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Polyethyleneimine functionalized platinum superstructures: enhancing hydrogen evolution performance by morphological and interfacial control

机译:聚乙烯亚胺官能化的铂上层结构:通过形态和界面控制提高析氢性能

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摘要

The electrocatalytic hydrogen evolution reaction (HER) is a highly promising green method for sustainable and efficient hydrogen production. So far, Pt nanocrystals are still the most active electrocatalysts for the HER in acidic media, although a tremendous search for alternatives has been done in the past decade. In this work, we synthesize polyethyleneimine (PEI) functionalized Pt superstructures (Pt-SSs@PEI) with tetragonal, hierarchical, and branched morphologies with a facile wet chemical reduction method. A series of physical characterizations are conducted to investigate the morphology, electronic structure, surface composition, and formation mechanism of Pt-SSs@PEI. Impressively, the as-prepared Pt-SSs@PEI show an unprecedented onset reduction potential (+64.6 mV vs. reversible hydrogen electrode) for the HER in strong acidic media due to the protonation of –NH2 groups in the PEI adlayers on the Pt surface, and they outperform all currently reported HER electrocatalysts. The work highlights a highly effective interface-engineering strategy for improving the electrocatalytic performance of Pt nanocrystals for the HER.
机译:电催化制氢反应(HER)是可持续发展和高效制氢的极有前途的绿色方法。到目前为止,Pt纳米晶体在酸性介质中仍然是HER活性最高的电催化剂,尽管过去十年来人们一直在寻找替代品。在这项工作中,我们用一种简便的湿式化学还原方法合成了具有四方,分层和分支形态的聚乙烯亚胺(PEI)功能化的Pt超结构(Pt-SSs @ PEI)。进行了一系列的物理表征,以研究Pt-SSs @ PEI的形态,电子结构,表面组成和形成机理。令人印象深刻的是,由于Pt表面PEI层中–NH2基团的质子化,在强酸性介质中,所制备的Pt-SSs @ PEI显示出前所未有的HER还原电位(与可逆氢电极相比为+64.6 mV)的性能优于目前报道的所有HER电催化剂。这项工作强调了一种有效的界面工程策略,可改善Pt纳米晶体对HER的电催化性能。

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