“…The s·i(s) curves remain oscillated near the zero axis, showing that the diffraction experiments and data treatment processes are reliable. , and this assignment is suggested by the crystal structure data [10]; The peak at 0.24 nm is ascribed to the Na + -H 2 O interactions within the first hydration shell of hydrated Na + ions on the basis of the crystal structure of NaBH 4 •2H 2 O [10], the previous findings from X-ray diffraction [11,12], computer simulation [13]and ab initio [14], and the sum of the ionic radius of Na + (0.102 nm) and the size of a water molecule (0.14 nm); The peak at about 0.29 nm can be ascribed to the H-Bonding of bulk water [15]; The second peak at 0.34 nm arises mainly from the octahedral vertexes of hydrated Na + (cis O-O Na+ ) according to (2) 1/2 r Na-O(1) =0.340 nm; The peak at 0.35 nm may be assign to B-W(I) the interaction of the hydrated BH 4 -and the interaction of the contact ion pair (CIP) of Na + and BH 4 -, Na-Na interaction with a hydrated dimmer sodium ions; the peak at 0.396 nm is due to the interaction between octahedral vertexes and O B -H 2 O(I) interaction in the hydrated B(OH) 4 -ion. The peak around 0.43 and 0.47 nm is due to the interactions of Na-O(2) and trans O-O(Na + ), respectively.…”