Addition Of MnO2 Research Articles

Synergistic effects of advanced MoSe2/MnO2 nanocomposite: Using direct yellow dye degradation for enhanced photocatalytic applications

MoSe2, a significant component within the class of transition metal dichalcogenides (TMDCs), boasts diverse photocatalysis characteristics. Herein, this research focuses on the hydrothermal approach to fabricate and thoroughly characterize Molybdenum diselenide (MoSe2) nanoparticles and Manganese dioxide (MnO2) nanoflakes as their co-catalyst with controllable morphologies size and enhanced photocatalytic activity. The samples were advanced characterizations such as SEM and HR-TEM to examine morphology, Powder X-ray diffraction (PXRD) to validate phase and crystal structure, Fourier transform infrared (FTIR) spectroscopy for analysing functional groups and bonds, and XPS for insights into elemental composition and chemical state of the nanocomposite. Due to the efficient separation of photogenerated electron-hole pairs facilitated by the rapid transfer of electrons by the addition of MnO2 and MoSe2/MnO2 nanocomposite demonstrates significantly enhanced photocatalytic performance and excellent stability in Direct Yellow (DY), a common pollutant found in industrial effluents. The MoSe2/MnO2 nanocomposite photocatalytic activity was 1.2–1.6 times higher than that of its individual components of MoSe2 and MnO2, indicating synergistic effects leading to enhanced performance. Consequently, this study illustrates that the MoSe2/MnO2 nanocomposite effectively degrades direct yellow dye under base conditions through photocatalysis.

Surface chemo-mechanics coupling of MnO2/Au layered composites under electrochemical environment

The intersection of surface mechanics and electrochemistry has gradually become a prominent topic in the realm of new energy research. To explore the influence of the electrochemical process on the stress of energy storage electrode composite, supercapacitor material manganese dioxide (MnO2) was selected as the coating and the MnO2/Au composites were prepared by the electrochemical deposition. The surface stress of MnO2/Au composites under different electrochemical modes and the stress variation law of MnO2 with varying thicknesses were determined. The addition of MnO2 could alter the stress response and the strain magnitude of the gold electrode with varied electrochemical potential. The reversible tensile strain within the Au surface during 0.3 ∼ 0.8 V charging was induced by the absorption of SO42−, while the compressive strain of the MnO2/Au composites was related to the extraction of Na+ ions resulting from the redox pseudocapacitance of MnO2. Notably, the produced stress exhibited a linear correlation with the capacitance. And the long-cycle tests revealed that as the specific capacitance of electrodes decreased, the induced tensile stress progressively diminished. This study emphasized the surface chemo-mechanics coupling of both the Au layer and MnO2/Au composites, which would provide a new approach to regulating surface strain in the solid–liquid interface.

Optimization of Energy Storage Performance in NaNbO3-Based High Entropy Ceramics via MnO Doping

Excellent comprehensive energy storage performance is essential to ensure a favorable application prospect for high entropy dielectric capacitors. In this work, the energy storage performance of 0.8(Na0.5Li0.5NbO3)-0.2(Sr0.5Bi0.5)(Fe0.5Ti0.25Zr0.25)O3 ceramics with high entropy was improved by incorporating various contents of MnO. The results show that with the addition of MnO, the relaxation behavior is enhanced, significantly improving energy storage performance, and a recoverable energy density of 7.93 J/cm³ and energy efficiency of 90.6% is achieved for [0.8(Na0.5Li0.5NbO3)-0.2(Sr0.5Bi0.5)(Fe0.5Ti0.25Zr0.25)O3]-0.05MnO under a 510 kV/cm electric field. Compared with non-MnO-doped ceramics, the size of the polar nanoregions (PNRs) is significantly reduced. It also shows remarkable stability to temperature and frequency. This study validates that integrating MnO effectively enhances the energy storage performance of high-entropy ceramics.

