Ion Coordination Research Articles

Tough and Fast‐Responding Fe3+‐Coordinated Poly (Acrylic Acid ‐N‐Isopropyl Acrylamide) Shape Memory Hydrogels

AbstractHydrogels with programmable shape memory hold great promise for applications in soft robots, smart medical devices, etc., but the preparation of tough and fast‐responding shape memory hydrogels remains challenging. In this work, Poly (acrylic acid ‐N‐isopropyl acrylamide) (3:1)‐Fe3+ (P(AA‐NIPAM)(3:1)‐Fe3+) hydrogels are obtained by monomer copolymerization and ionic coordination, which exhibited tough mechanical properties with a maximum tensile strength of 2.48 ± 0.08 MPa and a maximum elongation of 338.5 ± 19.6%. The hydrogel also demonstrated a good shape memory effect, with the hydrogel curled into a spiral shape recovering to 71.1% ± 5.9% in 30 s under the swelling effect of water, and the convoluted structure recovering to 95% in 4 s. The shape memory hydrogels prepared based on this method will provide an important reference value for the development of higher performance shape memory hydrogels.

Ni(II) and Cu(II) Ion Coordination by the Novel (2E,2′E)-N,N′-(2-Hydroxypropane-1,3-diyl)bis[(2-hydroxyimino)propanamide] Ligand in the Solid State and in Aqueous Medium

In the process of a systematic study of the bis-chelate oxime-amide ligands with different polymethylene spacers and their transition metal complexes, two new Ni(II) and Cu(II) complexes of the mhiea2poh ligand have been isolated, and their molecular and crystal structures determined by single crystal X-ray diffraction. Potentiometric titrations were performed on a range of aqueous solutions in both systems, which allowed the identification of various complex species and afforded their stability constants. ESR spectra of samples with optimised concentrations of complexes in Cu(II)–L–H system were recorded. A distinguishing feature of both systems is the dimerization of anionic pseudo-macrocyclic complexes. The latter is caused either by centrosymmetric hydrogen bonding of the hydroxy group on the propane spacer to the oximato oxygen of the opposing unit or by back-to-back π-stacking of planar complex units. ESR measurements indicated likely coupling of Cu-Cu paramagnetic centres in the dimers.

Cu/MOF-808 Catalyst for Transfer Hydrogenation of 5-Hydroxymethylfurfural to 2, 5-Furandimethanol with Formic Acid Mediation

Biomass platform compound 5-Hydroxymethylfurfural (HMF), with its low price and abundant source, can be used as a renewable resource to replace traditional petrochemicals. MOF-808(Zr) has tunable active sites and excellent stability under high temperatures and acidic as well as basic environments, and the unsaturated coordination of metal ions within its framework structure can exhibit Lewis acidity, facilitating catalytic transfer hydrogenation from HMF to 2, 5-Furandimethanol (BHMF). The hydrothermal–impregnation–reduction method was used to prepare Cu/MOF-808 catalysts with high catalytic performance. Formic acid was chosen as the hydrogen donor solvent. The selectivity and yield of BHMF were 75.65% and 71%, respectively, at 150 °C for 4 h. A reaction pathway for the catalytic hydrogen transfer of HMF to BHMF was proposed. The high activity and stability of the Cu/MOF-808 catalyst with dual active sites provide a viable method for feasible hydrogenation of HMF to high value-added compounds.

Computationally aided design of single‐ion‐conducting block copolymer electrolytes to boost lithium‐ion conductivity

AbstractIn this work, we implement a combinatory approach that integrates molecular dynamics (MD) simulation and a Gaussian process regression (GPR) algorithm to explore optimal design strategies for a generic single‐ion‐conducting block copolymer electrolyte (SIC‐BCPE) model system that covers a rich design parameter space inspired by recently established poly(ethylene oxide)‐based block copolymer electrolytes. The GPR algorithm is employed to efficiently reveal the relationships between the desired lithium‐ion conductivity and four design parameters reflecting both chain architectural control and specific tuning of molecular chemistry. Guided by the GPR results, an optimal combination of four parameter values is inferred, and MD simulation confirms that the corresponding SIC‐BCPE system produces relatively higher lithium‐ion conductivity. To further understand the influence of each molecular parameter on the trends of lithium‐ion conductivity, we analyse the proportion variation of different types of lithium‐ion coordination and identify a strong correlation between the ion coordination pattern and ionic conductivity. Due to its generality, we expect that the MD‐GPR combinatory approach reported in this work is applicable to a broad range of other polymer‐based ion transport systems. © 2024 Society of Chemical Industry.

