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Hexamethylenetetramine concentration effect on CaWO_4 for electrochemical hydrogen evolution reaction activity

机译:六亚甲基四胺浓度浓度效应Cawo_4用于电化学氢气进化反应活性

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摘要

Hexamethylenetetramine (HMT) assisted calcium tungstate nanostructures were successfully synthesized through co-precipitation method. The phase and material confirmation of scheelite type calcium tungstate nanostructures with tetragonal unit cell (a = 5.193 and c = 11.255) were done by employing X-ray diffraction (XRD). All the prepared electrocatalysts such as CW1, CW2 and CW3 crystallite sizes were 29.01, 24.86 and 17.40 nm respectively. The calculated band gap values were found to be 3.31, 3.31 and 3.27 eV for CW1, CW2 and CW3 materials respectively. Different morphology such as ball like and dumbbell shaped calcium tungstate were revealed by scanning electron microscopy (SEM). Surfactant largely plays a significant role to reduce nanostructures agglomeration. The specific surface area, pore volume and diameter of 0.1 M hexamethylenetetramine (HMT) assisted calcium tungstate nanostructure was about 24.7 m(2)/g, 0.141 cc/g and 3.365 nm. The surface area of the calcium tungstate nanostructures drastically enhanced hydrogen evolution reaction (HER) performance as recognized by linear sweep voltammetry. The overpotential values of CW1, CW2 and CW3 electrodes were 123, 115 and 102 mV respectively. Solution resistance (R-s) and charge transfer resistance (R-ct) of synthesized materials was finding out by electrochemical impedance spectroscopy and all prepared electrocatalyst estimated values were 1.07, 1.25, 1.34 Omega and 4.06, 1.62, 0.76 Omega respectively. The stability of 0.1 M hexamethylenetetramine (HMT) assisted CaWO4 was analyzed by 16 h and it exhibited excellent robustness without any decay. The synthesized CaWO4 material exhibited superior hydrogen evolution reaction (HER) activity and the prepared electrodes was capable electro catalysts in water splitting applications.
机译:通过共沉淀法成功地合成了六亚甲基四胺(HMT)辅助碳酮纳米结构。通过采用X射线衍射(XRD)来完成用四方单元电池(A = 5.193和C = 11.255)进行白钨矿型钙钨纳米结构的相和材料确认。所有制备的电催化剂如CW1,CW2和CW3微晶尺寸分别为29.01,24.86和17.40nm。 CW1,CW2和CW3材料分别发现计算的带隙值为3.31,3.31和3.27eV。通过扫描电子显微镜(SEM)揭示了诸如球状和哑铃形钙钨酸盐的不同形态。表面活性剂在很大程度上起到降低纳米结构集聚的重要作用。比表面积,孔体积和直径为0.1M六亚甲基四胺(HMT)辅助碳酸钙纳米结构约24.7m(2)/ g,0.141cc / g和3.365nm。钨酸钙纳米结构的表面积大幅增强了通过线性扫描伏安法识别的氢进化反应(其)性能。 CW1,CW2和CW3电极的过电值分别为123,115和102mV。合成材料的溶液电阻(R-S)和电荷转移电阻(R-CT)通过电化学阻抗光谱发现,所有制备的电催化剂估计值分别为1.07,1.25,1.34ω和4.06,1.62,0.76ω。通过16小时分析0.1M六亚甲基四胺(HMT)辅助Cawo4的稳定性辅助Cawo4,并且在没有任何腐烂的情况下表现出优异的鲁棒性。合成的Cawo4材料表现出优异的氢进化反应(其)活性,并且制备的电极能够在水分裂应用中电催化剂。

著录项

  • 来源
    《Fuel 》 |2021年第15期| 121781.1-121781.8| 共8页
  • 作者单位

    Alagappa Univ Dept Phys Karaikkudi Tamil Nadu India;

    Alagappa Univ Dept Phys Karaikkudi Tamil Nadu India;

    Sri Sivasubramaniya Nadar Coll Engn Dept Chem Engn Chennai 603110 Tamil Nadu India|Sri Sivasubramaniya Nadar Coll Engn Ctr Excellence Water Res CEWAR Chennai 603110 Tamil Nadu India;

    Alagappa Univ Dept Phys Karaikkudi Tamil Nadu India;

    Western Norway Univ Appl Sci Fac Sci & Engn N-5063 Bergen Norway;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Hexamethylenetetramines; Calcium tungstate; Hydrogen evolution reaction; Electrochemical; Catalyst;

    机译:六亚甲基四胺;钨酸钙;氢气进化反应;电化学;催化剂;

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