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Enhancing oxygen and hydrogen evolution activities of perovskite oxide LaCoO3 via effective doping of platinum

机译:通过有效掺杂铂增强钙钛矿氧化物LaCoO3的氧气和氢气逸出活性

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In this study, a series of perovskite oxides LaCo _(1? x ) Pt _( x ) O _(3? δ ) ( x = 0, 0.02, 0.04, 0.06, and 0.08) were prepared by the citric acid–ethylenediaminetetraacetic acid (CA–EDTA) complexing sol–gel method and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). Then, the samples were investigated as OER and HER bifunctional electrocatalysts in alkaline media. Compared with other catalysts, LaCo _(0.94) Pt _(0.06) O _(3? δ ) had good stability and presented more activity at a lower overpotential of 454 mV (at 10 mA cm ~(?2) ), a lower Tafel slope value of 86 mV dec ~(?1) and a higher mass activity of 44.4 A g ~(?1) for OER; it displayed a lower overpotential of 294 mV (at ?10 mA cm ~(?2) ), a lower Tafel slope value of 148 mV dec ~(?1) and a higher mass activity of ?34.5 A g ~(?1) for HER. The improved performance might depend on a larger ECSA, faster charge transfer rate and higher ratio of the highly oxidative oxygen species (O _(2) ~(2?) /O ~(?) ). Furthermore, the e _(g) orbital filling of Co approaching 1.2 in the B site might play a leading role.
机译:在这项研究中,通过柠檬酸-乙二胺四乙酸制备了一系列钙钛矿氧化物LaCo _(1?x)Pt _(x)O _(3?δ)(x = 0、0.02、0.04、0.06和0.08)。酸(CA-EDTA)络合溶胶-凝胶法,其特征在于X射线衍射(XRD),扫描电子显微镜(SEM),透射电子显微镜(TEM)和X射线光电子能谱(XPS)。然后,将样品作为碱性介质中的OER和HER双功能电催化剂进行研究。与其他催化剂相比,LaCo _(0.94)Pt _(0.06)O _(3?δ)具有良好的稳定性,并且在454 mV的较低过电势(在10 mA cm〜(?2)),较低的情况下表现出更多的活性。塔菲尔斜率值为86 mV dec〜(?1),对OER的质量活度更高,为44.4 A g〜(?1);它显示出较低的过电位294 mV(在?10 mA cm〜(?2)时),更低的Tafel斜率值148 mV dec〜(?1)和更高的质量活性?34.5 A g〜(?1)为了她。性能的提高可能取决于更大的ECSA,更快的电荷传输速率和更高比例的高氧化性氧(O _(2)〜(2?)/ O〜(?))。此外,B站点中Co的e _(g)轨道填充接近1.2可能起主导作用。

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