Anaerobic Catalyst Design for Alcohol Oxidation: Fine‐Tuning Copper/TEMPO with Bipyridine Proportions

In this study, we investigate the indirect electro‐oxidation of benzyl alcohol using the Copper/TEMPO catalytic system, which combines copper complexes with 2,2,6,6‐tetramethylpiperidin‐1‐oxyl (TEMPO) in an anaerobic medium. We reexamine the impact of bpy ligand proportions, exploring ratios of 1:1, 2:1, 3:1, and 4:1 on catalytic activity. Cyclic voltammetry and visible spectroscopy reveal distinct electrochemical characteristics and complex formations at different bpy ratios. Simulations uncover intricate energy equilibria involving ion coordination, varying with oxidation state and bpy proportion. Theoretical and experimental spectra align, supporting the proposed structures. The Brønsted base, triethylamine (TEA), essential in this anaerobic system, shows different voltammetric profiles with each ligand ratio, revealing key interactions with bpy complexes. In the presence of benzyl alcohol, the 1:1 and 2:1 ratios exhibit indirect catalytic activity, with the 2:1 ratio yielding significantly higher current densities. This establishes a new optimal condition where [Cu(bpy)₂]²⁺ formed in a 2:1 stoichiometry demonstrates superior activity with a lower redox potential, while maintaining labile coordination points for necessary interactions. Theoretical results also indicate weaker TEMPO coordination to [Cu(bpy)₂]²⁺.

Titanium Implant Modified With Zinc-Doped Carbon Dot Layer as an Innovative Coating for the Development of Local Drug Delivery System for Ciprofloxacin.

This study presents a new innovative drug delivery system for ciprofloxacin, which is based on the formation of a zinc-doped carbon dots layer on the surface of a titanium alloy (TiAl4V6). In the study, the effectiveness of the synthesis method of a zinc-doped carbon dots layer was determined. The distribution of the layer of carbon dots on the surface of the titanium alloy was investigated using the FT-IR mapping technique, which confirmed the efficiency of the synthesis. The effective synthesis of carbon dots and the coordination of zinc ions on their surface opens the possibility of sorption of ciprofloxacin, which results in a high application potential of the obtained biomaterial. The introduction of zinc cations on the surface of the carbon dots layer resulted in high sorption results of the active substance (40 μg of drug per 1 cm2 of implant). The release profile of ciprofloxacin from the modified surface of the titanium alloy indicates that this active substance can be released for up to 4 h. The biomaterial obtained in this work is also hydrophilic (about 40°), which was shown by the contact angle tests. This is an important feature and indicates a high application potential of the performed modification. The resulting layer has antibacterial properties. Growth inhibition for microorganisms such as Pseudomonas aeruginosa, Escherichia coli, Staphylococcus aureus, Bacillus cereus, and Candida albicans ranged from 74% to 96%. The creation of such a layer on the titanium alloy may reduce the risk of infection during the implantation procedure.

Salicylic acid-induced single-step synthesis of multimorphic anhydrous MgCO3 from brucite waste: Characterization, mechanism, and DFT calculation

The brucite production generates a large amount of powdered solid waste, which presents significant challenges for direct utilization. Utilizing brucite for CO2 mineralization enables solid waste reuse and CO2 utilization and storage. In this study, multimorphic anhydrous MgCO3 was synthesized from brucite solid waste and salicylic acid using a one-step method. The results indicate that higher temperatures and longer hydrothermal times favor the anhydrous MgCO3 formation. Cubic, hexagonal block and columnar anhydrous MgCO3 were synthesized by regulating the salicylic acid additions. The formation mechanism reveals that coordination between salicylic acid and Mg2+ inhibits Mg2+ hydration, preventing the hydrated MgCO3 formation. Phenol and phenolate anion derived from salicylic acid decomposition adsorb onto the anhydrous MgCO3 surfaces, regulating crystal growth. Characterization results and DFT calculations show that the salicylate, phenolate anion, and phenol form ionic coordination bonds and hydrogen bonds with Mg2+/anhydrous MgCO3, achieving chelation and adsorption, which modulate the phase transition and morphology of crystal. Anhydrous MgCO3 shows potential applications in flame retardancy, electronic component enhancement, photoelectrochemical energy storage, and wastewater treatment. This method represents a comprehensive green technology for CO2 reduction and anhydrous MgCO3 synthesis, shortening the preparation process for high-value-added magnesium products, and offering broad industrial prospects.

