Uncovering
the function of structured water in the interfacial
capacitance at the molecular level is the basis for the development
of the concept and model of the electric double layer; however, the
limitation of the available technology makes this task difficult.
Herein, using surface-enhanced infrared absorption spectroscopy combined
with electrochemistry, we revealed the contribution of the cleavage
of loosely bonded tetrahedral water to the enhancement of model membrane
capacitance. Upon further combination with ionic perturbation, we
found that the interface hydrogen bonding environment in the stern
layer was greatly significant for the light-induced cleavage of tetrahedral
water and thus the conversion of optical signals into electrical signals.
Our work has taken an important step toward gaining experimental insight
into the relationship between water structure and capacitance at the
bioelectric interface