Tris-imidazolinium-based porous poly(ionic liquid)s as an efficient catalyst for decarboxylation of cyclic carbonate to epoxide

A series of imidazolinium-based porous poly(ionic liquid)s (PILs) with different anions prepared by free-radical copolymerization of an arene-bridged tris-vinylimidazolium salt and divinylbenzene (DVB) were constructed. The as-prepared PILs were characterized by BET, SEM, TEM, TGA and Elemental Analysis (EA), and the results showed that they had plentiful ionic sites, and abundant and stable mesopores. In particular, the density of ionic sites and pore structure of PILs could be controlled by adjusting the content of DVB. Moreover, the PILs were used as efficient heterogeneous catalysts for the decarboxylation of cyclic carbonates to epoxides for the first time. Results showed that the catalytic activity of PILs was positively correlated with the nucleophilicity of the anions in PILs, and PDVB-[PhTVIM]Cl-1 with a chloride anion-enriched skeleton displayed the best catalytic performance. Without any solvent or cocatalyst, PDVB-[PhTVIM]Cl-1 achieved a TOF value of 108.1 h⁻¹ and the yield of butylene oxide of 89.6%, which was even better than the homogeneous IL-based catalysts (TOF value: 8.7 h⁻¹) that had been previously reported. Meanwhile, PDVB-[PhTVIM]Cl-1 also exhibited excellent recyclability and substrate compatibility.

The tris-imidazolium-based porous poly(ionic liquid)s with plentiful ionic sites prepared by free-radical polymerization exhibited superior catalytic performance toward the heterogeneous conversion of butylene carbonate to butylene oxide.     

Preparation of nitrogen-doped porous carbons for high-performance supercapacitor using biomass of waste lotus stems

In this study, advanced nitrogen-doped porous carbon materials for supercapacitor was prepared using low-cost and environmentally friendly waste lotus stems (denoted as LS-NCs). Nitrogen in the surface functionalities of LS-NCs was investigated using X-ray photoelectron spectroscopy analysis. The sum of pyridine nitrogen (N-6) and pyrrolic/pyridinic (N-5) contents accounted for 94.7% of the total nitrogen and significantly contributed to conductivity. Pore structure and surface area of activated carbons were measured using the Brunauer–Emmett–Teller method. A maximum specific surface area of 1322 m² g⁻¹ was achieved for LS-NCs. The porous carbons exhibited excellent electrochemical properties with a specific capacitance of 360.5 F g⁻¹ at a current density of 0.5 A g⁻¹ and excellent cycling stability (96% specific capacitance retention after 5000 cycles). The above findings indicate that taking advantage of the unique structure of abundant waste lotus stem provides a low-cost and feasible design for high-performance supercapacitors.

In this study, advanced nitrogen-doped porous carbon materials for supercapacitor was prepared using low-cost and environmentally friendly waste lotus stems (denoted as LS-NCs).     

One-pot synthesis of poly(ionic liquid)s with 1,2,3-triazolium-based backbones via clickable ionic liquid monomers

Clickable α-azide-ω-alkyne ionic liquid monomers were developed and subsequently applied to the one-pot synthesis of ionically conducting poly(ionic liquid)s with 1,2,3-triazolium-based backbones through a click chemistry strategy. This approach does not require the use of solvents, polymerisation mediators, or catalysts. The obtained poly(ionic liquid)s were characterized by NMR, differential scanning calorimetry, thermogravimetric analysis, and impedance spectroscopy analysis. Moreover, these poly(ionic liquid)s were cross-linked via N-alkylation with a dianion quarternizing agent to achieve enhanced ionic conductivity and mechanical strength. The resulting free-standing films showed a Young''s modulus up to 4.8 MPa and ionic conductivities up to 4.60 × 10⁻⁸ S cm⁻¹ at 30 °C. This facile synthetic strategy has the potential to expand the availability of poly(ionic liquid)s and promote the development of functional materials.

Clickable ionic liquid monomers realize the one-pot synthesis of ionically conducting poly(ionic liquid)s with 1,2,3-triazolium-based backbones via click chemistry.     