Phosphorylation Enables Nano‐Graphene for Tunable Artificial Synapses

AbstractFlexible and robust memristors with controllable resistance‐switching characteristics are important to neuromorphic computing. However, the nanomaterials‐based, solution‐processed resistance switching layer usually has poor reliability and tunability due to uneven morphology and invariable surface properties. Herein, phosphorylated graphene nanoflakes (phos‐GPs) are synthesized for high‐performance solution‐processed flexible memristors. In situ conductive atomic force microscopy reveals that the tightly stacked uniform nanoflakes and modified phosphorate groups jointly reduce the formation barrier of the conductive filaments. Furthermore, phosphorylation gives rise to surface silver ion coordination leading to enhanced radial growth of the conductive filaments. The memristor shows volatile characteristics in the Ag/phos‐GPs/ITO architecture and exhibits non‐volatile properties in the Ag/Ag+‐(phos‐GPs)/ITO structure. Both types of memristors display consistent I‐‐V curves during long‐term cycling and under repetitive mechanical bending, in addition to excellent synaptic plasticity. Moreover, ultrasmall nonlinearity is observed from non‐volatile long‐term synaptic potentiation and depression. By utilizing the tunable artificial synapses, the processes of memory‐forgetting and re‐recognition are simulated, and the image recognition tasks are accomplished by the artificial neural networks.

Extreme Toughening of Conductive Hydrogels Through Synergistic Effects of Mineralization, Salting-Out, and Ion Coordination Induced by Multivalent Anions.

Developing conductive hydrogels with both high strength and fracture toughness for diverse applications remains a significant challenge. In this work, an efficient toughening strategy is presented that exploits the multiple enhancement effects of anions through a synergistic combination of mineralization, salting-out, and ion coordination. The approach centers on a hydrogel system comprising two polymers and a cation that is highly responsive to anions. Specifically, polyvinyl alcohol (PVA) and chitosan quaternary ammonium (HACC) are used, as PVA benefits from salting-out effects and HACC undergoes ion coordination with multivalent anions. After just 1 h of immersion in an anionic solution, the hydrogel undergoes a dramatic improvement in mechanical properties, increasing by more than three orders of magnitude. The optimized hydrogel achieves high strength (26 MPa), a high Young's modulus (45 MPa), and remarkable fracture toughness (67.3 kJ m-2), representing enhancements of 860, 3200, and 1200 times, respectively, compared to its initial state. This breakthrough overcomes the typical trade-off between stiffness and toughness. Additionally, the ionic conductivity of the hydrogel enables reliable strain sensing and supports the development of durable supercapacitors. This work presents a simple and effective pathway for developing hydrogels with exceptional strength, toughness, and conductivity.

Unraveling the role of counter ions in shaping the structures of helical peptides in aqueous phase

AbstractHelical peptides, as well as proteins composed of helical peptides, play essential roles in various biological processes, including their functions as components of cell membranes and their interactions with biological membranes. Therefore, it is crucial to predict the propensity and structural characteristics of helices formed in solution or lipid environments for specific peptide sequences. Melittin and pexiganan are antimicrobial peptides (AMPs) that possess distinct sequence characteristics but exhibit similar structural properties in both solution and lipid environments. In this study, we conducted molecular dynamics simulations to investigate how the presence of counter ions creates differences in structural characteristics between these two peptides in solution. By analyzing the structures formed for each AMP using extended helical projections, we aimed to uncover the underlying principles governing the interaction between counter ions and peptide sequences, leading to the formation of stable structures. It was found that the coordination of counter ions effectively extends the helical surface and stabilizes the extended helix by reducing the electrostatic repulsion between charged residues. Our results demonstrate how sequence specificity influences helical structure formation in solution and provide an explanation for the varying degrees of synergistic effects exhibited by different helical AMPs.

