Nitrogen-Doped Hierarchical Porous Activated Carbon Derived from Paddy for High-Performance Supercapacitors

A facile and environmentally friendly fabrication is proposed to prepare nitrogen-doped hierarchical porous activated carbon via normal-pressure popping, one-pot activation and nitrogen-doping process. The method adopts paddy as carbon precursor, KHCO₃ and dicyandiamide as the safe activating agent and nitrogen dopant. The as-prepared activated carbon presents a large specific surface area of 3025 m²·g⁻¹ resulting from the synergistic effect of KHCO₃ and dicyandiamide. As an electrode material, it shows a maximum specific capacitance of 417 F·g⁻¹ at a current density of 1 A·g⁻¹ and very good rate performance. Furthermore, the assembled symmetric supercapacitor presents a large specific capacitance of 314.6 F·g⁻¹ and a high energy density of 15.7 Wh·Kg⁻¹ at 1 A·g⁻¹, maintaining 14.4 Wh·Kg⁻¹ even at 20 A·g⁻¹ with the energy density retention of 91.7%. This research demonstrates that nitrogen-doped hierarchical porous activated carbon derived from paddy has a significant potential for developing a high-performance renewable supercapacitor and provides a new route for economical and large-scale production in supercapacitor application.     

Bulk Heterojunction Solar Cell with Nitrogen-Doped Carbon Nanotubes in the Active Layer: Effect of Nanocomposite Synthesis Technique on Photovoltaic Properties

Nanocomposites of poly(3-hexylthiophene) (P3HT) and nitrogen-doped carbon nanotubes (N-CNTs) have been synthesized by two methods; specifically, direct solution mixing and in situ polymerization. The nanocomposites were characterized by means of transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray dispersive spectroscopy, UV-Vis spectrophotometry, photoluminescence spectrophotometry (PL), Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, thermogravimetric analysis, and dispersive surface energy analysis. The nanocomposites were used in the active layer of a bulk heterojunction organic solar cell with the composition ITO/PEDOT:PSS/P3HT:N-CNTS:PCBM/LiF/Al. TEM and SEM analysis showed that the polymer successfully wrapped the N-CNTs. FTIR results indicated good π-π interaction within the nanocomposite synthesized by in situ polymerization as opposed to samples made by direct solution mixing. Dispersive surface energies of the N-CNTs and nanocomposites supported the fact that polymer covered the N-CNTs well. J-V analysis show that good devices were formed from the two nanocomposites, however, the in situ polymerization nanocomposite showed better photovoltaic characteristics.     

Synthesis and Properties of Nitrogen-Doped Carbon Quantum Dots Using Lactic Acid as Carbon Source

Nitrogen-doped carbon quantum dots (N-CQDs) were synthesized in a one-step hydrothermal technique utilizing L-lactic acid as that of the source of carbon and ethylenediamine as that of the source of nitrogen, and were characterized using dynamic light scattering, X-ray photoelectron spectroscopy ultraviolet-visible spectrum, Fourier-transformed infrared spectrum, high-resolution transmission electron microscopy, and fluorescence spectrum. The generated N-CQDs have a spherical structure and overall diameters ranging from 1–4 nm, and their surface comprises specific functional groups such as amino, carboxyl, and hydroxyl, resulting in greater water solubility and fluorescence. The quantum yield of N-CQDs (being 46%) is significantly higher than that of the CQDs synthesized from other biomass in literatures. Its fluorescence intensity is dependent on the excitation wavelength, and N-CQDs release blue light at 365 nm under ultraviolet light. The pH values may impact the protonation of N-CQDs surface functional groups and lead to significant fluorescence quenching of N-CQDs. Therefore, the fluorescence intensity of N-CQDs is the highest at pH 7.0, but it decreases with pH as pH values being either more than or less than pH 7.0. The N-CQDs exhibit high sensitivity to Fe³⁺ ions, for Fe³⁺ ions would decrease the fluorescence intensity of N-CQDs by 99.6%, and the influence of Fe³⁺ ions on N-CQDs fluorescence quenching is slightly affected by other metal ions. Moreover, the fluorescence quenching efficiency of Fe³⁺ ions displays an obvious linear relationship to Fe³⁺ concentrations in a wide range of concentrations (up to 200 µM) and with a detection limit of 1.89 µM. Therefore, the generated N-CQDs may be utilized as a robust fluorescence sensor for detecting pH and Fe³⁺ ions.     

