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Probing hydrogen bond strength in liquid water by resonant inelastic X-ray scattering
KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Teoretisk kemi och biologi. KTH.
KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Teoretisk kemi och biologi.
Visa övriga samt affilieringar
(Engelska)Manuskript (preprint) (Övrigt vetenskapligt)
Abstract [en]

The potential energy surface is widely used powerful concept in chemical physics. However, direct experimental access to the local potential energy surface in liquid especially in systems  with strong hydrogen bonds is lacking. We develop general technique demonstrated  for liquid water how to reconstruct from state-of-the-art  sub-natural linewidth resonant inelastic X-ray scattering (RIXS)  the local distribution of OH potential energy curves,  separately for OH bonds with weak and strong hydrogen bond. By this we are able to look on the local structure by characterising  selectively the strength of the hydrogen bond. We present a detailed analysis of the formation of the vibrationally resolved RIXS of liquids using a classical/quantum formalism  based on a combination of {\it ab initio} molecular dynamics, density functional theory calculations and quantum nuclear wave packet propagation. Theory nicely explains shortening of the vibrational progression in liquid phase in comparison with RIXS of free water molecules seen in the experiment by fluctuation of the hydrogen bond  network and coherent excitation of both OH bonds.

Nationell ämneskategori
Teoretisk kemi Atom- och molekylfysik och optik
Identifikatorer
URN: urn:nbn:se:kth:diva-227951OAI: oai:DiVA.org:kth-227951DiVA, id: diva2:1205807
Anmärkning

QC 20180515

Tillgänglig från: 2018-05-15 Skapad: 2018-05-15 Senast uppdaterad: 2018-05-15Bibliografiskt granskad
Ingår i avhandling
1. Quantum Nuclear Dynamics in Resonant X-ray Scattering of Gas-Phase and Liquid Systems
Öppna denna publikation i ny flik eller fönster >>Quantum Nuclear Dynamics in Resonant X-ray Scattering of Gas-Phase and Liquid Systems
2018 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

This thesis focuses on the role of the nuclear degrees of freedom in X-ray induced molecular processes. An important part of it is devoted to establishing theoretical principles to model and interpret high-resolution resonant X-ray scattering experiments in gases and liquids. Our investigations address the resonant inelastic x-ray scattering (RIXS) of H2O(g), H2O(l) and CH3OH(g) and Auger emission induced by hard X-rays in CO(g). The simulations for gas-phase systems are based on a multi-mode wave packet formalism and on potential energy surfaces computed with multi-configurational approaches.

For liquid systems, we propose a classical/quantum formalism for simulating RIXS based on a combination of ab initio molecular dynamics, density functional theory calculations and quantum nuclear wave packet propagation. The developed model is able to reproduce the experimental observation of shortening of the vibrational progression in H2O(l).

We show that electronically-elastic RIXS has an intrinsic capability to map the potential energy surface and to carry out vibrational analysis of the electronic ground state in free molecules as well as liquids. For gas-phase water, we see that the landscape of different core-excited states cause the nuclear wave packet to be localized along specific directions thus allowing to reconstruct one-dimensional potential energy curves. For liquid water, we propose a model for deriving, from experiment, confidence intervals for the molecular potential energy curves along the OH bonds, which are determined by the local arrangement of the hydrogen bond network.

We also investigate the role of ultra-fast rotations induced by photoionization by hard X-rays. In this case, the ejection of a fast photoelectron results in an ultra-fast rotational motion of the molecule, which combined with the anisotropy of the Auger process causes the spectral profile to be split due to a dynamical Doppler effect.

Ort, förlag, år, upplaga, sidor
Stockholm: KTH Royal Institute of Technology, 2018. s. 88
Serie
TRITA-CBH-FOU ; 2018:24
Nyckelord
resonant inelastic X-ray scattering, X-ray absorption, water, methanol, CO, rotational doppler effect, recoil, wave packet, non-Franck-Condon effect, ultra-fast molecular dissociation, potential energy surface, hydrogen bond, liquid
Nationell ämneskategori
Teoretisk kemi Fysik Atom- och molekylfysik och optik
Forskningsämne
Teoretisk kemi och biologi
Identifikatorer
urn:nbn:se:kth:diva-227962 (URN)978-91-7729-806-9 (ISBN)
Disputation
2018-06-12, FA32, AlbaNova University Center, Roslagstullsbacken 21, Stockholm, 10:00 (Engelska)
Opponent
Handledare
Anmärkning

QC 20180515

Tillgänglig från: 2018-05-15 Skapad: 2018-05-15 Senast uppdaterad: 2018-05-16Bibliografiskt granskad

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Av författaren/redaktören
Vaz da Cruz, ViniciusGel'mukhanov, FarisCarvalho Couto, Rafael
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Teoretisk kemi och biologi
Teoretisk kemiAtom- och molekylfysik och optik

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