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通过溴化物诱导的电替换反应合成具有凹面结构的 Pd-Pt 双金属纳米晶体。

Synthesis of Pd-Pt bimetallic nanocrystals with a concave structure through a bromide-induced galvanic replacement reaction.

机构信息

Department of Biomedical Engineering, Washington University, St. Louis, Missouri 63130, United States.

出版信息

J Am Chem Soc. 2011 Apr 20;133(15):6078-89. doi: 10.1021/ja201156s. Epub 2011 Mar 25.

Abstract

This article describes a systematic study of the galvanic replacement reaction between PtCl(6)(2-) ions and Pd nanocrystals with different shapes, including cubes, cuboctahedrons, and octahedrons. It was found that Br(-) ions played an important role in initiating, facilitating, and directing the replacement reaction. The presence of Br(-) ions led to the selective initiation of galvanic replacement from the {100} facets of Pd nanocrystals, likely due to the preferential adsorption of Br(-) ions on this crystallographic plane. The site-selective galvanic replacement resulted in the formation of Pd-Pt bimetallic nanocrystals with a concave structure owing to simultaneous dissolution of Pd atoms from the {100} facets and deposition of the resultant Pt atoms on the {111} facets. The Pd-Pt concave nanocubes with different weight percentages of Pt at 3.4, 10.4, 19.9, and 34.4 were also evaluated as electrocatalysts for the oxygen reduction reaction (ORR). Significantly, the sample with a 3.4 wt.% of Pt exhibited the largest specific electrochemical surface area and was found to be four times as active as the commercial Pt/C catalyst for the ORR in terms of equivalent Pt mass.

摘要

本文系统研究了 PtCl(6)(2-)离子与不同形状的 Pd 纳米晶之间的电置换反应,包括立方体、十二面体和八面体。研究发现 Br(-)离子在引发、促进和定向置换反应中起着重要作用。Br(-)离子的存在导致电置换反应选择性地从 Pd 纳米晶的{100}面开始,这可能是由于 Br(-)离子优先吸附在这个晶面上。由于同时从{100}面溶解 Pd 原子,并在{111}面沉积生成的 Pt 原子,从而导致了具有凹面结构的 Pd-Pt 双金属纳米晶的选择性电置换。还评估了不同 Pt 重量百分比(3.4wt%、10.4wt%、19.9wt%和 34.4wt%)的 Pd-Pt 凹面纳米立方体作为氧还原反应(ORR)的电催化剂。显著的是,在 Pt 质量相当的情况下,具有 3.4wt%Pt 的样品表现出最大的比电化学表面积,对 ORR 的活性是商业 Pt/C 催化剂的四倍。

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