Effects of Pd ensemble size in dilute and single atom alloy PdAu catalysts for one-pot selective hydrogenation and reductive amination†

IF 4.4 3区 化学 Q2 CHEMISTRY, PHYSICAL
Kang Rui Garrick Lim, Toghrul Azizli, Selina K. Kaiser, Michael Aizenberg, Matthew M. Montemore and Joanna Aizenberg
{"title":"Effects of Pd ensemble size in dilute and single atom alloy PdAu catalysts for one-pot selective hydrogenation and reductive amination†","authors":"Kang Rui Garrick Lim, Toghrul Azizli, Selina K. Kaiser, Michael Aizenberg, Matthew M. Montemore and Joanna Aizenberg","doi":"10.1039/D5CY00441A","DOIUrl":null,"url":null,"abstract":"<p >In the one-pot reaction between nitroarenes, aldehydes, and hydrogen, the desired outcome is the selective hydrogenation of nitroarenes to form aminoarenes that condense with aldehydes to yield pharmaceutically relevant imines and <em>N</em>-alkylamines. One approach to facilitate the selective hydrogenation of nitroarenes over aldehydes involves using bimetallic catalysts with near equimolar ratios. However, structural characterization of metallic ensembles on the nanoparticle surface is challenging at such high alloying ratios, which hinders the elucidation of clear structure–property relationships. Here, we prepared a well-controlled series of dilute Pd-in-Au alloy catalysts with a fixed nanoparticle size as a model system to investigate the effects of surface Pd ensemble size, from single atoms to dimers and trimers, in the one-pot hydrogenation reaction between nitrobenzene and benzaldehyde as our probe reaction. The highest (near unity) selectivity to condensation products was achieved using the catalyst with the lowest Pd content prepared (Pd<small><sub>2</sub></small>Au<small><sub>98</sub></small>/SiO<small><sub>2</sub></small>), which predominantly exposed Pd single atoms on the nanoparticle surface as verified by surface-sensitive spectroscopy. Theoretical calculations reveal that Pd single atoms were inactive for benzaldehyde adsorption and thus enabled selective nitrobenzene hydrogenation. On the contrary, the adsorption of benzaldehyde became stronger than nitrobenzene for Pd trimers and larger ensembles, explaining the enhanced competitive adsorption from benzaldehyde in catalysts with increasing Pd content. Our results demonstrate that the commonly used (near equimolar) alloying ratio is rather arbitrary and may not necessarily produce the highest selectivity to condensation products. Instead, we illustrate how controlling the nanoscale Pd ensemble size on the nanoparticle surface tunes competitive kinetics to steer selectivity towards forming the desired condensation products.</p>","PeriodicalId":66,"journal":{"name":"Catalysis Science & Technology","volume":" 14","pages":" 4179-4193"},"PeriodicalIF":4.4000,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysis Science & Technology","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/cy/d5cy00441a","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

In the one-pot reaction between nitroarenes, aldehydes, and hydrogen, the desired outcome is the selective hydrogenation of nitroarenes to form aminoarenes that condense with aldehydes to yield pharmaceutically relevant imines and N-alkylamines. One approach to facilitate the selective hydrogenation of nitroarenes over aldehydes involves using bimetallic catalysts with near equimolar ratios. However, structural characterization of metallic ensembles on the nanoparticle surface is challenging at such high alloying ratios, which hinders the elucidation of clear structure–property relationships. Here, we prepared a well-controlled series of dilute Pd-in-Au alloy catalysts with a fixed nanoparticle size as a model system to investigate the effects of surface Pd ensemble size, from single atoms to dimers and trimers, in the one-pot hydrogenation reaction between nitrobenzene and benzaldehyde as our probe reaction. The highest (near unity) selectivity to condensation products was achieved using the catalyst with the lowest Pd content prepared (Pd2Au98/SiO2), which predominantly exposed Pd single atoms on the nanoparticle surface as verified by surface-sensitive spectroscopy. Theoretical calculations reveal that Pd single atoms were inactive for benzaldehyde adsorption and thus enabled selective nitrobenzene hydrogenation. On the contrary, the adsorption of benzaldehyde became stronger than nitrobenzene for Pd trimers and larger ensembles, explaining the enhanced competitive adsorption from benzaldehyde in catalysts with increasing Pd content. Our results demonstrate that the commonly used (near equimolar) alloying ratio is rather arbitrary and may not necessarily produce the highest selectivity to condensation products. Instead, we illustrate how controlling the nanoscale Pd ensemble size on the nanoparticle surface tunes competitive kinetics to steer selectivity towards forming the desired condensation products.

Abstract Image

稀原子和单原子合金PdAu催化剂中钯系综尺寸对一锅选择性加氢和还原胺化反应的影响
在硝基芳烃、醛和氢之间的一锅反应中,期望的结果是硝基芳烃选择性加氢形成氨基芳烃,氨基芳烃与醛缩合生成药学上相关的亚胺和n -烷基胺。一种促进硝基芳烃在醛上选择性加氢的方法涉及使用接近等摩尔比的双金属催化剂。然而,在如此高的合金含量下,纳米颗粒表面金属系综的结构表征具有挑战性,这阻碍了清晰的结构-性能关系的阐明。在此,我们制备了一系列控制良好的稀释钯金合金催化剂,并以固定的纳米颗粒大小为模型体系,研究了表面钯原子大小的影响,从单原子到二聚体和三聚体,在硝基苯和苯甲醛的一锅加氢反应中作为我们的探针反应。制备的钯含量最低的催化剂(Pd2Au98/SiO2)对缩合产物的选择性最高(接近一致),表面敏感光谱证实了钯主要暴露在纳米颗粒表面。理论计算表明,Pd单原子对苯甲醛的吸附不活跃,从而实现了硝基苯的选择性加氢。相反,苯甲醛对Pd三聚体的吸附比硝基苯更强,说明催化剂对苯甲醛的竞争吸附随着Pd含量的增加而增强。我们的研究结果表明,通常使用的(近等摩尔)合金化比是相当任意的,可能不一定产生最高的缩合产物选择性。相反,我们说明了如何控制纳米颗粒表面的纳米级Pd系综尺寸来调节竞争动力学,从而引导选择性地形成所需的缩合产物。
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
Catalysis Science & Technology
Catalysis Science & Technology CHEMISTRY, PHYSICAL-
CiteScore
8.70
自引率
6.00%
发文量
587
审稿时长
1.5 months
期刊介绍: A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis. Editor-in-chief: Bert Weckhuysen Impact factor: 5.0 Time to first decision (peer reviewed only): 31 days
×
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:604180095
Book学术官方微信