Hierarchical porous carbons from carboxylated coal-tar pitch functional poly(acrylic acid) hydrogel networks for supercapacitor electrodes

A gel carbonization strategy for the synthesis of hierarchical porous carbons (HPCs) from carboxylated coal-tar pitches (CCP) functional poly(acrylic acid) (PAA) hydrogel networks for advanced supercapacitor electrodes was reported. The amphiphilic CCP and PAA polymer could be easily self-assembled to gel by the major driving force of hydrogen bonding and π–π stacking. The HPCs containing interconnected macro-/meso-/micropores were fabricated by direct carbonization of the dried hydrogels. The resultant HPCs with a high specific surface area and total pore volume of 1294.6 m² g⁻¹ and 1.34 cm³ g⁻¹ respectively, as a supercapacitor electrode exhibit a high specific capacitance of 292 F g⁻¹ at 1.0 A g⁻¹ in two-electrode system. The electrode also exhibits ultra-long cycle life with a capacitance retention as high as 94.2% after 10 000 cycles, indicating the good electrochemical stability. Furthermore, the concept of such hierarchical architecture and synthesis strategy would expand to other materials for advanced energy storage systems, such as Na-ion batteries and metal oxides for supercapacitors.

As a supercapacitor electrode exhibit a high specific capacitance of 292 F g⁻¹ at 1.0 A g⁻¹.     

Three-dimensional ordered macroporous ZIF-8 nanoparticle-derived nitrogen-doped hierarchical porous carbons for high-performance lithium–sulfur batteries

Lithium–sulfur (Li–S) batteries have attracted considerable attention due to their ultra-high specific capacity and energy density. However, there are still problems to be resolved such as poor conductivity of sulfur cathodes and dissolution of polysulfides in organic electrolytes. Herein, a novel ZIF-8-derived nitrogen-doped connected ordered macro–microporous carbon (COM-MPC) was developed by a dual solvent-assisted in situ crystallization method within a face-centered cubic stacking sphere template, which acts as an advanced sulfur host for enhanced Li–S battery performance. Compared with the conventional predominant microporous C-ZIF-8, the unique hierarchical macro–microporous structure with nitrogen doping not only renders polysulfide intermediates enhanced entrapment by confining the effect of micropores and chemisorption of doping N atoms, but also facilitates electrolyte accessibility and efficient ion transport owing to the ordered macroporous structure. Benefitting from this, the COM-MPC@S cathode delivers a high initial specific capacity of 1498.5 mA h g⁻¹ and a reversible specific capacity of 1118.9 mA h g⁻¹. Moreover, the COM-MPC@S cathode exhibits 82.3% of capacity retention within 10th to 50th cycle at 0.5C and a large capacity of 608.5 mA h g⁻¹ after 50 cycles at a higher rate of 1C, and this enhanced cycling stability and rate capability demonstrate great practical application potential in Li–S battery systems.

Lithium–sulfur (Li–S) batteries have attracted considerable attention due to their ultra-high specific capacity and energy density.     

Template-free preparation of anthracite-based nitrogen-doped porous carbons for high-performance supercapacitors and efficient electrocatalysts for the oxygen reduction reaction

The conversion of coal into high-performance electrochemical energy materials, exemplified by electrodes and electrocatalysts for supercapacitors and fuel cells, is currently crucial to the advancement of high value-added, clean and non-fuel utilization of coal resources. In this work, anthracite-based nitrogen-doped porous carbon (ANPC) materials with well-defined pore architectures and adjustable nitrogen concentrations were prepared without any template: ANPC-1 by a one-step activation/doping process and ANPC-2 by a two-step process. The specific capacitance value of the ANPC-1 materials could attain a maximum of 346.0 F g⁻¹ at the current density of 0.5 A g⁻¹ in 6 M KOH. Supercapacitors composed of the ANPC-1 electrodes were able to achieve high energy densities up to 10.3 W h kg⁻¹ and 20.8 W h kg⁻¹, together with good charge/discharge stabilities of 95.4% and 91.3% after 5000 cycles, in KOH and Na₂SO₄ aqueous electrolytes, respectively. The ANPC-2 materials are more associated with the oxygen reduction reaction (ORR): one possessed a comparable ORR electrocatalytic activity to the commercial JM Pt/C (20% Pt) catalyst, and, moreover, its onset potential (0.96 V vs. RHE), half-wave potential (0.85 V vs. RHE), catalyst durability (95.9% activity retained after 40 000 s) and methanol tolerance were all superior to the benchmark electrocatalyst. This study provides a feasible route to rational design of coal-based multifunctional materials towards electrochemical energy storage and conversion.

