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NiO/MnO2
IONICS · 2024 · IF 2.4

NiO/MnO2 pompon-like hybrid structure for long-term electrode and supercapacitor

Yan Lichen,Chen Wei,Song Zehui,Xiao Li

A novel NiO/MnO 2 pompon-like hybrid structure was synthesized through a facile one-step hydrothermal in situ growth approach in this paper. NiO nanosheets grow on MnO 2 pompon-like microsphere to form typical hybrid structures which significantly increase the abundant active sites of electrode materials. The resulting NiO/MnO 2 electrode material exhibits an impressive specific capacity of 2706.1 F/g at a current density of 1 A/g. Remarkably, NiO/MnO 2 pompon-like hybrid structure shows excellent cycling performance and its capacity retention is maintained at 84.8% and the charge–discharge efficiency at 96% after 15,000 cycles. Even after undergoing 40,000 cycles, the electrode material maintains an outstanding charge–discharge efficiency of 95.2% with capacity retention of 69%, which revealing promising application as long-term electrode materials for supercapacitors.

CAS / MDL: 151-21-3
研究领域: 材料科学 · 能源存储
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ELECTROCHIMICA ACTA · 2017 · IF 4.798

One-pot microwave synthesis of NiO/MnO2 composite as a high-performance electrode material for supercapacitors

Yuhong Bi,Amit Nautiyal,Huaiping Zhang,Jujie Luo,Xinyu Zhang

A facile and energy efficient microwave synthesis of NiO/MnO 2 composite is presented in this study. The NiO nanoparticles (∼30 nm) and composite of NiO nanoparticles with nano-particle MnO 2 were grown on the surface of graphite. The morphologies and electrochemical performance of NiO@graphite and NiO/MnO 2 @graphite composite were tested and compared. The SEM results showed that addition of MnO 2 prevented the agglomeration of NiO nanoparticles. The electrochemical results of NiO/MnO 2 @graphite has demonstrated better performance than NiO@graphite, with higher specific capacitance of 102.78 mAh g −1 at 1 A g −1 and superior cycling stability with specific capacitance retention of 140% over more than 1500 cycles. The excellent electrochemical performance of NiO/MnO 2 @graphite makes it suitable for electrode material of supercapacitors .

CAS / MDL: 7782-42-5 6156-78-1
研究领域: 材料科学 · 电化学 · 纳米技术
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JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY · 2021 ·Vol. 96 ·期 6 ·1553-1560 · IF 3.174

NiO-MnO2/Nb2O5-TiO2 catalyzed reaction integration of butanal self-condensation and successive hydrogenation and its kinetics

Sibo Li,Jiaxun Zhang,Hualiang An,Guirong Wang,Xinqiang Zhao,Yanji Wang

BACKGROUND The reaction integration of butanal self-condensation and successive hydrogenation (that is, one-step synthesis of 2-ethylhexanol from butanal) is an efficiency way to simply process flow and reduce energy consumption for the commercial manufacture of 2-ethylhexanol (2EHO). In the present work, a NiO-MnO 2 /Nb 2 O 5 -TiO 2 catalyst was prepared for the integration reaction to reach a high 2-ethylhexanol selectivity. Furthermore, the reaction integration was investigated kinetically for the next scale-up. RESULTS A 2EHO selectivity of 90.0% was achieved at a complete conversion of butanal with the help of reduction-in-reaction technique in this reaction integration. The reaction rate of butanal is determined by the reversible aldol self-condensation reaction and its direct hydrogenation reaction. The reaction order with respect to butanal in the two reactions is, respectively, 2.004 and 1.004. The activation energy of the hydrogenation reaction is higher than that of the forward reaction of the self-condensation, suggesting the suppressive effect the reaction integration on the direct hydrogenation. CONCLUSION The reaction integration promotes butanal self-condensation and successive hydrogenation and it suppresses butanal direct hydrogenation by using NiO-MnO 2 /Nb 2 O 5 -TiO 2 catalyst with the help of reduction-in-reaction technique, giving rise to a pretty high selectivity of 2-ethylhexanol. The establishment of the integration reaction kinetics will lay the foundation for reactor design and analysis. © 2021 Society of Chemical Industry

CAS / MDL: 5593-70-4 9022-96-2
研究领域: 化学工程 · 催化化学 · 反应动力学
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