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Ferroferric oxide (Fe3O4) is regarded to be a promising high-capacity anode material for LIBs. However, the capacity attenuates fast and the rate performance is poor due to the dramatic pulverization and sluggish charge transfer properties. To solve these problems, a simple in situ encapsulation and composite method was successfully developed to construct carbon nanotube/nanorod/nanosheet-supported Fe3O4 nanoparticles. Owing to the hierarchical architecture design, the novel structure Fe3O4@C nanocomposites effectively enhance the charge transfer, alleviate pulverization, avoid the agglomeration of Fe3O4 nanoparticles, and also provide superior kinetics toward lithium storage, thereby showing significantly improved reversibility and rate performance. The carbon nanotube/nanorod supported core-shell structure Fe3O4@C nanocomposite displays outstanding high rate capability and stable cycling performance (reversible capability of 1006, 552 and 423 mA h g−1 at 0.2, 0.5 and 1 A g−1 after running 100, 300 and 500 cycles, respectively).

Advanced carbon materials have played an important function in the field of energy conversion and storage. The green and low-carbon synthesis of elemental carbon with controllable morphology and microstructure is the main problem for carbon materials. Herein, we develop a green and low-carbon method to synthesize porous carbon by reacting CO2 with LiAlH4 at low temperatures. The starting reaction temperatures are as low as 142, 121, and 104 °C for LiAlH4 reacting with 1, 30, and 60 bar CO2, respectively. For the elemental carbon, the porosity of elemental carbon gradually decreased, whereas its graphitization degree increased as the CO2 pressure increased from 1 bar to 60 bar. CO2 serves as one of the two reactants and the CO2 pressure can adjust the thermodynamic and kinetic properties of the formation reaction for synthesizing elemental carbon. The mechanism for CO2 pressure-dependent microstructure and morphology of carbon is discussed on the basis of the formation reaction of elemental carbon and gas blowing effect of H2 and CO2. The elemental carbon with different morphology and microstructure exhibits distinct electrochemical lithium storage performance including reversible capacity, rate capability, cycling stability, and Coulombic efficiency, owing to their different lithium storage mechanism. The elemental carbon synthesized at 30 bar CO2 delivers the highest reversible capacity of 506 mAh g−1 after 1000 cycles even at 1.0 A g−1. Advanced energy storage technology based on the green and low-carbon synthesis of carbon materials is a requisite for providing a stable and sustainable energy supply to meet the ever-growing demand for energy.