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Surface treated nickel phosphide nanosheet with oxygen as highly efficient bifunctional electrocatalysts for overall water splitting

机译:经表面处理的磷化镍纳米片,具有氧气作为高效的双功能电催化剂,可用于整体水分解

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The development of high catalytic activity, earth-abundant, low-cost, and long-term stability electrocatalysts is highly desirable. In this study, oxygen surface treated Ni2P nanosheets as bifunctional catalysts for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is proposed based on density functional theory calculations. The mechanism of the enhanced electrocatalytic performance was investigated by considering oxygen adsorption and substitution of surface phosphorus on the Ni2P nanosheets surface. The results show that six O adsorption and six O substitution Ni2P exhibit excellent electrocatalytic performance because of their tuned Gibbs free energy and overpotential for hydrogen/oxygen evolution reaction being just -0.21 eV/0.27 V and - 0.15 eV/0.45 V, respectively. Additionally, due to the reducing of total potential, the catalysts can present better OER performance in alkaline media. The bicatalytic activities of O adsorption and O substitution can be well-explained by an amendatory p band-center model, which is also suitable for a broad class of surface engineering systems. This theoretical study not only provides vital insights into the enhanced mechanism of the bifunctional activities of water splitting but also helps to prescribe the principles for designing high performance multifunctional electrocatalysts.
机译:迫切需要开发高催化活性,富含地球的,低成本和长期稳定性的电催化剂。在这项研究中,基于密度泛函理论计算,提出了将氧气表面处理过的Ni2P纳米片作为双功能催化剂用于氢气释放反应(HER)和氧气释放反应(OER)。通过考虑氧的吸附和Ni2P纳米片表面上表面磷的取代,研究了增强电催化性能的机理。结果表明,六个O吸附和六个O取代Ni2P表现出优异的电催化性能,这是因为它们的吉布斯自由能和氢/氧释放反应的超电势分别仅为-0.21 eV / 0.27 V和-0.15 eV / 0.45V。另外,由于总电势的降低,催化剂在碱性介质中可以表现出更好的OER性能。 O吸附和O取代的双催化活性可以通过修正的p带中心模型得到很好的解释,该模型也适用于各种表面工程系统。这项理论研究不仅为水分解双功能活性的增强机理提供了重要的见解,而且还有助于规定设计高性能多功能电催化剂的原理。

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