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We herein describe a simple and efficient one-pot synthesis approach to prepare crystalline polycarbonate–polyester diblock copolymers by copolymerizing tetrachlorophthalic anhydride, CO2, and ethylene oxide using a metal-free catalyst. The block copolymers possess a melting point as high as 169 °C and two distinct glass transition temperatures. It is also possible to control the length and composition of the copolymers, thereby customizing their crystallinity and physical performance. [ABSTRACT FROM AUTHOR]

The cathode affects the capacity, working voltage, and cost of lithium-ion batteries. Although the binder is a small part of the cathode material, it is particularly important to the performance of the batteries. Therefore, the design and development of polymer binders with different structures and characteristics is an important topic. In this paper, an NCM811 cathode (PPC-NCM) was prepared by a solvent-free method using poly (propylene carbonate) (PPC) as the binder, with an active substance loading of 10 mg/cm2. To explore the effect of the PPC binder on the electrochemical performance of the NCM811 cathode, the discharge capacity was 112.2 mAh/g with a 76.1% capacity retention after cycling more than 200 cycles at 1 C, which has a significantly better cycling performance than that of a PVDF-NCM/Li battery. The PPC/NCM/graphite full cells were also assembled to demonstrate the practical application potential of this work. It was shown that PPC as a binder can improve the cycling stability of NCM811/Li and NCM811/graphite full cells. The PPC binder used in the NCM811 cathode not only makes it extremely easy to prepare dry electrodes, but also makes it very simple to recover the electrode material by heating in the case of battery failure. This paper provides a new idea for the industrialization and development of a novel binder. [ABSTRACT FROM AUTHOR]

The polycondensation of carbon dioxide and diols under atmospheric pressure has significant appeal, thus making the study of catalysts in this process very important. Here, a series of CeO2-X catalysts (X = 9/11/13) with surface modification by basic sites was synthesized via simple impregnation in KOH solution. The structure and morphology of the CeO2-X catalysts remained unchanged after KOH treatment. However, the specific surface area of modified catalysts showed a slight decrease compared with the unmodified samples due to the notable enhancement of basic sites on the surface, resulting in improvement of CO2 adsorption capacity. Furthermore, the catalytic performance of the resultant CeO2-X catalysts was evaluated by solvent-free polymerization of 1,6-hexanediol (HDO) and CO2 at atmospheric pressure (0.1 MPa) using a well-designed reaction apparatus. As a result, the modified catalysts exhibited better performance for CO2 activation due to the existence of abundant basic sites on the surfaces, while CeO2-11 possessed the most favorable catalytic activity and displayed an enhancement of approximately 50% in production compared with that of unmodified CeO2. [ABSTRACT FROM AUTHOR]

High-temperature proton exchange membrane fuel cells (HT-PEMFCs) have become one of the important development directions of PEMFCs because of their outstanding features, including fast reaction kinetics, high tolerance against impurities in fuel, and easy heat and water management. The proton exchange membrane (PEM), as the core component of HT-PEMFCs, plays the most critical role in the performance of fuel cells. Phosphoric acid (PA)-doped membranes have showed satisfied proton conductivity at high-temperature and anhydrous conditions, and significant advancements have been achieved in the design and development of HT-PEMFCs based on PA-doped membranes. However, the persistent issue of HT-PEMFCs caused by PA leaching remains a challenge that cannot be ignored. This paper provides a concise overview of the proton conduction mechanism in HT-PEMs and the underlying causes of PA leaching in HT-PEMFCs and highlights the strategies aimed at mitigating PA leaching, such as designing crosslinked structures, incorporation of hygroscopic nanoparticles, improving the alkalinity of polymers, covalently linking acidic groups, preparation of multilayer membranes, constructing microporous structures, and formation of micro-phase separation. This review will offer a guidance for further research and development of HT-PEMFCs with high performance and longevity. [ABSTRACT FROM AUTHOR]