Hazardous Petroleum Sludge-Derived Nitrogen and Oxygen Co-Doped Carbon Material with Hierarchical Porous Structure for High-Performance All-Solid-State Supercapacitors

Rational design and sustainable preparation of high-performance carbonaceous electrode materials are important to the practical application of supercapacitors. In this work, a cost-effective synthesis strategy for nitrogen and oxygen co-doped porous carbon (NOC) from petroleum sludge waste was developed. The hierarchical porous structure and ultra-high surface area (2514.7 m² g⁻¹) of NOC electrode materials could provide an efficient transport path and capacitance active site for electrolyte ions. The uniform co-doping of N and O heteroatoms brought enhanced wettability, electrical conductivity and probably additional pseudo-capacitance. The as-obtained NOC electrodes exhibited a high specific capacitance (441.2 F g⁻¹ at 0.5 A g⁻¹), outstanding rate capability, and cycling performance with inconspicuous capacitance loss after 10,000 cycles. Further, the assembled all-solid-state MnO₂/NOC asymmetrical supercapacitor device (ASC) could deliver an excellent capacitance of 119.3 F g⁻¹ at 0.2 A g⁻¹ under a wide potential operation window of 0–1.8 V with flexible mechanical stability. This ASC device yielded a superior energy density of 53.7 W h kg⁻¹ at a power density of 180 W kg⁻¹ and a reasonable cycling life. Overall, this sustainable, low-cost and waste-derived porous carbon electrode material might be widely used in the field of energy storage, now and into the foreseeable future.     

Optically Controlled Supercapacitors: Functional Active Carbon Electrodes with Semiconductor Particles

Supercapacitors, S-C—capacitors that take advantage of the large capacitance at the interface between an electrode and an electrolyte—have found many short-term energy applications. The parallel plate cells were made of two transparent electrodes (ITO), each covered with a semiconductor-embedded, active carbon (A-C) layer. While A-C appears black, it is not an ideal blackbody absorber that absorbs all spectral light indiscriminately. In addition to a relatively flat optical absorption background, A-C exhibits two distinct absorption bands: in the near-infrared (near-IR and in the blue. The first may be attributed to absorption by the OH⁻ group and the latter, by scattering, possibly through surface plasmons at the pore/electrolyte interface. Here, optical and thermal effects of sub-μm SiC particles that are embedded in A-C electrodes, are presented. Similar to nano-Si particles, SiC exhibits blue band absorption, but it is less likely to oxidize. Using Charge-Discharge (CD) experiments, the relative optically related capacitance increase may be as large as ~34% (68% when the illuminated area is taken into account). Capacitance increase was noted as the illuminated samples became hotter. This thermal effect amounts to <20% of the overall relative capacitance change using CD experiments. The thermal effect was quite large when the SiC particles were replaced by CdSe/ZnS quantum dots; for the latter, the thermal effect was 35% compared to 10% for the optical effect. When analyzing the optical effect one may consider two processes: ionization of the semiconductor particles and charge displacement under the cell’s terminals—a dipole effect. A model suggests that the capacitance increase is related to an optically induced dipole effect.     

Synthesis of Hollow Calcium Carbonate Microspheres by a Template Method for DOX Loading and Release with Carbon Dots Photosensitivity

Calcium carbonate, as the main inorganic component of human bones and teeth, has good biocompatibility and bioactivity and finds increasing applications in the field of bone drug carriers. In this study, hollow calcium carbonate microspheres were synthesized by a water hydrothermal method using folic acid as a template. Before drug loading, the prepared calcium carbonate microspheres were subjected to aminidation, carboxylation, and vinylenimine modification. The hollow calcium carbonate microspheres loaded with doxorubicin hydrochloride (DOX) were further incorporated with light-emitting carbon quantum dots(CQDs) and hyaluronic acid (HA). The result showed that the drug loading capacity in the as-prepared calcium carbonate was 179.064 mg/g. In the simulated solutions of cellular metabolism containing various concentrations of reduced glutathione(GSH), the sustained release of DOX was confirmed qualitatively by the luminescence of the CQDs. The DOX release rate was measured quantitively by UV absorption spectra. The highest release rate reached 85.99% in a simulated solution of 0.005 mol/L GSH solution, and the release rate could vary intelligently with the concentration.     

