Detection of Aqueous Solvated Electrons Produced by Photoemission from Solids Using Transient Absorption Measurements.

Solvated electrons in water have long been of interest to chemists. While readily produced using intense multiphoton excitation of water and/or irradiation with high-energy particles, the possible role of solvated electrons in electrochemical and photoelectrochemical reactions at electrodes has been controversial. Recent studies showed that excitation of electrons to the conduction band of diamond leads to barrier-free emission of electrons into water. While these electrons can be inferred from the reactions they induce, direct detection by transient absorption measurements provides more direct evidence. Here, we present studies demonstrating direct detection of solvated electrons produced at diamond electrode surfaces and the influence of electrochemical potential and solution-phase electron scavengers. We further present a more detailed analysis of experimental conditions needed to detect solvated electrons emitted from diamond and other solid materials through transient optical absorption measurements.

High-Density Covalent Grafting of Spin-Active Molecular Moieties to Diamond Surfaces.

Functionalization of diamond surfaces with TEMPO and other surface paramagnetic species represents one approach to the implementation of novel chemical detection schemes that make use of shallow quantum color defects such as silicon-vacancy (SiV) and nitrogen-vacancy (NV) centers. Yet, prior approaches to quantum-based chemical sensing have been hampered by the absence of high-quality surface functionalization schemes for linking radicals to diamond surfaces. Here, we demonstrate a highly controlled approach to the functionalization of diamond surfaces with carboxylic acid groups via all-carbon tethers of different lengths, followed by covalent chemistry to yield high-quality, TEMPO-modified surfaces. Our studies yield estimated surface densities of 4-amino-TEMPO of approximately 1.4 molecules nm-2 on nanodiamond (varying with molecular linker length) and 3.3 molecules nm-2 on planar diamond. These values are higher than those reported previously using other functionalization methods. The ζ-potential of nanodiamonds was used to track reaction progress and elucidate the regioselectivity of the reaction between ethenyl and carboxylate groups and surface radicals.

Impact of Electrocatalyst Activity and Ion Permeability on Water-Splitting Photoanodes.

Electrocatalyst (EC)-modified semiconductor (SC) photoelectrodes are key elements of solar water-splitting systems. The SC|EC interface affects the composite photoelectrode behavior but is poorly understood. We uncover the role of EC activity and SC|EC interface properties using a range of metal (Ni, Fe, Ni-Fe, Co, Ir) oxide or (oxy)hydroxide ECs deposited on model single-crystal n-TiO2 photoanodes. The impedance and photoelectrochemical response of the system was nearly independent of EC oxygen evolution activity if the catalyst was deposited electrochemically as an ion-permeable (oxy)hydroxide or hydrous oxide. When dense oxides (e.g., ion-impermeable) ECs were used, the response depended strongly on the EC. These data demonstrate that the EC and SC interface structures are more important than the EC activity in determining the composite photoanode response, confirming recent SC|EC interface simulations for ion-permeable ECs. These results thus inform the design of high-performance water-oxidizing photoanodes with direct SC|EC interfaces.