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An incorporation of the hydrogen bond (O:H O or HB) cooperativity notion, contact angle detection, and the differential phonon spectrometrics (DPS) has enabled us to gain refined information on the HCl, KCl and KOH solvation resolved solute-solvent molecular interactions and the solution surface stresses. Results show that ionic polarization stiffens the solvent H O bond phonon from 3200 to 3480 cm −1 in the hydration shells. The HO − in alkaline solution, however, shares not only the same H O phonon redshift of compressed water from 3200 to < 3100 cm −1 but also the dangling bonds of H 2 O surface featured at 3610 cm −1 . Salt and alkaline solvation enhances the solution surface stress by K + and Cl − ionic polarization. The excessive H + proton in acid solution forms a H↔H anti-HB that depresses the solution surface stress, instead. The solute capability of transforming the fraction of the O:H O bonds of the solvent matrix is featured by: f H = 0 and f x ∝ 1-exp(-C/C 0 ) (x = HO − , K + and Cl − ) towards saturation. Exercises not only confirm the presence of the H↔H anti-HB point fragilization, the O:⇔:O super-HB point compression, and ionic polarization dominating the performance of the respective HCl, KOH, and KCl solutions, but also demonstrate the power of the DPS that enables high resolution of solute-solute-solvent interactions and correlation between HB relaxation and solution surface stress. [ABSTRACT FROM AUTHOR]