Synthesis, characterization and adsorption of Pb(Ⅱ), Cd(Ⅱ) and Cu(Ⅱ) by red mud/polyacrylic acid/sodium carboxymethyl cellulose hydrogel

Heavy metal pollution in water and pollution hazards caused by red mud disposal are urgent environmental problems to be solved. Red mud waste can be utilized as resources by preparing hydrogels. By employing free radical polymerization, a red mud/polyacrylate/sodium carboxymethyl cellulose hydrogel (RMAAC) was synthesized using red mud (RM) as the main component, sodium carboxymethyl cellulose (SCMC) as the grafting substrate, N, N’-methylene bisacrylamide (MBA) as the crosslinking agent, and potassium persulfate (KPS) as the initiator. The proportions of MBA, KPS, and SCMC were optimized using the response surface method. The adsorption kinetics and isothermal adsorption model were applied to analyze the adsorption characteristics, while XRD, FTIR, SEM-EDS, and XPS characterization methods were employed to study the adsorption mechanism. The results demonstrated that the optimal proportions of MBA, KPS, and SCMC in RMAAC were determined to be 0.15 %, 0.2 %, and 1.5 %, respectively, and the addition of 0.5 % RM to enhance the adsorption performance of the hydrogel. The adsorption processes of Pb(II), Cd(II), and Cu(II) by RMAAC followed the pseudo-second-order kinetic model and the Langmuir model, suggesting chemisorption through a single molecular layer as the main adsorption mechanism. The maximum theoretical adsorption capacities of the three heavy metal ions at 25°C were determined to be 730.16, 292.71, and 215.37 mg/g, respectively. It was found that RMAAC exhibited a higher affinity toward Pb(II) compared to Cu(II) and Cd(II). Characterization analyses revealed that ion exchange and coordination chelation were the predominant mechanisms involved in the adsorption of Pb(II), Cd(II), and Cu(II) by RMAAC.

A polyamide-facilitated soldering approach for Mini LED precise alignment leveraging 3D interfacial networks

Driven by the need for improved quality, energy efficiency, and visual innovation, display technology has evolved from CRT to Mini LED. However, the transfer process in Mini LED assembly poses challenges in precision. This study addressed the displacement issue during the transfer process by investigating the synergistic effects of solder and functional organic chemicals. Through the Mini LED assembly process, with the Mini LED size measuring 150 μm (length) ∗ 100 μm (width) ∗ 70 μm (thickness), polyamide was identified as a facilitator for precise alignment, which enhanced self-alignment capabilities by 68.8 % and improved the accuracy on self-aligned distance from 12.5 μm to 21.1 μm in Mini LED packaging. Through the powder coalescence approach, further extensive analysis using XPS, SEM, FTIR, and DSC reveals the synergistic effects. It supports the proposed three-dimensional polyamide-tin ion coordination interfacial network construction mechanism that facilitates solder-to-solder self-alignment and coalescence. This study provides insight into such a polymer-metal ion 3D coordination network for Mini LED precise alignment, which is promising for mass production.

Charge Separation-Engineered Piezoelectric Ultrathin Nanorods Modulate Tumor Stromal Microenvironment and Enhance Cell Immunogenicity for Synergistically Piezo-Thermal-Immune Therapy.

The tumor microenvironment (TME) is characterized by hypoxia and low immunogenicity, with a dense and rigid extracellular matrix (ECM) that impedes the diffusion of therapeutic agents and immune cells, thereby limiting the efficacy of immunotherapy. To overcome these challenges, an oxygen defect piezoelectric-photothermal sensitizer, bismuth vanadate nanorod-supported platinum nanodots (BVP) is developed. The integration of platinum enhances the photothermal effect and improves charge separation efficiency under ultrasound, leading to increased heat generation and the production of reactive oxygen species (ROS) and oxygen. Platinum also catalyzes the conversion of hydrogen peroxide in the TME to oxygen, which serves as both a ROS source and a means to alleviate tumor hypoxia, thereby reversing the immunosuppressive TME. Moreover, the coordination of bismuth ions with glutathione further amplifies cellular oxidative stress. The generated heat and ROS not only denature the collagen in the ECM, facilitating the deeper penetration of BVP into the tumor but also induce immunogenic cell death in tumor cells. Through the "degeneration and penetration" strategy, photoacoustic therapy effectively activates immune cells, inhibiting both tumor growth and metastasis. This study introduces a pioneering approach in the design of antitumor nanomedicines aimed at reversing the immunosuppressive characteristics of the TME.

In Situ Preparation of MnO2 on the Catechol/Silane-Coated Polypropylene Nonwoven Fabrics for Effective Removal of Cationic Dyes.

