ABSTRACT
Aqueous zinc ion batteries (ZIBs) have been considered promising energy storage systems due to their excellent electrochemical performance, environmental toxicity, high safety and low cost. However, uncontrolled dendrite growth and side reactions at the zinc anode have seriously hindered the development of ZIBs. Herein, we prepared the carbon nanoparticles layer coated zinc anode with (103) crystal plane preferential oriented crystal structure (denoted as C@RZn) by a facile one-step vapor deposition method. The preferential crystallographic orientation of (103) crystal plane promotes zinc deposition at a slight angle, effectively preventing the formation of Zn dendrites on the surface. In addition, the hydrophobic layer of carbon layer used as an inert physical barrier to prevent corrosion reaction and a buffer during volume changes, thus improving the reversibility of the zinc anode. As a result. the C@RZn anode achieves a stable cycle performance of more than 3000 h at 1 mA cm-2 with CE of 99.77 % at 5 mA cm-2. The full battery with C@RZn anode and Mn-doped V6O13 (MVO) cathode show stability for 5000 cycles at the current density of 5 A g-1. This work provides a new approach for the design of multifunctional interfaces for Zn anode.
ABSTRACT
It is a great challenge to achieve both high specific capacity and high energy density of supercapacitors by designing and constructing hybrid electrode materials through a simple but effective process. In this paper, we proposed a hierarchically nanostructured hybrid material combining Zn0.76Co0.24S (ZCS) nanoparticles and Co(OH)2 (CH) nanosheets using a two-step hydrothermal synthesis strategy. Synergistic effects between ZCS nanoparticles and CH nanosheets result in efficient ion transports during the charge-discharge process, thus achieving a good electrochemical performance of the supercapacitor. The synthesized ZCS@CH hybrid exhibits a high specific capacity of 1152.0 C g-1 at a current density of 0.5 A g-1 in 2 M KOH electrolyte. Its capacity retention rate is maintained at â¼ 70.0% when the current density is changed from 1 A g-1 to 10 A g-1. A hybrid supercapacitor (HSC) assembled from ZCS@CH as the cathode and active carbon (AC) as the anode displays a capacitance of 155.7 F g-1 at 0.5 A g-1, with a remarkable cycling stability of 91.3% after 12,000cycles. Meanwhile, this HSC shows a high energy density of 62.5 Wh kg-1 at a power density of 425.0 W kg-1, proving that the developed ZCS@CH is a promising electrode material for energy storage applications.
ABSTRACT
MnCo2O4 is regarded as a good electrode material for supercapacitor due to its high specific capacity and good structural stability. However, its poor electrical conductivity limits its wide-range applications. To solve this issue, we integrated the MnCo2O4 with Ni3S4, which has a good electrical conductivity, and synthesized a MnCo2O4/Ni3S4 nanocomposite using a two-step hydrothermal process. Comparing with individual MnCo2O4 and Ni3S4, the MnCo2O4/Ni3S4 nanocomposite showed a higher specific capacity and a better cycling stability as the electrode for the supercapacitor. The specific capacity value of the MnCo2O4/Ni3S4 electrode was 904.7 C g-1 at 1 A g-1 with a potential window of 0-0.55 V. A hybrid supercapacitor (HSC), assembled using MnCo2O4/Ni3S4 and active carbon as the cathode and anode, respectively, showed a capacitance of 116.4 F g-1 at 1 A g-1, and a high energy density of 50.7 Wh kg-1 at 405.8 W kg-1. Long-term electrochemical stability tests showed an obvious increase of the HSC's capacitance after 5500 charge/discharge cycles, reached a maximum value of â¼162.7% of its initial value after 25,000 cycles, and then remained a stable value up to 64,000 cycles. Simultaneously, its energy density was increased to 54.2 Wh kg-1 at 380.3 W kg-1 after 64,000 cycles.