Vanadium oxides as cathode for zinc-ion batteries have attracted much attention because of their high theoretical capacity,flexible layered structure and abundant resources.However,cathodes are susceptible to the coll...Vanadium oxides as cathode for zinc-ion batteries have attracted much attention because of their high theoretical capacity,flexible layered structure and abundant resources.However,cathodes are susceptible to the collapse of their layered structure and the dissolution of vanadium after repeated long cycles,which worsen their capacities and cycling stabilities.Herein,a synergistic engineering of calcium-ion intercalation and polyaniline coating was developed to achieve the superior electrochemical performance of vanadium pentoxide for zinc-ion batteries.The pre-intercalation of calcium-ion between vanadium pentoxide layers as pillars increase the crystal structure’s stability,while the polyaniline coating on the cathodes improves the conductivity and inhibits the dissolution of vanadium.This synergistic engineering enables that the battery system based-on the polyaniline coated calcium vanadate cathode to deliver a high capacity of 406.4 mAh·g^(−1)at 1 A·g^(−1),an ultralong cycle life over 6000 cycles at 10 A·g^(−1)with 93%capacity retention and high-rate capability.The vanadium oxide cathode with synergistic engineering of calcium-ion intercalation and polyaniline coating was verified to effectively improve the electrochemical performance of zinc-ion batteries.展开更多
Potassium ion hybrid capacitors(PIHC)have promising applications in medium and large-scale energy storage systems due to their high energy/power density,abundant potassium resource and low cost.However,the slow kineti...Potassium ion hybrid capacitors(PIHC)have promising applications in medium and large-scale energy storage systems due to their high energy/power density,abundant potassium resource and low cost.However,the slow kinetics of battery-type anodes originating from the large-size K+results in a mismatch between the two electrodes,rendering the modest energy density of PIHC.Herein,we first develop an electrospinning strategy to successfully synthesize fibrous precursor by using the HNO_(3)pre-oxidized low-softening-point coal pitch as the low-cost raw material.With further carbonization or KOH activation,the two types of carbon nanofibers(CNF)are fabricated as anode and cathode materials,respectively,towards the dual-carbon PIHC devices.Thanks to its threedimensional interconnected porous conducting network and large layer spacing,the resulted CNF anode material is endowed with high reversible capacities,excellent rate and long cycle stability.Meanwhile,the activated CNF cathode with a large surface area of 2169 m^(2)·g^(-1)exhibits excellent capacitive performance.A PIHC constructed with the two fibrous electrodes delivers an energy density of110.0 Wh·kg^(-1)at 200.0 W kg^(-1),along with a capacitance retention of 83.5%after 10,000 cycles at 1.0 A·g^(-1).The contribution here provides a cost-efficiency avenue and platform for advanced dual-carbon PIHC.展开更多
Novel and highly durable air cathode electrocatalyst with three dimensional (3D)-clam-shaped structure, MnO2 nanotubes-supported Fe2O3 (Fe2O3/MnO2) composited by carbon nanotubes (CNTs) ((Fe2O3/ MnO2)3/4-(C...Novel and highly durable air cathode electrocatalyst with three dimensional (3D)-clam-shaped structure, MnO2 nanotubes-supported Fe2O3 (Fe2O3/MnO2) composited by carbon nanotubes (CNTs) ((Fe2O3/ MnO2)3/4-(CNTs)1/4) is synthesized using a facile hydrothermal process and a following direct heat- treatment in the air. The morphology and composition of this catalyst are analyzed using scanning elec- tronic microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD) and energy dispersive X-ray spectroscopy (EDX). The morphology characteristics reveal that flower-like Fe2O3 parti- cles are highly dispersed on both MnO2 nanotubes and CNT surfaces, coupling all three components firmly. Electrochemical measurements indicate that the synergy of catalyst exhibit superior bi- functional catalytic activity for both oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) as well as stability than Pt/C and lrO2 catalysts. Using these catalysts for air-cathodes, both primary and rechargeable zinc-air batteries (ZABs) are assembled for performance validation. In a primary ZAB, this 3D-clamed catalyst shows a decent open circuit voltage (OCV, -1.48 V) and a high discharge peak power density (349 mW cm 2), corresponding to a coulomhic efficiency of 92%. In a rechargeahle ZABs with this bifunctional catalyst, high OCV (〉1.3 V) and small charge-discharge voltage gap (〈1.1 V) are achieved along with high specific capacity (780 mAh g 1 at 30 mA cm-2) and robust cycle-life (1,390 cycles at cycle profile of 20 mA/10 min).展开更多
基金This work was supported by the National Natural Science Foundation of China(Grant Nos.22101309,52103277 and U1804126)the Key Scientific and Technological Project of Henan Province(Grant No.222102240001)the Startup Research of Henan Academy of Sciences(Grant No.231817001).
