Abstract

Metal halide perovskites (MHPs) with environment-dependent optoelectronic properties can provide a new platform for highly sensitive and active gas sensor materials. While MHPs are a crystalline semiconductor with high carrier mobility and long carrier diffusion length, the formation of efficient channels for charge carriers can be hindered by the intrinsic point defects and impurities as well as grain boundaries in the solution-cast films with an uncontrolled morphology. Furthermore, a precise control of nanostructured MHP materials and their distribution with respect to device electrodes still remains challenging, which requires tedious efforts for additional fabrication. Herein, we demonstrate that the dielectrophoresis process can allow for self-alignment of single-crystalline MHP nanowires (NWs) with a uniform spatial distribution and orientation on interdigitated electrodes. We found that MAPbBr3 NWs array sensors exhibited the highest sensitivity (∼120% and τ = 40 s at 100 ppm) for H2S gas molecules among oxidizing (NO2) and reducing gases (NH2 and H2S), whereas no significant response was observed for MAPbCl3 NWs. The MAPbBr3 NW array-based sensor showed a long time stability exceeding one month with less than 20% derivation during first two weeks. The characteristic response of MHP NWs array significantly depends on the interaction of oxygen molecules adsorbed at their surface with the environmental target species, in which their surface conductivity can be modulated by the variation of trap states related to surface defects. Our work demonstrates a simple and facile route to synthesis and self-alignment of MHP NWs for chemiresistive gas sensors, broadening the range of technological applications of MHPs.

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