The demand for compact energy storage devices necessitates the development of high-performance anode materials directly integrated with current collectors, minimizing or eliminating the need for binders or additives. With its layered structure and high theoretical capacity, molybdenum disulfide (MoS2) is regarded as a promising anode material for lithium-ion batteries (LIBs). Here, we report chemical vapor deposition (CVD) growth of self-integrated, vertically aligned MoS2 nanosheets with embedded molybdenum dioxide (MoO2) directly on a molybdenum foil and explore its potential as an anode material for LIBs. The results show that the formation of the MoO2/MoS2 hybrid structure occurs through partial conversion of the initially grown MoO2 crystals to MoS2 layers under controlled sulfurization reactions. The self-integrated hybrid material, devoid of additional conductive or binder agents, exhibits remarkably efficient transfer of ions and electrons, facilitated by the high electrical conductivity of MoO2 and exposed active sites of MoS2. Electrochemical studies reveal an impressive areal capacity of 253 μA h cm-2 for the MoO2/MoS2 hybrid material on a molybdenum foil. In addition, the Li-ion diffusion coefficient value is estimated to be 0.798 × 10-10 and 1.14 × 10-10 cm2/s for the delithiation and lithiation processes, respectively. The capacity of LIBs can be significantly enhanced by engineering the MoO2/MoS2 anode material, making it a promising candidate for overcoming the limitations of single-anode materials. Our findings show that CVD can be a potential approach toward the fabrication of binder and conducting agent-free anodes directly on current collectors for advanced LIBs.
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