“…Here, because the redox potential of almost all organic compounds is significantly more negative than that of OH radicals, once OH radicals are formed and reach the molecule to be oxidized, no differentiation according to the exact type of the chemical species should be expected 51. Therefore, rate enhancement can be obtained by facilitating adsorption in close proximity to the photocatalytic sites, as demonstrated when using inert substrates, such as zeolites,52 silica,53 activated carbon,54, 55 and even CNTs 29. Moreover, by controlling adsorption, it is possible to achieve specificity, either by selective physisorption at the vicinity of the sites (“adsorb and shuttle”)56–58 or by molecular imprinting on the surface of the photocatalyst 59…”