Acting as supercapacitor electrodes and ORR electrocatalysts, anthracite-based nitrogen-doped porous carbons are prepared by one/two-step activation/doping processes.     

Self-template/activation nitrogen-doped porous carbon materials derived from lignosulfonate-based ionic liquids for high performance supercapacitors

A simple ion exchange reaction of sodium lignosulfonate (SLS) and 1-allyl-3-methyl imidazolium chloride ([Amim]Cl) produced a new polymeric ionic liquid [Amim]LS and NaCl, and the mixture was successfully used as a precursor to prepare a nitrogen-doped porous carbon material via direct carbonization without any additional activation agent or template. It was believed that the in situ produced NaCl during the precursor synthesis process acted as the self-template and in self-activation. The introduction of imidazolium ionic liquid into the precursor raised the nitrogen content of the obtained carbon material up to 4.68% for a high yield of [Amim]LS-700 carbon material up to 34.6%. The effect of carbonization temperature on the structures and electrochemical properties of the prepared carbon were also studied systematically. It was found that the carbon material exhibits a superior gravimetric capacitance up to 230 F g⁻¹ (0.1 A g⁻¹) at the carbonization temperature of 700 °C, a good energy density of 7.99 W h kg⁻¹ at the power density of 25 W Kg⁻¹, and an excellent cycling stability of 90.3% after 20 000 cycles. This work provides a new path for the value-added utilization of biomass coupled with the field of electrochemical energy storage.

Without any additional template or activation agent, a high N-doped porous carbon was easily prepared by a simple ion exchange reaction and a following carbonization, and showed excellent electrochemical performance as a supercapacitor electrode.     

The influence of the polymerization approach on the catalytic performance of novel porous poly (ionic liquid)s for green synthesis of pharmaceutical spiro-4-thiazolidinones

Although poly (ionic liquids) (PILs) have attracted great research interest owing to their various applications, the performance of nanoporous PILs has been rarely developed in the catalysis field. To this end, a micro–mesoporous PIL with acid–base bifunctional active sites was designed and fabricated by two different polymerization protocols including hydrothermal and classical precipitation polymerization in this paper. Based on our observations, hydrothermal conditions (high temperature and pressure) enabled the proposed sonocatalyst to possess a great porous structure with a high specific surface area (S_BET: 315 m² g⁻¹) and thermal stability (around 450 °C for 45% weight loss) through strengthening cross-linking. In a comparative study, the preferred nanoporous PIL was selected and utilized as the sonocatalyst in a multicomponent reaction of isatins, primary amines, and thioglycolic acid. In the following, a variety of new and known pharmaceutical spiro-4-thiazolidinone derivatives were synthesized at room temperature and obtained excellent yields (>90%) within short reaction times (4–12 min) owing to the substantial synergistic effect between ultrasound irradiation and magnetically separable catalyst.

Sustainable synthesize of a new mesoporous poly (ionic liquid) as acid–base bifunctional catalyst for environmental being preparation of monospiro derivatives has been developed.     

Self-standing cellulose nanofiber/poly(3,4-ethylenedioxythiophene):poly(4-styrenesulfonate)/ionic liquid actuators with superior performance

