Ni/TiO 2 catalysts with different morphologies (granular, sheet, tubular and spherical) were prepared. Hydrogen was generated from ethanol aqueous-phase reforming over Ni/TiO 2 in a water-ethanol-m-chloronitrobenzene reaction system and directly applied into m-chloronitrobenzene catalytic hydrogenation. Thereby, in-situ liquid-phase hydrogenation of m-chloronitrobenzene over Ni/TiO 2 without addition of molecular hydrogen was successful. Compared with granular, sheet and spherical Ni/TiO 2 , the nanotubular Ni/TiO 2 prepared from one-step hydrothermal reaction had larger specific surface area, smaller and uniformly-distributed pore sizes and more Lewis acid sites. In-situ liquid-phase hydrogenation of m-chloronitrobenzene experiments showed the nanotubular Ni/TiO 2 had the highest catalytic activity, which was ascribed to both catalyst morphology and acid sites. Firstly, the nanotubular structure endowed the catalysts with a nanoscale confinement effect and thereby high catalytic performance. Secondly, the Lewis acid sites not only accelerated water-gas shift reaction, enhancing the ethanol aqueous-phase reforming activity for hydrogen generation, but also promoted the adsorption and hydrogenation of-NO 2 on the active sites of the catalysts.