Herein, carbon dots/octahedral molybdenum disulfide hybrids (CDs@1T-MoS 2 ) were successfully fabricated via a facile hydrothermal method by the induction of carbon dots. In this method, CDs as a core in this system were first synthesized via hydrothermal method of citric acid (CA). Their morphology and properties were analyzed using X-Ray diffraction (XRD), Raman spectroscopy, Xray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) measurements. Results indicated that the high yield (about 78%) and ultrathin sheets octahedral 1T-MoS 2 were obtained by introducing CDs fabricated by hydrothermal CA. Importantly, this work effectively solves the aggregation of nonsubstituted MoS 2 sheets via in-situ formation, intercalation and exfoliation of CDs and achieves MoS 2 sheet-based electrode materials with big specific surface area and high specific capacitance as well as good rate capability and excellent cycling stability. Among binary CDs@1T-MoS 2 hybrids, the S4 hybrid especially exhibits the highest specific capacitance of 380 F/g at a current density of 0.5 A/g and the best cycle stability with keeping 97% after 2000 charge-discharge cycles. The outstanding performances of the CDs@1T-MoS 2 hybrids were mainly attributed to the awesome synergistic effects between CDs and 1T-MoS 2 . And these multifunctional CDs@1T-MoS 2 hybrids have great potential applications in supercapacitance electrode material, microwave adsorption, and catalytic degradation. K E Y W O R D S carbon dots (CDs), electrochemical performances, hydrothermal method, octahedral molybdenum disulfide (1T-MoS 2 )