4.8 Article

Enhanced Davydov Splitting in Crystals of a Perylene Diimide Derivative

期刊

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
卷 8, 期 6, 页码 1118-1123

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.7b00283

关键词

-

资金

  1. Bolton Fund at Lafayette College
  2. EXCEL Program at Lafayette College
  3. NSF [DMR-1505437]
  4. Direct For Mathematical & Physical Scien
  5. Division Of Materials Research [1505437] Funding Source: National Science Foundation

向作者/读者索取更多资源

We report the polarized absorption spectra of high quality, thin crystals of a perylene diimide (PDI) species with branched side chains (B2). The absorption spectrum shows exemplary polarization-dependent H-like and J-like aggregate behavior upon orthogonal excitation, with a sizable Davydov splitting (DS) of 1230 cm(-1) and peak to peak splitting of 3040 cm(-1). The experimental results are compared to theoretical calculations with remarkable agreement. The theoretical analysis of the polarized absorption spectra shows evidence of a high degree of intermolecular charge transfer, which, along with Coulombic coupling, conspires to create the unprecedented DS for this family of dye molecules. The large polarization dependence of the electronic spectra is attributed to the unique twisted crystal structure, in which a substantial rotational displacement exists between neighboring chromophores within a pi-stack. These results highlight the strong intermolecular geometry in PDI systems.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Biophysics

IR Spectroscopy Can Reveal the Mechanism of K+ Transport in Ion Channels

Steven E. Strong, Nicholas J. Hestand, Alexei A. Kananenka, Martin T. Zanni, J. L. Skinner

BIOPHYSICAL JOURNAL (2020)

Article Chemistry, Physical

Unusual Non-Kasha Photophysical Behavior of Aggregates of Push-Pull Donor-Acceptor Chromophores

Chuwei Zhong, David Bialas, Frank C. Spano

JOURNAL OF PHYSICAL CHEMISTRY C (2020)

Article Chemistry, Physical

Frenkel-Holstein Hamiltonian applied to absorption spectra of quaterthiophene-based 2D hybrid organic-inorganic perovskites

Svenja M. Janke, Mohammad B. Qarai, Volker Blum, Frank C. Spano

JOURNAL OF CHEMICAL PHYSICS (2020)

Article Chemistry, Multidisciplinary

A Thermostable Protein Matrix for Spectroscopic Analysis of Organic Semiconductors

George A. Sutherland, Daniel Polak, David J. K. Swainsbury, Shuangqing Wang, Frank C. Spano, Dirk B. Auman, David G. Bossanyi, James P. Pidgeon, Andrew Hitchcock, Andrew J. Musser, John E. Anthony, P. Leslie Dutton, Jenny Clark, C. Neil Hunter

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2020)

Review Chemistry, Multidisciplinary

Excitons and Polarons in Organic Materials

Raja Ghosh, Frank C. Spano

ACCOUNTS OF CHEMICAL RESEARCH (2020)

Article Chemistry, Physical

Vibronic exciton model for low bandgap donor-acceptor polymers

Mohammad Balooch Qarai, Xin Chang, F. C. Spano

JOURNAL OF CHEMICAL PHYSICS (2020)

Article Chemistry, Physical

HJ-aggregates of donor-acceptor-donor oligomers and polymers

Xin Chang, Mohammad Balooch Qarai, Frank C. Spano

Summary: A vibronic exciton model was developed to explain the spectral signatures of HJ-aggregates in oligomers and polymers with donor-acceptor-donor repeat units. The model shows that single chains with enhanced intrachain order exhibit J-behavior, while positive H-promoting interchain Coulomb interactions in aggregates attenuate the vibronic ratio. The ratio formula derived previously for P3HT aggregates was shown to also apply to (DAD)(N) aggregates with slight modifications.

JOURNAL OF CHEMICAL PHYSICS (2021)

Article Chemistry, Physical

A Holstein-Peierls Approach to Excimer Spectra: The Evolution from Vibronically Structured to Unstructured Emission

April L. Bialas, Frank C. Spano

Summary: Excimers are commonly found in many organic systems, with broad, structureless, and red-shifted emission. A theoretical model based on a Holstein-Peierls Hamiltonian is proposed to explain absorption and photoluminescence in molecular dimers, showing that excimer emission can be induced through local or nonlocal intermolecular coupling. Incorporating both types of coupling successfully reproduces absorption and excimer emission spectra.

JOURNAL OF PHYSICAL CHEMISTRY C (2022)

Article Chemistry, Physical

Understanding Bipolarons in Conjugated Polymers Using a Multiparticle Holstein Approach

Mohammad Balooch Qarai, Raja Ghosh, Frank C. Spano

Summary: The Holstein-based model has been expanded to include singlet bipolarons in conjugated polymers with nondegenerate ground states. The mid-IR band for bipolarons is red-shifted by up to 0.2 eV compared to single polarons, reflecting enhanced hole delocalization in the bound bipolaron complex. This observation is in good agreement with recent measurements on electrochemically doped P3HT.

JOURNAL OF PHYSICAL CHEMISTRY C (2021)

Correction Chemistry, Physical

Confirmation of the Origins of Panchromatic Spectra in Squaraine Thin Films Targeted for Organic Photovoltaic Devices (vol 119, pg 18964, 2015)

Nicholas J. Hestand, Chenyu Zheng, Anirudh Raju Penmetcha, Brandon Cona, Jeremy A. Cody, Frank C. Spano, Christopher J. Collison

JOURNAL OF PHYSICAL CHEMISTRY C (2022)

Article Chemistry, Physical

Intermolecular Charge Transfer in H- and J-Aggregates of Donor-Acceptor-Donor Chromophores: The Curious Case of Bithiophene-DPP

Xin Chang, Mohammad Balooch Qarai, Frank C. Spano

Summary: A vibronic exciton model is used to describe low-energy electronic excitations in slip-stack aggregates. The study reveals that J- and H-aggregate behavior in these aggregates is driven by intermolecular charge transfer rather than Coulomb coupling as assumed in the Kasha model. Additionally, both J- and H-aggregates exhibit red-shifted behavior.

JOURNAL OF PHYSICAL CHEMISTRY C (2022)

Correction Chemistry, Physical

HJ-aggregates of donor-acceptor-donor oligomers and polymers(vol 155, 034905, 2021)

Xin Chang, Mohammad Balooch Qarai, Frank C. Spano

JOURNAL OF CHEMICAL PHYSICS (2022)

Article Chemistry, Physical

Multipolaron Complexes in Conducting Polymers: The Importance of Hole-Hole Repulsion in Charge Delocalization

Mohammad Balooch Qarai, Raja Ghosh, Nicholas J. Hestand, Frank C. Spano

Summary: Theoretical investigation of multipolaron complexes in p-doped poly(3-hexylthiophene) films, where stationary dopant anions are positioned on both sides of the polymer chain within the lamellar region, was conducted. Complexes as large as tetrapolarons, consisting of four anions and an equal number of mobile holes, were considered. It was found that the mid-IR absorption band (P1) red-shifts and the hole ionization potential decreases as the complex grows in size, from a single polaron to a tetrapolaron. This behavior mainly arises from enhanced hole delocalization due to hole-hole repulsion and has significant implications for charge transport in organic materials.

JOURNAL OF PHYSICAL CHEMISTRY C (2023)

暂无数据