In situ high-energy synchrotron X-ray diffraction revealing precipitation reaction kinetics of silver ions with mixed halide ions

被引:7
|
作者
Liu, Qi [1 ]
Li, Zheng [1 ]
Okasinski, John S. [2 ]
Ren, Yang [2 ]
Sun, Yugang [1 ]
机构
[1] Argonne Natl Lab, Ctr Nanoscale Mat, Argonne, IL 60439 USA
[2] Argonne Natl Lab, Xray Sci Div, Adv Photon Source, Argonne, IL 60439 USA
关键词
AG-AT-AGCL; HYDROGEN GENERATION; NANOWIRES; EFFICIENT; PHOTOCATALYST; NANOPARTICLES; CONVERSION; FIBERS; GROWTH; BR;
D O I
10.1039/c5tc01306b
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Precipitation of silver ions simultaneously with chloride and bromide ions in ethylene glycol at a mild temperature (e.g., 60 degrees C) has been successfully demonstrated for the synthesis of silver chlorobromide (AgClxBr1-x, 0 < x < 1) nanoparticles, which is realized by injecting a AgNO3 solution into a solution containing both halogen ions. The injection rate of the AgNO3 solution has been determined to be critical for controlling the uniformity of AgClxBr1-x nanoparticles. Time-resolved in situ high-energy synchrotron X-ray diffraction has been applied, for the first time, to quantitatively monitor the reaction kinetics of nanocrystal formation. The real-time results shed light on the fact that the injection rate of AgNO3 solution significantly influences the nucleation and growth processes, and thus the quality of resulting AgClxBr1-x nanoparticles. Specifically, fast injection enables the complete addition of AgNO3 solution to the reaction solution before the nucleation process starts, leading to a good separation of nucleation and growth and thus the formation of uniform AgClxBr1-x nanocubes with well-defined composition and narrow size distribution. By contrast, slow injection results in a continuous addition of AgNO3 solution to the reaction solution even after nucleation starts, leading to continuous multiple nucleation/growth processes and thus the formation of AgClxBr1-x nanoparticles with broad dimensional and morphological distributions.
引用
收藏
页码:7492 / 7498
页数:7
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