Previous studies have confirmed that MnOx removes heavy metal ions and organic pollutants from water with dual effects of adsorption and oxidation coupling, significantly improving the ability to remove impurities. Nanometal oxides have a highly reactive surface but tend to agglomerate during preparation and are challenging to recycle after use. A common method is to combine nano-MnO2 with Fe3O4 to prepare magnetic materials for easy recycling. Our previous research has confirmed that catechol (CA) and (3-aminopropyl) triethoxysilane (KH550) can be co-deposited on the surface of polypropylene nonwovens to form a stable CK coating under alkaline conditions. In addition, the coating has many active groups, including hydroxyl groups, amino groups, etc. This study further investigates the secondary reactivity of CK coatings. The coordination of catechol groups and metal ions was used to anchor manganese ions to the coating. Meanwhile, the hydroxyl and amino groups were used to reduce manganese ions to Mn4+ in situ to prepare PP-(CK-MnO2). We found that the sample had an excellent decolorization effect on cationic dyes but was limited to anionic dyes. The decolorization mechanism of cationic dyes was further discussed. The results showed that the decolorization of cationic dyes had a dual effect of adsorption and oxidative degradation. Under acidic conditions, its oxidation properties were enhanced. It can be used as a highly effective decolorizing agent for cationic dyes, and the decolorization behavior is consistent with the first-order kinetics. As the pH increases, its oxidation properties gradually decrease. Although the electrostatic adsorption effect was enhanced, the overall decolorization performance was significantly reduced. Recycling experiments have proved that it can maintain >90% removal rate after five cycles. This study also demonstrated that the CK coating has dopamine-like properties, which can coordinate with metal ions to prepare metal-organic hybrid materials.

Induction of ectosome formation by binding of phospholipases D from Loxosceles venoms to endothelial cell surface: Mechanism of interaction

Members of the phospholipase D (PLD) superfamily found in Loxosceles spider venoms are potent toxins with inflammatory and necrotizing activities. They degrade phospholipids in cell membranes, generating bioactive molecules that activate skin cells. These skin cells, in turn, activate leukocytes involved in dermonecrosis, characterized by aseptic coagulative necrosis. Although the literature has advanced in understanding the structure-function relationship, the cell biology resulting from the interactions of these molecules with cells remains poorly understood. In this study, we show that different cells exposed to recombinant PLDs bind these molecules to their plasma membrane, leading to the subsequent organization of extracellular microvesicles/ectosomes. The binding occurs as quickly as five minutes or less after exposure, increases over time, and eventually, the PLDs are expelled from the cell surface without generating cytotoxicity. PLDs are not endocytosed, nor do they spatially colocalize with acidic organelles in the intracellular environment. At least two regions of PLDs – the domain involved in magnesium ion coordination and the choline binding site – appear to play a role in cell surface binding and ectosome organization. However, the amino acids involved in catalysis do not participate in these events. The binding of these PLDs to the cell membrane, independent of catalytic activity, is sufficient to trigger intracellular signaling and enhance the expression of the pro-inflammatory IL-8 gene. These results are supported by the observation that isoforms of PLDs lacking catalytic activity induce an inflammatory response in vivo when injected into the skin of rabbits, without causing dermonecrosis. Our data indicate that these PLDs bind to the surface of target cells, promoting the organization of extracellular vesicles/ectosomes. Subsequently, these events activate pro-inflammatory genes and induce an inflammatory response in vivo. The binding to cells is not dependent on amino acids involved in catalysis but rather on amino acids involved in magnesium coordination. The binding of PLDs to the cell surface, formation of ectosomes, and activation of cells appear to initiate signals involved in inflammatory responses that can lead to dermonecrosis in accidents. This correlation is supported by experimental observations indicating that the events of toxin binding to cells, formation of microvesicles, and inflammatory responses observed both in vitro and in vivo are interconnected.

Thermal and Luminescent Properties of Multi-Ligand Complexes of Europium(III) with Pyrazine-2-carboxylic Acid

Eu(III) compounds with pyrazine-2-carboxylic acid and nitrogen- and phosphorus-containing neutral ligands were synthesized. Using the methods of chemical elemental and thermal analysis and IR spectroscopy, the composition of the complexes and the method of coordination of carboxylate ions were established. The most thermally stable compounds have been identified. The luminescent characteristics of complex compounds have been studied. It was found that the maximum luminescence intensity is characteristic of europium(III) pyrazinate with triphenylphosphine oxide. The morphological structure and dispersion of the complexes were determined.