This paper describes new actuators with cellulose nanofiber/poly(3,4-ethylenedioxythiophene):poly(4-styrenesulfonate)/ionic liquid (CNF/PEDOT:PSS/IL) structures. Devices containing these structures exhibit higher strain and maximum generated stress than those based on only PEDOT:PSS/IL. The new actuator system contains an electrode, which is an electrochemical capacitor, and which consists of both a faradaic capacitor (FC) and a small electric double-layer capacitor (EDLC), i.e., PEDOT:PSS. This combined capacitor plays the role of an FC and a base polymer, and the CNF skeleton is used in the place of carbon nanotubes (CNTs). This device therefore functions differently from traditional CNT/PVdF–HFP/IL actuators, which are only used as EDLC units and from PEDOT:PSS/vapor-grown carbon nanofibers (VGCF)/IL actuators, which are used as hybrid (FC and EDLC) units. The developed films are novel, robust, and flexible, and demonstrate potential as actuator materials for wearable energy-conversion devices. A double-layer charging kinetic model, which is similar to that previously proposed for PEDOT:PSS/CNT/IL actuators, is developed to explain the oxidation and reduction of PEDOT:PSS. This model successfully simulates the frequency-dependent displacement response of actuators.

This paper describes new actuators with cellulose nanofiber/PEDOT:PSS/ionic liquid (CNF/PEDOT:PSS/IL) structures. These devices show superior performance with respect to strain and maximum generated stress compared to those containing PEDOT:PSS/IL.     

Thermo-responsive draw solute for forward osmosis process; poly(ionic liquid) having lower critical solution temperature characteristics

We synthesized poly(4-vinylbenzyltributylammonium hexanesulfonate) (P[VBTBA][HS]), a poly(ionic liquid) that shows lower critical solution temperature (LCST), via the anion exchange reaction of poly(4-vinylbenzyltributylammonium chloride) (P[VBTBA][Cl]) with sodium hexanesulfonate in order to investigate its suitability as a draw solute for the forward osmosis (FO) process. P[VBTBA][Cl] was obtained by the free radical polymerization of (4-vinylbenzyltributylammonium chloride [VBTBA][Cl]) monomer acquired by the Menshutkin reaction. The FO performance and recovery properties of the synthesized materials were systematically investigated. For example, the LCST of P[VBTBA][HS] was observed to be ∼17 °C at 20 wt%, while no LCST was observed for [VBTBA][Cl] monomer and P[VBTBA][Cl] polymer before the anion exchange reaction, indicating that P[VBTBA][HS] can be recovered from the aqueous solution by heating it to above its LCST. Moreover, in an active layer facing the feed solution (AL-FS) system containing 20 wt% aqueous P[VBTBA][HS] solution at 15 °C, the water flux and reverse solute flux of P[VBTBA][HS] were found to be ∼5.85 L m⁻² h⁻¹ and 1.13 g m⁻² h⁻¹, respectively. Therefore, we studied the feasibility of using the poly(ionic liquid), a homopolymer having LCST characteristics, as a draw solute in the FO process.

A poly(ionic liquid) having lower critical solution temperature characteristics was synthesized to investigate its suitability as a draw solute for forward osmosis.     

High ionic conduction,toughness and self-healing poly(ionic liquid)-based electrolytes enabled by synergy between flexible units and counteranions

Polymer electrolytes offer great potential for emerging wearable electronics. However, the development of a polymer electrolyte that has high ionic conductivity, stretchability and security simultaneously is still a considerable challenge. Herein, we reported an effective approach for fabricating high-performance poly(ionic liquids) (PILs) copolymer (denoted as PIL-BA) electrolytes by the interaction between flexible units (butyl acrylate) and counteranions. The introduction of butyl acrylate units and bis(trifluoromethane-sulfonyl)imide (TFSI⁻) counteranions can significantly enhance the mobility of polymer chains, resulting in the effective improvement of ion transport, toughness and self-healability. As a result, the PIL-BA copolymer-based electrolytes containing TFSI⁻ counterions achieved the highest ionic conductivity of 2.71 ± 0.17 mS cm⁻¹, 1129% of that of a PIL homopolymer electrolyte containing Cl⁻ counterions. Moreover, the PIL-BA copolymer-based electrolytes also exhibit ultrahigh tensile strain of 1762% and good self-healable capability. Such multifunctional polymer electrolytes can potentially be applied for safe and stable wearable electronics.

Polymer electrolytes offer great potential for emerging wearable electronics.     

