ATP hydrolysis releases a significant amount of energy primarily due to two key factors: the breaking of the phosphodiester bond between the terminal phosphate and ADP, and the resulting changes in electrostatic interactions and entropy. When the bond is broken, it alleviates the electrostatic repulsion between negatively charged phosphate groups, making the reaction enthalpically favorable. Additionally, the reaction is entropically favorable because cells maintain a high ATP/ADP ratio. It is important to note that the Pi-ADP bond is not accurately described as "storing" energy; instead, it is characterized as unstable with high potential energy. The hydrolysis process leads to the formation of more stable bonds, resulting in energy release. The weak P-O-P bond in ATP prevents spontaneous hydrolysis, requiring catalysts for the reaction to occur efficiently.