We report the formation and observation of an electron liquid in
Sr2−xLaxTiO4, the quasi-two-dimensional counterpart of SrTiO3,
through reactive molecular-beam epitaxy and {\it in situ} angle-resolved
photoemission spectroscopy. The lowest lying states are found to be comprised
of Ti 3dxy orbitals, analogous to the LaAlO3/SrTiO3 interface and
exhibit unusually broad features characterized by quantized energy levels and a
reduced Luttinger volume. Using model calculations, we explain these
characteristics through an interplay of disorder and electron-phonon coupling
acting co-operatively at similar energy scales, which provides a possible
mechanism for explaining the low free carrier concentrations observed at
various oxide heterostructures such as the LaAlO3/SrTiO3 interface