The sustainable biopolymer, poly(lactide) (PLA), has been intensely researched over the past decades because of its excellent biodegradability, renewability, and sustainability. The boundless potential of this sustainable biopolymer could resolve the adverse negative impact caused by the petroleum-based polymers. However, the inherent drawback of PLA such as brittleness, low heat distortion temperature, and slow recrystallization rate narrowed the broad applications in biomedical, automotive, and structural fields. In this study, we successfully synthesized a PHB-based filler (PHB-di-rub) displaying synergetic functions of (1) effective nucleation and (2) extreme toughening of the PLA matrix at only 5% (1.5 wt % PHB content). Remarkably, the storage modulus improves by 15%; tensile elongation extends by 57-fold (300% strain) and toughness by 38-fold while maintaining its original strength and stiffness. Likewise, 10% of PHB-di-rub (3 wt % PHB content) has an even higher improvement with a storage modulus improvement by 32%, elongation by 128-fold (680% strain), and toughness by 84-fold, with a marginal change in strength and stiffness. NMR results confirmed the structure of PHB-di-rub, where PHB acts as the rigid core and the poly(lactide-cocaprolactone) (DLA-co-CL) random copolymer confers the flexibility. DSC, WAXD, and POM display the excellent nucleating ability of PHB-di-rub. SEM shows the morphology of elongated fibrils structure with strong matrix−filler interaction and homogeneous filler dispersion. SAXS, WAXS, and WAXD elucidate the extreme toughening mechanism to be a combination of rubber-induced crazing effect and highly orientated PLA matrix with PHB-di-rub. The Herman's orientation function further quantifies the extreme elongation (680%) owing to the perfect alignment. This highly biodegradable biocomposite with high strength and toughness shows potential in replacing the current petroleum-based polymers, which open up to broader prospects in the biomedical, automotive, and structural application.

The future of green electronics possessing great strength and toughness proves to be a promising area of research in this technologically advanced society. This work develops the first fully bendable and malleable toughened polylactic acid (PLA) green composite by incorporating a multifunctional polyhydroxybutyrate rubber copolymer filler that acts as an effective nucleating agent to accelerate PLA crystallization and performs as a dynamic plasticizer to generate massive polymer chain movement. The resultant biocomposite exhibits a 24‐fold and 15‐fold increment in both elongation and toughness, respectively, while retaining its elastic modulus at >3 GPa. Mechanism studies show the toughening effect is due to an amalgamation of massive shear yielding, crazing, and nanocavitation in the highly dense PLA matrix. Uniquely distinguished from the typical flexible polymer that stretches and recovers, this biocomposite is the first report of PLA that can be “bend, twist, turn, and fold” at room temperature and exhibit excellent mechanical robustness even after a 180° bend, attributes to the highly interconnected polymer network of innumerable nanocavitation complemented with an extensively unified fibrillar bridge. This unique trait certainly opens up a new horizon to future sustainable green electronics development.

Inspired by the biomineralization of unicellular diatoms, a biomimetic approach based on template (pluronic F127 micelle cluster)-induced self-assembly of α-cyclodextrin is developed to create hierarchical porous graphitic carbon spheres via hydrothermal treatment followed by pyrolysis. The as-obtained carbon spheres combine the features required for high-power electrode materials in lithium-ion batteries (LIBs), such as high degree of graphitization, large surface area with hierarchically distributed pore sizes as well as doping with heteroatoms, which synergistically contribute to their impressive electrochemical properties. When applied as an anode for LIBs, the carbon spheres exhibit high reversible capacity (ca. 700 mA h g–1 at 50 mA g–1), good cycling stability, and remarkably outstanding high-rate performance (ca. 600, 450, and 290 mA h g–1 obtained at a current density of 1, 10, and 30 A g–1, respectively), which is among the best of present pure carbon materials for LIBs applications. The fabrication process is straightforward and cost-effective, providing a new methodology for the tailored design of carbon materials with enhanced power densities for energy storage applications.