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Strontium Vanadium Oxide-Hydrides: 'Square-Planar' Two-Electron Phases

机译:锶钒氧化物氢化物:“方平面”两电子相

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A series of strontium vanadium oxide-hydride phases prepared by utilizing a low-temperature synthesis strategy in which oxide ions in Sr_(n+1)V_nO_(3n+1) (n = ∞, 1, 2) phases are topochemically replaced by hydride ions to form SrVO2H, Sr2VO3H, and Sr3V2O5H2, respectively. These new phases contain sheets or chains of apex-linked V~(3+)O4 squares stacked with SrH layers/chains, such that the n = ∞ member, SrVO2H, can be considered to be analogous to "infinite-layer" phases, such as Sr_(1-x)Ca_xCuO2 (the parent phase of the high-T_c cuprate superconductors), but with a d~2 electron count. All three oxide-hydride phases exhibit strong antiferromagnetic coupling, with SrVO2H exhibiting an antiferromagnetic ordering temperature, T_N>300 K. The strong antiferromagnetic couplings are surprising given they appear to arise from π-type magnetic exchange.
机译:利用低温合成策略制备的一系列锶钒氧化物氢化物相,其中Sr_(n + 1)V_nO_(3n + 1)(n =∞,1,2)相中的氧化物离子被氢化物拓扑化学取代离子分别形成SrVO2H,Sr2VO3H和Sr3V2O5H2。这些新相包含由SrH层/链堆叠的顶点连接的V〜(3+)O4正方形薄片或链,因此n =∞成员SrVO2H可被视为类似于“无限层”相,例如Sr_(1-x)Ca_xCuO2(高T_c铜酸盐超导体的母相),但电子数为ad〜2。所有三个氧化物-氢化物相均表现出强反铁磁耦合,其中SrVO2H表现出反铁磁有序温度T_N> 300K。强反铁磁耦合令人惊讶,因为它们似乎是由π型磁交换引起的。

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