The effect of MnO2 additive on the microstructure and mechanical properties of magnesium aluminate spinel

AbstractIn this study, varying amounts of MnO2 up to 5 wt.% were added to magnesium aluminate spinel (MA) bodies using a solid‐state sintering method at 1200–1600°C. The effect of MnO2 addition on the phase composition, microstructure, distribution of elements, and ionic valence of MA was investigated via X‐ray diffraction, scanning electron microscopy, energy‐dispersive spectroscopy, and X‐ray photoelectron spectroscopy, respectively. The results showed that Mg2+ ions in MA crystals were replaced by Mn2+ ions, resulting in the formation of the (Mg1‐xMnx)Al2O4 solid solution. The distorted crystal structures promoted the sintering reactions, and the mechanical characteristics of MA were greatly improved by the solid solution strengthening process. When the additive amount of MnO2 was 5 wt.% and the sintered temperature reached at 1600°C, excess manganese ions hardly dissolved into the lattice of MA. And these ions were only distributed at the grain boundaries of MgAl2O4, forming a “barrier” that hindered the migration and diffusion of particles, thereby suppressing the sintering process and weakening the mechanical strength of MA.

The ancient glass decoloration technology based on the Fe-Mn redox pairs revived to improve the chemical stability of Fe2O3-containing borosilicate glass for medical application

MnO has been used for the decoloration of glasses containing iron oxide impurity since ancient times, based on the oxidation-reduction of Fe-Mn redox pairs (Fe2++Mn3+→Fe3++Mn2+). In this work, it was evidenced that a combinative addition of Fe2O3 and MnO into borosilicate glasses for pharmaceutical packaging application induced the above reaction and improved the water resistance of glass. As a comparative study, the structure of glasses with the inclusion of either MnO or Fe2O3 and both of them as well as the valence, coordination of Fe and Mn ions in the glasses were fully investigated by using FTIR, Raman, NMR, EPR, PL and UV–Vis–NIR spectroscopy. It was concluded that the single addition of Fe2O3 or MnO had a similar depolymerization effect on the glass structure, while the co-addition of Fe2O3 and MnO exhibited a synergistic effect, which led to the increase of glass network connectivity due to oxidation-reduction of Fe/Mn redox pairs and consequently the improvement of water resistance of the glasses.

Phase and defect structures of MnO2‐doped 75BiFeO3–25BaTiO3 ceramics and their effects on electrical properties

AbstractBismuth ferrite (BiFeO3)‐based high‐temperature piezoelectric ceramics have high Curie temperatures and excellent thermal stability; however, their applications are limited by inadequate piezoelectric performance due to large coercive fields and high leakage conduction. This study investigates the impact of MnO2 doping on the phase transition, defect structure, domain morphology, as well as the dielectric, ferroelectric, and electrical conduction behaviors of 75BiFeO3–25BaTiO3 ceramics sintered under an oxygen atmosphere. A structural transformation from distorted rhombohedral to pseudo‐cubic symmetry was observed with increasing MnO2 content, accompanied by domain fragmentation. MnO2 doping at an appropriate level inhibited defects such as and . Regarding electrical properties, the reduction in rhombohedral distortion and enhancement in the pseudo‐cubic phase after MnO2 doping resulted in decreased remanent polarization and electrostrain, which could potentially hinder piezoelectric response. However, appropriate MnO2 doping effectively reduced leakage conduction, significantly enhancing the poling efficiency of the ceramics. The maximum d33 value of 107 pC/N and kp of 0.36 were achieved at an MnO2 doping content of 0.1 wt.%. Excessive MnO2 addition may generate defect dipoles, as indicated by increased coercive field (Ec) and dielectric loss. The observed increase in high‐temperature resistivity with MnO2 content is primarily attributed to reduced grain size and increased concentration of mobile defects. This study provides valuable insights for further research on the application of 75BiFeO3–25BaTiO3 systems in high‐temperature piezoelectric devices.

Microwave‐sintered mullite structural ceramics based on low‐grade bauxite applied for fracturing proppants

AbstractThis study aimed to assess the feasibility of manufacturing fracturing proppants by microwave sintering and using low‐grade bauxite as raw material. The effects of microwave hotspot SiC and sintering additive MnO2 content on the performance of the mullite‐based structural materials were studied, respectively. The optimum sintering condition was determined by single‐factor experiments. The sintering process and mechanism were explored based on the analysis of physicochemical properties, phase transitions, and microstructure. The results showed that (1) mullite ceramic composites could be successfully prepared only with SiC added and with poor interparticle bonding microstructure. (2) With the addition of MnO2 and CaO, the granular‐shaped mullite crystals transformed into rod‐like mullite crystals, forming a net structure. (3) As the input power increased, the overfast sintering rate would reduce proppants' mechanical properties, and it was also necessary to select a reasonable sintering time to avoid overburning. (4) When the mass ratio of MnO2:CaO:SiC:bauxite was 2:1.5:12:84.5 and under the sintering condition of 1000 W, 2 h, the performance (breakage ratio of 8.5% under 28 MPa closed pressure, apparent density of 2.58 g/cm3, turbidity of 52 FTU, and acid solubility of 6.77%) could meet the requirements of the Chinese Petroleum and Gas Industry Standard (SY/T 5108–2014). This study provides a powerful way for reducing the fracturing cost, which not only improves the low‐grade bauxite utilization scale within the ceramic industry, but also expands the application of microwave sintering technology in mullite structural materials for the petroleum and gas industry.

