Pt介花水裂解电催化剂的合成

S. Razak, V. Fauzia, S. Budi, M. Khotib
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摘要

电催化水分解被认为是一种有希望的技术,在生产氢作为负担得起的绿色能源。电催化剂用于提高析氢反应(HER)和析氧反应(OER)的动力学。与其他贵金属相比,铂(Pt)在酸或碱电解质中作为HER电催化剂具有最高的效率和稳定性。文献研究表明,纳米结构Pt的电催化效率受晶面形状、尺寸和表面的影响很大。为此,本研究在涂有氧化铟锡(ITO)的玻璃基板上进行了方波脉冲(SWP)电沉积,在两种不同的电解质溶液(KCl和KCl+H2SO4)中进行了铂颗粒的合成,以获得表面上一定的晶体面。结果表明:硫酸电解质(HSO4−和SO42-)中存在一定的离子,会影响Pt颗粒的生长;这些离子促进了各向异性、花状颗粒的形成,而使用KCl本身作为电解质只产生球形的Pt颗粒。我们的Pt介孔花(MFs)在HER中表现出更好的催化性能,并且比Pt介孔球(MSs)具有更低的过电位和斜率。这一结果可能是由于高指数面(220)和(311)的存在,它们作为活性位点可以破坏化合物的键链。另一方面,Pt MSs的主要晶面是(100)和(002),这对OER的催化活性更有利。
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Synthesis of Pt mesoflowers as electrocatalysts for water splitting
Electrocatalytic water splitting is considered a hopeful technology in the production of hydrogen as affordable green energy. Electrocatalysts are used to enhance the electrokinetics of the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). Compared to other noble metals, platinum (Pt) has the highest efficiency and stability in HER electrocatalyst in acid or base electrolytes. Literature studies show that the electrocatalytic efficiency of nanostructured Pt is greatly affected by the shape, size, and surface of the crystal facets. For this reason, this research carried out the synthesis of Pt particles on a glass substrate coated with indium tin oxide (ITO) using square-wave pulse (SWP) electrodeposition with two variations in the electrolyte solution (KCl and KCl+H2SO4) to obtain certain crystal facets on the surface. The results show that the growth of Pt particles was affected by the presence of certain ions in the sulfuric acid electrolyte (HSO4− and SO42-). These ions promoted the formation of anisotropic, flower-like particles, while using KCl by itself as an electrolyte produced only spherically shaped Pt particles. Our Pt mesoflowers (MFs) showed better catalytic performance in the HER and a lower overpotential and slope than the Pt mesospheres (MSs). This result might be due to the presence of the high-index facets (220) and (311), which work as active sites that can break the bonding chains of compounds. On the other hand, the dominant crystal facets of the Pt MSs are (100) and (002), which are more favorable for the catalytic activity of the OER.
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