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To do it, we feed all their energy terms with different sets of orbitals obtained previously from self\u2010consistent density functional theory calculations using several exchange\u2010correlation functionals (e.g., PBE, PBE0, PBEH&H), or directly with HF\u2010PBE orbitals, to see their effect on selected datasets for atomization and reaction energies, the latter proned to marked self\u2010interaction errors. We find that the PBE\u2010QIDH double\u2010hybrid model shows a great consistency, as the best results are always obtained for the set of orbitals corresponding to its hybrid scheme, which prompts us to recommend this model without any other fitting or reparameterization. \u00a9 2017 Wiley Periodicals, Inc.<\/jats:p>","DOI":"10.1002\/jcc.24788","type":"journal-article","created":{"date-parts":[[2017,4,10]],"date-time":"2017-04-10T11:17:59Z","timestamp":1491823079000},"page":"1509-1514","source":"Crossref","is-referenced-by-count":3,"title":["Determining the role of the underlying orbital\u2010dependence of PBE0\u2010DH and PBE\u2010QIDH double\u2010hybrid density functionals"],"prefix":"10.1002","volume":"38","author":[{"given":"Juan Carlos","family":"Sancho\u2010Garc\u00eda","sequence":"first","affiliation":[{"name":"Departamento de Qu\u00edmica F\u00edsica Universidad de Alicante Alicante E\u201003080 Spain"}]},{"given":"\u00c1ngel 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