Preparation of Electrode Materials Based on Carbon Cloth via Hydrothermal Method and Their Application in Supercapacitors

Supercapacitors have the unique advantages of high power density, fast charge and discharge rates, long cycle life, high safety, and reliability, and are increasingly being used for applications including automobiles, rail transit, communication equipment, digital electronics, and aerospace equipment. The supercapacitor industry is currently in a stage of rapid development; great breakthroughs have also been made in improving the performance of supercapacitors and the expansion of their application. Electrode technology is the core of supercapacitors. Transition-metal compounds have a relatively high theoretical capacity and have received widespread attention as electrode materials for supercapacitors. In addition, there is a synergistic effect between the different components of various electrode composite materials. Due to their superior electrochemical performance, supercapacitors are receiving increasing research attention. Flexible supercapacitors have been hailed for their good plasticity, resulting in a development boom. This review article mainly outlines the development process of various electrode materials, including carbon materials, conductive polymers, metal compounds, and composite materials, as well as flexible electrode materials based on carbon cloth.     

DABCO Derived Nitrogen-Doped Carbon Nanotubes for Oxygen Reduction Reaction (ORR) and Removal of Hexavalent Chromium from Contaminated Water

Though chemically-derived reduced graphene oxide (CDG) from graphite oxide (GO) precursors is a widely practiced procedure for the large-scale production of graphene, the quality and quantity of thus obtained CDG is dependent on the reduction strategy used. In this work, we report an all-solid-state, residue-free, microwave process for the reduction of graphene oxide and subsequent growth of carbon nanotube ‘separators’ from a single precursor, namely DABCO (1,4-diazabicyclo[2.2.2]octane). The utility of our newly developed technique in efficiently and effectively reducing graphene oxide and in growing nitrogen-doped carbon nanotubes via catalysts like palladium and iron into unique mesoporous, 3-D hierarchical carbon nanostructures is demonstrated. The applicability of the thus obtained palladium embedded in Pd@NCNT-rGO nanoarchitectures for the oxygen reduction reaction (ORR) is investigated. When carbon fiber (CF) was used as the substrate, three-dimensional Fe@NCNT-CF were obtained, whose capability as versatile adsorbents for hexavalent chromium ion removal from contaminated waters was also demonstrated.     

Nitrogen-Doped Porous Carbon from Biomass with Efficient Toluene Adsorption and Superior Catalytic Performance

The chemical composition and surface groups of the carbon support affect the adsorption capacity of toluene. To investigate the effect of catalyst substrate on the catalytic performance, two different plant biomasses, banana peel and sugarcane peel, were used as carbon precursors to prepare porous carbon catalyst supports (Cba, Csu, respectively) by a chemical activation method. After decorating PtCo₃ nanoparticles onto both carbon supports (Cba, Csu), the PtCo₃-su catalyst demonstrated better catalytic performance for toluene oxidation (T₁₀₀ = 237 °C) at a high space velocity of 12,000 h⁻¹. The Csu support possessed a stronger adsorption capacity of toluene (542 mg g⁻¹), resulting from the synergistic effect of micropore volume and nitrogen-containing functional groups, which led to the PtCo₃-su catalyst exhibiting a better catalytic performance. Moreover, the PtCo₃-su catalyst also showed excellent stability, good water resistance properties, and high recyclability, which can be used as a promising candidate for practical toluene catalytic combustion.     

Electrochemical Improvement of the MWCNT/Al Electrodes for Supercapacitors

An original technique of chemical deposition (CVD) by catalytic pyrolysis of ethanol vapor was used to directly grow multiwall carbon nanotubes (MWCNTs) layers on aluminum foil. The grown nanotubes had excellent adhesion and direct electrical contact to the aluminum substrate. This material was perfect for use in electrochemical supercapacitors. In this work, the possibility of a significant increase in the specific capacity of MWCNTs by simple electrochemical oxidation was investigated. The optimal conditions for improving the characteristics of the MWCNT/Al electrodes were found. Electrochemical treatment of MWCNT/Al electrodes in a 0.005 M Na₂SO₄ solution at a potential of 4–5 V for 20–30 min increased the specific capacity of MWCNTs from 30 F/g to 140 F/g. The properties of modified nanotubes were investigated by X-ray photoelectron spectroscopy, cyclic voltammetry (CV), and impedance spectroscopy. A significant increase in the concentration of oxygen-containing functional groups on the surface of MWCNTs was found as a result of electrochemical oxidation. The modified MWCNT/Al electrodes maintained excellent stability to multiple charge–discharge cycles. After 20,000 CVs, the capacity loss was less than 5%. Thus, the results obtained significantly expanded the possibilities of using MWCNT/Al composite materials obtained by the method of direct deposition of carbon nanotubes on aluminum foil as electrodes for supercapacitors.     

