TG-DTA, TEM, and IR were used to investigate the thermal decomposition behavior of poly(N-vinyl-2-pyrrolidone) (PVP). The TG-DTA results show that the thermal decomposition behavior of PVP on platinum (Pt) is quite different from that of pure PVP. For pure PVP, 95.25% is decomposed when the temperature is increased up to 500°C; while under the same experimental condition, PVP coated on the Pt nanoparticles is only 66.7% decomposed. This is further supported by IR measurement. TEM results exhibited that the partially decomposed PVP still plays a role in stabilizing Pt nanoparticles: after heating treatment at 500°C for half an hour, the platinum nanoparticles did not aggregate heavily.

Nanocellulose, extracted from the most abundant biomass material cellulose, has proved to be an environmentally friendly material with excellent mechanical performance owing to its unique nano-scaled structure, and has been used in a variety of applications as engineering and functional materials. The great biocompatibility and biodegradability, in particular, render nanocellulose promising in biomedical applications. In this review, the structure, treatment technology and properties of three different nanocellulose categories, i.e., nanofibrillated cellulose (NFC), nanocrystalline cellulose (NCC) and bacterial nanocellulose (BNC), are introduced and compared. The cytotoxicity, biocompatibility and frontier applications in biomedicine of the three nanocellulose categories were the focus and are detailed in each section. Future prospects concerning the cytotoxicity, applications and industrial production of nanocellulose are also discussed in the last section.

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In this work, we carefully designed and synthesized a series of novel polyelectrolyte-functionalized carbon dots (CDs-PEI-X) by a facile and reversible phase transfer method based on the protonation reaction and anion exchange process executed on the surface of polyethylenimine-grafted CDs (CDs-PEI), where X denotes the anionic moieties of polyelectrolyte shells including hexafluorophosphate (PF 6 − ), bis(trifluoromethane)sulfonimide (NTf 2 − ), oleate (OL − ), and bis(salicylato)borate (BScB − ), respectively. Attributed to the favorable compatibility of these anions and polyethylene glycol (PEG) molecules, the hydrophobic CDs-PEI-X displayed excellent dispersibility and long-term stability in PEG200 base oil. Subsequently, the tribological behaviors of CDs-PEI-X as the lubricant additives of PEG200 were systematically investigated. It was proved that the anionic moieties of the polyelectrolyte shells of CDs-PEI-X played a crucial role in regulating their tribological behaviors. Particularly, CDs-PEI-OL was confirmed as an optimal additive, exhibiting the best lubricity, outstanding load-bearing capacity, long service life, and remarkable operational stability under boundary lubrication regime. Based on the tribological evaluations and worn surface analyses, the lubrication mechanism of CDs-PEI-OL was mainly attributed to the formation of the organic−inorganic hybrid adsorption film, the protective tribofilm, and its nanolubrication functions as scrollable "ball-bearing", i.e., the synergistic lubrication effects of surface polyelectrolyte shells and carbon cores. This study provides a feasible and versatile strategy to rapidly and effectively tailor the surface chemistry of CDs and discloses the essential contribution of carbon cores and surface groups on the lubrication process, which facilitates the development of advanced CDs-based nanolubricant additives.

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