In this work, the oxidation mechanism of hypophosphite anion ( H2PO2
- ) in acidic and alkaline media in the
presence of Ni(II) specie was investigated by using electrochemical impedance spectroscopy (EIS) and density
functional theory (DFT). In EIS, three major electrochemical processes in the electroless deposition process
were found, when the solution pH ranged from 5.5 to 9.5. To understand the microscopic mechanisms involved,
all participate species in the reaction pathways were calculated by the DFT method along with a natural bond
orbital (NBO) analysis. Two emulating reactions were demonstrated: Path (I) passes through a primary
dehydrogenation (D-RP), and Path (II) includes a primary addition of OH- (A-RP) on the hypophosphite
anion. By comparison of the energy levels of all species, it can be concluded that Path (II) is energetically
favorable under both acidic and alkaline conditions. The DFT and NBO analysis can provide strong evidence
for the loops detected in the EIS, especially especially for the inductive loop (IL-M) in the medium-frequency
domain that is caused by the formation of [NiI−H3PO2(OH)] and the capacitive loop (CL-L) in the low-frequency domain by [H2PO2(OH)]. The combination of electrochemical analysis (EIS) and first principle
theory (DFT) analysis proves that it is helpful to explore the nature of the interaction between anodic and
cathodic reactions in the electroless deposition process.