One-step soaking strategy toward mechanical double-network hydrogel

Double-network (DN) hydrogels, which comprise noncovalent interacting networks, are highly sought after due to their controlled compositions and environmental friendliness. However, the complex preparation methods hinder the application of these hydrogels. In this study, we present a simple and feasible approach for fabricating hybrid PAA-CS DN hydrogels by post-treating the PAA-CS composite hydrogels with CuSO4 solutions to induce the formation of physical networks through CS chain entanglement. The composite hydrogel, composed of chitosan (CS) and polyacrylic acid (PAA), readily transforms into a DN hydrogel after soaking in a CuSO4 solution, thanks to in situ formation of chain entanglements, hydrogen bonds, and ionic coordination. The resulting hybrid DN hydrogels exhibit porous networks, high tensile strength, and exceptional toughness. This facile but effective soaking method can be universally applied to fabricate mechanically robust hydrogels, modulate noncovalent interactions, and broaden their potential applications.

Metal Ion Sensing by Tetraloop-like RNA Fragment: Role of Compact Intermediates with Non-Native Metal Ion-RNA Inner-Shell Contacts.

Divalent metal ions influence the folding and function of ribonucleic acid (RNA) in the cells. The mechanism of how RNA structural elements in riboswitches sense specific metal ions is unclear. RNA interacts with ions through two distinct binding modes: direct interaction between the ion and RNA (inner-shell (IS) coordination) and indirect interaction between the ion and RNA mediated through water molecules (outer-shell (OS) coordination). To understand how RNA senses metal ions such as Mg2+ and Ca2+, we studied the folding of a small RNA segment from the Mg2+ sensing M-Box riboswitch using computer simulations. This RNA segment has the characteristics of a GNRA tetraloop motif and interestingly requires the binding of a single Mg2+ ion. The folding free energy surface of this simple tetraloop system is multidimensional, with a population of multiple intermediates where the tetraloop and cation interact through IS and OS coordination. The partially folded compact tetraloop intermediates form multiple non-native IS contacts with the metal ion. Thermal fluctuations should break these strong non-native IS contacts so that the tetraloop can fold to the native state, resulting in higher folding free energy barriers. Ca2+ undergoes rapid OS to IS transitions and vice versa due to its lower charge density than Mg2+. However, the ability of Ca2+ to stabilize the native tetraloop state is weaker, as it could not hold the loop-closing nucleotides together due to its weaker interactions with the nucleotides. These insights are critical to understanding the specific ion sensing mechanisms in riboswitches, and the predictions are amenable for verification by nuclear magnetic resonance (NMR) experiments.

A study on the influence of geometric coordination of cobalt ions on the structural, physical and optical properties of borosilicate glass

A study on the influence of geometric coordination of cobalt ions on the structural, physical and optical properties of borosilicate glass

Solvent-free mechanochemical synthesis of Mg-gallic acid complex for the fabrication of high-performance supercapacitor porous carbon

At molecular level, it is challenging to construct a porous carbon from magnesium based template and low cost precursor by a facile route for supercapacitive energy storage, e.g. solvent-free approach because the coordination of magnesium ion with organic ligands usually needs participation of solvent. Herein, a balling milling mediated coordination of magnesium acetate and gallic acid was developed in the absence of solvent to prepare porous carbon. The key of the present strategy lies in the generation of volatile HAc, orienting the reaction in a favorable direction for the formation of complexes. The resultant porous carbon (denoted BGMC) owns a high microporostiy ratio (24.2 % vs template-free derived ones of 11.1 %), open accessed microstructure and hydrophobic character. As electrode for supercapacitor, in aqueous electrolyte, the BGMC based supercapacitor achieves a high energy density of 19.2 Wh kg−1@900 W kg−1, while, in organic electrolyte of 1.0 M TEABF4/AN, the symmetric device based on BGMC delivers energy in a wide voltage window of 0–3.5 V with large energy of 34.4 Wh kg−1@1750 W kg−1, which is superior to those of recently reported carbon based devices. And more, at high current density of 10 A g−1, the BGMC device can resist continual charge/discharge for 30 000 cycles, showing an excellent cycling stability. Our strategy involving solvent-freely coordination of template and precursor molecule to prepare porous carbon open up a route with facile, scalable and easy-operable attributes towards the preparation of functional porous carbon.