MnO2 Nanoflowers Research Articles

A highly permeable nanoplatform based on functionalized carbon dots for synergistic reactive oxygen/nitrogen species tumor therapy

Reactive oxygen species (ROS)-based antitumor strategies, particularly chemodynamic therapy, have garnered considerable attention. However, challenges such as difficulties in achieving deep penetration, relatively low H2O2 levels in the tumor microenvironment, the requirement for low pH by the Fenton reaction, and their short lifespan have impeded satisfactory therapeutic outcomes. Hence, we have developed a nanoplatform with enhanced permeability that not only generates significant amounts of ROS but also converts them into longer-lasting reactive nitrogen species (RNS), thereby improving tumor therapy efficacy. In our study, carbon dots were functionalized by doping with gold atoms and grafting nitrosoglutathione (GSNO) to form ACN, which exhibits glucose oxidase-like properties and enables laser-responsive NO release. ACN and indocyanine green (ICG) were then loaded onto MnO2 nanoflowers to form MnO2@AI. Upon arrival at the tumor site, MnO2 reacts with H2O2 and GSH, leading to its degradation and the subsequent release of ACN, which is characterized by three permeation-promoting properties: ultra-small size, positive charge, and NO content. In addition, ACN promotes H2O2 production through glucose metabolism and reduces pH, both of which enhance the Fenton-like reaction of MnO2, thereby amplifying ROS generation. The ICG in MnO2@AI enhances its photothermal properties, leading to the responsive release of NO from GSNO grafted onto ACN, which then reacts with the increased ROS to generate more toxic RNS. Collectively, the approach described herein offers substantial potential for advancing the treatment of malignant tumors.

Enhanced formaldehyde oxidation of plywood using MnO2 nanoflowers supported on porous hydrothermal carbon at ambient temperature

MnO2 nanoflowers were supported on porous hydrothermal carbon via in situ loading and used for the catalytic oxidation of formaldehyde from plywood manufactured with UF adhesive. The prepared MnO2 had a δ-type structure. The use of hydrothermal carbon (Hcs) improved the dispersion of active components in the materials and provided space for the catalytic reactions. Hcs/MnO2 exhibited catalytic activity and stability during formaldehyde oxidation at room temperature. The formaldehyde removal efficiency reached 90.43 % in 30 min. The Hcs/MnO2 had more oxygen vacancies than the MnO2 catalyst, providing more abundant active substances such as -OH, O2-, O- and other active substances to promote the catalytic reaction. The effects of Hcs/MnO2 on the formaldehyde emission and the mechanical properties of plywood were investigated. The MOR, MOE and bonding strength of the Hcs/MnO2-loaded plywood with 9 % Hcs were 51.1 MPa, 2994 MPa, and 0.8 MPa, respectively. After 28 d of exposure, the formaldehyde emitted from the plywood treated with Hcs/MnO2 decreased to 0.023 mg/m3, which fulfilled the requirement for ENF grading. The controlled release of free formaldehyde from plywood by Hcs/MnO2 was reflected by changes in mass transfer and catalytic oxidation. The manganese oxides in the micropores of the wood reduced the diffusion coefficient of free formaldehyde and hindered migration through the substrate. Once the concentration of formaldehyde decreased to a certain level, it was degraded by Hcs/MnO2, thus removing formaldehyde from the source.

Multiwalled carbon nanotubes decorated ɛ-MnO2 nanoflowers cathode with oxygen defect for aqueous zinc-ion batteries

As a potential cathode for aqueous zinc-ion batteries, the low electrical conductivity and poor electrochemical kinetics of MnO2 limit its further development and application. Herein, multiwalled carbon nanotubes decorated MnO2 nanoflowers with hexagonal structure (ɛ-MnO2/MWCNTs) were synthesized by one-step co-precipitation method. The ɛ-MnO2/MWCNTs inherit the advantages of highly conductive MWCNTs and nanostructured MnO2, thus showing excellent zinc-ion storage capacity. The ɛ-MnO2/MWCNTs display high invertible capacity of 335.6 mAh/g at 0.2 A/g after 150 cycles, and long-term capacity of 115.7 mAh/g at 2.0 A/g after 4000 cycles. The results of kinetics tests further reveal that the MWCNTs decoration can reduce polarization of MnO2 and accelerate its reaction kinetics. Thanks to these merits, the ɛ-MnO2/MWCNTs hold great potential for high performance eco-friendly batteries cathode material.

