Stable–liquid contact electrification (SL-CE) has emerged as a particular pathway for driving interfacial chemistry, but the rules governing how triboelectric polarity {couples} with electrolyte id to control response exercise stay poorly understood. On this examine, triboelectricity-driven chemistry at strong–liquid interfaces was examined utilizing two consultant supplies positioned at far ends of the triboelectric collection, and paired with cationic or anionic dyes. It was discovered that adsorption and the formation of {an electrical} double layer may end in suppressed interfacial cost switch, resulting in markedly diminished, and in some circumstances totally inhibited, era of reactive oxygen species. These findings set up a mechanistic framework for triboelectric polarity–electrolyte coupling, highlighting the pivotal function of floor physicochemical properties in governing SL-CE and providing normal design rules for optimizing triboelectricity-driven chemical reactions.
