Solution Phase Synthesis of Indium Gallium Phosphide Alloy Nanowires

被引:43
作者
Kornienko, Nikolay [1 ]
Whitmore, Desire D. [1 ]
Yu, Yi [1 ]
Leone, Stephen R. [1 ,2 ,4 ]
Yang, Peidong [1 ,3 ,5 ,6 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Phys, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Dept Mat Sci Engn, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Div Chem Sci, Berkeley, CA 94720 USA
[5] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Div Mat Sci, Berkeley, CA 94720 USA
[6] Kavli Energy Nanosci Inst, Berkeley, CA 94720 USA
关键词
nanowire; alloy; solution phase synthesis; LIQUID-SOLID SYNTHESIS; HYDROGEN-PRODUCTION; RAMAN-SCATTERING; SURFACTANT-FREE; INP NANOWIRES; GROWTH; GAP; PHOTOLUMINESCENCE; LUMINESCENCE; SEMICONDUCTORS;
D O I
10.1021/nn507335j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The tunable physical and electronic structure of III-V semiconductor alloys renders them uniquely useful for a variety of applications, including biological imaging, transistors, and solar energy conversion. However, their fabrication typically requires complex gas phase instrumentation or growth from high-temperature melts, which consequently limits their prospects for widespread implementation. Furthermore, the need for lattice matched growth substrates in many cases confines the composition of the materials to a narrow range that can be epitaxially grown. In this work, we present a solution phase synthesis for indium gallium phosphide (InxGa1-xP) alloy nanowires, whose indium/gallium ratio, and consequently, physical and electronic structure, can be tuned across the entire x= 0 to x = 1 composition range. We demonstrate the evolution of structural and optical properties of the nanowires, notably the direct to indirect band gap transition, as the composition is varied from InP to GaP. Our scalable, low-temperature synthesis affords compositional, structural, and electronic tunability and can provide a route for realization of broader InxGa1-xP applications.
引用
收藏
页码:3951 / 3960
页数:10
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