Electronic and atomic structures of vacancies and protons in hydroxyapatite (HAp) were analyzed by using first-principles band structure calculations. From total energies of super-cells for monoclinic HAp, defect formation energies and equilibrium concentrations were evaluated, assuming chemical equilibrium between HAp and aqueous solution saturated with respect to HAp. It was found that interstitial and Ca-substitutional protons form H2O groups or acid phosphates of HPO42- and were stabilized by making H-bonds with adjacent PO43- groups. Moreover, defect association considerably decreased the defect formation energies, and, in particular, interstitial protons bonded to OH− groups become most stable when associated with Ca-substitutional protons. Due to abundant formation of the associated defect comprising interstitial and Ca-substitutional protons, Ca contents in HAp decrease with lowering pH, which explains pH dependence of Ca/P molar ratios of HAp observed experimentally.

Theoretical Investigation of the Defect Formation Mechanism Relevant to Nonstoichiometry in Hydroxyapatite. K.Matsunaga: Physical Review B, 2008, 77[10], 104106 (14pp)