natural abundance, and operational safety, which is considered to be one of the most promising next-generation batteries. [3] However, Zn anode in the mildly acidic condition is plagued by notorious dendritic growth, inevitable corrosion, as well as hydrogen evolution due to thermodynamic instability, which gives rise to a low coulombic efficiency and poor cycling reversibility during the plating/stripping process. [4] Similar to Li/Na metal batteries, the Zn 2+ ion prefers to form nuclei at dislocated sites due to relatively high potential, and subsequent zinc ions deposit at initial nucleation sites with higher curvature and lower activation energy, further growing into protuberances. The sharp tips of protuberances with the considerably higher electric field would serve as charge center, eventually resulting in furious dendrites growth after long-term accumulation. [5] Most disturbingly, the persistent dendrites growth would result in loose porous morphology and a mass of "dead Zn", which further exacerbates the interfacial parasitic reaction due to excessive exposure between the electrolyte and Zn anode. [6] Therefore, uniform Zn deposition and less contact with water are of great significance to achieving the long cycle life of the Zn anode.Recently, to obtain a robust zinc anode, modification of electrolyte/anode interfaces has been proposed to suppress the formation of Zn dendrites. Electrolyte engineering, [7] including regulation of the electrolyte composition and introduction of additive, one easy and effective strategy, is adopted to enhance the stability of zinc anode via tailoring solvated structure or forming a solid electrolyte interface. However, expensive costs for highly concentrated electrolytes and continual consumption of functional additives seriously impede the large-scale practical application of ZMBs. Another strategy of amending Zn anode structure, such as surface-preferred crystal plane and nano-sized Zn anode, has attracted a great deal of attention, which could greatly reduce the nucleation barrier leading to the inhibition of dendrites growth. [8] Unsatisfactorily, regulating the preferred orientation crystal involves complicated operation techniques, and nano-structured Zn with extensive specific area results in excessive contact between electrode and electrolyte, which may aggravate hydrogen evolution reaction (HER) and Zn corrosion. In addition to the above two strategies to solve the issue of zinc dendrites, constructing an artificial interfacial layer with a similar function to SEI via ex situ coating or in situ growth has been widely studied to ameliorate problems of electrode/electrolyte interface. [9] The metal coating layer exhibits strong affiliationThe practical implementation of Zn metal anodes with high volumetric capacity is seriously plagued by the dendritic growth and accompanying interfacial parasitic reactions. Herein, high yield carbon dots (CDs) with abundant polar functional groups (CHO and CN), as a functional artificial interface layer, are rationally de...