Enhancing the catalytic performance of Cu/ZnO/Al2O3 catalyst in methanol synthesis from biomass‐derived syngas with CeO2, MnO2 and ZrO2 as promoters

AbstractThe performance of Cu/ZnO/Al2O3 (CZA) catalysts promoted by addition of CeO2, MnO2 or ZrO2 in direct methanol production from unconventional syngas was experimentally investigated. The unconventional syngas used in this study contain 25% H2, 25% CO, 20% CH4, 20% CO2 and 10% N2, representing biomass‐derived syngas cultivated from an industrial wood chips pyrolysis plant. The catalysts were synthesised using co‐precipitation technique and tested for methanol synthesis in a fixed‐bed reactor. The activity test of the catalysts showed that the addition of CeO2 or ZrO2 to the CZA catalyst improved the methanol yield, albeit with lower selectivity, whereas adding MnO2 enhanced methanol selectivity but decreased the methanol yield. ZrO2‐promoted catalyst showed the best‐improved activity and stability. The calcined and spent catalysts were characterised using X‐ray diffraction (XRD), N2 physisorption, N2O chemisorption, hydrogen temperature‐programmed reduction (H2‐TPR) and X‐ray photoelectron spectroscopy (XPS). The characterisation results indicate that the catalytic activity is dependent on Cu dispersion, Cu‐active surface area, the catalyst reducibility, Brunauer–Emmett–Teller (BET) surface area and the Cu0/Cu+ ratio. In contrast, catalyst stability was related to the proportion of Cu+ among all surface Cu species.

Significant enhancement of ferroelectric performance in lead-free NaNbO3 ceramics

The comparable free energy between antiferroelectric (AFE) and ferroelectric (FE) phases in NaNbO3 (NN) leads to unstable ferroelectricity, restricting future applications for energy storage devices. In this work, lead-free NN ceramics based on different sintering aids have been rigorously synthesized and the microstructural, dielectric, and ferroelectric properties of this system have been thoroughly examined. It is found that a tiny amount of sintering aids effectively lowers the sintering temperature and manipulates the grain growth, as well as plays an essential role in the stability of FE phase in NN ceramics. The tunable ferroelectricity is observed in NN: CuO as sintering aids results in a hardening effect, whereas MnO2 addition promotes softening behavior. More interestingly, introducing 1 wt% MnO2 as sintering aids results in strong ferroelectricity with high polarization (Pm) of 84.6 μC/cm2 stabilized by a stimulated electric field (Ef) as low as 60 kV/cm. This is significantly better than other NN-based ceramics (Pm is smaller than 40 μC/cm2 and Ef is higher than 90 kV/cm in the NN-based systems reported earlier). Our findings demonstrate the potential of sintering aids in tailoring the ferroelectric performance of lead-free NN ceramics, offering insights into the development of environmentally friendly ferroelectric materials.

Characteristics of humification, functional enzymes and bacterial community metabolism during manganese dioxide-added composting of municipal sludge

The aim of this study was to assess effects of MnO2 addition (CK-0%, T1-2% and T2-5%) on humification and bacterial community during municipal sludge (MS) composting. The results suggested that MnO2 addition inhibited the growth of Nitrospira but stimulated Nonomuraea, Actinomadura, Streptomyces and Thermopolyspora, facilitating the lignocellulose degradation and humification with the increase in organic matter degradation by 13.8%–19.2% and humic acid content by 10.9%–20.6%. Compared to CK, the abundances of exoglucanase (EC:3.2.1.91), endo-1,4-beta-xylanase (EC:3.2.1.136) and endomannanase (EC:3.2.1.78) increased by 88–99, 52–66 and 4–15 folds, respectively. However, 5%-MnO2 induced the enrichment of Mizugakiibacter that harms the environment of agricultural production. The addition of 2%-MnO2 was recommended for MS composting. Furthermore, metabolic function analysis indicated that MnO2 addition altered amino acid and carbohydrate metabolism, especially enhancing propanoate metabolism and butanoate metabolism but inhibiting citrate cycle. Structural equation modeling revealed that Nonomuraea and Actinomadura were the main drivers for lignocellulose degradation. This study provided theoretical guidance in regulating humification via MnO2 for MS composting.

