Regulating the local microenvironment of active sites to increase their specific CO2 concentration and pH gradient, is a promising approach to optimize the electrochemical CO2 reduction reaction (eCO(2)RR). However, currently reported morphological strategies display an uncertainty to the compatibility and distribution between catalytic sites and their microenvironment. Here, a uniform spatial-separation metal-organic framework (MOF) layer between active sites and bulk electrolyte is proposed, which enables each active site to locate in a similarly favorable microenvironment. Zinc oxide (ZnO) nanorods (NR), a representative electrocatalyst for eCO(2)RR, is covered with a Zeolitic imidazolate framework-8 (ZIF-8) thin layer to serve as a model system. The prepared ZnO NR@ZIF-8 exhibits an enhanced Faradaic efficiency toward CO at a wide range of potentials and reaches a maximum FE of CO (85%) at -1.05 V versus reversible hydrogen electrode, which is one of the best records till date. Moreover, the hydrophobic ZIF-8 layer protects ZnO against self-reduction. Such performance benefits from the porous ZIF-8 shell with high CO2 affinity, realizing efficient CO2 access and retaining an increased local pH near ZnO active sites.