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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2023 ·Vol. 34 ·期 24 ·1707 · IF 2.8

Enhancement of electrochemical properties of porous rGO by controlled growth CoFe2O4 nanoparticles

Van Ngo Hoanh,Nguyen Hung Tran,Le Hieu Trung,Le Thanh Huu,Vu Thien Tri,Pham Kien Trung,Phung Thinh Xuan

A study area in supercapacitor research is the design and manufacturing of composite electrode materials that combine the advantages of various materials. The rGO/CoFe 2 O 4 composite material is produced by growing cobalt ferrite particles on the surface of rGO using a simple and highly efficient thermal reduction technique. The results show that the electrochemical properties of rGO are significantly improved by the incorporation of cobalt ferrite. rGO sheets are used as supporting frameworks for the CoFe 2 O 4 nanoparticles, while the CoFe 2 O 4 particles provide more active sites for redox reactions. The prepared rGO/CoFe 2 O 4 show excellent electrochemical properties, with a high specific capacitance of 283 F/g at a current density of 0.1 A/g and a specific capacitance retention of 90.5% after 1000 cycles. The attractive performances exhibited by rGO/CoFe 2 O 4 composites make them potential electrode materials for supercapacitors in future.

研究领域: 材料科学 · 电化学 · 纳米科技 · 能源存储 · 功能材料
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ELECTROCHIMICA ACTA · 2017 · IF 4.798

Cu/Ce0.6Mn0.3Fe0.1O2-δ membrane fuel electrode fabricated by infiltration method for solid oxide electrochemical cells

Limin Liu,Yong Wang,Xiaoliang Zhou,Yixuan Yang,Chao Ma,Yuan Li,Chen Wang,Xiaohong Zhao,Bin Li

A cermet fuel electrode Cu/Ce 0.6 Mn 0.3 Fe 0.1 O 2-δ (Cu/CMF) is proposed for a reversible solid oxide electrochemical cell (SOC) with CO/CO 2 as the shuttle. Cu is inert for the carbon deposition and CMF is electrochemically active for CO oxidation and CO 2 reduction. The electrode polarization resistances in CO at 700, 750 and 800   °C are 0.328, 0.207 and 0.155   Ω cm 2 , respectively, presenting high electrochemical activity towards CO oxidation. The maximal power densities can reach up to 303.3, 482.2 and 691.9   mW/cm 2 at 700, 750 and 800   °C, respectively. When the reversible SOCs are operated in solid oxide electrolysis cell mode, the polarization resistance of the electrolysis cell for pure CO 2 reduction at 800   °C has the minimal value of 0.126   Ω cm 2 at 1.8   V. At 2.0   V, the current densities can reach up to 0.584 1.219 and 2.204   A/cm 2 at 700, 750 and 800   °C, respectively. The durability of the cell in CO for as long as 200   h indicates the electrode has remarkable stability. And the short-term stability characteristics for CO 2 electrolysis at different voltages illustrate that the cell performs well below 2.0   V. The harsh reducing environment at 2.0   V may be detrimental to the Cu/CMF electrode.

研究领域: 电化学 · 能源材料 · 功能陶瓷 · 催化化学 · 可再生能源 · 电化学能量转换
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Nanoscale · 2019 ·Vol. 11 ·期 34 ·15881-15891 · IF 6.97

Porous diatomite-mixed 1,4,5,8-NTCDA nanowires as high-performance electrode materials for lithium-ion batteries

Yong Xu,Jun Chen,Ze'en Xiao,Caixia Ou,Weixia Lv,Lihong Tao,Shengwen Zhong

A porous composite electrode composed of diatomite-mixed 1,4,5,8-naphthalenetetracarboxylic dianhydride (NTCDA) is prepared by electrostatic spinning technology. Compared with traditional coated electrodes without diatomite mixing, the obtained composite electrode materials have higher porosity, larger specific surface area and faster lithium ion transport channels, which makes them exhibit better electrochemical performance, such as smaller impedance, higher capacity, and better cycling stability and rate performance. The electrospun diatomite-mixed 1,4,5,8-NTCDA composite (ED-1,4,5,8-NTCDA) electrode shows an initial coulombic efficiency of 77.2%, which is much higher than that of the electrospun 1,4,5,8-NTCA (E-1,4,5,8-NTCDA) electrode without diatomite mixing (63.8%) and the coated 1,4,5,8-NTCA (C-1,4,5,8-NTCDA) electrode (48.3%). Moreover, the ED-1,4,5,8-NTCDA electrode displays an initial discharge capacity of 1106.5 mA h g−1, which is much higher than that of the E-1,4,5,8-NTCDA electrode (546.0 mA h g−1) and the C-1,4,5,8-NTCDA electrode (185.4 mA h g−1). After 200 cycles, the capacity of the ED-1,4,5,8-NTCDA electrode remains at 1008.5 mA h g−1 with a retention ratio of 91.2%, which is also much higher than that of 753.2 mA h g−1 for the E-1,4,5,8-NTCDA electrode and 288.1 mA h g−1 for the C-1,4,5,8-NTCDA electrode. Even at a higher current density of 1500 mA g−1, its capacity remains above 508.9 mA h g−1. The ED-1,4,5,8-NTCDA electrode presents superior performance, which opens up a promising new approach for further utilization of organic materials as electrode materials in rechargeable lithium-ion batteries.

研究领域: 材料科学 · 电化学 · 纳米科技 · 能源存储 · 功能材料
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