MnO2 enhanced low temperature HCHO sensing performance of SnO2

The exploration of gas sensing materials holds significant importance for practical applications. This work introduces a novel SnO2/MnO2 nanocomposite designed to achieve formaldehyde monitoring at ppb level with a relative low temperature. The as prepared sensor demonstrates a response of 8.1–50 ppb formaldehyde at 100 °C. These remarkable formaldehyde sensing capabilities were explained by the heterojunction structure of the composite, and the low-temperature catalytic properties of MnO2. Moreover, in-situ infrared reflectance spectroscopy was employed to investigate the underlying mechanism by monitoring the evolution of reaction intermediates, and the result suggested that the addition of MnO2 can reduce the ineffective occupation of active sites and promote the generation of intermediate intermediates.

Z-Type Heterojunction MnO2@g-C3N4 Photocatalyst-Activated Peroxymonosulfate for the Removal of Tetracycline Hydrochloride in Water.

A Z-type heterojunction MnO2@g-C3N4 photocatalyst with excellent performance was synthesized by an easy high-temperature thermal polymerization approach and combined with peroxymonosulfate (PMS) oxidation technology for highly efficient degrading of tetracycline hydrochloride (TC). Analysis of the morphological structural and photoelectric properties of the catalysts was achieved through different characterization approaches, showing that the addition of MnO2 heightened visible light absorption by g-C3N4. The Mn1-CN1/PMS system showed the best degradation of TC wastewater, with a TC degradation efficiency of 96.97% following 180 min of treatment. This was an approximate 38.65% increase over the g-C3N4/PMS system. Additionally, the Mn1-CN1 catalyst exhibited excellent stability and reusability. The active species trapping experiment indicated •OH and SO4•- remained the primary active species to degrade TC in the combined system. TC degradation pathways and intermediate products were determined. The Three-Dimensional Excitation-Emission Matrix (3DEEM) was employed for analyzing changes in the molecular structure in TC photocatalytic degradation. The biological toxicity of TC and its degradation intermediates were investigated via the Toxicity Estimation Software Test (T.E.S.T.). The research offers fresh thinking for water environment pollution treatment.

Effect of MnO2 addition on structure, electrical and optical properties of Ba(Fe0.5Nb0.5)O3 ceramics

Admixture of Ba(Fe0.5Nb0.5)O3 (BFN) ceramics with different content of MnO2 (0, 0.5, 1.0, 1.5 and 2.0 wt.%) powder were processed through conventional solid-state reaction route. The XRD characterization of all sintered samples confirmed the formation of a single cubic perovskite structure.MnO2 acts as sintering aid, which significantly enhances grain size of the BFN ceramics. The room temperature dielectric constant and conductivity of the MnO2 modified BFN ceramics were suppressed compared to the pure BFN ceramics. However, the dielectric constant increases with the increase in temperature above 250 ?C. The relaxation activation energy (>0.6 eV) and high dielectric constant (?104 at temperature above 250 ?C) of the MnO2 modified BFN ceramics were explained on the basis of ionization of oxygen vacancies, mobile oxygen vacancies and polaron hopping between multiple oxidation states of manganese (Mn2+ and Mn3+). A narrow band gap of 1.45 eV was observed in the 1.5 wt.% MnO2 modified BFN ceramics.

Effect of MnO addition on chemical durability, glass-crystal transition, thermal, structural, optical, EPR, and color properties of Na2O-CaO-P2O5 ternary glass system

This paper investigates the effect of CaO substitution for MnO on the physicochemical properties in 25Na2O-(30-x)CaO-xMnO-45P2O5 (0 ≤ x ≤ 30 mol%) glass system. These materials were elaborated by the conventional melt-quenching technique at 1050 °C. Free-manganese glass is colorless, while the glasses containing manganese are purple. X-ray diffraction (XRD) confirmed the amorphous state of the studied glasses and showed that the annealing of these glasses leads to a mixture of crystalline phases. Replacing Ca-O bonds with more covalent Mn-O ones in the vitreous matrix increased density (ρ) and glass transition temperature (Tg), indicating the strength of the glass network. Infrared and Raman spectroscopies revealed the existence of PO3, PO2 and PO4 units with P-O-P linkages in the glassy network. EPR spectra exhibited absorptions centered at g ≈ 2, characteristic of isolated Mn2+ ions in distorted octahedral coordination and the optical absorption spectra disclosed bands due to Mn2+ and Mn3+ ions. Decreasing the band gap energy values (Eg) with increasing MnO content agrees with strengthening the vitreous network. Chemical durability results showed the existence of ionic exchanges between distilled water and the studied glasses, and good water resistance is detected for glasses with low Mn content (x = 5 and 10 mol%).