A series of CO2-based thermoplastic polyurethanes (TPUs) were prepared using CO2-based poly(polycarbonate) diol (PPCDL), 4,4′-methylenebis (cyclohexyl isocyanate) (HMDI), and polypropylene glycol (PPG and 1,4-butanediol (BDO) as the raw materials. The mechanical, thermal, optical, and barrier properties shape memory behaviors, while biocompatibility and degradation behaviors of the CO2-based TPUs are also systematically investigated. All the synthesized TPUs are highly transparent amorphous polymers, with one glass transition temperature at ~15–45 °C varying with hard segment content and soft segment composition. When PPG is incorporated into the soft segments, the resultant TPUs exhibit excellent self-healing and shape memory performances with the average shape fixity ratio and shape recovery ratio as high as 98.9% and 88.3%, respectively. Furthermore, the CO2-based TPUs also show superior water vapor permeability resistance, good biocompatibility, and good biodegradation properties, demonstrating their pretty competitive potential in the polyurethane industry applications. [ABSTRACT FROM AUTHOR]

Degradable and high-barrier plastic packaging materials draw more attention with the development of a social economy and the demands of environmental protection. In this study, poly(propylene carbonate phthalate) (PPC-P) and poly(butylene adipate-co-terephthalate) (PBAT) blends with different ratios were designed and prepared, marked as PPC-P/PBAT. Chain extenders were introduced into the blends, and the mechanical properties, thermal properties, and barrier properties of the composites were studied. The 75PPC-P/PBAT with 2% extenders represent the best performance. The addition of the chain extender has significantly improved the thermal stability and tensile elongation of PPC-P/PBAT. On this basis, the PPC-P/PBAT composite film was coated with PVA and borax using the dipping and pulling method. The oxygen barrier properties have been further improved for the composite film with a coating layer. Considering the characteristics of biodegradability and a high-barrier property, the 75PPC-P/PBAT/2MDI@Gly blend coated with 2 wt% PVA and 3 wt% borax exhibits potential as a superior food/pharmaceutical plastic packaging material with excellent tensile and barrier properties. [ABSTRACT FROM AUTHOR]

To address the challenges posed by the narrow oxidation decomposition potential window and the characteristic of low ionic conductivity at room temperature of solid polymer electrolytes (SPEs), carbon dioxide (CO2), epichlorohydrin (PO), caprolactone (CL), and phthalic anhydride (PA) were employed in synthesizing di-block copolymer PCL-b-PPC and PCL-b-PPCP. The carbonate and ester bonds in PPC and PCL provide high electrochemical stability, while the polyether segments in PPC contribute to the high ion conductivity. To further improve the ion conductivity, we added succinonitrile as a plasticizer to the copolymer and used the copolymer to assemble lithium metal batteries (LMBs) with LiFePO4 as the cathode. The LiFePO4/SPE/Li battery assembled with PCL-b-PPC electrolyte exhibited an initial discharge-specific capacity of 155.5 mAh·g−1 at 0.5 C and 60 °C. After 270 cycles, the discharge-specific capacity was 140.8 mAh·g−1, with a capacity retention of 90.5% and an average coulombic efficiency of 99%, exhibiting excellent electrochemical performance. The study establishes the design strategies of di-block polymer electrolytes and provides a new strategy for the application of LMBs. [ABSTRACT FROM AUTHOR]

High-energy-density Li-CO2 batteries are promising candidates for large-capacity energy storage systems. However, the development of Li-CO2 batteries has been hindered by low cycle life and high overpotential. In this study, we propose a CO2-based thermoplastic polyurethane (CO2-based TPU) with CO2 adsorption properties and excellent self-healing performance to replace traditional polyvinylidene fluoride (PVDF) as the cathode binder. The CO2-based TPU enhances the interfacial concentration of CO2 at the cathode/electrolyte interfaces, effectively increasing the discharge voltage and lowering the charge voltage of Li-CO2 batteries. Moreover, the CO2 fixed by urethane groups (-NH-COO-) in the CO2-based TPU are difficult to shuttle to and corrode the Li anode, minimizing CO2 side reactions with lithium metal and improving the cycling performance of Li-CO2 batteries. In this work, Li-CO2 batteries with CO2-based TPU as the multifunctional binders exhibit stable cycling performance for 52 cycles at a current density of 0.2 A g−1, with a distinctly lower polarization voltage than PVDF bound Li-CO2 batteries. [ABSTRACT FROM AUTHOR]

