催化作用
纳米颗粒
金属有机骨架
碳纤维
材料科学
多孔性
氧还原反应
氮气
无机化学
金属
化学工程
氧气
核化学
化学
纳米技术
电化学
物理化学
冶金
有机化学
电极
复合材料
复合数
吸附
工程类
作者
Wenling Gu,Changshuai Shang,Jing Li,Erkang Wang
标识
DOI:10.1002/celc.201700632
摘要
Abstract Herein, a porous nitrogen‐doped carbon material (NH 2 ‐MIL‐101‐C) derived from the metal‐organic frameworks (MOFs) of NH 2 ‐MIL‐101 ([Fe 3 OX(NH 2 ‐BDC) 3 ] n , X: OH, NH 2 ‐BDC: 2‐aminoterephthalic acid) is applied as a corrosion‐resistant support matrix for the growth of Pt nanoparticles (NH 2 ‐MIL‐101‐C@Pt). The Pt nanoparticles could be uniformly and steadily deposited on the porous carbon support matrix, owing to their strong interactions, which effectively inhibited agglomeration of the nanoparticles. NH 2 ‐MIL‐101‐C@Pt is tested for the possible factors as an excellent oxygen reduction reaction (ORR) catalyst in basic medium. Compared to the commercial Pt/C catalyst, enhanced ORR activity and greater long‐time durability is obtained when using the NH 2 ‐MIL‐101‐C@Pt catalyst. In addition, it is proved that the enhanced activity should be ascribed to the alternate local electron density of Pt in the NH 2 ‐MIL‐101‐C@Pt catalyst, which convincingly change the d‐band center of Pt compared to the Fermi level and promotes faster ORR kinetics.
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