Radiation shielding features of Na2O–P2O5 glasses doped with MnO experimentally and using FLUKA and Phy-X

This research focused on examining the radiation shielding performance of (50% - x/2)P2O5-(50%-x/2)Na2O-xMnO (where x = 0, 5, 15, 25, and 33 mol%) glass system. The shielding review covered the radiation of photons, electrons, particles of heavy-charged, and neutrons. Hence, multiple parameters such as coefficient of mass attenuation (μm), transmission and buildup factors (HVL, MFP, EBF, and EABF), effective atomic number for samples (Zeff), and removal cross-section for fast neutron (FNRCS) of the selected samples were investigated. The results are determined experimentally and by employing FLUKA Monte Carlo software and Phy-X (ZeXTRA and PSD) theoretical programs. A relative discrepancy (RD) and a root-mean-square error (RMSE) were applied to verify the deviation between FLUKA and Phy-X values. An excellent agreement is noticed between measured, simulated, and calculated results. The research revealed that increasing MnO content improves the gamma, electron and heavy charged particle shielding efficiency of studied glasses. Although the addition of MnO has an insignificant impact on FNRCS (from 0.086 to 0.092 cm−1), obtained results identified the relationship between the packing density and shield ability against neutrons for ternary phosphate glasses. We found that the HVL values dropped from 13.898 cm to 11.568 cm at 15 MeV. A range of 7–12 for gamma, 8–12 for electron, 10–11 for proton, 10–11 for alpha, and 9–11 for carbon ion was the maximum value of Zeff that could be obtained. These glasses' shielding behaviors were contrasted with those of conventional materials. Accordingly, the sample with the highest mole fraction (x = 33 %) has higher shielding efficiency than ordinary concrete, Pyrex, and RS253-G18. Finally, the studied glass system can be a good compromise between highest effectiveness of shielding, lowest fabrication cost and environment-friendly shield.

Effect of sintering aid combined vacuum infiltration on the properties of Al2O3-based ceramics via binder jetting

Binder Jetting (BJ) technology enables cost-effective and efficient fabrication of complex Al2O3-based ceramic components. However, in the process of manufacturing Al2O3-based ceramics using BJ, issues such as high sintering temperatures and relatively low sintered strength and relative density are encountered. In this study, we investigated the MnO2 sintering aid in combination with TiO2 sol-gel vacuum infiltration to introduce a MnO-TiO2-Al2O3 ternary sintering system, which could reduce the sintering temperature and enhance the strength and relative density of Al2O3-based ceramics. Through single-factor and response surface experiments, the effects of MnO2 addition, green body sintering temperature, infiltration time, and infiltration vacuum level on the properties and reinforcement mechanism of BJ Al2O3-based ceramics were studied. The research results revealed that with 10% MnO2 addition, a sintering temperature of 1450 °C, infiltration time of 60 s, and infiltration vacuum level of 24 KPa, the bending strength and sintered relative density of Al2O3-based ceramics reached 113.79 MPa and 78.13%, respectively. The bending strength was 48 times higher than that of the Al2O3 ceramic samples without sintering aid composite infiltration treatment, and the sintered relative density was improved by 41.85%.

Preparation of polypropylene with photothermal conversion and hydrophilicity by one-step impregnation for efficient interfacial water evaporation

Solar-driven interfacial water evaporation is a technology that is currently attracting significant interest for tackling freshwater scarcity. However, the creation of porous membranes with photothermal conversion and hydrophilicity remains a challenging task. This study utilizes melt-blown polypropylene nonwoven (PP), a substrate with high porosity, low cost and high yield, to prepare evaporation membranes exhibiting photothermal conversion properties. The PP surface was treated with a one-step impregnation method to produce both shell and nanoparticles containing MnO2−x. The addition of MnO2−x grants the PP membranes both photothermal conversion and hydrophilicity simultaneously. Sunlight absorption efficiency of PP membranes covered with MnO2−x (M-PP) is 85.83%, and its hydrophilicity and porosity enable it to form an ultra-thin layer of water during evaporation, promoting rapid escape of vapors. Evaporation rate of M-PP membranes reach 1.02 kg m−2 h−1, much higher than that of PP and bulk water. In addition, M-PP membranes have excellent corrosion resistance, which is potentially valuable in treating wastewater and desalinating seawater.

