We experimentally determine the redox reactions during (de-)lithiation of the SnO 2 working electrode cycled in (Li 2 S) 3 −P 2 S 5 solid electrolyte by combining operando X-ray photoelectron spectroscopy and in situ X-ray absorption spectroscopy. Specifically, we have accurately determined the composition changes in the SnO 2 working electrode upon cycling and identified the onset voltage formation of the various phases. Starting from the open-circuit potential, we find that, on lithiation, the Sn M-edge absorption spectra reveal unequivocally the formation of SnO x (x ≤ 1) and Li 2 SnO 3 already at a potential of 1.6 V vs Li + /Li, while Sn 3d/Sn 4d, O 1s, and Li 1s core-level spectra show the formation of Sn 0 and Li 2 O along the first potential plateau at 0.8 V vs Li + /Li and of Li 8 SnO 6 at lower potentials. Below 0.6 V vs Li + /Li, an alloying reaction takes place until the end of the lithiation process at 0.05 V vs Li + /Li, as shown by the formation of Li x Sn. During delithiation, both the conversion and alloying reactions are found to be partially reversible, starting by the re-formation of Sn 0 at 0.3 V vs Li + /Li and followed by the re-formation of Li 8 SnO 6 and SnO x above 0.5 V vs Li + /Li. The conversion and alloying reactions are found to overlap during both lithiation and delithiation. Finally, we validate the theoretical prediction for the SnO 2 conversion and alloy (de-)lithiation reactions and clarify the open questions about their reaction mechanism.