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Hu, Wei
Publikationer (3 of 3) Visa alla publikationer
Hu, W., Duan, S. & Luo, Y. (2017). Theoretical modeling of surface and tip-enhanced Raman spectroscopies. Wiley Interdisciplinary Reviews. Computational Molecular Science, 7(2), Article ID UNSP e1293.
Öppna denna publikation i ny flik eller fönster >>Theoretical modeling of surface and tip-enhanced Raman spectroscopies
2017 (Engelska)Ingår i: Wiley Interdisciplinary Reviews. Computational Molecular Science, ISSN 1759-0876, E-ISSN 1759-0884, Vol. 7, nr 2, artikel-id UNSP e1293Artikel, forskningsöversikt (Refereegranskat) Published
Abstract [en]

Raman spectroscopy is a powerful technique in molecular science because of the ability of providing vibrational 'finger-print'. The developments of the surfaceenhanced Raman spectroscopy (SERS) and tip-enhanced Raman spectroscopy (TERS) have significantly improved the detection sensitivity and efficiency. However, they also introduce complications for the spectral assignments, for which advanced theoretical modeling has played an important role. Here we summarize some of our recent progresses for SERS and TERS, which generally combine both solid-state physics and quantum chemistry methods with two different schemes, namely the cluster model and the periodic boundary condition (PBC) model. In the cluster model, direct Raman spectra calculations are performed for the cluster taken from the accurate PBC structure. For PBC model, we have developed a quasianalytical approach that enables us to calculate the Raman spectra of entire system. Under the TERS condition, the non-uniformity of plasmonic field in real space can drastically alter the interaction between the molecule and the light. By taking into account the local distributions of the plasmonic field, a new interaction Hamiltonian is constructed and applied to model the super-high-resolution Raman images of a single molecule. It shows that the resonant Raman images reflect the transition density between ground and excited states, which are generally vibrational insensitive. The nonresonant Raman images, on the other hand, allow to visualize the atomic movement of individual vibrational modes in real space. The inclusion of non-uniformity of plasmonic field provides ample opportunities to discover new physics and new applications in the future. 

Ort, förlag, år, upplaga, sidor
WILEY, 2017
Nationell ämneskategori
Kemi
Identifikatorer
urn:nbn:se:kth:diva-206709 (URN)10.1002/wcms.1293 (DOI)000399013100003 ()2-s2.0-85007367855 (Scopus ID)
Anmärkning

QC 20170508

Tillgänglig från: 2017-05-08 Skapad: 2017-05-08 Senast uppdaterad: 2017-05-08Bibliografiskt granskad
Liang, L., Hu, W., Xue, Z. & Shen, J.-W. -. (2017). Theoretical study on the interaction of nucleotides on two-dimensional atomically thin graphene and molybdenum disulfide. FlatChem, 2, 8-14
Öppna denna publikation i ny flik eller fönster >>Theoretical study on the interaction of nucleotides on two-dimensional atomically thin graphene and molybdenum disulfide
2017 (Engelska)Ingår i: FlatChem, ISSN 2452-2627, Vol. 2, s. 8-14Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

In this work, the interaction between single nucleotide and polynucleotides composed of different nucleotides and two-dimensional (2D) materials (graphene and MoS2) were investigated through first principles calculations and molecular dynamics (MD) simulation. The binding energy strength between single nucleotide and graphene is G > C > A > T, and it is G > A > C > T between single nucleotide and MoS2, derived from density function density (DFT) calculations. The binding strength between polynucleotide and graphene is A6 > G6 > T6 > C6, and the order is G6 > A6 > C6 > T6 of binding strength between polynucleotide and MoS2, calculated from molecular dynamics simulation. The average binding free energy for different single nucleotide A, T, C, G (polynucleotides A6, T6, C6, G6) on graphene sheet is −4.17 kcal/mol (-10.04 kcal/mol), and it is about −2.29 kcal/mol (-2.24 kcal/mol) on MoS2 surface. The binding strength for different single nucleotide (polynucleotides) on graphene sheets is around 2 times (4 times) stronger than that between nucleotide (polynucleotides) and MoS2 surface. The different absorption strength of nucleotides on these two-dimensional materials may be utilized for different promising applications.

Ort, förlag, år, upplaga, sidor
Elsevier B.V., 2017
Nyckelord
Density functional theory, Free energy calculation, Graphene, MoS2, Two-dimensional material
Nationell ämneskategori
Teoretisk kemi
Identifikatorer
urn:nbn:se:kth:diva-216538 (URN)10.1016/j.flatc.2017.02.001 (DOI)2-s2.0-85019620591 (Scopus ID)
Anmärkning

Funding details: 21403049, NSFC, National Natural Science Foundation of China; Funding details: 21503186, NSFC, National Natural Science Foundation of China; Funding details: 21674032, NSFC, National Natural Science Foundation of China; Funding text: We acknowledge financial support by the National Natural Science Foundation of China (Grant Nos. 21503186, Nos. 21403049, 21674032), Qianjiang Talents Program of Zhejiang Provice (Nos. QJD1602011).

QC 20171124

Tillgänglig från: 2017-11-24 Skapad: 2017-11-24 Senast uppdaterad: 2017-11-24Bibliografiskt granskad
Liang, L., Hu, W., Zhang, Z. & Shen, J.-W. (2016). Theoretic Study on Dispersion Mechanism of Boron Nitride Nanotubes by Polynucleotides. SCIENTIFIC REPORTS, 6, Article ID 39747.
Öppna denna publikation i ny flik eller fönster >>Theoretic Study on Dispersion Mechanism of Boron Nitride Nanotubes by Polynucleotides
2016 (Engelska)Ingår i: SCIENTIFIC REPORTS, ISSN 2045-2322, Vol. 6, artikel-id 39747Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Due to the unique electrical and mechanical properties of boron nitride nanotubes (BNNT), BNNT has been a promising material for many potential applications, especially in biomedical field. Understanding the dispersion of BNNT in aqueous solution by biomolecules is essential for its use in biomedical applications. In this study, BNNT wrapped by polynucleotides in aqueous solution was investigated by molecular dynamics (MD) simulations. Our results demonstrated that the BNNT wrapped by polynucleotides could greatly hinder the aggregation of BNNTs and improve the dispersion of BNNTs in aqueous solution. Dispersion of BNNTs with the assistance of polynucleotides is greatly affected by the wrapping manner of polynucleotides on BNNT, which mainly depends on two factors: the type of polynucleotides and the radius of BNNT. The interaction between polynucleotides and BNNT(9, 9) is larger than that between polynucleotides and BNNT(5, 5), which leads to the fact that dispersion of BNNT(9, 9) is better than that of BNNT(5, 5) with the assistance of polynucleotides in aqueous solution. Our study revealed the molecular-level dispersion mechanism of BNNT with the assistance of polynucleotides in aqueous solution. It shades a light on the understanding of dispersion of single wall nanotubes by biomolecules.

Ort, förlag, år, upplaga, sidor
Nature Publishing Group, 2016
Nationell ämneskategori
Fysikalisk kemi
Identifikatorer
urn:nbn:se:kth:diva-200210 (URN)10.1038/srep39747 (DOI)000390866400001 ()2-s2.0-85006992037 (Scopus ID)
Anmärkning

QC 20170202

Tillgänglig från: 2017-02-02 Skapad: 2017-01-23 Senast uppdaterad: 2017-02-02Bibliografiskt granskad
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