Safe Synthesis of InP Quantum Dots for Biological Applications

Abstract

Semiconductor nanocrystals (also known as quantum dots) have been extensively studied because of their unique optical properties which makes them promising candidates for bio imaging and bio sensing. II-VI semiconductor quantum dots are commonly used in biomedical applications because of their near unit quantum yields and narrow emission profiles. Despite these advantages, II-VI semiconductor nanocrystals contain toxic metals. As a result, III-V semiconductor nanocrystals such as InP are promising replacements for cadmium-based semiconductor nanocrystals. However, the synthesis of bright InP quantum dots with narrow size distribution is challenging mainly due to the use of overly reactive phosphorus precursors like tris(trimethylsilyl) phosphine (TMS)3P. This reagent is also highly flammable. We employed less pyrophoric sterically encumbered tris(triethylsilyl) phosphine and tris(tributylsilyl) phosphine for the synthesis and observed that quantum yield and the emission color saturation (fwhm) of InP nanocrystals are improved compared to those prepared with (TMS)3P, but not up to the levels realized with CdSe. HF treatment is often employed as a post-synthetic treatment to improve the optical properties of quantum dots. We demonstrate that ammonium bifluoride is a safer alternative to extremely hazardous HF. Ammonium bifluoride etched InP core dots were further passivated to create InP/ZnSeS core-shell quantum dots that were later water-solubilized and functionalized for biological applications. Figure 1