Abstract
Discovered almost two decades ago, the solution–liquid–solid (SLS) method for semiconductor nanowire synthesis has proven to be an important route to high-quality, single-crystalline anisotropic nanomaterials. In execution, the SLS technique is similar to colloidal quantum-dot synthesis in that it entails the injection of chemical precursors into a hot surfactant solution, but mechanistically it is considered the solution-phase analogue to vapour–liquid–solid (VLS) growth. Both SLS and VLS methods make use of molten metal nanoparticles to catalyse the nucleation and elongation of single-crystalline nanowires. Significantly, however, the methods differ in how chemical precursors are introduced to the metal catalysts. In SLS, precursors are added in a one-off fashion in a flask, whereas in VLS they are carried by a flow of gas through the reaction chamber, and by-products are removed similarly. The ability to dynamically control the introduction of reactants and removal of by-products in VLS synthesis has enabled a degree of synthetic control not possible with SLS growth. We show here that SLS synthesis can be transformed into a continuous technique using a microfluidic reactor. The resulting flow-based SLS (‘flow-SLS’) platform allows us to slow down the synthesis of nanowires and capture mechanistic details concerning their growth in the solution phase, as well as synthesize technologically relevant axially heterostructured semiconductor nanowires, while maintaining the propensity of SLS for accessing ultrasmall diameters below 10 nm.
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Acknowledgements
R.L. was supported by a Los Alamos National Laboratory (LANL) Laboratory Directed Research and Development (LDRD) Program's Director's Postdoctoral Research Fellowship. R.L. is currently supported by the National Science and Technology Development Agency of Thailand (NSTDA), through which some of the data analysis was completed. K.P. was supported in part by LANL Center for Integrated Nanotechnologies (CINT) postdoctoral funding. N.A.S., R.M.D., D.J.W. and J.A.H. acknowledge support from the LANL LDRD programme. J.K.B. was funded by LANL CINT. This work was performed in large part at CINT, a US Department of Energy (DOE) Office of Science Nanoscale Science Research Center and User Facility. LANL, an affirmative action equal opportunity employer, is operated by Los Alamos National Security, LLC, for the National Nuclear Security Administration of the US DOE under contract DE-AC52-06NA25396.
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J.A.H. conceived the concept of ‘flow-SLS’. N.A.S. and J.A.H. designed the flow-SLS chip in collaboration with the subcontractor (Dolomite). N.A.S. performed the initial flow-SLS semiconductor nanowire syntheses, and R.L. and K.P. performed the syntheses reported here, under the guidance of J.A.H. R.L. conducted SEM imaging and performed measurements of semiconductor nanowire dimensions with contributions from K.P. The data were analysed and interpreted by R.L. and J.A.H. R.L. performed all calculations, mathematical modelling and curve fitting to establish the combined Gibbs–Thomson/diffusion-limited flow-SLS growth model. R.L. and J.A.H. wrote the manuscript with contributions from K.P. R.M.D. conducted high-angle annular dark-field scanning transmission electron microscopy imaging and obtained the line scan profile of the segmented semiconductor nanowire using energy-dispersive X-ray analysis, while D.J.W. conducted high-resolution transmission electron microscopy imaging, obtained selected area diffraction patterns, analysed the semiconductor nanowire crystal structure and determined growth directions. J.K.B. prepared the Bi-coated Si substrates.
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Laocharoensuk, R., Palaniappan, K., Smith, N. et al. Flow-based solution–liquid–solid nanowire synthesis. Nature Nanotech 8, 660–666 (2013). https://doi.org/10.1038/nnano.2013.149
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DOI: https://doi.org/10.1038/nnano.2013.149
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