Abstract
Investigating proton transport at the interface in an excited state facilitates the mechanistic investigation and utilization of nanomaterials. However, there is a lack of suitable tools for in-situ and interfacial analysis. Here we addresses this gap by in-situ observing the proton transport of graphene quantum dots (GQDs) in an excited state through reduction of magnetic resonance relaxation time. Experimental results, utilizing 0.1 mT ultra-low-field nuclear magnetic resonance relaxometry compatible with a light source, reveal the light-induced proton dissociation and acidity of GQDs' microenvironment in the excited state (Hammett acidity function: -13.40). Theoretical calculations demonstrate significant acidity enhancement in -OH functionalized GQDs with light induction ( pK∗apKa*<math><mi>p</mi> <msubsup><mrow><mi>K</mi></mrow> <mrow><mi>a</mi></mrow> <mrow><mo>*</mo></mrow> </msubsup> </math> = -4.62, stronger than that of H2SO4). Simulations highlight the contributions of edge and phenolic -OH groups to proton dissociation. The light-induced superacidic microenvironment of GQDs benefits functionalization and improves the catalytic performances of GQDs. Importantly, this work advances the understanding of interfacial properties of light-induced sp2-sp3 carbon nanostructure and provides a valuable tool for exploring catalyst interfaces in photocatalysis.