催化作用
材料科学
可逆氢电极
电化学
氢溢流
化学工程
电极
氢
合金
反应性(心理学)
铂金
纳米技术
工作电极
冶金
金属
物理化学
化学
有机化学
病理
替代医学
工程类
医学
作者
Luan Liu,Yan Wang,Yongzhi Zhao,Yong Wang,Zili Zhang,Tong Wu,Wanjun Qin,Sijia Liu,Baorui Jia,Haoyang Wu,Deyin Zhang,Xuanhui Qu,Manish Chhowalla,Mingli Qin
标识
DOI:10.1002/adfm.202112207
摘要
Abstract Maximizing the Pt utilization is important for the widescale implementation of Pt‐based hydrogen evolution reaction (HER) electrocatalysts, owing to the scarcity of Pt. Here, three‐component heterostructured HER catalysts with ultrahigh Pt mass activity in which hollow PtCu alloy nanospheres are supported on an array of WO 3 on Cu foam, are reported. It has been pointed out that the use of Pt counter electrode in a three‐electrode configuration in evaluating catalysts’ HER performances in acidic media carries the risk of contaminating the working electrode in previous reports. Here, the authors rationally utilize this “contaminating” to “activate” low‐HER‐activity materials, maximizing the Pt utilization. As a result, ultrahigh Pt mass activity is achieved, that is 1.35 and 10.86 A mg −1 Pt at overpotentials of 20 and 100 mV, respectively, 27 and 13 times higher than those of commercial Pt/C catalysts, outperforming some state‐of‐the‐art Pt‐single‐atom catalysts. The hollow sphere structure and PtCu alloying increase the number and reactivity of active sites. Density function calculations and electrochemical experiments reveal that the synergy between WO 3 and Pt is also responsible for the high HER activity where the hydrogen spillover effect triggers the Volmer–Heyrovsky mechanism and promotes the rapid removal of H * from Pt to re‐expose the active sites.
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