In two-dimensional (2D) semiconducting transition metal dichalcogenides (TMDs), new electronic phenomena such as tunable bandgaps 1-3 and strongly bound excitons and trions emerge from strong many-body effects [4][5][6] , beyond the spin and valley degrees of freedom induced by spin-orbit coupling and by lattice symmetry 7 . Combining single-layer TMDs with other 2D materials in van der Waals heterostructures offers an intriguing means of controlling the electronic properties through these many-body effects, by means of engineered interlayer interactions [8][9][10] . Here, we use micro-focused angle-resolved photoemission spectroscopy (microARPES) and in situ surface doping to manipulate the electronic structure of single-layer WS 2 on hexagonal boron nitride (WS 2 /h-BN). Upon electron doping, we observe an unexpected giant renormalization of the spin-orbit splitting of the single-layer WS 2 valence band, from 430 meV to 660 meV, together with a bandgap reduction of at least 325 meV, attributed to the formation of trionic quasiparticles. These findings suggest that the electronic, spintronic and excitonic properties are widely tunable in 2D TMD/h-BN heterostructures, as these are intimately linked to the quasiparticle dynamics of the materials [11][12][13] . Coulomb interactions in 2D materials are several times stronger than in their 3D counterparts. In 2D TMDs, this is most directly evidenced by the presence of excitons with binding energies an order of magnitude higher than in the bulk 4 . Although the excitons in these 2D materials have been widely studied by optical techniques 13 , the impact of strong electron-electron interactions on the quasiparticle band structure remains unclear. Theory predicts that many-body effects will influence the spin-orbit splitting around the valenceband maximum (VBM) and conduction-band minimum (CBM) 14 . Although these should be observable by ARPES, a direct probe of many-body effects 15 , measurements so far have mainly focused on the layer-dependence of the single-particle spectrum and the direct bandgap transition in 2D TMD systems, including epitaxial single- . Unfortunately, the lateral size of mechanically assembled heterostructures is usually of the order of 10 μ m, much smaller than the beam spot of typical ARPES setups (≳ 100 μ m). Furthermore, sample charging on insulating bulk h-BN substrates would complicate ARPES experiments.We overcome these challenges as follows. We realize a high-quality 2D semiconductor-insulator interface by mechanically transferring a relatively large (~100 μ m) single-layer WS 2 crystal onto a thin flake of h-BN that has itself been transferred onto a degenerately doped TiO 2 substrate, as depicted in Fig. 1a. Sample charging is avoided because there is electrical contact from the continuous single-layer WS 2 flake to both the h-BN and the conductive TiO 2 . Figure 1b is an optical microscope image of the sample, including a flake of h-BN, approximately 100 μ m wide, surrounded by several transferred flakes of single-layer WS 2 on the Ti...