Nanophase Evolution at Semiconductor/Electrolyte Interface in Situ Probed by Time-Resolved High-Energy Synchrotron X-ray Diffraction

被引:24
|
作者
Sun, Yugang [1 ]
Ren, Yang [2 ]
Haeffner, Dean R. [2 ]
Almer, Jonathan D. [2 ]
Wang, Lin [3 ]
Yang, Wenge [3 ]
Truong, Tu T. [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
[3] Carnegie Inst Sci, Geophys Lab, HPSync, Argonne, IL 60439 USA
关键词
Time-resolved X-ray diffraction; in situ probing; galvanic reaction; silver nanoplates; GOLD NANOPARTICLES; SUPERCRITICAL WATER; GROWTH; GAAS; NUCLEATION; SCATTERING; CELLS; PHOTOCATHODES; PHOTOCURRENT; SPECTROSCOPY;
D O I
10.1021/nl102458k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Real-time evolution of nanoparticles grown at the semiconductor/electrolyte interface formed between a single crystalline n-type GaAs wafer and an aqueous solution of AgNO3 has been studied by using high-energy synchrotron X-ray diffraction. The results reveal the distinct nucleation and growth steps involved in the growth of anisotropic Ag nanoplates on the surface of the GaAs wafer. For the first time, a quick transit stage is observed to be responsible for the structural transformation of the nuclei to form structurally stable seeds that are critical for guiding their anisotropic growth into nanoplates. Reaction between a GaAs wafer and AgNO3 solution at room temperature primarily produces Ag nanoplates on the surface of the GaAs Wafer in the dark and at room temperature. In contrast, X-ray irradiation can induce charge separation in the GaAs wafer to drive the growth of nanoparticles made of silver oxy salt (Ag7NO11) and silver arsenate (Ag3AsO4) at the semiconductor/electrolyte interface if the GaAs wafer is illuminated by the X-ray and reaction time is long enough.
引用
收藏
页码:3747 / 3753
页数:7
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