High mobility is a crucial requirement for a large variety of electronic device applications. The state-of-the-art for high quality graphene devices is based on heterostructures made with graphene encapsulated in > 80 nm-thick flakes of hexagonal boron nitride (hBN). Unfortunately, scaling up multilayer hBN while precisely controlling the number of layers remains an elusive challenge, resulting in a rough material unable to enhance the mobility of graphene. This leads to the pursuit of alternative, scalable materials, which can be simultaneously used as substrate and encapsulant for graphene. Tungsten disulfide (WS2) is a transition metal dichalcogenide, which was successfully grown in large (∼mm-size) multi-layers by chemical vapour deposition. However, the resistance vs gate voltage characteristics when gating graphene through WS2 exhibit largely hysteretic shifts of the charge neutrality point (CNP) in the order of ∆n ∼2.6•10 11 cm −2 , hindering the use of WS2 as a reliable encapsulant. The hysteresis originates due to the charge traps from sulfur vacancies present in WS2. In this work, we report for the first time the use of WS2 as a substrate and the overcoming of hysteresis issues by chemically treating WS2 with a super-acid, which passivates these vacancies and strips the surface from contaminants. The hysteresis is significantly reduced below the noise level by at least a factor five (to ∆n <5•10 10 cm −2 ) and, simultaneously, the roomtemperature mobility of WS2-encapsulated graphene is as high as ∼6.2•10 4 cm −2 V −1 s −1 at a carrier density n ∼1•10 12 cm −2 . Our results promote WS2 to a valid alternative to hBN as encapsulant for high-performance graphene devices.