{"title":"大块Pt电沉积超高Pt质量活性析氢催化剂","authors":"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","doi":"10.1002/adfm.202112207","DOIUrl":null,"url":null,"abstract":"<p>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<sub>3</sub> 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<sup>−1</sup><sub>Pt</sub> 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<sub>3</sub> 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<sup>*</sup> from Pt to re-expose the active sites.</p>","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"32 20","pages":""},"PeriodicalIF":19.0000,"publicationDate":"2022-02-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"37","resultStr":"{\"title\":\"Ultrahigh Pt-Mass-Activity Hydrogen Evolution Catalyst Electrodeposited from Bulk Pt\",\"authors\":\"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\",\"doi\":\"10.1002/adfm.202112207\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>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<sub>3</sub> 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<sup>−1</sup><sub>Pt</sub> 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<sub>3</sub> 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<sup>*</sup> from Pt to re-expose the active sites.</p>\",\"PeriodicalId\":112,\"journal\":{\"name\":\"Advanced Functional Materials\",\"volume\":\"32 20\",\"pages\":\"\"},\"PeriodicalIF\":19.0000,\"publicationDate\":\"2022-02-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"37\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Functional Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/adfm.202112207\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/adfm.202112207","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 37
摘要
由于Pt的稀缺性,最大限度地提高Pt的利用率对于大规模实现基于Pt的析氢反应(HER)电催化剂至关重要。本文报道了具有超高Pt质量活性的三组分异质结构HER催化剂,其中空心PtCu合金纳米球被支撑在Cu泡沫上的WO3阵列上。在之前的报道中已经指出,在酸性介质中使用三电极配置的Pt对电极来评估催化剂的HER性能有污染工作电极的风险。在这里,作者合理地利用这种“污染”来“激活”低her活性的材料,最大限度地利用Pt。结果表明,该催化剂在过电位为20 mV和100 mV时的Pt质量活度分别为1.35和10.86 a mg - 1Pt,比商业Pt/C催化剂高27倍和13倍,优于一些最先进的Pt单原子催化剂。空心球结构和PtCu合金化提高了活性位点的数量和反应活性。密度函数计算和电化学实验表明,WO3和Pt之间的协同作用也是高HER活性的原因,其中氢溢出效应触发Volmer-Heyrovsky机制,促进Pt上H*的快速去除,使活性位点重新暴露。
Ultrahigh Pt-Mass-Activity Hydrogen Evolution Catalyst Electrodeposited from Bulk Pt
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 WO3 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−1Pt 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 WO3 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.
期刊介绍:
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