Precursor reactivity differentiation for single-step preparation of Ag2Se@Ag2S core–shell nanocrystals with distinct absorption and emission properties enabling sensitive near-infrared photodetection

To obtain dual active near-infrared (NIR) nanomaterial with strong absorption and emission properties, we report herein a novel precursor reactivity differentiation strategy, i.e., utilizing 1-octadecene (ODE)–Se having the ability to react with Ag salts much stronger and faster than ODE–thiourea, for single-step preparation of Ag 2 Se@Ag 2 S nanocrystals (NCs). With this strategy, we were able to synthesize high-quality Ag 2 Se@Ag 2 S NCs with both excellent NIR absorption and emission properties. Particularly, these nanocrystals possess a rather strong and sharp excitonic absorption peak with a full width at half maximum less than 70 nm and a maximum fluorescence quantum yield as high as 24.3%. Their appealing optical properties and structural features were founded to be highly dependent on the Se to S precursor ratio in the reaction solutions, owing to such a ratio exerting a direct influence on the core sizes and shell thicknesses of the as-formed NCs. Taking advantage of their remarkable NIR absorption properties, self-powered photoelectrochemical-type photodetectors based on the as-prepared Ag 2 Se@Ag 2 S NCs were successfully fabricated, which demonstrate a much better response performance and photostability in comparison with those based on Ag 2 Se NCs.