文摘Vanadium oxides as cathode for zinc-ion batteries have attracted much attention because of their high theoretical capacity,flexible layered structure and abundant resources.However,cathodes are susceptible to the collapse of their layered structure and the dissolution of vanadium after repeated long cycles,which worsen their capacities and cycling stabilities.Herein,a synergistic engineering of calcium-ion intercalation and polyaniline coating was developed to achieve the superior electrochemical performance of vanadium pentoxide for zinc-ion batteries.The pre-intercalation of calcium-ion between vanadium pentoxide layers as pillars increase the crystal structure’s stability,while the polyaniline coating on the cathodes improves the conductivity and inhibits the dissolution of vanadium.This synergistic engineering enables that the battery system based-on the polyaniline coated calcium vanadate cathode to deliver a high capacity of 406.4 mAh·g^(−1)at 1 A·g^(−1),an ultralong cycle life over 6000 cycles at 10 A·g^(−1)with 93%capacity retention and high-rate capability.The vanadium oxide cathode with synergistic engineering of calcium-ion intercalation and polyaniline coating was verified to effectively improve the electrochemical performance of zinc-ion batteries.
基金financially supported by the National Natural Science Foundation of China(Nos.52072151 and 52171211)Taishan Scholars(No.ts201712050)+2 种基金Jinan Independent Innovative Team(No.2020GXRC015)the Natural Science Doctoral Foundation of Shandong Province(No.ZR2019BB057)the Major Program of Shandong Province Natural Science Foundation(No.ZR2021ZD05)。
文摘Potassium ion hybrid capacitors(PIHC)have promising applications in medium and large-scale energy storage systems due to their high energy/power density,abundant potassium resource and low cost.However,the slow kinetics of battery-type anodes originating from the large-size K+results in a mismatch between the two electrodes,rendering the modest energy density of PIHC.Herein,we first develop an electrospinning strategy to successfully synthesize fibrous precursor by using the HNO_(3)pre-oxidized low-softening-point coal pitch as the low-cost raw material.With further carbonization or KOH activation,the two types of carbon nanofibers(CNF)are fabricated as anode and cathode materials,respectively,towards the dual-carbon PIHC devices.Thanks to its threedimensional interconnected porous conducting network and large layer spacing,the resulted CNF anode material is endowed with high reversible capacities,excellent rate and long cycle stability.Meanwhile,the activated CNF cathode with a large surface area of 2169 m^(2)·g^(-1)exhibits excellent capacitive performance.A PIHC constructed with the two fibrous electrodes delivers an energy density of110.0 Wh·kg^(-1)at 200.0 W kg^(-1),along with a capacitance retention of 83.5%after 10,000 cycles at 1.0 A·g^(-1).The contribution here provides a cost-efficiency avenue and platform for advanced dual-carbon PIHC.
基金supported by the National Natural Science Foundation of China(U1510120)Natural Science Foundation of Shanghai(14ZR1400700)+2 种基金the Project of Introducing Overseas Intelligence High Education of China(2017-2018)the Graduate Thesis Innovation Foundation of Donghua University(EG2017031,EG2016034)the College of Environmental Science and Engineering,State Environmental Protection Engineering Centre for Pollution Treatment and Control in Textile Industry,Donghua University
文摘Novel and highly durable air cathode electrocatalyst with three dimensional (3D)-clam-shaped structure, MnO2 nanotubes-supported Fe2O3 (Fe2O3/MnO2) composited by carbon nanotubes (CNTs) ((Fe2O3/ MnO2)3/4-(CNTs)1/4) is synthesized using a facile hydrothermal process and a following direct heat- treatment in the air. The morphology and composition of this catalyst are analyzed using scanning elec- tronic microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD) and energy dispersive X-ray spectroscopy (EDX). The morphology characteristics reveal that flower-like Fe2O3 parti- cles are highly dispersed on both MnO2 nanotubes and CNT surfaces, coupling all three components firmly. Electrochemical measurements indicate that the synergy of catalyst exhibit superior bi- functional catalytic activity for both oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) as well as stability than Pt/C and lrO2 catalysts. Using these catalysts for air-cathodes, both primary and rechargeable zinc-air batteries (ZABs) are assembled for performance validation. In a primary ZAB, this 3D-clamed catalyst shows a decent open circuit voltage (OCV, -1.48 V) and a high discharge peak power density (349 mW cm 2), corresponding to a coulomhic efficiency of 92%. In a rechargeahle ZABs with this bifunctional catalyst, high OCV (〉1.3 V) and small charge-discharge voltage gap (〈1.1 V) are achieved along with high specific capacity (780 mAh g 1 at 30 mA cm-2) and robust cycle-life (1,390 cycles at cycle profile of 20 mA/10 min).