Fully exposed Pd species on nanodiamond/graphene hybrid support for the efficient toluene hydrogenation reaction

EcoEnergy Pub Date : 2023-11-23 DOI:10.1002/ece2.13
Yue Wang, Linlin Wang, Jingwang Zhang, Xiangbin Cai, Jiangyong Diao, Lini Yang, Hongyang Liu
{"title":"Fully exposed Pd species on nanodiamond/graphene hybrid support for the efficient toluene hydrogenation reaction","authors":"Yue Wang,&nbsp;Linlin Wang,&nbsp;Jingwang Zhang,&nbsp;Xiangbin Cai,&nbsp;Jiangyong Diao,&nbsp;Lini Yang,&nbsp;Hongyang Liu","doi":"10.1002/ece2.13","DOIUrl":null,"url":null,"abstract":"<p>Liquid organic hydrogen carriers have emerged as promising hydrogen storage systems, offering notable advantages over conventional storage and utilization efficiency methods. However, designing a catalyst that operates at low temperatures and remains cost-effective poses a significant challenge. We successfully synthesized Pd species (single atoms, fully exposed clusters, and nanoparticles) on a nanodiamond/graphene (ND@G) hybrid support for toluene hydrogenation. The structure of as-developed Pd catalyst was investigated by HAADF-STEM, X-ray absorption fine structure, Raman, XRD, XPS, and other characterizations. Remarkably, the Pd<sub>n</sub>/ND@G catalyst achieved a toluene conversion rate of 99.3% (100°C, 2.0 MPa H<sub>2</sub>) without loss of catalytic ability after 5 runs, which exhibited excellent catalytic performance and stable activity. Furthermore, the Pd<sub>n</sub>/ND@G catalyst exhibited an apparent activation energy as low as 62.36 ± 3.33 kJ mol<sup>−1</sup> and an initial turnover frequency of 33.1 h<sup>−1</sup> at 100°C. By adjusting the size and metal-dependent effects, we have achieved enhanced catalytic performance for toluene hydrogenation, thus paving the way for the design of efficient liquid organic hydrogen storage catalysts.</p>","PeriodicalId":100387,"journal":{"name":"EcoEnergy","volume":"1 1","pages":"207-214"},"PeriodicalIF":0.0000,"publicationDate":"2023-11-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ece2.13","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"EcoEnergy","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ece2.13","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Liquid organic hydrogen carriers have emerged as promising hydrogen storage systems, offering notable advantages over conventional storage and utilization efficiency methods. However, designing a catalyst that operates at low temperatures and remains cost-effective poses a significant challenge. We successfully synthesized Pd species (single atoms, fully exposed clusters, and nanoparticles) on a nanodiamond/graphene (ND@G) hybrid support for toluene hydrogenation. The structure of as-developed Pd catalyst was investigated by HAADF-STEM, X-ray absorption fine structure, Raman, XRD, XPS, and other characterizations. Remarkably, the Pdn/ND@G catalyst achieved a toluene conversion rate of 99.3% (100°C, 2.0 MPa H2) without loss of catalytic ability after 5 runs, which exhibited excellent catalytic performance and stable activity. Furthermore, the Pdn/ND@G catalyst exhibited an apparent activation energy as low as 62.36 ± 3.33 kJ mol−1 and an initial turnover frequency of 33.1 h−1 at 100°C. By adjusting the size and metal-dependent effects, we have achieved enhanced catalytic performance for toluene hydrogenation, thus paving the way for the design of efficient liquid organic hydrogen storage catalysts.

Abstract Image

完全暴露在纳米金刚石/石墨烯杂化载体上的Pd物种用于高效的甲苯加氢反应
液态有机氢载体是一种很有前途的储氢系统,与传统的储氢和利用效率方法相比具有显着的优势。然而,设计一种在低温下工作并保持成本效益的催化剂是一个重大挑战。我们成功地在纳米金刚石/石墨烯(ND@G)杂化载体上合成了Pd物种(单原子,完全暴露的簇和纳米粒子)用于甲苯氢化。采用HAADF-STEM、x射线吸收精细结构、拉曼、XRD、XPS等表征手段对钯催化剂的结构进行了表征。值得注意的是,Pdn/ND@G催化剂在100℃、2.0 MPa H2条件下运行5次后,甲苯转化率达到99.3%,且没有损失催化能力,表现出优异的催化性能和稳定的活性。此外,Pdn/ND@G催化剂在100℃下的表观活化能低至62.36±3.33 kJ mol−1,初始周转频率为33.1 h−1。通过调整尺寸和金属依赖效应,我们实现了甲苯加氢催化性能的增强,从而为高效液态有机储氢催化剂的设计铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信