Abstract:Hollow mesoporous hetero-NiCo2S4/Co9S8 submicro-spindles were fabricated in high yield, and delivered excellent pseudocapacitance with high energy density and desirable cycling duration at high rates for advanced hybrid supercapacitors.
“…5e. The ASCs can deliver a high energy density of 37.3 W h kg −1 at a power density of 800 W kg −1 and still maintain as high as 21.3 W h kg −1 while at a high power density of 8 kW kg −1 , which is higher than previously reported ASCs [45][46][47][48][49]. The cycling performance of the Co 3 O 4 @ZnCo 2 O 4 ||AC ASCs was performed at a current density of 5 A g −1 (Fig.…”
“…5e. The ASCs can deliver a high energy density of 37.3 W h kg −1 at a power density of 800 W kg −1 and still maintain as high as 21.3 W h kg −1 while at a high power density of 8 kW kg −1 , which is higher than previously reported ASCs [45][46][47][48][49]. The cycling performance of the Co 3 O 4 @ZnCo 2 O 4 ||AC ASCs was performed at a current density of 5 A g −1 (Fig.…”
“…Furthermore, the SC retention observed here for the hybrid is compared, and even superior to other NCS-based hybrid supercapacitors, such as asymmetric NCS//C (≈23% SC degradation at 5 mA cm −2 after 5000 cycles), [51] NiCo sulfide arrays on Ni foam//AC (≈26.9% SC degradation at 32 mA cm −2 after 3000 cycles), [54] NCS nanotube@NiMn layered double hydroxide arrays/graphene sponge//VN/graphene sponge (≈15.5% SC degradation at 20 mA cm −2 after 5000 cycles), [55] NCS nanosheets//AC (≈20.9% SC degradation at 80 mA cm −2 after 6000 cycles), [4] NCS//AC (≈14.4% SC degradation at 7.5 mA cm −2 after 4000 cycles), [31] Ni/ Co layered double hydroxide@NCS@graphene@Ni foam//AC (≈12.2% SC degradation at 6 A g −1 after 3000 cycles) devices, [56] www.advelectronicmat.de Adv. [57] With the current further up to an even large current density of 3.0 A g −1 , the SC still can be kept as large as ≈86 F g −1 , ≈95% capacitance retention after continuous 2000 cycles. Mater.…”
Section: Electrochemical Performance Of the Ncs-mds//ac Hybrid Supercmentioning
In this contribution, a facile two‐step hydrothermal protocol to prepare hierarchical uniform hollow mesoporous NiCo2S4 microdumbbells (NCS‐MDs) for advanced supercapacitors is developed. Physicochemical investigations reveal that the as‐obtained NCS‐MDs with mesoporous channels in nanoshells possess high‐content Co(III) and Ni(III) species, large surface area (≈80 m2 g−1)/pore volume (≈0.12 m3 g−1), and high tap density (≈0.8 g cm−3). When evaluated as an attractive pseudocapacitive electrode, the unique NCS‐MDs with mass loading of 7 mg cm−2 exhibit remarkable gravimetric/volumetric specific capacitances of ≈912 F g−1 (≈729 F cm−3) at 3 A g−1, and even ≈767 F g−1 (≈613 F cm−3) at high current density of 10 A g−1. Additionally, capacitive degradations of ≈13% and ≈18% are observed over 5000 continous cycles at current rates of 6 and 10 A g−1, respectively. Furthermore, a high‐energy‐density hybrid device is fabricated by using hollow NCS‐MDs and biomass‐derived activated carbon as positive and negative electrodes, respectively, and delivers striking energy density of ≈35.4 Wh kg−1 at power density of ≈381.2 W kg−1, and excellent electrochemical stability at various rates over 11 000 consecutive cycles. These fascinating features strongly highlight that the as‐resulted hollow mesoporous NCS‐MDs could be highly anticipated as a promising electrode platform for next‐generation hybrid supercapacitors.
“…Especially, the self-template method is an efficient approach to generate MMSs with hollow nanostructures. [28,30,75,79,82,83,87] When synthesizing Mo-or W-containing MMSs using these solutionbased methods, (NH 4 ) 2 Mo(W)S 4 is generally used as both Mo(W) and S sources. [29,48,63,89] The gas sulfidation method is another facile approach to synthesize MMSs.…”
Section: Wwwadvenergymatdementioning
confidence: 99%
“…In general, a self-template method involves the synthesis of template precursors and subsequent sulfidation treatment process through ion-exchange reactions and/or Kirkendall effect. Up to present, numerous intriguing templates have been developed, including mixed metal oxide, [72,73] mixed metal hydroxide, [74,75] layered double hydroxide (LDH), [76,77] mixed metal carbonate, [78,79] mixed metal glycerate, [28,80,81] mixed metal carbonate hydroxide, [27,82] mixed metal acetate hydroxide, [83] mixed metal silicate, [84,85] and metal-organic frameworks (MOFs). [86][87][88] These self-engaged templates could directly determine the shape, size, and composition of the resultant MMSs.…”
Section: Wwwadvenergymatdementioning
confidence: 99%
“…[28,72,75,[78][79][80][81][82][83][84][85][130][131][132][133][134] Up to now, various strategies have been developed to synthesize hollow nanostructured nickel cobalt sulfides with diverse nanostructures. Temple-engaged approach is probably the most effective strategy to construct hollow nanostructured nickel cobalt sulfides with controlled composition, size, morphology, shell thickness, internal void size, and interior complexity.…”
Mixed metal sulfides (MMSs) have attracted increased attention as promising electrode materials for electrochemical energy storage and conversion systems including lithium‐ion batteries (LIBs), sodium‐ion batteries (SIBs), hybrid supercapacitors (HSCs), metal–air batteries (MABs), and water splitting. Compared with monometal sulfides, MMSs exhibit greatly enhanced electrochemical performance, which is largely originated from their higher electronic conductivity and richer redox reactions. In this review, recent progresses in the rational design and synthesis of diverse MMS‐based micro/nanostructures with controlled morphologies, sizes, and compositions for LIBs, SIBs, HSCs, MABs, and water splitting are summarized. In particular, nanostructuring, synthesis of nanocomposites with carbonaceous materials and fabrication of 3D MMS‐based electrodes are demonstrated to be three effective approaches for improving the electrochemical performance of MMS‐based electrode materials. Furthermore, some potential challenges as well as prospects are discussed to further advance the development of MMS‐based electrode materials for next‐generation electrochemical energy storage and conversion systems.
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