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dc.contributor.authorFiedler, Johannes
dc.contributor.authorPersson, Clas
dc.contributor.authorBoström, Mathias
dc.contributor.authorBuhmann, Stefan Yoshi
dc.date.accessioned2018-09-03T13:40:04Z
dc.date.available2018-09-03T13:40:04Z
dc.date.created2018-04-24T20:50:49Z
dc.date.issued2018
dc.identifier.citationJournal of Physical Chemistry A. 2018, 122 (19), 4663-4669.nb_NO
dc.identifier.issn1089-5639
dc.identifier.urihttp://hdl.handle.net/11250/2560552
dc.description.abstractDispersion forces, especially van der Waals forces as interactions between neutral and polarizable particles act at small distances between two objects. Their theoretical origin lies in the electromagnetic interaction between induced dipole moments caused by the vacuum fluctuations of the ground-state electromagnetic field. The resulting theory well describes the experimental situation in the limit of the point dipole assumption. At smaller distances, where the finite size of the particles has to be taken into account, this description fails and has to be corrected by higher orders of the multipole expansion, such as quadrupole moments and so on. With respect to the complexity of the spatial properties of the particles this task requires a considerable effort. In order to describe the van der Waals interaction between such particles, we apply the established method of a spatially spread out polarizability distribution to approximate the higher orders of the multipole expansion. We thereby construct an effective theory for effects from anisotropy and finite size on the van der Waals potential.nb_NO
dc.language.isoengnb_NO
dc.publisherAmerican Chemical Societynb_NO
dc.titleOrientational dependence of the van der Waals interactions for finite-sized particlesnb_NO
dc.typeJournal articlenb_NO
dc.description.versionsubmittedVersionnb_NO
dc.source.pagenumber4663-4669nb_NO
dc.source.volume122nb_NO
dc.source.journalJournal of Physical Chemistry Anb_NO
dc.source.issue19nb_NO
dc.identifier.doi10.1021/acs.jpca.8b01989
dc.identifier.cristin1581393
dc.relation.projectNorges forskningsråd: 250346nb_NO
dc.description.localcodeThis article will not be available due to copyright restrictions (c) 2018 by American Chemical Societynb_NO
cristin.unitcode194,64,25,0
cristin.unitnameInstitutt for energi- og prosessteknikk
cristin.ispublishedtrue
cristin.fulltextpreprint
cristin.qualitycode2


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