Carbon-coated silicon/graphite oxide composites as anode materials for highly stable lithium-ion batteries.

Silicon (Si) has been widely investigated as an anode material for lithium-ion batteries (LIBs) due to its high theoretical capacity. However, the huge volume expansion and low electrical conductivity limit its practical application to some extent. Here, we prepared silicon/reduced graphene oxide/amorphous carbon (Si/G/C) anode materials for lithium-ion batteries using a facile synergistic cladding layer. The protective effect of different carbon layers was explored and it was found that ternary composites have excellent electrochemical properties. In this work, the surface of Si was first modified using ammonia, and the positively charged Si was tightly anchored to the graphene sheet layer. In contrast, amorphous carbon was used as a reinforcing coating for further coating to synergistically build up the cladding layer of Si NPs with graphene oxide. The ternary composite (Si/G/C) material greatly ensures the structural integrity of the composites and shows excellent cycling as well as rate performance compared to Si/reduced graphene oxide and Si/carbon composites. For the Si/G/C composite, at a current density of 1 A g-1, it can be stably cycled over 267 times with 70% capacity retention (only 0.0711% capacity reduction per cycle).

Rational synthesis of 3D coral-like ZnCo2O4 nanoclusters with abundant oxygen vacancies for high-performance supercapacitors.

Transition metal oxides with high theoretical capacitance are regarded as desired electrode materials for supercapacitors, however, the poor conductivity and sluggish charge transfer kinetics constrain their electrochemical performance. The three-dimensional (3D) coral-like ZnCo2O4 nanomaterials with abundant oxygen vacancies were synthesized through a facile hydrothermal method and chemical reduction approach. The introduced oxygen vacancies can provide more active sites and lower the energy barrier, thereby facilitating the kinetics of surface reactions. Furthermore, the abundant oxygen vacancies in metal oxides can function as shallow donors to facilitate charge carrier diffusion, resulting in a faster ion diffusion rate and superior electrochemical conductivity. The electrochemical performance of ZnCo2O4 was optimized by the introduction of oxygen vacancies. The ZnCo2O4 nanoclusters, reduced by 0.5 M NaBH4 (ZnCo2O4-0.5), exhibit a specific capacitance of 2685.7 F g-1 at 1 A g-1, which is nearly twice that of the pristine ZnCo2O4 (1525.7 F g-1 at 1 A g-1). The ZnCo2O4-0.5 exhibits an excellent rate capacity (81.9% capacitance retention at 10 A g-1) and a long cycling stability (72.6% specific capacitance retention after 10 000 cycles at 3 A g-1). Furthermore, the asymmetric supercapacitor (ASC, ZnCo2O4-0.5 nanoclusters//active carbon) delivers a maximum energy density of 50.2 W h kg-1 at the power density of 493.7 W kg-1 and an excellent cycling stability (75.3% capacitance retention after 3000 cycles at 2 A g-1), surpassing the majority of previously reported ZnCo2O4-based supercapacitors. This work is important for revealing the pivotal role of implementing the defect engineering regulation strategy in achieving optimization of both electrochemical activity and conductivity.

Facile synthesis of morphology-controlled hybrid structure of ZnCo2O4 nanosheets and nanowires for high-performance asymmetric supercapacitors.

Controllable synthesis of electrode materials with desirable morphology and size is of significant importance and challenging for high-performance supercapacitors. Herein, we propose an efficient hydrothermal approach to controllable synthesis of hierarchical porous three-dimensional (3D) ZnCo2O4 composite films directly on Ni foam substrates. The composite films consisted of two-dimensional (2D) nanosheets array anchored with one-dimensional (1D) nanowires. The morphologies of ZnCo2O4 arrays can be easily controlled by adjusting the concentration of NH4F. The effect of NH4F in the formation of these 3D hierarchical porous ZnCo2O4 nanosheets@nanowires films is systematically investigated based on the NH4F-independent experiments. This unique 3D hierarchical structure can help enlarge the electroactive surface area, accelerate the ion and electron transfer, and accommodate structural strain. The as-prepared hierarchical porous ZnCo2O4 nanosheets@nanowires films exhibited inspiring electrochemical performance with high specific capacitance of 1289.6 and 743.2 F g-1 at the current density of 1 and 30 A g-1, respectively, and a remarkable long cycle stability with 86.8% capacity retention after 10 000 cycles at the current density of 1 A g-1. Furthermore, the assembled asymmetric supercapacitor using the as-prepared ZnCo2O4 nanosheets@nanowires films as the positive electrode and active carbon as negative electrode delivered a high energy density of 39.7 W h kg-1 at a power density of 400 W kg-1. Our results show that these unique hierarchical porous 3D ZnCo2O4 nanosheets@nanowires films are promising candidates as high-performance electrodes for energy storage applications.