IF 2.4 4区 化学 Q3 CHEMISTRY, PHYSICAL
Ionics Pub Date : 2025-01-27 DOI:10.1007/s11581-025-06091-w
Yuanmeng Wang, Fan Yang, Xinyu Zhu, Yidi Zhou, Wenhao Peng, Yu Tang, Shaorou Ke, Bozhi Yang, Shujie Yang, Xiaowen Wu, Yangai Liu, Ruiyu Mi, Zhaohui Huang, Xin Min, Minghao Fang
{"title":"Biochar-anchored PtPd bimetallic nanoparticle catalyst for high-efficient hydrogen evolution reaction","authors":"Yuanmeng Wang,&nbsp;Fan Yang,&nbsp;Xinyu Zhu,&nbsp;Yidi Zhou,&nbsp;Wenhao Peng,&nbsp;Yu Tang,&nbsp;Shaorou Ke,&nbsp;Bozhi Yang,&nbsp;Shujie Yang,&nbsp;Xiaowen Wu,&nbsp;Yangai Liu,&nbsp;Ruiyu Mi,&nbsp;Zhaohui Huang,&nbsp;Xin Min,&nbsp;Minghao Fang","doi":"10.1007/s11581-025-06091-w","DOIUrl":null,"url":null,"abstract":"<div><p>PtPd bimetallic catalysts have garnered significant attention in the field of hydrogen production via water electrolysis due to their excellent catalytic performance and promising application prospects. There is an urgent need to develop a direct synthesis method for highly efficient and stable PtPd-based nanocatalysts. In this study, a PtPd bimetallic nanoparticle/biochar composite catalyst was synthesized by combining the impregnation method and high-temperature carbonization in situ co-reduction techniques. Leveraging the micro-confinement effect of the biomass cell membrane/wall structure, the PtPd bimetallic nanoparticles were in situ anchored onto the surface of the biomass nitrogen-doped carbon material through the action of ionic chemical bonds. The addition of Pd modulated the electronic structure of Pt, and the synergistic interaction between Pt and Pd, along with the interaction between the PtPd alloy and the C-N support, generated multiple active sites, significantly enhancing the electrocatalytic hydrogen evolution reaction (HER) efficiency. The synthesized PtPd@C-N catalyst exhibited excellent hydrogen evolution activity and long-term stability in 0.5 M H<sub>2</sub>SO<sub>4</sub>. Among them, Pt<sub>65</sub>Pd<sub>35</sub>@C-N achieved a mass activity of 3.56 A/mg at an overpotential of 50 mV, far surpassing that of Pt@C-N, Pd@C-N prepared under the same conditions and is 16 times higher than the mass activity of commercial Pt/C. This study provides a new idea for the preparation of binary alloy nanocatalysts and demonstrates potential application prospects in the fields of energy conversion and storage.</p></div>","PeriodicalId":599,"journal":{"name":"Ionics","volume":"31 3","pages":"2715 - 2725"},"PeriodicalIF":2.4000,"publicationDate":"2025-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ionics","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11581-025-06091-w","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

摘要

铂钯双金属催化剂因其优异的催化性能和广阔的应用前景,在电解水制氢领域备受关注。目前迫切需要开发一种直接合成高效、稳定的铂钯基纳米催化剂的方法。本研究结合浸渍法和高温碳化原位共还原技术,合成了铂钯双金属纳米颗粒/生物炭复合催化剂。利用生物质细胞膜/壁结构的微粘合效应,通过离子化学键的作用,将铂钯双金属纳米颗粒原位锚定在生物质掺氮碳材料表面。钯的加入调控了铂的电子结构,铂与钯之间的协同作用以及铂钯合金与 C-N 支持物之间的相互作用产生了多个活性位点,显著提高了电催化氢进化反应(HER)的效率。合成的 PtPd@C-N 催化剂在 0.5 M H2SO4 中表现出优异的氢进化活性和长期稳定性。其中,Pt65Pd35@C-N 在过电位为 50 mV 时的质量活性达到 3.56 A/mg,远远超过了在相同条件下制备的 Pt@C-N、Pd@C-N,是商用 Pt/C 质量活性的 16 倍。这项研究为制备二元合金纳米催化剂提供了新思路,并展示了其在能量转换和储存领域的潜在应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biochar-anchored PtPd bimetallic nanoparticle catalyst for high-efficient hydrogen evolution reaction

PtPd bimetallic catalysts have garnered significant attention in the field of hydrogen production via water electrolysis due to their excellent catalytic performance and promising application prospects. There is an urgent need to develop a direct synthesis method for highly efficient and stable PtPd-based nanocatalysts. In this study, a PtPd bimetallic nanoparticle/biochar composite catalyst was synthesized by combining the impregnation method and high-temperature carbonization in situ co-reduction techniques. Leveraging the micro-confinement effect of the biomass cell membrane/wall structure, the PtPd bimetallic nanoparticles were in situ anchored onto the surface of the biomass nitrogen-doped carbon material through the action of ionic chemical bonds. The addition of Pd modulated the electronic structure of Pt, and the synergistic interaction between Pt and Pd, along with the interaction between the PtPd alloy and the C-N support, generated multiple active sites, significantly enhancing the electrocatalytic hydrogen evolution reaction (HER) efficiency. The synthesized PtPd@C-N catalyst exhibited excellent hydrogen evolution activity and long-term stability in 0.5 M H2SO4. Among them, Pt65Pd35@C-N achieved a mass activity of 3.56 A/mg at an overpotential of 50 mV, far surpassing that of Pt@C-N, Pd@C-N prepared under the same conditions and is 16 times higher than the mass activity of commercial Pt/C. This study provides a new idea for the preparation of binary alloy nanocatalysts and demonstrates potential application prospects in the fields of energy conversion and storage.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Ionics
Ionics 化学-电化学
CiteScore
5.30
自引率
7.10%
发文量
427
审稿时长
2.2 months
期刊介绍: Ionics is publishing original results in the fields of science and technology of ionic motion. This includes theoretical, experimental and practical work on electrolytes, electrode, ionic/electronic interfaces, ionic transport aspects of corrosion, galvanic cells, e.g. for thermodynamic and kinetic studies, batteries, fuel cells, sensors and electrochromics. Fast solid ionic conductors are presently providing new opportunities in view of several advantages, in addition to conventional liquid electrolytes.
×
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