The present article experimentally establishes the governing influence of electric fields on the evaporation kinetics of pendant droplets of conducting liquids. It has been shown that the evaporation kinetics of pendant droplets of saline solutions can be largely augmented by the application of an external alternating electric field. The evaporation behaviour is modulated by increase in the field strength as well as the field frequency. The classical diffusion driven evaporation model is found insufficient in predicting the improved evaporation rates. The change in surface tension due to field constraint is also observed to be insufficient for explaining the observed physics. Consequently, the internal hydrodynamics of the droplet is probed employing particle image velocimetry. It is revealed that the electric field induces enhanced internal advection, which is the cause behind the improved evaporation rates. An analytical model based on scaling approach has been proposed to understand the role of internal electrohydrodynamics, electro-thermal and the electro-solutal effects. Stability maps reveal that the electrohydrodynamic advection is caused nearly equally by the electro-solutal and electro-thermal effects and are the dominant transport mechanisms within the droplet.The model is able to illustrate the influence played by the governing thermal and solutal Marangoni number, the electro-Prandtl and electro-Schmidt number, and the associated Electrohydrodynamic number. The magnitude of the internal circulation can be well predicted by the proposed model, which thereby validates the proposed mechanism. The present revelations may find strong implications in droplet modulation using electric fields in micro and macroscale transport phenomena domains.