RESUMO
ZnWO4@NiCo2O4 core-shell nanosheet array composites are synthesized on nickel foam via a two-step hydrothermal method. The optimal conditions, including a Ni(NO3)2·6H2O to Co(NO3)2·6H2O molar ratio of 2 : 1, 12 hours reaction time, and 120 °C temperature, yield a specific capacitance of 875 C g-1 at 1 A g-1. The electrode also maintains 81.1% capacitance after 10 000 cycles. The material's performance is attributed to its core-shell structure, which enhances ion diffusion and electron transport. This study presents a viable approach for high-performance supercapacitor electrodes.
RESUMO
The electrocatalytic performance of a Fe65Co10Si12.5B12.5 Fe-based compounds toward alkaline hydrogen evolution reaction (HER) is enhanced by dealloying. The dealloying process produced a large number of nanosheets on the surface of NS-Fe65Co10Si12.5B12.5, which greatly increased the specific surface area of the electrode. When the dealloying time is 3 h, the overpotential of NS-Fe65Co10Si12.5B12.5 is only 175.1 mV at 1.0 M KOH and 10 mA cm-2, while under the same conditions, the overpotential of Fe65Co10Si12.5B12.5 is 215 mV, which is reduced. In addition, dealloying treated electrodes also show better HER performance than un-dealloying treated electrodes. With the increase in Co doping amount, the overpotential of the hydrogen evolution reaction decreases, and the hydrogen evolution activity is the best when the addition amount of Co is 10%. This work not only provides a basic understanding of the relationship between surface activity and the dealloying of HER catalysts, but also paves a new way for doping transition metal elements in Fe-based electrocatalysts working in alkaline media.
RESUMO
Titanium dioxide (TiO2) photocatalytic technology has the advantages of high catalytic activity, high chemical stability, nontoxicity, and low cost. Therefore, it finds widespread applications in the degradation of organic pollutants in water, antibacterial, environmental purification, and other fields. In this study, we have obtained a photocatalyst by modifying nanoTiO2 with the photosensitizer thioxanthone. The light-harvesting units of thioxanthone and nanoTiO2 can work synergistically to capture light energy. As a heterogeneous photocatalytic material, it can efficiently degrade organic dyes such as Rhodamine B, methyl blue and methyl orange. Specifically, the degradation rate of 0.1 mmol/L Rhodamine B can reach 97% after 35 min of irradiation, and methyl blue and methyl orange can also reach 98 and 56%, respectively.
RESUMO
CuCo2S4 as a spinel-structured transition metal sulfide is a highly effective HER catalyst due to its excellent endurance, low overpotential, and low Tafel slope. In this work, the CuCo2S4/Ni foam (NF) catalysts with various morphologies have been successfully synthesized by controlling the ratio of urea and ammonium fluoride (NH4F) based on the hydrothermal method. Urea and NH4F ratio exhibit a great influence on the microstructure and the HER catalytic performance of CuCo2S4/NF catalysts is discussed in detail.
RESUMO
It is essential for energy storage and conversion systems to construct electrodes and electrocatalysts with superior performance. In this work, ZnCo2S4@Ni(OH)2 nanowire arrays are synthesized on nickel foam by hydrothermal methods. As a supercapacitor electrode, the ZnCo2S4@Ni(OH)2 structure exhibits a specific capacitance of 1,263.0C g-1 at 1 A g-1. The as-fabricated ZnCo2S4@Ni(OH)2//active carbon device can achieve a maximum energy density of 115.4 Wh kg-1 at a power density of 5,400 W kg-1. As electrocatalysts, the ZnCo2S4@Ni(OH)2 structure delivers outstanding performance for oxygen evolution reaction (an overpotential of 256.3 mV at 50 mA cm-2), hydrogen evolution reaction (141.7 mV at 10 mA cm-2), overall water splitting (the cell voltage of 1.53 V at 50 mA cm-2), and a high stability for 13 h.
RESUMO
NiMoO4 is an excellent candidate for supercapacitor electrodes, but poor cycle life, low electrical conductivity, and small practical capacitance limit its further development. Therefore, in this paper, we fabricate NiMoO4@MnCo2O4 composites based on a two-step hydrothermal method. As a supercapacitor electrode, the sample can reach 3000 mF/cm2 at 1 mA/cm2. The asymmetric supercapacitor (ASC), NiMoO4@MnCo2O4//AC, can be constructed with activated carbon (AC) as the negative electrode, the device can reach a maximum energy density of 90.89 mWh/cm3 at a power density of 3726.7 mW/cm3 and the capacitance retention can achieve 78.4% after 10,000 cycles.
RESUMO
In this study, a two-step hydrothermal method is used to prepare NiCo2O4@NiMoO4 nanoscale materials for periodic stability supercapacitors. The synthesized product can be directly used as the electrode material of the supercapacitor, and its specific capacitance is 685.7 C g-1. The composite electrode NiCo2O4@NiMoO4 is used as the positive electrode and the hybrid capacitor is assembled. Meanwhile, at the power density of 4050 W kg-1, the energy density is 96.3 W h kg-1, and the capacitance retention is 100% after 10 000 cycles. At the same time, when the composite is used as a catalyst, it exhibits OER overvoltage (300 mV), HER overvoltage (170 mV) and a low battery voltage of 1.65 V at 10 mA cm-2. After 14 hours of long-term use, NiCo2O4@NiMoO4 maintained good stability, indicating that its structure further improved the electrochemical performance, providing a great advantage for the study of low-cost electrode materials for overall water splitting.