Abstract

The synthesis of lead sulfide nanocrystals within a solution processable sulfur ‘inverse vulcanization’ polymer thin film matrix was achieved from the in situ thermal decomposition of lead(II) n-octylxanthate, [Pb(S2COOct)2]. The growth of nanocrystals within polymer thin films from single-source precursors offers a faster route to networks of nanocrystals within polymers when compared with ex situ routes. The ‘inverse vulcanization’ sulfur polymer described herein contains a hybrid linker system which demonstrates high solubility in organic solvents, allowing solution processing of the sulfur-based polymer, ideal for the formation of thin films. The process of nanocrystal synthesis within sulfur films was optimized by observing nanocrystal formation by X-ray photoelectron spectroscopy and X-ray diffraction. Examination of the film morphology by scanning electron microscopy showed that beyond a certain precursor concentration the nanocrystals formed were not only within the film but also on the surface suggesting a loading limit within the polymer. We envisage this material could be used as the basis of a new generation of materials where solution processed sulfur polymers act as an alternative to traditional polymers.

Highlights

  • The in situ growth of nanomaterials from single-source precursors in polymers offers a potentially shorter route to thin films of bi-continuous phases of inorganic nanocrystals and polymers, by growing the nanocrystals in the polymer rather than synthesizing them ex situ followed by incorporation into the polymer

  • We present the synthesis of PbS nanocrystals in a solution processable sulfur polymer from the in situ decomposition of lead(II) n-octylxanthate, [Pb(S2COOct)2]

  • Films of a solution processable sulfur polymer containing networks of PbS nanocrystals have been produced via spin coating of sulfur polymers with lead(II) n-octylxanthate, [Pb(S2COOct)2], and the subsequent heating of the films

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Summary

Introduction

The in situ growth of nanomaterials from single-source precursors in polymers offers a potentially shorter route to thin films of bi-continuous phases of inorganic nanocrystals and polymers, by growing the nanocrystals in the polymer rather than synthesizing them ex situ followed by incorporation into the polymer. The substrate is heated causing the decomposition of the precursor to given nanocrystals in the polymer film (scheme 1). This has the advantage over ex situ routes as surface ligands, a necessity for colloidal stability, can be avoided improving contact between the particles and polymer in the film, a particular advantage when producing bulk heterojunction photovoltaics [1]. Potential applications for nanocrystal-containing thin films include: solar cells [9,10,12,13,14,15], catalysis [16,17,18], absorptive optical filters [19,20], sensors [21,22,23,24,25] and antimicrobial surfaces [26,27,28,29]

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