原子层沉积
催化作用
氧还原
纳米颗粒
图层(电子)
材料科学
化学工程
选择性
碳纤维
铂金
粒径
粒子(生态学)
碳纳米管
氧还原反应
纳米技术
无机化学
沉积(地质)
化学
电化学
电极
物理化学
复合材料
有机化学
地质学
古生物学
工程类
海洋学
复合数
生物
沉积物
作者
Jie Gan,Jiankang Zhang,Baiyan Zhang,Wenyao Chen,Dongfang Niu,Yong Qin,Xuezhi Duan,Xinggui Zhou
标识
DOI:10.1016/j.jechem.2019.09.024
摘要
Understanding carbon-supported Pt-catalyzed oxygen reduction reaction (ORR) from the perspective of the active sites is of fundamental and practical importance. In this study, three differently sized carbon nanotube-supported Pt nanoparticles (Pt/CNT) are prepared by both atomic layer deposition (ALD) and impregnation methods. The performances of the catalysts toward the ORR in acidic media are comparatively studied to probe the effects of the sizes of the Pt nanoparticles together with their distributions, electronic properties, and local environments. The ALD-Pt/CNT catalysts show much higher ORR activity and selectivity than the impregnation-Pt/CNT catalysts. This outstanding ORR performance is ascribed to the well-controlled Pt particle sizes and distributions, desirable Pt0 4f binding energy, and the Cl-free Pt surfaces based on the electrocatalytic measurements, catalyst characterizations, and model calculations. The insights reported here could guide the rational design and fine-tuning of carbon-supported Pt catalysts for the ORR.
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