(Dated: today) N-doped SrO seems to be one of the model systems for d 0 magnetism, in which magnetism (or ideally, ferromagnetism) was ascribed to the localized N 2p spins mediated by delocalized O 2p holes. Here we offer a different view, using density functional calculations. We find that N-doped SrO with solely substitutional N impurities as widely assumed in the literature is unstable, and instead that a pairing state of substitutional and interstitial N impurities is significantly more stable and has a much lower formation energy than the former by 6.7 eV. The stable (N sub -N int ) 2− dimers behave like a charged (N 2 ) 2− molecule and have each a molecular spin=1. However, their spin-polarized molecular levels lie well inside the wide band gap of SrO and thus the exchange interaction is negligibly weak. As a consequence, N-doped SrO could not be ferromagnetic but paramagnetic. PACS numbers: 75.50.Pp, 71.20.b, 71.70.d, 71.15.Mb In extensive search of magnetic semiconductors, d 0 ferromagnet recently draws a lot of attention [1][2][3][4][5][6][7][8][9][10]. It has no magnetic transition-metal or rare-earth element present and is free of the issue of clustering of magnetic elements, which, however, has been quite often addressed for transition-metal doped semiconductors. Thus, an observed d 0 ferromagnetism could be intrinsic, and it is important both technologically and in the viewpoint of fundamental physics.Very recently, a group of density functional calculations [11][12][13][14][15][16][17][18][19][20] suggest that when N *