Facile Synthesis of Carbon Nanospheres with High Capability to Inhale Selenium Powder for Electrochemical Energy Storage

Carbon–selenium composite positive electrode (CSs@Se) is engineered in this project using a melt diffusion approach with glucose as a precursor, and it demonstrates good electrochemical performance for lithium–selenium batteries. X-ray diffraction (XRD) and scanning electron microscopy (SEM) with EDS analysis are used to characterize the newly designed CSs@Se electrode. To complete the evaluation, electrochemical characterization such as charge–discharge (rate performance and cycle stability), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS) tests are done. The findings show that selenium particles are distributed uniformly in mono-sized carbon spheres with enormous surface areas. Furthermore, the charge–discharge test demonstrates that the CSs@Se cathode has a rate performance of 104 mA h g⁻¹ even at current density of 2500 mA g⁻¹ and can sustain stable cycling for 70 cycles with a specific capacity of 270 mA h g⁻¹ at current density of 25 mA g⁻¹. The homogeneous diffusion of selenium particles in the produced spheres is credited with an improved electrochemical performance.     

In Situ Dry Chemical Synthesis of Nitrogen-Doped Activated Carbon from Bamboo Charcoal for Carbon Dioxide Adsorption

In this work, nitrogen-doped bamboo-based activated carbon (NBAC) was in situ synthesized from simply blending bamboo charcoal (BC) with sodamide (SA, NaNH₂) powders and heating with a protection of nitrogen flow at a medium temperature. The elemental analysis and X-ray photoelectron spectra of as-synthesized NBAC showed quite a high nitrogen level of the simultaneously activated and doped samples; an abundant pore structure had also been determined from the NBACs which has a narrow size distribution of micropores (<2 nm) and favorable specific surface area that presented superb adsorption performance. The fcarbon dioxide (CO₂) adsorption of the NBACs was measured at 0 °C and 25 °C at a pressure of 1 bar, whose capture capacities reached 3.68–4.95 mmol/g and 2.49–3.52 mmol/g, respectively, and the maximum adsorption could be observed for NBACs fabricated with an SA/BC ratio of 3:1 and activated at 500 °C. Further, adsorption selectivity of CO₂ over N₂ was deduced with the ideal adsorbed solution theory ((IAST), the selectivity was finally calculated which ranged from 15 to 17 for the NBACs fabricated at 500 °C). The initial isosteric heat of adsorption (Qst) of NBACs was also determined at 30–40 kJ/mol, which suggested that CO₂ adsorption was a physical process. The results of ten-cycle adsorption-desorption experimentally confirmed the regenerated NBACs of a steady CO₂ adsorption performance, that is, the as-synthesized versatile NBAC with superb reproducibility makes it a perspective candidate in CO₂ capture and separation application.     

Deep Eutectic Solvent for Facile Synthesis of Mn3O4@N-Doped Carbon for Aqueous Multivalent-Based Supercapacitors: New Concept for Increasing Capacitance and Operating Voltage

The capacitance and operating voltage of supercapacitors as well as their energy density have been increased by development of different materials and electrolytes. In this paper, two strategies, for the first time, were used to improve energy density: Mn₃O₄- and N-dual doped carbon electrode and aqueous mixture of multivalent ions as electrolyte. Mn₃O₄- and N-dual doped carbon was prepared by a novel and cost-effective procedure using deep eutectic solvent. XRD, XPS, and FTIR confirmed presence of Mn₃O₄ and nitrogen, while SEM and EDS elemental mapping showed micrometer-sized nanosheets with uniform distribution of C, O, N, and Mn atoms. Charge storage behavior of carbon was tested in aqueous multivalent-based electrolytes and their mixture (Ca²⁺-Al³⁺). Regarding both specific capacitance and workable voltage, the Ca²⁺-Al³⁺ mixed electrolyte was found as the best optimal solution. The calcium addition to the Al-electrolyte allows the higher operating voltage than in the case of individual Al(NO₃)₃ electrolyte while the addition of Al³⁺ ion in the Ca(NO₃)₂ electrolyte improves the multivalent-ion charge storage ability of carbon. As a result, the specific energy density of two-electrode Mn₃O₄@N-doped carbon//Al(NO₃)₂+Ca(NO₃)₂//Mn₃O₄@N-doped carbon supercapacitor (34 Wh kg⁻¹ at 0.1 A g⁻¹) overpasses the reported values obtained for Mn-based carbon supercapacitors using conventional aqueous electrolytes.     

