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Dopant influence on phase and electrochemical performance of molybdenum sulfide nanostructures

机译:掺杂对硫化钼纳米结构的相和电化学性能的影响

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MoS_2 nanostructure was successfully synthesized by employing one step solvothermal route for electrochemical water splitting applications. Generally, MoS_2 nanostructures played a very important role in electrochemical energy field due to its unique physical and chemical properties [1]. In the present study, bare and Ni incorporated MoS_2 nanostructures were synthesized via solvothermal route and the rhombohedral phase formation for bare and 5% Ni doped MoS2 was confirmed by X-ray diffraction (XRD) study. On further increasing the dopant concentration as 10%, the phase transformation was strongly influenced and thereby the rhombohedral phase was turned as monoclinic Mo_2S_3 phase and was evidenced by strong diffraction peak of plane (-101). The phase changing mechanism of Ni dopant on MoS_2 nanostructures was also revealed. The luminescent nature of the synthesized nanostructures was studied by photoluminescence (PL) spectra. FTIR result clearly demonstrated the Mo-S vibration of two different phases. SEM images clearly revealed the clumsy growth of nanorods for both the phases of nanostructures. The electrochemical water splitting efficiency of different phase molybdenum sulfides have been explored by cyclic voltammetry (CV), linear sweep voltammetry (LSV), electrochemical impedance spectroscopy (EIS) and chronoampherometry (CA) studies. The best efficient 10% Ni doped Mo_2S_3 electrode governed the specific capacitance of 1207 F/g at 10 mV/s scan rate with higher current density of 193 mA/g with good conductivity. Moreover, the very good electrochemical stability was reported for the efficient electrode for 18 h with zero percent decay of its activity even after 18 h of excellent electrochemical water oxidation process. Mechanism of dopant and phase nature on electrochemical performance of the electrode was revealed. Hence, the favorable phase, dopant and morphology of molybdenum sulfide nanostructures for electrochemical water splitting applications were explored in this study.
机译:通过采用电化学水分裂应用的一步溶液途径成功地合成MOS_2纳米结构。通常,由于其独特的物理和化学性质,MOS_2纳米结构在电化学能场中起着非常重要的作用[1]。在本研究中,通过溶液通过溶液合成裸裸和Ni掺入的MOS_2纳米结构,通过X射线衍射(XRD)研究证实了裸露和5%Ni掺杂MOS2的菱形相形成。在进一步增加掺杂剂浓度为10%时,相变强烈影响,从而使菱形相变为单斜晶体MO_2S_3相,并且通过平面的强衍射峰(-101)来证明。还揭示了MOS_2纳米结构NI掺杂剂的相变机制。通过光致发光(PL)光谱研究了合成纳米结构的发光性质。 FTIR结果清楚地证明了两种不同阶段的MO-S振动。 SEM图像清楚地揭示了纳米结构阶段的纳米棒的笨拙生长。通过循环伏安法(CV),线性扫描伏安法(LSV),电化学阻抗谱(EIS)和ChronoAnhermetry(CA)研究探索了不同相钼硫化物的电化学水分解效率。最佳有效的10%Ni掺杂Mo_2S_3电极在10 mV / s扫描速率下控制了1207 f / g的特定电容,电流密度为193mA / g,导电性良好。此外,即使在优异的电化学水氧化过程18小时后,其活性为18小时的高效电极为18小时的高效电极,均为非常好的电化学稳定性。揭示了掺杂剂和相性质对电极电化学性能的机理。因此,本研究探讨了电化学水分解应用硫化钼纳米结构的有利相,掺杂剂和形态。

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