Practical high‐voltage lithium metal batteries hold promise for high energy density applications, but face stability challenges in electrolytes for both 4 V‐class cathodes and lithium anode. To address this, we delve into the positive impacts of two crucial moieties in electrolyte chemistry: fluorine atom (‐F) and cyano group (‐CN) on the electrochemical performance of polyether electrolytes and lithium metal batteries. Cyano‐bearing polyether electrolytes possess strong solvation, accelerating Li+ desolvation with minimal SEI impact. Fluorinated polyether electrolytes possess weak solvation, and stabilize the lithium anode via preferential decomposition of F‐segment, exhibiting nearly 6000‐h stable cycling of lithium symmetric cell. Furthermore, the electron‐withdrawing properties of ‐F and ‐CN groups significantly bolster the high‐voltage tolerance of copolymer electrolyte, extending its operational range up to 5 V. This advancement enables the development of 4 V‐class lithium metal batteries compatible with various cathodes, including 4.45 V LiCoO2, 4.5 V LiNi0.8Co0.1Mn0.1O2, and 4.2 V LiNi0.5Co0.2Mn0.3O2. These findings provide insights into design principles centered around polymer components for high‐performance polymer electrolytes. [ABSTRACT FROM AUTHOR]

Poly(propylene carbonate-co-phthalate) (PPC-P) is an amorphous copolymer of aliphatic polycarbonate and aromatic polyester; it possesses good biodegradability, superior mechanical performances, high thermal properties, and excellent affinity with CO2. Hence, we fabricate PPC-P foams in an autoclave by using subcritical CO2 as a physical blowing agent. Both saturation pressure and foaming temperature affect the foaming behaviors of PPC-P, including CO2 adsorption and desorption performance, foaming ratio, cell size, porosity, cell density, and nucleation density, which are investigated in this research. Moreover, the low-cost PPC-P/nano-CaCO3 and PPC-P/starch composites are prepared and foamed using the same procedure. The obtained PPC-P-based foams show ultra-high expansion ratio and refined microcellular structures simultaneously. Besides, nano-CaCO3 can effectively improve PPC-P's rheological properties and foamability. In addition, the introduction of starch into PPC-P can lead to a large number of open cells. Beyond all doubt, this work can certainly provide both a kind of new biodegradable PPC-P-based foam materials and an economic methodology to make biodegradable plastic foams. These foams are potentially applicable in the packaging, transportation, and food industry. [ABSTRACT FROM AUTHOR]

How to optimize and regulate the distribution of phosphoric acid in matrix, and pursuing the improved electrochemical performance and service lifetime of high temperature proton exchange membrane (HT‐PEMs) fuel cell are significant challenges. Herein, bifunctional poly (p‐terphenyl‐co‐isatin piperidinium) copolymer with tethered phosphonic acid (t‐PA) and intrinsic tertiary amine base groups are firstly prepared and investigated as HT‐PEMs. The distinctive architecture of the copolymer provides a well‐designed platform for rapid proton transport. Protons not only transports through the hydrogen bond network formed by the adsorbed free phosphoric acid (f‐PA) anchored by the tertiary amine base groups, but also rely upon the proton channel constructed by the ionic cluster formed by the t‐PA aggregation. Thorough the design of the structure, the bifunctional copolymers with lower PA uptake level (<100%) display prominent proton conductivities and peak power densities (99 mS cm−1, 812 mW cm−2 at 160 °C), along with lower PA leaching and higher voltage stability, which is a top leading result in disclosed literature. The results demonstrate that the design of intermolecular acid–base‐pairs can improve the proton conductivity without sacrificing the intrinsic chemical stability or mechanical property of the thin membrane, realizing win‐win demands between the mechanical robustness and electrochemical properties of HT‐PEMs. [ABSTRACT FROM AUTHOR]