An interfacial synergism effect of Pd–g-C3N4 in Pd/g-C3N4 for highly active and selective hydrogenation of 4-nitrophenol

IF 3.5 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR Dalton Transactions Pub Date : 2023-11-06 DOI:10.1039/D3DT03471B
Liqing Li, Xin Deng, Jiani He, Huan Zhang, Li Li and Lihua Zhu
{"title":"An interfacial synergism effect of Pd–g-C3N4 in Pd/g-C3N4 for highly active and selective hydrogenation of 4-nitrophenol","authors":"Liqing Li, Xin Deng, Jiani He, Huan Zhang, Li Li and Lihua Zhu","doi":"10.1039/D3DT03471B","DOIUrl":null,"url":null,"abstract":"<p >Herein, we report that Pd nanoparticles (NPs) anchored on graphitic nitride carbon (Pd/g-C<small><sub>3</sub></small>N<small><sub>4</sub></small>) catalysts with various Pd contents (1.55 wt%, 0.14 wt%, 0.04 wt%) are successfully prepared <em>via</em> a simple NaBH<small><sub>4</sub></small> reduction method, exhibiting excellent catalytic activity and selectivity toward 4-aminophenol (4-AP) in 4-nitrophenol (4-NP) selective hydrogenation. 4-NP is completely converted to 4-AP (yield ∼ 100%) under quite moderate reaction conditions (40 °C, 2.0 MPa H<small><sub>2</sub></small> and 5 min) over the 1.55 wt% Pd/g-C<small><sub>3</sub></small>N<small><sub>4</sub></small> catalyst, with a high reaction rate <em>r</em> = 134.4 mol<small><sub>4-NP</sub></small> mol<small><sub>Pd</sub></small><small><sup>−1</sup></small> min<small><sup>−1</sup></small>. The excellent catalytic performance can be attributed to the following reasons: (1) a higher ratio of Pd(0)/Pd<small><sup><em>n</em>+</sup></small> provides much more exposed active sites for the potential adsorption and activation of the reactants, which is beneficial for increasing the reaction rate and catalytic activity; (2) Pd NPs are highly dispersed on g-C<small><sub>3</sub></small>N<small><sub>4</sub></small> due to the strong interaction of Pd–N or Pd–C; (3) the interfacial synergism effect between Pd NPs and g-C<small><sub>3</sub></small>N<small><sub>4</sub></small> enables the effective adsorption and activation of H<small><sub>2</sub></small> (4-NP) at Pd (g-C<small><sub>3</sub></small>N<small><sub>4</sub></small>), promoting the catalytic hydrogenation of 4-NP and improving their catalytic properties. In addition, this catalyst has superior reusability.</p>","PeriodicalId":71,"journal":{"name":"Dalton Transactions","volume":" 47","pages":" 17974-17980"},"PeriodicalIF":3.5000,"publicationDate":"2023-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dalton Transactions","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2023/dt/d3dt03471b","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0

Abstract

Herein, we report that Pd nanoparticles (NPs) anchored on graphitic nitride carbon (Pd/g-C3N4) catalysts with various Pd contents (1.55 wt%, 0.14 wt%, 0.04 wt%) are successfully prepared via a simple NaBH4 reduction method, exhibiting excellent catalytic activity and selectivity toward 4-aminophenol (4-AP) in 4-nitrophenol (4-NP) selective hydrogenation. 4-NP is completely converted to 4-AP (yield ∼ 100%) under quite moderate reaction conditions (40 °C, 2.0 MPa H2 and 5 min) over the 1.55 wt% Pd/g-C3N4 catalyst, with a high reaction rate r = 134.4 mol4-NP molPd−1 min−1. The excellent catalytic performance can be attributed to the following reasons: (1) a higher ratio of Pd(0)/Pdn+ provides much more exposed active sites for the potential adsorption and activation of the reactants, which is beneficial for increasing the reaction rate and catalytic activity; (2) Pd NPs are highly dispersed on g-C3N4 due to the strong interaction of Pd–N or Pd–C; (3) the interfacial synergism effect between Pd NPs and g-C3N4 enables the effective adsorption and activation of H2 (4-NP) at Pd (g-C3N4), promoting the catalytic hydrogenation of 4-NP and improving their catalytic properties. In addition, this catalyst has superior reusability.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Pd/g-C3N4在Pd/g-C3N4中的界面协同作用增强对硝基苯酚的高活性选择性加氢
在此,我们报道了通过简单的NaBH4还原方法成功地制备了锚定在不同钯含量(1.55wt%、0.14wt%、0.04wt%)的石墨氮化碳(Pd/g-C3N4)催化剂上的钯纳米粒子(NP),对4-氨基苯酚(4-AP)的4-硝基苯酚(4-NP)选择性加氢表现出优异的催化活性和选择性。在1.55wt%Pd/g-C3N4催化剂上,在相当温和的反应参数(40°C,2.0MPa H2和5分钟)下,4-NP完全转化为4-AP(产率⁓100%)。反应速率r=134.4mol4-NPmolPd-1min-1。优异的催化性能可归因于:1)较高的Pd(0)/Pdn+比例为反应物的潜在吸附和活化提供了更多暴露的活性位点,有利于提高反应速率和催化活性;2) Pd-NP通过Pd-N或Pd-C的强相互作用高度分散在g-C3N4上;3) Pd NPs与g-C3N4之间的界面协同作用使H2(4-NP)在Pd(g-C3N4)上有效吸附和活化,促进4-NP的催化加氢,提高其催化性能。此外,该催化剂具有优异的可重复使用性。
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 去求助
来源期刊
Dalton Transactions
Dalton Transactions 化学-无机化学与核化学
CiteScore
6.60
自引率
7.50%
发文量
1832
审稿时长
1.5 months
期刊介绍: Dalton Transactions is a journal for all areas of inorganic chemistry, which encompasses the organometallic, bioinorganic and materials chemistry of the elements, with applications including synthesis, catalysis, energy conversion/storage, electrical devices and medicine. Dalton Transactions welcomes high-quality, original submissions in all of these areas and more, where the advancement of knowledge in inorganic chemistry is significant.
期刊最新文献
Rubidium vanadium(III) vanadyl(IV) phosphate, Rb3V3+(V4+O)(PO4)(H0.5PO4)2: crystal chemistry and low-dimensional magnetism Distinguishing between aquo and hydroxo coordination in molecular copper complexes by 1H and 17O ENDOR spectroscopy The coordination chemistry and anticancer activity of organo-ruthenium(II), -iridium(III) and -rhodium(III) complexes with sulfonyl-substituted thiourea ligands Application of a simple copper(II) complex compound as an epinephrine selective voltammetric sensor in the presence of uric acid in aqueous conditions Dual chalcogenide coordination engineering on a self-supported alloy electrode for enhanced hydrogen evolution reaction
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1