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核壳结构Ni@Pt氧还原反应电催化剂的形貌与成分工程

Topographical and compositional engineering of core-shell Ni@Pt ORR electro-catalysts.

作者信息

Leteba Gerard M, Mitchell David R G, Levecque Pieter B J, van Steen Eric, Lang Candace I

机构信息

Catalysis Institute, Department of Chemical Engineering, University of Cape Town Cape Town 7700 South Africa

School of Engineering, Macquarie University Sydney NSW 2109 Australia.

出版信息

RSC Adv. 2020 Aug 7;10(49):29268-29277. doi: 10.1039/d0ra05195k. eCollection 2020 Aug 5.

Abstract

Complex faceted geometries and compositional anisotropy in alloy nanoparticles (NPs) can enhance catalytic performance. We report on the preparation of binary PtNi NPs a co-thermolytic approach in which we optimize the synthesis variables, which results in significantly improved catalytic performance. We used scanning transmission electron microscopy to characterise the range of morphologies produced, which included spherical and concave cuboidal core-shell structures. Electrocatalytic activity was evaluated using a rotating disc electrode (1600 rpm) in 0.1 M HClO; the electrocatalytic performance of these Ni@Pt NPs showed significant (∼11-fold) improvement compared to a commercial Pt/C catalyst. Extended cycling revealed that electrochemical surface area was retained by cuboidal PtNi NPs post 5000 electrochemical cycles (0.05-1.00 V, SHE). This is attributed to the enclosure of Ni atoms by a thick Pt shell, thus limiting Ni dissolution from the alloy structures. The novel synthetic strategy presented here results in a high yield of Ni@Pt NPs which show excellent electro-catalytic activity and useful durability.

摘要

合金纳米颗粒(NPs)中复杂的多面体形貌和成分各向异性能够提高催化性能。我们报道了二元PtNi NPs的制备,采用共热解方法,通过优化合成变量,显著提高了催化性能。我们使用扫描透射电子显微镜来表征所产生的形貌范围,其中包括球形和凹面立方核壳结构。在0.1 M HClO中使用旋转圆盘电极(1600 rpm)评估电催化活性;与商业Pt/C催化剂相比,这些Ni@Pt NPs的电催化性能有显著(约11倍)提高。长时间循环表明,在5000次电化学循环(0.05 - 1.00 V,标准氢电极)后,立方体形PtNi NPs的电化学表面积得以保留。这归因于Ni原子被厚的Pt壳层包裹,从而限制了Ni从合金结构中的溶解。本文提出的新型合成策略可高产率制备出具有优异电催化活性和良好耐久性的Ni@Pt NPs。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4e4/9055937/f5faea0fcffb/d0ra05195k-s1.jpg

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