材料科学
催化作用
铂金
甲酸
扫描隧道显微镜
电化学
循环伏安法
氧化物
化学工程
无机化学
纳米技术
物理化学
电极
化学
冶金
有机化学
工程类
作者
Jiwhan Kim,Chi‐Woo Roh,Suman Kalyan Sahoo,Sungeun Yang,Junemin Bae,Jeong Woo Han,Hyunjoo Lee
标识
DOI:10.1002/aenm.201701476
摘要
Abstract Single atomic Pt catalyst can offer efficient utilization of the expensive platinum and provide unique selectivity because it lacks ensemble sites. However, designing such a catalyst with high Pt loading and good durability is very challenging. Here, single atomic Pt catalyst supported on antimony‐doped tin oxide (Pt1/ATO) is synthesized by conventional incipient wetness impregnation, with up to 8 wt% Pt. The single atomic Pt structure is confirmed by high‐angle annular dark field scanning tunneling electron microscopy images and extended X‐ray absorption fine structure analysis results. Density functional theory calculations show that replacing Sb sites with Pt atoms in the bulk phase or at the surface of SbSn or ATO is energetically favorable. The Pt1/ATO shows superior activity and durability for formic acid oxidation reaction, compared to a commercial Pt/C catalyst. The single atomic Pt structure is retained even after a harsh durability test, which is performed by repeating cyclic voltammetry in the range of 0.05–1.4 V for 1800 cycles. A full cell is fabricated for direct formic acid fuel cell using the Pt1/ATO as an anode catalyst, and an order of magnitude higher cell power is obtained compared to the Pt/C.
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