Chemical Dynamics Laboratory, RIKEN Advanced Science Institute, Wako 351-0198, Japan.
Phys Chem Chem Phys. 2011 Jan 14;13(2):413-7. doi: 10.1039/c0cp01636e. Epub 2010 Nov 10.
High-resolution soft X-ray photoelectron spectra of liquid water (H(2)O and D(2)O) were measured using a liquid beam photoelectron spectrometer. The 1a(1) (O1s) band and the lowest valence 1b(1) band had single peaks, which is not consistent with the split 1b(1)→ 1a(1) of the X-ray emission band of liquid water if the splitting is assumed to originate from level shifts in two different hydrogen bonding structures. The second valence 3a(1) band of liquid water exhibited a flat top implying that two bands exist underneath a broad feature, which is similar to the case of the 3a(1) band of amorphous ice. The energy splitting between the two 3a(1) bands is estimated to be 1.38 eV (H(2)O) and 1.39 eV (D(2)O). Ab initio calculations suggest that the large splitting of the 3a(1) band is characteristic of water molecules that function as both proton donor and acceptor. The overall result is consistent with the conventional model of a tetrahedral hydrogen-bonding network in liquid water.
使用液体射流光电离电子能谱仪,我们对液态水(H₂O 和 D₂O)的高分辨率软 X 射线光电子能谱进行了测量。1a(1)(O1s)带和最低价 1b(1)带都只有单个峰,如果假定劈裂源于两种不同氢键结构中的能级移动,那么这与液态水的 X 射线发射带的劈裂 1b(1)→1a(1)不一致。液态水的第二个价 3a(1)带呈现平顶,这意味着在一个宽特征下存在两个带,这与非晶冰的 3a(1)带的情况相似。两个 3a(1)带之间的能量劈裂估计为 1.38 eV(H₂O)和 1.39 eV(D₂O)。从头算计算表明,3a(1)带的大劈裂是质子供体和受体功能的水分子的特征。整体结果与液态水中四面体氢键网络的传统模型一致。