Limiting resources of fossil fuels and environmental issues inevitably require more efficient utilization of solar energy. Photocatalytic production of hydrogen is identified as one of the most promising routes for developing clean and sustainable energy. However, engineering of low-cost materials exhibiting high catalytic activity in the entire range of solar spectrum is still a challenge. Here we report, for the first time, simple, easily scalable and environmentally friendly synthesis of stable Ti@TiO 2 core-shell nanoparticles exhibiting photocatalytic activity in hydrogen production under Vis/NIR light irradiation without any noble metals. Stable to oxidation core-shell Ti@TiO 2 nanoparticles have been obtained by the simultaneous actions of ultrasound and hydrothermal treatment on air-passivated titanium metal nanoparticles in pure water. The obtained material is composed of quasi-spherical Ti particles (20-80 nm) coated by 5-15 nm crystals of defect-free anatase with small amounts of rutile. In contrast to pristine TiO 2 , the Ti@TiO 2 nanoparticles extend the photo response from UV to NIR light region due to the light absorption by nonplasmonic Ti core. In MeOH-H 2 O solutions, the Ti@TiO 2 nanoparticles exhibit the strongest catalytic activity in H 2 formation under joint effect of Vis/NIR light and heat. Isotopic study using MeOH-D 2 O solutions suggested the reaction mechanism involving electron holes accumulation in semiconducting TiO 2 shell via charge separation and multiple charge-transfer steps that follow Ti interband transition. The electron transport from Ti core presumably occurs through the junctions between TiO 2 crystals at the surface of core-shell nanoparticles.