Activated Carbon Modification towards Efficient Catalyst for High Value-Added Products Synthesis from Alpha-Pinene

DT0-activated carbons modified with HCl and HNO₃ acids, which were used for the first time in the catalytic process of alpha-pinene isomerization, are presented in this study. The carbon materials DT0, DT0_HCl, DT0_HNO₃, and DT0_HCl_HNO₃ were examined with the following methods: XRF, SEM, EDX, XPS, FT-IR, XRD, and N₂ adsorption at −196 °C. It was shown that DT0_HCl_HNO₃-activated carbon was the most active material in the alpha-pinene isomerization process. Detailed studies of alpha-pinene isomerization were carried out over this carbon by changing the reaction parameters such as time (5–180 min) and temperature (60–175 °C). The 100% conversion of alpha-pinene was achieved at the temperature of 160 °C and catalyst content of 5 wt% after 3 h over the DT0_HCl_HNO₃ catalyst. Camphene and limonene were the main products of the alpha-pinene isomerization reaction.     

Synthesis and Characterization of Novel Hybrid Flocculants Based on Potato Starch Copolymers with Hollow Carbon Spheres

Novel carbon nanofiller-based starch-g-polyacrylamide hybrid flocculation materials (St-PAM-CS) were in situ prepared using potato starch (St), acrylamide (AM), and hollow mesoporous carbon spheres (CSs; diameters of 300–400 nm). Structures of different St-PAM-CS systems were characterized by Fourier transform infrared (FTIR) spectroscopy, X-Ray diffraction (XRD), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), laser scanning microscopy (LSM), and particle size analysis. The flocculation tests were evaluated by removing high turbidity kaolin suspension—initial absorbance 1.84. The effect of the St to AM molar ratio, doses, and content of CSs in hybrids on flocculation efficiency were examined. Satisfactory flocculation efficiency was obtained for all hybrids with 1 wt.% of the CS component. The highest reduction of the kaolin suspension absorbance (to 0.06) was observed for a 3 mL dose of the starch hybrid with the highest AM content. Additionally, St-PAM-CS showed a reduction in the sludge volume in time. The hybrids reached better flocculation efficiency in relation to the reference systems without CSs. The proposed flocculation mechanism (considering bridging, patching, and formation of hydrogen bonds) has been confirmed by the recorded results.     

Detection of Cobalamin and In Vitro Cell Imaging Based on Nitrogen-Doped Yellow Fluorescent Carbon Dots with Nano Architectonics

As novel fluorescent nanomaterials, carbon dots have attracted increasing research attention because of their simple synthesis, robust fluorescence, low toxicity, and easy functionalisation. Previous research was focused on preparing carbon dots from biomass and chemical materials; however, most of these carbon dots exhibited blue fluorescence. Moreover, the fluorescence quantum yield was generally low, significantly limiting their application in biological imaging. To broaden the application scope of carbon dots, this study prepared long-wavelength emitting nano-carbon dots that exhibited increased quantum yield. Novel N-doped yellow fluorescent nano-carbon dots (Y-CDs) were synthesised via a hydrothermal method using L-tartaric acid and urea as the precursors. The Y-CDs had a high quantum yield (15.9%) and demonstrated photostability at various pHs, temperatures, and ionic strengths. The Y-CDs could detect cobalamin effectively and selectively, showing a linear relationship between fluorescence intensity and cobalamin concentration. The related coefficient was 0.997, and the detection limit was 2.101 μmol/L. In addition, the Y-CDs were successfully used as an imaging probe for MDA-MB-231 cells. Therefore, the Y-CDs developed in this study can be used for cobalamin detection and cell imaging.     

