电催化剂
化学
催化作用
铂金
氯
甲醇
量子点
金属
化学工程
纳米技术
无机化学
电化学
物理化学
有机化学
电极
材料科学
工程类
作者
Lan Hui,Xueting Zhang,Yurui Xue,Xi Chen,Yan Fang,Chengyu Xing,Yuxin Liu,Xuchen Zheng,Yuncheng Du,Chao Zhang,Feng He,Yuliang Li
摘要
The development of efficient and durable electrocatalysts is the only way to achieve commercial fuel cells. A new, efficient method was utilized for epitaxial growth of gold quantum dots using atomically platinum chlorine species with porous graphdiyne as a support (PtCl2Au(111)/GDY), for obtaining successful multicomponent quantum dots with a size of 2.37 nm. The electrocatalyst showed a high mass activity of 175.64 A mgPt-1 for methanol oxidation reactions (MORs) and 165.35 A mgPt-1 for ethanol oxidation reactions (EORs). The data for this experiment are 85.67 and 246.80 times higher than those of commercial Pt/C, respectively. The catalyst also showed highly robust stability for MORs with negligible specific activity decay after 110 h at 10 mA cm-2. Both structure characterizations and theoretical calculations reveal that the excellent catalytic performance can be ascribed to the chlorine introduced to modify the d-band structure on the Pt surface and suppression of the CO poisoning pathway of the MOR. Our results indicate that an atomically dispersed metal species tailoring strategy opens up a new path for the efficient design of highly active and stable catalysts.
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