Abstract

Powder X-ray diffraction is one of the key techniques used to characterize the inorganic structure of colloidal nanocrystals. The comparatively low scattering factor of nuclei of the organic capping ligands and their propensity to be disordered has led investigators to typically consider them effectively invisible to this technique. In this report, we demonstrate that a commonly observed powder X-ray diffraction peak around q=1.4{AA}^{-1} observed in many small, colloidal quantum dots can be assigned to well-ordered aliphatic ligands bound to and capping the nanocrystals. This conclusion differs from a variety of explanations ascribed by previous sources, the majority of which propose an excess of organic material. Additionally, we demonstrate that the observed ligand peak is a sensitive probe of ligand shell ordering. Changes as a function of ligand length, geometry, and temperature can all be readily observed by X-ray diffraction and manipulated to achieve desired outcomes for the final colloidal system.

Highlights

  • Powder X-ray diffraction is one of the key techniques used to characterize the inorganic structure of colloidal nanocrystals

  • InCl3 has been shown to partially displace indium myristate from indium phosphide quantum dot surfaces in a Ztype ligand exchange[8], while hydrofluoric acid (HF) protonates the carboxylates on the quantum dot surface and replaces them with fluorine[34]

  • The quantum dot was capped with ordered myristate ligands at ligand densities that have been observed for indium phosphide quantum dots (Fig. 1c)[7,8,35]

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Summary

Introduction

Powder X-ray diffraction is one of the key techniques used to characterize the inorganic structure of colloidal nanocrystals. We elected to analyze experimental and simulated powder X-ray diffraction of different ligand treatments on indium phosphide quantum dots, where this previously unassigned peak is prominent. With increasing quantum dot size, the relative intensity of the ligand peak decreased in both experimental (Fig. 2b), and simulated powder X-ray diffraction patterns (Fig. 2c).

Results
Conclusion
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