 USA
[4] Univ Penn, Dept Phys & Astron, Philadelphia, PA 19104 USA
基金
美国国家科学基金会;
关键词
doped nanocrystals; superlattice; lanthanides; luminescence; PHASE; SIZE; NANOCRYSTALS; NAYF4-YB; ER; GOLD; NANOPARTICLES; SUPERLATTICES; LUMINESCENCE; CRYSTALLINE; PHOSPHORS;
D O I
10.1073/pnas.1008958107
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We report a one-pot chemical approach for the synthesis of highly monodisperse colloidal nanophosphors displaying bright upconversion luminescence under 980 nm excitation. This general method optimizes the synthesis with initial heating rates up to 100 degrees C/minute generating a rich family of nanoscale building blocks with distinct morphologies (spheres, rods, hexagonal prisms, and plates) and upconversion emission tunable through the choice of rare earth dopants. Furthermore, we employ an interfacial assembly strategy to organize these nanocrystals (NCs) into superlattices over multiple length scales facilitating the NC characterization and enabling systematic studies of shape-directed assembly. The global and local ordering of these superstructures is programmed by the precise engineering of individual NC's size and shape. This dramatically improved nanophosphor synthesis together with insights from shape-directed assembly will advance the investigation of an array of emerging biological and energy-related nanophosphor applications.
引用
收藏
页码:22430 / 22435
页数:6
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