Core−shell {nanocarbon-coated/TiO 2 } hybrids (C@ TiO 2 ) were developed through a double-nozzle flame spray pyrolysis (DN-FSP) process. By optimizing the DN-FSP parameters, we have achieved control over the subnanometric thickness of the carbon shell as well as the anatase/rutile ratio within the TiO 2 . A library of C@ TiO 2 hybrids, with varying carbon contents and sp 2 /sp 3 ratios, has been produced. These optimized C@TiO 2 hybrids are capable of performing efficient photocatalytic hydrogen production from water, exceeding 400 μmol g −1 h −1 , without the need for any noble-metal cocatalyst. HR-TEM has demonstrated that the DN-FSP process facilitates the formation of a nanocarbon shell and carbon nanodots in close contact with the TiO 2 surface. XRD and Raman spectra indicate that this close carbon/TiO 2 interface promotes the formation of a TiO 2 rutile/anatase interphase. EPR spectroscopy shows that the carbon/TiO 2 nanohybrids stabilize reduced Ti 3+ sites at the interface. Moreover, an in situ EPR study of the photoinduced holes/ electrons demonstrates that the nanocarbon moieties act as a very efficient acceptor of the photogenerated electrons. In this way, the highly efficient photocatalytic performance of C@TiO 2 nanohybrids is attributed to the formation of a Z-scheme assembly of {rutile/anatase/carbon} nanophases. From a technological perspective, this work highlights the potential of the DN-FSP process for the scalable synthesis of functional photocatalytic (carbon/metal oxide) nanomaterials.