Electrochemical sensor formed from poly(3,4-ethylenedioxyselenophene) and nitrogen-doped graphene composite for dopamine detection

In this study, an electrochemical sensor for dopamine (DA) detection has been developed by a composite of poly(3,4-ethylenedioxyselenophene) (PEDOS) and nitrogen-doped graphene (PEDOS/N-Gr) using an in situ polymerization method. Its structure and properties were then compared with those of the composites of poly(3,4-ethylenedioxythiophene) (PEDOT)/nitrogen-doped graphene (PEDOT/N-Gr), which were prepared by the same methods. FT-IR, Raman, UV-vis, XPS, mapping and SEM investigated the structure and morphology of these composites. These revealed that PEDOS/N-Gr had a higher conjugation degree than PEDOT/N-Gr. The synergetic effect between PEDOS and N-Gr was beneficial for the formation of a homogenous surface coating. The cyclic voltammetry (CV) and differential pulse voltammetry (DPV) methods were conducted for electrochemical detection of DA. Compared with PEDOT/N-Gr, the PEDOS/N-Gr displayed an enhanced sensitivity and electrocatalytic performance for DA detection with linear ranges of 0.008–80 μM (PEDOT/N-Gr: 0.04–70 μM) and limits of detection (LOD) of 0.0066 μM (S/N = 3) (PEDOT/N-Gr: 0.018 μM (S/N = 3)).

An electrochemical sensor for dopamine detection has been fabricated using a composite of PEDOS and N-Gr. The results of actual samples showed that the composite of PEDOS/N-Gr has excellent recovery (95.40–100.14%) for human serum and urine samples.     

A novel l-histidine based ionic liquid (LHIL) as an efficient corrosion inhibitor for mild steel

A novel l-histidine based ionic liquid (LHIL) was developed and successfully synthesized. Its structure was confirmed by Fourier-transform infrared spectroscopy, UV-vis spectroscopy, X-ray photoelectron spectroscopy, ¹H-NMR and high-resolution mass spectrometry. The outstanding corrosion inhibition effect of the LHIL on mild steel in 1 M hydrochloric acid was thoroughly evaluated by Tafel plots, electrochemical impedance spectroscopy, and localized electrochemical strategies. The results revealed that the corrosion of mild steel was effectively suppressed by the adsorption of LHIL on its surface, and the best inhibition efficiency reached 98.8%. The adsorption behavior of LHIL on steel obeyed the Langmuir adsorption isotherm, which involved both chemisorption and physisorption. Theoretical calculations indicated the strong chemisorption of LHIL on steel, as proved by the low energy gap (ΔE = 0.0522 eV) and high binding energy (E_binding = 303.47 kcal mol⁻¹), which clearly confirmed the effectiveness of LHIL for steel protection.

A novel l-histidine based ionic liquid (LHIL) was developed and successfully synthesized.     

High-performance cellulose nanofibers,single-walled carbon nanotubes and ionic liquid actuators with a poly(vinylidene fluoride-co-hexafluoropropylene)/ionic liquid gel electrolyte layer

This study describes new actuators with cellulose nanofibers, single-walled carbon nanotubes and ionic liquids (CNFs/SWCNTs/ILs) and examines the electrochemical and electromechanical properties of CNF/SWCNT/IL gel hybrid actuators. Further, the effects of the CNF species present on the electrode and the electrolyte layer species of poly(vinylidene fluoride-co-hexafluoropropylene) (PVdF(HFP)) or CNF/IL on the electrochemical and electromechanical properties of the low-voltage electroactive polymer actuators are investigated. The CNF/SWCNT/IL structure revealed a network of highly entangled CNFs and SWCNTs. The results indicated that the CNF/SWCNT/IL electrodes and the PVdF(HFP)/IL electrolyte actuators can significantly outperform the CNF/SWCNT/IL electrodes and the CNF/IL electrolyte actuators. PVdF(HFP) was considered to be a better polymer electrolyte than CNF. Further, the frequency dependences of the displacement responses of these CNF/SWCNT/IL electrode actuators were successfully simulated using a double-layered charging kinetic model. The equivalent circuit models exhibited by the PVdF(HFP)/IL electrolyte actuators are different when compared to those exhibited by the CNF/IL electrolyte actuators. Based on the results of this study, the CNF/SWCNT/IL electrodes and the PVdF(HFP)/IL electrolyte actuators are promising for application as electrochemical materials that are useful in real-world applications, including wearable and energy-conversion devices.

