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Although lubricants play an essential role in reducing wear and friction in mechanical systems, environmental issues persist. In the past decades, Ionic Liquids (ILs) have arisen as environmentally friendly alternatives to conventional lubricants and additives. ILs are low–volatile and non-flammable salts that possess low melting points (below 100 ºC). Their tunable properties, achieved by selecting the appropriate cation and anion, make them ideal candidates for different applications, including lubricants. In recent times, Protic Ionic Liquids (PILs) have attracted attention in the tribological community as a cost-effective alternative to conventional aprotic counterparts. In this work, a choline-amino acid ionic liquid, derived only from renewable, biodegradable, and biocompatible products, was synthesized, and investigated as both neat lubricant and additive to non-polar oil. The lubricating properties of [CHO][GLY] were studied both as a neat lubricant and as a 1 wt. % additive to a polyalphaolefin (PAO) oil using a ball-on-flat reciprocating friction tester. AISI 52100 steel disks were tested against AISI 52100 steel balls using either [CHO][GLY] or the mixture of PAO+[CHO][GLY]. For comparison purposes, the commercially available base oil, PAO, was also tested. Preliminary results showed no major differences in friction between the lubricants used. Nevertheless, the addition of 1 wt.% to the PAO demonstrated a remarkable 30% reduction in wear on the steel disk. This encouraging improvement in anti-wear characteristics raises the potential advancement of lubrication technology with the choline-amino acid ionic liquid, coupled with its environmentally friendly nature. Energy-dispersive X-ray (EDX) spectroscopy, non-contact profilometry, and scanning electron microscopy (SEM) were used to study the worn steel surfaces and elucidate the wear mechanisms. 

Efficient nanomaterials for artificial photosynthesis require fast and robust unidirectional electron transfer (ET) from photosensitizers through charge-separation and accumulation units to redox-active catalytic sites. We explored the ultrafast time-scale limits of photo-induced charge transfer between a Ru(II)tris(bipyridine) derivative photosensitizer and PpcA, a 3-heme c-type cytochrome serving as a nanoscale biological wire. Four covalent attachment sites (K28C, K29C, K52C, and G53C) were engineered in PpcA enabling site-specific covalent labeling with expected donor-acceptor (DA) distances of 4–8 Å. X-ray scattering results demonstrated that mutations and chemical labeling did not disrupt the structure of the proteins. Time-resolved spectroscopy revealed three orders of magnitude difference in charge transfer rates for the systems with otherwise similar DA distances and the same number of covalent bonds separating donors and acceptors. All-atom molecular dynamics simulations provided additional insight into the structure-function requirements for ultrafast charge transfer and the requirement of van der Waals contact between aromatic atoms of photosensitizers and hemes in order to observe sub-nanosecond ET. This work demonstrates opportunities to utilize multi-heme c-cytochromes as frameworks for designing ultrafast light-driven ET into charge-accumulating biohybrid model systems, and ultimately for mimicking the photosynthetic paradigm of efficiently coupling ultrafast, light-driven electron transfer chemistry to multi-step catalysis within small, experimentally versatile photosynthetic biohybrid assemblies.