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Biodegradable and biocompatible 3D printable biomaterials with tunable mechanical properties and degradation rate adapted to target tissues were urgently required to manufacture scaffolds for tissue regeneration. Herein, a strategy based on a series of copolymers are proposed where the mechanical and degradation properties can be optimized regarding the specific biological application. With this purpose, poly($\epsilon$-caprolactone)-poly(ethylene glycol)-poly($\epsilon$-caprolactone) (PCL-PEG-PCL, PCEC) triblock co-polymers with high molecular weight were synthesized by using PEG with a wide range of molecular weight (from 0.6 kg/mol to 35 kg/mol) as macroinitiators. PCEC copolymers exhibited tunable mechanical properties with an elastic modulus in the range 338-705 MPa and a degradation rate from 60% mass loss after 8 h to 70% mass loss after 23 days in accelerated tests, as well as excellent cytocompatibility and cell attachment after culture with mouse fibroblast L929 cells. The mechanisms responsible for these properties were ascertained by means of different techniques to ascertain the structure-property relationship in PCEC copolymers. Furthermore, it was shown that it is possible to manufacture PCEC scaffolds by 3D printing with excellent dimensional accuracy and controlled microporosity. This study provides a promising strategy to design, select, and fabricate copolymers with tunable mechanical properties and degradation rate for tissue engineering applications.

Layer-by-Layer (LbL) assembly was attractive as a versatile tool to address the flammability of cotton, while the washing fastness of LbL coating stayed an issue. Aiming to tackle this issue, LbL layers consisted of phenylphosphonic acid (PHA) and 3-aminopropyltriethoxysilane (APTES) was deposited on polydopamine (PDA)-coated cotton. The prepared cotton reached 31.4% of limiting oxygen index (LOI), and extinguished immediately after removing the ignitor. Peak of heat release rate (pHRR) attenuated around 36 % compared with pure cotton. A combined barrier and quenching mechanisms were proposed. Moreover, enhanced washing durability (24.1% of LOI) was achieved even after 50 detergent laundering cycles. A facile, boosted LbL approach with proposed {\pi}-{\pi} stacking interactions between PDA abundant aromatic structures and benzene ring in PHA from LbL layers, is first to put forward to construct durable efficient flame retardant (FR) cotton. This work attempted to enlighten more thoughts and design for durable FR cotton fabrics.

We developed a novel pathway to highly efficiently synthesize the [60]Fullerene (C$_{60}$)-Cyclodextrin (CD) complex, which is termed as solvent-induced reversible recognition. Three kinds of typical complexes, namely, C$_{60}$-2GUA$^+$-$\alpha$-CD, C$_{60}$-2GUA$^+$-$\beta$-CD and C$_{60}$-4OH-$\beta$-CD, were synthesized. The chemical structure of all complexes was fully confirmed by Fourier transform infrared spectroscopy, Nuclear magnetic resonance (NMR), UV-Vis spectroscopy and the solubility test. Furthermore, crystalline status and thermal degradation were recorded by X-ray diffraction and Thermogravimetric analysis, respectively. Both the NMR and ESI-MS results clearly confirmed the 1:1 complex of C$_{60}$ derivatives with CD. The pathway overcame the preparation limitation of traditional complex, and was extended to the prepare $\alpha$-CD containing complex. To the best of our knowledge, it is the first time to report $\alpha$-CD related complex. The geometric relation between C$_{60}$ and CD for all the three kinds of complexes were analyzed. We can achieve high efficiency to obtain solid-state complex products, which lays the foundation for the widely practical application of complex and provides enough experimental basis for the advanced application of C$_{60}$ and CD in supramolecular assembly. Notably, the solvent-induced reversibility and ionic instability of the complex provides a new possibility for the molecular recognition-based sensing.

A novel fully bio-based Poly (Glycerol-Itaconic acid) (PGI) was designed and highly efficiently synthesized by solvent-free polycondensation. The Poly (ethylene glycol) (PEG) was used as the phase change materials (PCM) working substance and encapsulated by the sustainable PGI supporter. PEG chains were tightly encapsulated with the PGI supporting material mainly under hydrogen bonds due to the structural compatibility between PGI and PEG. The PCMs can achieve high form stability and high phase change enthalpies in the same kinds of PCMs. Furthermore, the phase change temperatures and enthalpies of the PCMs can be adjusted conveniently by regulating the PEG content and molecular weight. Notably, this process extremely facilitates the realization of efficient mass production due to the eco-friendly nature, high efficiency and low cost.

The development of thermal energy storage materials is the most attractive strategy to harvest the solar energy and increase the energy utilization efficiency. Phase change materials (PCMs) have received much attention in this research field for several decades. Herein, we reported a new kind of PCM micro topological structure, design direction, and the ultra-flexible, form-stable and smart PCMs, polyrotaxane. The structure of polyrotaxane was fully confirmed by 1H nuclear magnetic resonance,attenuated total reflection-fourier transform infrared and X-ray diffraction. Then the tensile properties,thermal stability in the air, phase change energy storage and shape memory properties of the films were systematically analyzed. The results showed that all the mechanical performance, thermal stability in air and shape memory properties of polyrotaxanes were enhanced significantly compared to those of polyethylene oxide (PEO). The form stability at temperatures above the melting point of PEO significantly increased with the {\alpha}-CD addition. Further with the high phase transition enthalpy and excellent cycle performance, the polyrotaxane films are therefore promising sustainable and advanced form-stable phase change materials for thermal energy storage. Notably, its ultra-high flexibility, remolding ability and excellent shape memory properties provide a convenient way for the intelligent heat treatment packaging of complex and flexible electronic devices. In addition, this is a totally novel insight for polyrotaxane application and new design method for form-stable PCMs.

Metal halide perovskites (MHPs) based phosphor-converted light-emitting diodes (pc-LEDs) are limited by the low MHP stability under storage/operation conditions. A few works have recently stablished the in-situ synthesis of MHPs into polymer matrices as an effective strategy to enhance MHPs stability with a low-cost fabrication. However, this is limited within petrochemical-based polymers. Herein, the first in-situ ambient preparation of highly luminescent and stable MHPs-bio-polymer filters (MAPbBr3 nanocrystals as emitter and poly(L-lactide acid) (PLLA) as matrix) with arbitrary areas (up to ca. 300 cm2) is reported. The MAPbBr3-PLLA phosphors feature a narrow emission (25 nm) with excellent photoluminescence quantum yields (more than 85%) and stabilities under ambient storage, water, and thermal stress. This is corroborated in green pc-LEDs featuring a low efficiency roll-off, excellent operational stability of ca. 600 h, and high luminous efficiencies of 65 lm W-1 that stand out the prior art (e.g., average lifetime of 200 h at 50 lm W-1). The filters are further exploited to fabricate white-emitting pc-LEDs with efficiencies of ca. 73 lm W-1 and x/y CIE color coordinates values of 0.33/0.32. Overall, this work stablishes a straightforward (one-pot/in-situ) and low-cost preparation (ambient/room temperature) of highly efficient and stable MHP-bio-polymer phosphors for highly performing and more sustainable lighting devices.