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Although the nanosheet of molybdenum(IV) disulfide (MoS) has been widely recognized as a high-performance green nanoadditive for friction reduction and wear resistance, its low isolated yield and poor colloidal stability in lubricating base oils have become bottlenecks for practical tribological applications. In this work, we report the synthesis of α-lipoate functionalized triblock copolymers and their utilization in directly dispersing bulky MoS as a form of oleogels. The resulting polymer-inorganic composite oleogels are characterized by microscopic imaging, small-angle X-ray scattering, and rheology, demonstrating that the bulky MoS is exfoliated in situ into nanosheets driven by multiple Mo-S coordinating bonds. Notably, this process does not require preexfoliation or separate synthesis of MoS nanosheets. The polymer-nanosheet networks exhibit long-term dispersible and colloidal stability in base oils and excellent lubricating properties. Furthermore, the degree of MoS exfoliation increases with the degree of polymerization of the α-lipoate-containing blocks, resulting in enhanced lubricating performance of composite oleogels. The improved lubricity is attributed to a thicker protective tribofilm enriched with MoS nanosheets formed on the rubbing surface. More importantly, the direct use of bulk MoS as a lubricant additive with the assistance of α-lipoate-containing triblock copolymers establishes a facile strategy for the design of highly efficient green lubricants.
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http://dx.doi.org/10.1021/acsami.5c01620 | DOI Listing |
ACS Macro Lett
September 2025
State Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science, Fudan University, Shanghai 200433, China.
Poly(3-hexylthiophene) (P3HT)-based complex topological copolymers have attracted a great deal of attention for their unique electrical and optical properties. In this contribution, the P3HT-based Janus fibers with controlled lengths were innovatively prepared by sequential crystallization-driven self-assembly (CDSA) of poly(--butylstyrene)--polyisoprene--poly(3-hexylthiophene) (PBS--PI--P3HT) triblock copolymer, cross-linking of the interlayer PI region, and dissociation of fibers in good solvent. The comprehensive characterizations showed that the PBS/P3HT Janus fibers have nearly half the width of PBS--PI--P3HT fibers and fiber lengths close to or slightly shorter than those of PBS--PI--P3HT fibers, indicating that the Janus fibers with adjustable lengths could be prepared in a large window range.
View Article and Find Full Text PDFACS Macro Lett
September 2025
Department of Chemistry, Yonsei University, Seoul 03722, Republic of Korea.
Alkyne groups provide exceptional versatility for functionalization in macromolecular systems. However, the controlled anionic ring-opening polymerization (AROP) of epoxide monomers bearing terminal alkynes remains challenging due to the lability of alkynes under strongly basic conditions. Herein, we present a controlled AROP of glycidyl propargyl ether enabled by Lewis pair organocatalysis, employing a phosphazene base and triethylborane.
View Article and Find Full Text PDFRegen Ther
December 2025
Univ Toulouse, Inserm, ToNIC, Toulouse, France.
Background: Brain regeneration after injury is a challenge being tackled by numerous therapeutic strategies in pre-clinical development. There is growing interest in scaffolds implanted in brain lesions. Developments in 3D printing offer the possibility of designing complex structures of varying compositions adapted to tissue anatomy.
View Article and Find Full Text PDFJ Chem Theory Comput
September 2025
National Laboratory of Solid State Microstructure, Department of Physics, Nanjing University, Nanjing 210093, China.
Single-chain nanoparticles (SCNPs) represent a class of folded macromolecules that mimic biologically derived structures through the covalent cross-linking of polymer backbones. This study explores the interactions between SCNPs and lipid bilayers, focusing on the modulation of the membrane permeability and lipid dynamics. By employing coarse-grained Monte Carlo simulations, we investigate the behavior of diblock, triblock, and random copolymers of varying hydrophobicities and cross-linking densities in contact with lipid membranes.
View Article and Find Full Text PDFJ Phys Chem A
August 2025
Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, Maryland 21218, United States.
Polymer-networked nanoparticles are a promising alternative to silicon semiconductors for the realization of neuromorphic computing platforms. Variations in the interaction between gold nanoparticles (AuNPs) and polyelectrolyte linkers lead to the controlled formation of engineered nanoparticle network (ENPN) structures exhibiting a broad range of topologies and dynamics. Using dissipative particle dynamics (DPD) simulations, we designed triblock copolymers with polyelectrolyte ends that can selectively attach to each of two AuNPs and bridged them together through a middle polymer segment (or block).
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