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Efficient catalytic reduction of the main greenhouse gas CO2into high value-added chemicals is an important measure to alleviate the greenhouse effect and energy depletion. Metal nitrogen (M-N4) macrocyclic complexes have attracted increasing attention in the field of electrocatalytic CO2reduction (CO2RR) due to the precise adjustment of the catalytic active site according to the requirements and the flexible modification of the external ligand structure. Nevertheless, the poor activity and low selectivity of reduction products restrict their widespread application in electrocatalytic CO2RR. Herein, a combination of nanoscale and molecular level method has been developed to construct easily obtainable 4NH2-NiPc/NH2-CNT hybrid material, in which amino groups are connected to provide electrons toward the central Ni-N4site to promote the electrocatalytic CO2RR catalytic activity. As a result, the catalyst 4NH2-NiPc/NH2-CNT mainly produces CO in the electrocatalytic CO2RR, which exhibits a Faradaic efficiency of CO (FECO) higher than 92 % within a wide overpotential range of −0.70 to −0.95 V vs. RHE, and provides excellent stability with a current density of 12 mA cm−2at −0.80 V vs. RHE. In addition, 4NH2-NiPc/NH2-CNT reaches its maximum FECOvalue of 96 % at −0.8 V vs. RHE, which is approximately 3.1 times that of the original unmodified NiPc/CNT, demonstrating excellent promotion of electrochemical performance. Similarly, compared to NiPc/CNT without amino modification, the current density of 4NH2-NiPc/NH2-CNT exceeds it by more than twice. The research results indicate that promoting role of electron substituted amino groups in catalysis dispersion and electronic environment coordination. This study proposes a promising strategy of introducing amino groups into molecular catalysts and hybridizing with carbon nanotube to enhance the electrocatalytic conversion of CO2to deep reduction products.