Actualization of the hydrogen (H₂) economy and decarbonization goals can be achieved with feasible large-scale H₂ geo-storage. Geological formations are heterogeneous, and their wetting characteristics play a crucial role in the presence of H₂, which controls the pore-scale distribution of the fluids and sealing capacities of caprocks. Organic acids are readily available in geo-storage formations in minute quantities, but they highly tend to increase the hydrophobicity of storage formations. However, there is a paucity of data on the effects of organic acid concentrations and types on the H₂-wettability of caprock-representative minerals and their attendant structural trapping capacities. Geological formations contain organic acids in minute concentrations, with the alkyl chain length ranging from C₄ to C₂₆. To fully understand the wetting characteristics of H₂ in a natural geological picture, we aged mica mineral surfaces as a representative of the caprock in varying concentrations of organic molecules (with varying numbers of carbon atoms, lignoceric acid C₂₄, lauric acid C₁₂, and hexanoic acid C₆) for 7 days. To comprehend the wettability of the mica/H₂/brine system, we employed a contact-angle procedure similar to that in natural geo-storage environments (25, 15, and 0.1 MPa and 323 K). At the highest investigated pressure (25 MPa) and the highest concentration of lignoceric acid (10^-2 mol/L), the mica surface became completely H₂ wet with advancing (θ_a= 106.2°) and receding (θ_r=97.3°) contact angles. The order of increasing θ_a and θ_r with increasing organic acid contaminations is as follows: lignoceric acid > lauric acid > hexanoic acid. The results suggest that H₂ gas leakage through the caprock is possible in the presence of organic acids at higher physio-thermal conditions. The influence of organic contamination inherent at realistic geo-storage conditions should be considered to avoid the overprediction of structural trapping capacities and H₂ containment security.