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High-performance porous polyimide (PI) monoliths, including PI aerogels, sponges, and foams, have become one of the hotspots in both researching and applications due to their superior properties such as high porosity, outstanding mechanical and thermal stability, low dielectric constant and thermal conductivity. Up to now, various fabricating methods and applicating situations for PI porous monolith materials have been reported. From the viewpoint of molecular chemistry, porous structure construction, as well as the functional modification, the property optimization and adjustment are feasible, endowing PI monoliths with promising potential for different practical applications (e.g. sensors, low-k materials, thermal management, energy field and utilization, absorption and filtration, photonic utilization, etc.). In this review, the recent progress of porous PI monoliths was summarized in detail based on the fabrication methods, functional modifications, as well as multi-functional applications. Besides, the future perspectives of this field were also provided for reference. Apart from presenting an overview of progress made in the field of PI porous monoliths, this review could also be meaningful for those researching topics which have similarity within. [ABSTRACT FROM AUTHOR]

Quantitative explanation on the improved mechanical properties of aligned electrospun polyimide (PI) nanofibers as the increased imidization temperatures is highly required. In this work, polarized FT-IR spectroscopy is applied to solve this problem. Based on the polarized FT-IR spectroscopy and the molecular model in the fibers, the length of the repeat unit of PI molecule, the angle between the fiber axis and the symmetric stretching direction of carbonyl group on the imide ring, and the angle between the PI molecular axis and fiber axis are all investigated. The Mark-Howink equation is used to calculate the number-average molar mass of PI molecules. The orientation states of PI molecules in the electrospun nanofibers are studied from the number-average molar mass of PI molecules and the average fiber diameter. Quantitative analysis of the orientation factor of PI molecules in the electrospun nanofibers is performed by polarized FT-IR spectroscopy. [ABSTRACT FROM AUTHOR]

Hierarchical porous carbon-based electrodes, benefiting from their facilitated ion diffusion and electron conduction, have demonstrated enormous potential in supercapacitors. The preparation of hierarchical carbons with uniformity and appropriate porosity, however, still remains a grand challenge, which hinders their widespread applications. Herein, a hierarchical porous polyimide-derived carbon electrode (CPC-Fe/Zn) has been fabricated by employing bimetallic salts (Fe/Zn) as precursor and template to activate the cellulose/polyimide (PI) carbon (CPC). Originating from suitable distribution of mesopores and micropores, the obtained CPC-Fe/Zn delivers a high specific capacitance of 420 F/g at a current density of 1 A/g. Moreover, a symmetric supercapacitor device assembled with CPC-Fe/Zn exhibits delivers an energy density of 35.5 Wh/kg at a power density of 800 W/kg. Even at a larger current density of 20 A/g, the specific capacitance retention of such device still remains 92.5 % after 10,000 cycles, showing the rate performance and stability. This work has proposed a bimetallic salts template-assisted strategy to precisely modulate of the pore structure of carbon electrodes, which provides a promising platform to design superior electrodes for various electrochemical systems. [Display omitted] • The hierarchically porous structure of the material can be modulated precisely. • The symmetric supercapacitor exhibited a remarkable energy density of 35.5 Wh/kg @ 1000 W/kg. • The specific capacitance retention of symmetric supercapacitor reached 92.5 % after 10,000 cycles. [ABSTRACT FROM AUTHOR]

Mechanical properties of polyimide (PI) electrospun nanofibers could be improved by increasing imidization temperatures. However, the intrinsic mechanism on this phenomenon is highly required, which is helpful to improve mechanical properties of electrospun nanofibers by external thermal treatment. In this work, single electrospun PI nanofibers (SNF-PI) with different imidization temperatures were prepared. The nanofiber morphology was studied by SEM and AFM and the mechanical properties were measured by single fiber micro-tensile test. Polarized Raman Spectroscopy was applied to determine the PI molecular orientation in SNF-PI. The molecular orientation factor provides directly explanation on the effect of imidization temperatures on the mechanical properties of SNF-PI. [ABSTRACT FROM AUTHOR]

• Single PI/rGO composite nanofiber by in-situ polymerization and in-situ thermal conversion. • Tensile strength of single nanofiber up to 4.2 GPa (PI/rGO-1.0% single nanofiber). • Modulus of single nanofiber up to 121 GPa (PI/rGO-1.2% single nanofiber). • Homogeneous dispersion of rGO by in-situ strategies. • In-situ strategies enhance the interfacial interaction between rGO and PI fibrous matrix. High mechanical performance electrospun polymeric nanofibers are highly desired for practical applications, especially as reinforcements for composites. However, most of the electrospun polymeric nanofibers present tensile strength < 3 GPa. To overcome such limitation, this work successfully prepared single rGO reinforced polyimide composite nanofiber with tensile strength up to 4.2 GPa (PI/rGO-1.0%) and modulus up to 121 GPa (PI/rGO-1.2%) by applying in-situ polymerization, electrospinning, and in-situ thermal conversion. These mechanical properties are higher than other polymer-based electrospun nanofibers, and 45% and 236% higher than those of neat PI single nanofiber, respectively. The in-situ strategies provide the homogeneous dispersion of rGO in single electrospun nanofibers and enhance the interfacial interaction between rGO and PI. In addition, the PI/rGO composite nanofibers also present excellent thermal stability with glass transition temperature (T g) > 295 °C, and the 5% thermal decomposition temperature (T 5%) > 539 °C. This work would open a new route for the preparation of high performance electrospun nanofibers for composites. [ABSTRACT FROM AUTHOR]