Growing Tungsten Nanophases on Carbon Spheres Doped with Nitrogen. Behaviour as Electro-Catalysts for Oxygen Reduction Reaction

This work shows the preparation of carbon nanospheres with a high superficial nitrogen content (7 wt.%), obtained by a simple hydrothermal method, from pyrocatechol and formaldehyde, around which tungsten nanophases have been formed. One of these nanophases is tungsten carbide, whose electro-catalytic behavior in the ORR has been evaluated together with the presence of nitrogen surface groups. Both current and potential kinetic density values improve considerably with the presence of tungsten, despite the significant nitrogen loss detected during the carbonization treatment. However, the synergetic effect that the WC has with other electro-catalytic metals in this reaction cannot be easily evaluated with the nitrogen in these materials, since both contents vary in opposite ways. Nevertheless, all the prepared materials carried out oxygen electro-reduction by a mixed pathway of two and four electrons, showing remarkable electro-catalytic behavior.     

Hard Carbon Embedded with FeSiAl Flakes for Improved Microwave Absorption Properties

Carbon-based composites have been proven to be strong candidates for microwave absorbers in recent years. However, as an important member, magnetic hard carbon (HC)-based composites have rarely been studied in the field of microwave absorption. In this study, HC embedded with FeSiAl (FeSiAl@HC) was synthesized by pyrolyzing a mixture of FeSiAl flakes and phenolic resin (PR). The as-synthesized HC-FeSiAl exhibited a layered structure, and the detailed microstructures were modified by changing the mass ratio of FeSiAl flakes and PR. Thus, the as-synthesized HC-FeSiAl exhibited tunable magnetic properties, wealthy functional groups, excellent thermal stability, and enhanced microwave absorption properties. The optimal minimum reflection loss is lower up to −36.1 dB, and the effective absorption bandwidth is wider up to 11.7 GHz. These results indicated that HC-FeSiAl should be a strong candidate for practical applications of microwave absorption, which may provide new insight into the synthesis of magnetic HC-based composites.     

Solid-State Synthesis of Polyaniline/Single-Walled Carbon Nanotubes: A Comparative Study with Polyaniline/Multi-Walled Carbon Nanotubes

The polyaniline/single-walled carbon nanotubes (PANI/SWNTs) composites with a content of SWNTs varying from 8 wt% to 32 wt% were synthesized using a solid-state synthesis method. The structure and morphology of the samples were characterized by fourier transform infrared (FTIR) spectra, ultraviolet-visible (UV-vis) absorption spectra, X-ray diffraction (XRD) and transmission electron microscopy (TEM). The electrochemical performances of the composites were investigated by galvanostatic charge–discharge and cycling stability measurements. The structure and properties of PANI/SWNTs were compared with those of PANI/multi-walled carbon nanotubes (PANI/MWNTs) prepared under the same polymerization conditions. The results from FTIR and UV-vis spectra showed that the composites with SWNTs displayed a higher oxidation and doping degree than pure PANI, which is similar to that of PANI/MWNTs. The morphological studies revealed that PANI/SWNTs did not display any rod-like and granular-like features, which appeared in PANI/MWNTs. The galvanostatic charge–discharge measurements indicated that the specific capacitance of PANI/SWNTs is not higher than that of PANI/MWNTs, but the PANI/SWNTs exhibited higher cycling stability and more stable electrochemical behavior in neutral and alkaline electrolytes than PANI/MWNTs.     

Co-Existence of Iron Oxide Nanoparticles and Manganese Oxide Nanorods as Decoration of Hollow Carbon Spheres for Boosting Electrochemical Performance of Li-Ion Battery

Here, we report that mesoporous hollow carbon spheres (HCS) can be simultaneously functionalized: (i) endohedrally by iron oxide nanoparticle and (ii) egzohedrally by manganese oxide nanorods (Fe_xO_y/MnO₂/HCS). Detailed analysis reveals a high degree of graphitization of HCS structures. The mesoporous nature of carbon is further confirmed by N₂ sorption/desorption and transmission electron microscopy (TEM) studies. The fabricated molecular heterostructure was tested as the anode material of a lithium-ion battery (LIB). For both metal oxides under study, their mixture stored in HCS yielded a significant increase in electrochemical performance. Its electrochemical response was compared to the HCS decorated with a single component of the respective metal oxide applied as a LIB electrode. The discharge capacity of Fe_xO_y/MnO₂/HCS is 1091 mAhg⁻¹ at 5 Ag^–1, and the corresponding coulombic efficiency (CE) is as high as 98%. Therefore, the addition of MnO₂ in the form of nanorods allows for boosting the nanocomposite electrochemical performance with respect to the spherical nanoparticles due to better reversible capacity and cycling performance. Thus, the structure has great potential application in the LIB field.