This study describes new actuators with cellulose nanofibers, single-walled carbon nanotubes and ionic liquids (CNFs/SWCNTs/ILs) and examines the electrochemical and electromechanical properties of the CNF/SWCNT/IL gel hybrid actuators.     

Synthesis of poly(ionic liquid) for trifunctional epoxy resin with simultaneously enhancing the toughness,thermal and dielectric performances

Poly(ionic liquid) (PIL), integrating the characteristics of both polymers and ionic liquid, is synthesized and employed to modify diglycidyl-4,5-epoxy-cyclohexane-1,2-dicarboxylate (TDE-85). With the addition of PIL, the fracture toughness, and thermal and dielectric performances of TDE-85 were discovered to be simultaneously improved, meanwhile the tensile modulus and strength is increased. Upon an optimal loading of 3 wt% PIL, the critical stress intensity factor (K_IC), tensile modulus and strength are raised by 92.9%, 13.3% and 10.7%, respectively. Multi-toughening mechanisms due to spherical domains of PIL formed in TDE-85 during curing are responsible for the improved toughness. Moreover, the dielectric and thermal properties of TDE-85 are also enhanced by adding PIL. With the optimal addition of 5 wt% PIL, the dielectric constant of the composites is enhanced by 62.5%, the glass transition temperature is increased by 16.58 °C and the residual weight of carbon is increased by 59%.

This work will provide a strategy to obtain epoxy with relatively high toughness, thermal and dielectric properties.     

Imidazolium based ionic liquid stabilized foams for conformance control: bulk and porous scale investigation

Foams are typically used as a divergent fluid for conformance control in order to divert the fluid flow from a high-permeable zone into a low-permeable zone. Nevertheless, the stability of the foam still remains a challenge due to the presence of antifoaming crude oil and the harsh environment of the reservoir, such as high-temperature, high-salinity, and high-pressure. In this study, we investigated the stability and efficacy of various surfactant generated foams with ionic liquid (IL) additives. Intrinsically, the study is targeted to represent the conditions of Arab-D reservoir formations, which are abundant in Saudi Arabian oilfields. In this, we have screened several parameters that influence foam stability like the type of foamer gases (CO₂, N₂, and air), type of ILs, type of surfactants (nonionic, anionic, cationic, and zwitterionic), concentration, salinity (formation brine, low salinity brine, and seawater brine), temperature, etc. The stability of the generated foams was analyzed in both bulk and porous scale media. The bulk foam study has demonstrated that only a very minor concentration of ILs (50–500 ppm) shows a greater improvement in both the foamability and foam stability. The stability of the foam in the presence of the studied ILs and surfactants increases by more than 50% compared to their neat surfactant solution. A similar response was also witnessed in the dynamic foaming experiments at high-temperature, high-pressure, and high-salinity. The current work also involves the determination of the foam morphology, including structure, size, shape, gas–water interface and the lamellae size for different systems with and without ILs, which helps to understand the stability mechanism of the foams with and without ILs. Confocal and optical microscopic images of the foam structure of various systems reveal that these ILs are successful in reducing the size of bubbles and increasing the lamellae size. It is very clear that the addition of ILs generates the surfactant layered-ILs, and they tend to arrange themselves in the lamellae, and at the liquid–gas interface, thereby decreasing the rate of film drainage at the lamellae and delaying the bubble rupture point. This led to the observed enhanced foam stability. Thus, we would like to conclude that the ILs investigated here improved the foam stability by their adsorption at the foam lamella which further helped in preventing liquid drainage and film thinning.

Ionic liquid aggregates at the gas–liquid interface.     

