Abstract

The lack of highly efficient, cost effective and stable ammonia gas sensors functionable at room temperature even in extreme humid environments poses significant challenge for the future generation gas sensors. The prime factors that impede the development of such next generation gas sensors are the strong interference of humidity and sluggish selectivity. Herein, we fabricated tungsten doped molybdenum disulphide/reduced graphene oxide composite by an in-situ hydrothermal method to exploit the adsorption, dissolution (solubility), ionization and transmission process of ammonia and thereby to effectuate its trace level detection even in indispensable humid environments. The protype based on 5 at.% Tungsten doped MoS2/RGO (W5) gas sensor exhibited 3.8-fold increment in its response to 50 ppm of ammonia when the relative humidity varied from 20 % to 70 % with ultra-high selectivity at room temperature. The as prepared gas sensor revealed a practical detection limit down to 1 ppm with a substantial response and rapid recovery time. Furthermore, W5 gas sensor exhibited a 42-fold increment in response to 50 ppm of ammonia relative to its pristine (MoS2/RGO) MG composite with a RH of 70 %. The proton hopping mechanism accountable for such an enormous enhancement in ammonia sensing and its potential for breath sensor are briefly annotated.

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