Phase structure, domain structure, thermal stability, and high-temperature piezoelectric response of BiFeO3–BaTiO3 lead-free piezoelectric ceramics

High-temperature lead-free piezoceramics with a large piezoelectric constant d33 and a high depolarization temperature Td have long been a target of ferroelectric researchers. In this work, (1-x)BiFeO3-xBaTiO3 ceramics with MnO2 and Li2CO3 additives (BF-xBT) were fabricated with traditional ceramic preparation technology. The best piezoelectric ferroelectric properties and thermal stability d33 = 185 pC/N, Pr = 33.152 μC/cm2, Tc = 470 °C, and Td = 460 °C were obtained for x = 0.32. The tetragonal (T) phase content of BF-xBT ceramics increases gradually with an increase of BT content, and the temperature stability improves. In particular, an in-situ d33 test indicates that BF-xBT ceramics have large piezoceramics coefficients with d33 = 450.5 pC/N at a temperature of T = 334 °C. Piezo force microscopy and transmission electron microscopy tests show that nanodomains and polar nanoregions play a key role in the improvement of piezoelectric response. BF-xBT ceramics appear to be the most promising candidates to replace PZT ceramics in high-temperature applications.

Adhesion properties and formaldehyde emissions of MnO2/UF nanocomposite adhesives

Urea-formaldehyde (UF) resins are the most used resins in manufacturing particleboards. However, UF resins are susceptible to hydrolytic degradation, which causes formaldehyde emission and limits their use as wood panel adhesives for interior applications. In this study, we investigated the effects of the addition of nano MnO2 into urea-formaldehyde resin (UF) on the physicomechanical properties and formaldehyde emission of the bonded plywood. Two UF resins (a conventional as control and an innovative one with MnO2 nanoparticles (UFL)) were analyzed for their specifications with FTIR measurements both in their cured state. Differential scanning calorimetry (DSC) analysis was used to investigate the curing process. The formaldehyde emission decreased by 72.8 %, and the 3 h hot water soaking wet tensile shear strength improved by 74.5 % with the addition of 1.2 % (w/w)MnO2 nanoparticles compared to the UF resin control.

Multiprocess 3D printing of sodium-ion batteries via vat photopolymerization and direct ink writing

In this work, the ability to print shape-conformable batteries with multi-process additive manufacturing is reported. Vat photopolymerization (VPP) 3D printing process is employed to manufacture gel polymer electrolytes (GPEs) for sodium-ion batteries (SIBs), while direct ink writing process is used to prepare positive electrodes. The sodium-ion chemistry has proven to be an adequate substitute to lithium-ion due to the availability of resources and their potential lower production cost and enhanced safety. Three-dimensional printing technologies have the potential to revolutionize the production of shape-conformable batteries with intricate geometries that have been demonstrated to increase the specific surface area of the electrode and ion diffusion, thus leading to improved power performances. This study shows the preparation of composite UV-photocurable resins with different polymer matrix-to-liquid electrolyte ratios, designed to act as GPEs once printed via VPP. The impact of the liquid electrolyte ratio within the GPEs is thoroughly examined through a variety of electrochemical techniques. The exposure time printing parameter is optimized to ensure adequate print accuracy of the GPE. Using the optimized resin composition as material feedstock, shape-conformable 3D printed GPE exhibiting an ionic conductivity of 3.3 × 10−3 S·cm−1 at room temperature and a stability window up to 4.8 V vs. Na0/Na+ is obtained. In parallel, a composite ink loaded with Na0.44MnO2 and conductive additives is developed to 3D print via direct ink writing positive electrodes. After demonstrating the functionality of the independent 3D printed components in SIBs, the last part of this work is focused on combining the 3D printed Na0.44MnO2 electrode and the 3D printed GPE into the same battery cell to pave the way towards the manufacturing of a complete 3D printed battery thanks to different additive manufacturing processes.