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通过选择性电化学锡沉积方法制备用于聚合物电解质燃料电池的表面调控纳米 SnO2/Pt3Co/C 阴极催化剂。

Surface-Regulated Nano-SnO2/Pt3Co/C Cathode Catalysts for Polymer Electrolyte Fuel Cells Fabricated by a Selective Electrochemical Sn Deposition Method.

机构信息

Faculty for Integrated Arts and Sciences, The University of Tokushima , Minamijosanjima, Tokushima 770-8502, Japan.

Japan Synchrotron Radiation Research Institute , SPring-8, Sayo, Hyogo 679-5198, Japan.

出版信息

J Am Chem Soc. 2015 Oct 14;137(40):12856-64. doi: 10.1021/jacs.5b04256. Epub 2015 Oct 5.

DOI:10.1021/jacs.5b04256
PMID:26412503
Abstract

We have achieved significant improvements for the oxygen reduction reaction activity and durability with new SnO2-nanoislands/Pt3Co/C catalysts in 0.1 M HClO4, which were regulated by a strategic fabrication using a new selective electrochemical Sn deposition method. The nano-SnO2/Pt3Co/C catalysts with Pt/Sn = 4/1, 9/1, 11/1, and 15/1 were characterized by STEM-EDS, XRD, XRF, XPS, in situ XAFS, and electrochemical measurements to have a Pt3Co core/Pt skeleton-skin structure decorated with SnO2 nanoislands at the compressive Pt surface with the defects and dislocations. The high performances of nano-SnO2/Pt3Co/C originate from efficient electronic modification of the Pt skin surface (site 1) by both the Co of the Pt3Co core and surface nano-SnO2 and more from the unique property of the periphery sites of the SnO2 nanoislands at the compressive Pt skeleton-skin surface (more active site 2), which were much more active than expected from the d-band center values. The white line peak intensity of the nano-SnO2/Pt3Co/C revealed no hysteresis in the potential up-down operations between 0.4 and 1.0 V versus RHE, unlike the cases of Pt/C and Pt3Co/C, resulting in the high ORR performance. Here we report development of a new class of cathode catalysts with two different active sites for next-generation polymer electrolyte fuel cells.

摘要

我们通过一种新的选择性电化学锡沉积方法,对 SnO2-纳米岛/Pt3Co/C 催化剂进行了战略构建,使其在 0.1 M HClO4 中的氧还原反应活性和耐久性得到了显著提高。具有 Pt/Sn = 4/1、9/1、11/1 和 15/1 的纳米 SnO2/Pt3Co/C 催化剂通过 STEM-EDS、XRD、XRF、XPS、原位 XAFS 和电化学测量进行了表征,具有 Pt3Co 核/Pt 骨架-皮肤结构,在压缩的 Pt 表面上用缺陷和位错装饰 SnO2 纳米岛。纳米 SnO2/Pt3Co/C 的高性能源自 Pt 皮肤表面(位点 1)的高效电子修饰,这是由 Pt3Co 核和表面纳米 SnO2 的 Co 以及压缩 Pt 骨架-皮肤表面上 SnO2 纳米岛的外围位点(更多活性位点 2)的独特性质共同作用的结果,其活性远高于 d 带中心值的预期。与 Pt/C 和 Pt3Co/C 相比,纳米 SnO2/Pt3Co/C 的白线峰值强度在 0.4 至 1.0 V 相对于 RHE 的电位上下操作中没有滞后,这导致了高 ORR 性能。在这里,我们报告了一类具有两种不同活性位点的新型阴极催化剂的开发,用于下一代聚合物电解质燃料电池。

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