Capitalistic Chemistry

IF 3.3 3区 化学 Q2 CHEMISTRY, PHYSICAL The Journal of Physical Chemistry C Pub Date : 2025-03-05 DOI:10.1021/acs.jpcc.5c00660
Lars G.M. Pettersson
{"title":"Capitalistic Chemistry","authors":"Lars G.M. Pettersson","doi":"10.1021/acs.jpcc.5c00660","DOIUrl":null,"url":null,"abstract":"The concept of “bond strength” is of essence for modeling every kind of reactive chemistry. Particularly within the field of catalysis and surface science, the interaction strength of adsorbates to surfaces affects the activity, selectivity, and stability of intermediates and transition states. Here, we introduce a simple approach to chemical reactions through an analogy with business. We regard rehybridization as the <i>investment</i> a molecule makes to prepare its electronic and geometrical structure to form new bonds. The resulting bond strength is the total <i>proceeds</i> from bond formation, and the difference (exothermicity) is the <i>profit</i>. The predictive power lies in the fact that any change in the electronic structure to prepare for bond formation requires the involvement of specific excited states. Thus, with knowledge of the energy needed for this excitation (investment) and the strength of the resulting interaction one can predict whether a specific reaction or bonding mode will be favored. We apply this concept to rationalize observed binding modes at surfaces and the often observed large structural changes even for “weakly” chemisorbed systems and finally to justify using small metal clusters to correct chemisorption energies from periodic DFT calculations.","PeriodicalId":61,"journal":{"name":"The Journal of Physical Chemistry C","volume":"67 1","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2025-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Physical Chemistry C","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.jpcc.5c00660","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

The concept of “bond strength” is of essence for modeling every kind of reactive chemistry. Particularly within the field of catalysis and surface science, the interaction strength of adsorbates to surfaces affects the activity, selectivity, and stability of intermediates and transition states. Here, we introduce a simple approach to chemical reactions through an analogy with business. We regard rehybridization as the investment a molecule makes to prepare its electronic and geometrical structure to form new bonds. The resulting bond strength is the total proceeds from bond formation, and the difference (exothermicity) is the profit. The predictive power lies in the fact that any change in the electronic structure to prepare for bond formation requires the involvement of specific excited states. Thus, with knowledge of the energy needed for this excitation (investment) and the strength of the resulting interaction one can predict whether a specific reaction or bonding mode will be favored. We apply this concept to rationalize observed binding modes at surfaces and the often observed large structural changes even for “weakly” chemisorbed systems and finally to justify using small metal clusters to correct chemisorption energies from periodic DFT calculations.

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
求助全文
约1分钟内获得全文 去求助
来源期刊
The Journal of Physical Chemistry C
The Journal of Physical Chemistry C 化学-材料科学:综合
CiteScore
6.50
自引率
8.10%
发文量
2047
审稿时长
1.8 months
期刊介绍: The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.
期刊最新文献
Praseodymium-Doped Cerium Oxide (PrxCe1–xO2−δ) Nanoparticles with High Water Dispersibility: The Nature of Pr-Related Optical Transitions Studied by MCD Spectroscopy Theoretical Modeling of Direct Z-Scheme B,F-Doped g-C3N4/CoN4 Composites for Promoting Photocatalytic Water Splitting Reaction High-Throughput Screening of Dense Boron Nitride Structures from Structural Templates Potential-Dependent Atomic Dissolution and Segregation of Cu and Pt Surfaces Structure Thermal Domain Size in μm-Thick Single Crystalline Sapphire Wafer Uncovered by Low-Momentum Phonon Scattering
×
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