Novel poly(arylene ether ketone)/poly(ethylene glycol)-grafted poly(arylene ether ketone) composite microporous polymer electrolyte for electrical double-layer capacitors with efficient ionic transport

Polymer electrolytes have attracted considerable research interest due to their advantages of shape control, excellent safety, and flexibility. However, the limited use of traditional polymer electrolytes in electric double-layer capacitors due to their unsatisfactory ionic conductivities and poor mechanical properties makes them difficult to operate for long periods of time in large-scale energy storage. Therefore, we fabricated a high-performance microporous electrolyte based on poly(arylene ether ketone) (PAEK)/poly(ethylene glycol)-grafted poly(arylene ether ketone) (PAEK-g-PEG) using a certain amount of carboxylated chitosan with a high electrolyte uptake rate of 322 wt% and a high ionic conductivity of 2 × 10⁻² S cm⁻¹ at room temperature. A symmetric solid-state supercapacitor that uses activated carbon as electrodes and a composite microporous polymer film as the electrolyte shows a high specific capacitance of 134.38 F g⁻¹ at a current density of 0.2 A g⁻¹, while liquid electrolytes demonstrate a specific capacitance of 126.92 F g⁻¹. Energy density of the solid-state supercapacitor was 15.82% higher than that of the liquid supercapacitor at a current density of 5 A g⁻¹. In addition, the solid-state supercapacitor exhibited excellent cycling stability of over 5000 charge/discharge cycles at a current density of 1 A g⁻¹. Furthermore, solid-state supercapacitors display lower self-discharge behavior with an open-circuit potential drop of only 36% within 70 000 s, which is significantly better than that of conventional supercapacitors (52% @ 70 000 s), at a charging current density of 1 mA cm⁻². The satisfactory results indicated that the PAEK/PAEK-g-PEG composite microporous polymer film demonstrates high potential as an electrolyte material in practical applications of solid-state and portable energy storage devices.

Polymer electrolytes have attracted considerable research interest due to their advantages of shape control, excellent safety, and flexibility.     

Waste wool derived nitrogen-doped hierarchical porous carbon for selective CO2 capture

The goal of this research is to develop a low-cost porous carbon adsorbent for selective CO₂ capture. To obtain advanced adsorbents, it is critical to understand the synergetic effect of textural characteristics and surface functionality of the adsorbents for CO₂ capture performance. Herein, we report a sustainable and scalable bio-inspired fabrication of nitrogen-doped hierarchical porous carbon by employing KOH chemical activation of waste wool. The optimal sample possesses a large surface area and a hierarchical porous structure, and exhibits good CO₂ adsorption capacities of 2.78 mmol g⁻¹ and 3.72 mmol g⁻¹ at 25 °C and 0 °C, respectively, under 1 bar. Additionally, this sample also displays a moderate CO₂/N₂ selectivity, an appropriate CO₂ isosteric heat of adsorption and a stable cyclic ability. These multiple advantages combined with the low-cost of the raw material demonstrate that this sample is an excellent candidate as an adsorbent for CO₂ capture.

In this work, N-doped hierarchical porous carbon has been successfully fabricated by KOH activation of waste wool. The optimal sample exhibits good CO₂ adsorption capacity under atmospheric pressure (1 bar), as well as excellent CO₂/N₂ selectivity.     

Green synthesis of nitrogen-doped multiporous carbons for oxygen reduction reaction using water-caltrop shells and eggshell waste

A green synthesis method is proposed for the preparation of nitrogen-doped multiporous carbons (denoted as N-MPCs) from water-caltrop shell (WCS) using eggshell waste as both a nitrogen-dopant and an activating agent. It is shown that the surface area, porosity, yield and nitrogen content of the as-prepared N-MPCs can be easily controlled by adjusting the activation temperature. Moreover, in oxygen reduction reaction (ORR) tests performed in O₂-saturated 0.1 M KOH_(aq) electrolyte containing 1.0 M methanol, the N-MPC catalysts show a high ORR stability and good resistance to methanol corrosion. In addition, as a cathode material in Al–air battery tests, the N-MPCs achieve a power density of 16 mW g⁻¹ in a saturated NaCl_(aq) electrolyte. Overall, the results show that the N-MPCs have a promising potential as a green and sustainable material for ORR catalysis applications.

A green synthetic method is proposed for the preparation of nitrogen-doped multiporous carbons (denoted as N-MPCs) from water-caltrop-shell (WCS) biochar by using eggshell waste as both a nitrogen-dopant and an activating agent.