oxidation reaction on the anode, while the oxygen undergoes a reduction reaction on the cathode. However, the sluggish kinetics and instability of oxygen reduction reaction (ORR) electrocatalysts, especially in the practical acidic and oxidation environments, have severely hindered their further developments. Therefore, engineering ORR electrocatalysts with high activity and good stability is desired to promote energy transformation efficiency. By far, the most popular ORR electrocatalysts are the costly platinum group metal (PGM)-derived ones. However, the use of expensive, unsatisfied stability, and scarce PGM materials as ORR electrocatalyst limits the developments of this field. [8][9][10][11][12][13][14][15][16][17][18] To improve catalytic efficiency and cut the high expenditure, various strategies have been studied in recent years. Among them, electrocatalysts based on the metal-N-C (M-N-C) structures have attracted extensive attention in recent years due to their unique electronic structure to bind with the intermediates, abundant substitutional metal elements, maximum atomic utilization efficiency, as well as excellent stability. [19][20][21][22][23][24][25] Besides, compared to ORR electrocatalysts loaded with nanoclusters or nanoparticles, the M-N-C presents unambiguous catalytic sites and facile synthesis, which help the understanding of ORR mechanisms by precise theoretical calculations and in Exploring highly active, stable electrocatalysts with earth-abundant metal centers for the oxygen reduction reaction (ORR) is essential for sustainable energy conversion. Due to the high cost and scarcity of platinum, it is a general trend to develop metal-N-C (M-N-C) electrocatalysts, especially those prepared from the zeolite imidazolate framework (ZIF) to replace/minimize usage of noble metals in ORR electrocatalysis for their amazingly high catalytic efficiency, great stability, and readily-tuned electronic structure. In this review, the most pivotal advances in mechanisms leading to declined catalytic performance, synthetic strategies, and design principles in engineering ZIF-derived M-N-C for efficient ORR catalysis, are presented. Notably, this review focuses on how to improve intrinsic ORR activity, such as M-N x -C y coordination structures, doping metal-free heteroatoms in M-N-C, dual/ multi-metal sites, hydrogen passivation, and edge-hosted M-N x . Meanwhile, how to increase active sites density, including formation of M-N complex, spatial confinement effects, and porous structure design, are discussed. Thereafter, challenges and future perspectives of M-N-C are also proposed. The authors believe this instructive review will provide experimental and theoretical guidance for designing future, highly active ORR electrocatalysts, and facilitate their applications in diverse ORR-related energy technologies.