Two nitrogen-rich azo-bridged porphyrin porous organic polymers (Azo-Por-Bpy-POP and Azo-Por-Dadp-POP) with high surface areas were prepared by coupling 5,10,15,20-tetra(p-nitrophenyl)-porphyrin with the aromatic amines of 2,2'-bipyridine-5,5'-diamine (Bpy) and diaminodiphenyl (Dadp). Azo-Por-Bpy-POP and Azo-Por-Dadp-POP display high photocatalytic reduction activity for CO2 to CO under visible-light irradiation without a sacrificial reagent or metal co-catalyst. Azo-Por-Bpy-POP exhibits the highest photoreduction for CO2 with CO as the only carbonaceous reduction product with a production rate of 38.75 μmol g-1 h-1. Theoretical investigations indicate a stronger electrostatic interaction between CO2 and Azo-Por-Bpy-POP than Azo-Por-Dadp-POP, which favors CO2 photoreduction.