Time-resolved surface-enhanced resonance Raman spectroscopy can selectively probe the molecular structure and dynamics of the active sites of redox proteins that are immobilized on self-assembled monolayers on Ag electrodes (see picture). As shown for the protein cytochrome c, this method is capable of analyzing complex interfacial processes in terms of electron transfer and non-Faradaic reactions.
No takes yet. Share an insight, caveat, or question.
Murgida et al. (2001) studied this question.
Synapse has enriched 5 related papers. Consider them for comparative context: