The preparation of copper-based heterogeneous catalysts dedicated to the hydrogenation of CO2 to methanol typically relies on multi-step procedures carried out in batch. These steps are precisely tailored to introduce the active phase (Cu) and the promoters (e.g. zinc, gallium) onto a preformed support, to maximize catalyst performance. However, each process step-often carried out in batch-can be associated with the formation of waste and with the consumption of energy, thereby negatively impacting the environmental performance of the overall catalyst preparation procedure. Here, we propose a direct and continuous production process for the synthesis of efficient catalysts for the CO2 to methanol reaction. Gallium-and zinc-promoted mesoporous Cu-SiO2 catalysts are prepared in one step by the aerosol-assisted sol-gel process. The catalysts consist of spherical microparticles and feature high specific surface area and pore volume, with interconnected pores of about 6 nm. A strong promoting effect of Ga and Zn is highlighted, boosting the selectivity for methanol at the expense of CO. Upon calcination, we show that Cu species-initially trapped in the silica matrix-undergo a migration towards the catalyst surface and a progressive sintering. After optimization, the catalysts obtained via such direct route compete with the best catalysts reported in the literature and obtained via multi-step approaches. File list (2) download file view on ChemRxiv Debecker CO2 MeOH aerosol Cu Ga Zn SiO2-preprint.pdf (1.82 MiB) download file view on ChemRxiv Debecker CO2 MeOH aerosol Cu Ga Zn SiO2-GA.docx (238.46 KiB) CO 2 hydrogenation to methanol with Ga-and Zn-doped mesoporous Cu/SiO 2 catalysts prepared by the aerosol-assisted sol-gel process