Facile Ligand Exchange of Ionic Ligand-Capped Amphiphilic Ag<sub>2</sub>S Nanocrystals for High Conductive Thin Films
Yun‐Mo Sung, Hyun Beom Kim, Ji Heon Kim, Yoona Noh, Jaesang Yu, Jaesung Yang, Tae Hyun Kim, Juwon Oh
Abstract
A surface ligand modification of colloidal nanocrystals (NCs) is one of the crucial issues for their practical applications because of the highly insulating nature of native long-chain ligands. Herein, we present straightforward methods for phase transfer and ligand exchange of amphiphilic Ag 2 S NCs and the fabrication of highly conductive films. S-terminated Ag 2 S (S–Ag 2 S) NCs are capped with ionic octylammonium (OctAH + ) ligands to compensate for surface anionic charge, S 2–, of the NC core. An injection of polar solvent, formamide (FA), into S–Ag 2 S NCs dispersed in toluene leads to an additional envelopment of the charged S–Ag 2 S NC core by FA due to electrostatic stabilization, which allows its amphiphilic nature and results in a rapid and effective phase transfer without any ligand addition. Because the solvation by FA involves a dissociation equilibrium of the ionic OctAH + ligands, controlling a concentration of OctAH + enables this phase transfer to show reversibility. This underlying chemistry allows S–Ag 2 S NCs in FA to exhibit a complete ligand exchange to Na + ligands. The S–Ag 2 S NCs with Na + ligands show a close interparticle distance and compatibility for uniformly deposited thin films by a simple spin-coating method. In photoelectrochemical measurements with stacked Ag 2 S NCs on ITO electrodes, a 3-fold enhanced current response was observed for the ligand passivation of Na + compared to OctAH +, indicating a significantly enhanced charge transport in the Ag 2 S NC film by a drastically reduced interparticle distance due to the Na + ligands.