Journal
PHYSICAL REVIEW B
Volume 89, Issue 4, Pages -Publisher
AMER PHYSICAL SOC
DOI: 10.1103/PhysRevB.89.045140
Keywords
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Funding
- U. K. Engineering and Physical Sciences Research Council (EPSRC)
- KAKENHI [23104714, 22104011, 25600156]
- Tokuyama Science Foundation
- Grants-in-Aid for Scientific Research [25600156, 22104011, 26287063] Funding Source: KAKEN
- Engineering and Physical Sciences Research Council [EP/J017639/1, EP/K037870/1, EP/F032773/1] Funding Source: researchfish
- EPSRC [EP/F032773/1, EP/K037870/1, EP/J017639/1] Funding Source: UKRI
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The nonadditive dispersion contribution to the binding energy of three one-dimensional (1D) wires is investigated using wires modeled by (i) chains of hydrogen atoms and (ii) homogeneous electron gases. We demonstrate that the nonadditive dispersion contribution to the binding energy is significantly enhanced compared with that expected from Axilrod-Teller-Muto-type triple-dipole summations and follows a different power-law decay with separation. The triwire nonadditive dispersion for 1D electron gases scales according to the power law d(-beta), where d is the wire separation, with exponents beta(r(s)) smaller than 3 and slightly increasing with r(s) from 2.4 at r(s) = 1 to 2.9 at r(s) = 10, where r(s) is the density parameter of the 1D electron gas. This is in good agreement with the exponent beta = 3 suggested by the leading-order charge-flow contribution to the triwire nonadditivity, and is a significantly slower decay than the similar to d(-7) behavior that would be expected from triple-dipole summations.
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