In this work, we obtain two ruthenium(ii) complexes with Schiff base cavities that exhibit significantly enhanced electrochemiluminescence (ECL) intensity and quantum efficiency due to Ru(bpy)3(2+) in aqueous solution, without the addition of tri-n-propylamine (TPrA). The great increase in ECL intensity is confirmed to be due to the electrochemical oxidation of phenolic hydroxyl groups and the resonant structure of imino radicals. Thus, the electrons are transferred intramolecularly to the Ru(iii) center, leading to efficient generation of the excited state of Ru(ii)*. Subsequently, we find that Co(2+) bonding with the salen cavity can selectively and quickly quench the ECL signal. Furthermore, we study the mechanism of the process by which Co(2+) hinders the oxidation of phenolic groups and blocks the electron transfer from imino radicals to the Ru center. Thus, a highly sensitive and selective ECL probe for the recognition of Co(2+) was developed with a stable response over a concentration range of 0.9 μM to 6.3 μM and a detection limit as low as 21 nM.

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Carbon dots (CDs) have lately inspired extensive interest in tribology, especially in the field of friction modifiers. However, it remains an enormous challenge to obtain satisfactory compatibility between CDs and base oils without laborious and tedious chemical modifications. In this work, for the first time, we reported a scalable and sustainable synthesis of CDs from easily and cheaply available biomass via a one-pot solvothermal route, which used ethanol as the renewable reaction medium and H 2 O 2 as the clean oxidant. Typically, ginkgo leaves acting as the precursors were converted into CDs with an ultrahigh yield of 85.3%. As expected, the ginkgo leaf-derived CDs, abbreviated as GCDs, displayed excellent dispersibility, durable stability, and attractive fluorescence-emission behavior in PEG200. The as-prepared GCDs as additives for PEG200 exhibited remarkable lubricity, favorable loadcarrying ability, and long operating life under boundary lubrication. Particularly, the antiwear and friction-reducing performances of PEG200 were promoted by 70.5% and 34.7%, respectively, when only 0.20 wt % of GCDs was blended. Confirmed by the tribological investigations and surface detection of wear tracks, the essential lubrication mechanism of GCDs was chiefly associated with the generation of GCD-inserted tribochemical films with a thickness of about 80 nm and their nanolubrication functions, that is, the synergistic effects of surface organic moieties and carbonaceous cores. This study establishes a technically simple, feasible, versatile, cost-effective, and green methodology to produce CD-based friction modifiers toward PEG synthetic base oils for tribological applications.