Laccase mimetics as sensing elements for amperometric assay of 5-hydroxyindoleacetic acid in urine

Monitoring of the levels of 5-hydroxyindole-3-acetic acid (5-HIAA) is of significant importance for diagnostics of carcinoid tumors. We propose simple catalytic electrochemical sensors for the determination of 5-HIAA in urine using laccase and its mimetics. Laccase-like nanozymes (LacNZs) were synthesized via a chemical reduction, and resulting PtMn and MnO2 nanoflowers (NFs) demonstrated laccase-like activity similar to the laccase from the Trametes zonata. In addition, these LacNZs showed enhanced stability under a wide range of pH (3.0–7.5), temperatures (4–70 °C), and ionic strengths (up to 500 mM NaCl). The developed PtMn NF/graphite electrode, similar to a laccase/graphite electrode, can detect 5-HIAA with a high sensitivity (25 000 ± 12 A·M−1·m−2 and 1900 ± 9 A·M−1·m−2, respectively) and have linear ranges of 0.3 – 15 μM and 2 – 50 μM. The sensors work at low working potentials with a detection limit of 0.16 and 1.4 μM, covering the normal and pathologic ranges of 5-HIAA (1–50 μM) content in urine. They have been successfully applied to 5-HIAA assay in urine samples of people with various diseases and revealed good recovery values and reproducibility. Additionally, the LacNZ-sensor has the best stability and can be used up to 20 days.

Immobilization of MnO2 nanoflowers on coils using direct heating method for organic pollutant remediation

The immobilization of catalysts on supporting substrates for the removal of organic pollutants is a crucial strategy for mitigating catalyst loss during wastewater treatment. This study presented a rapid and cost-effective direct heating method for synthesizing MnO2 nanoflowers on coil substrates for the removal of organic pollutants. Traditional methods often require high power, expensive equipment, and long synthesis times. In contrast, the direct heating approach successfully synthesized MnO2 nanoflowers in just 10 min with a heating power of approximately 40 W·h after the heating power and duration were optimized. These nanoflowers effectively degraded 99% Rhodamine B in 60 min with consistent repeatability. The catalytic mechanisms are attributed to crystal defects in MnO2, which generate electrons to produce H2O2. Mn2+ ions in the acidic solution further dissociate H2O2 molecules into hydroxyl radicals (·OH). The high efficiency of this synthesis method and the excellent reusability of MnO2 nanoflowers highlight their potential as a promising solution for the development of supporting MnO2 catalysts for organic dye removal applications.

Restricted and epitaxial growth of MnO2-x nano-flowers in/out carbon nanofibers for long-term cycling stability supercapacitor electrodes

Carbon nanofibers (CFs) have been widely applied as electrodes for energy storage devices owing to the features of increased contact area between electrodes and electrolyte, and shortened transmission route of electrons. However, the poor electrochemical activity and severe waste of space hinder their further application as supercapacitors electrodes. In this work, MnO2−x nanoflowers restricted and epitaxial growth in/out carbon nanofibers (MnO2/MnO@CF) were prepared as excellent electrode materials for supercapacitors. With the synergistic effect of uniquely designed structure and the introduction of MnO and MnO2 nanoflowers, the prepared interconnected MnO2/MnO@CF electrodes demonstrated satisfactory electrochemical performance. Furthermore, the MnO2/MnO@CF//activated carbon (AC) asymmetric supercapacitor offered an outstanding long-term cycle stability. Besides, kinetic analysis of MnO2/MnO@CF-90 was conducted and the diffusion-dominated storage mechanism was well-revealed. This concept of “internal and external simultaneous decoration” with different valence states of manganese oxides was proven to improve the electrochemical performance of carbon nanofibers, which could be generalized to the preparation and performance improvement of other fiber-based electrodes.

All‐In‐One Self‐Floating Wood‐Based Solar‐Thermal Evaporators for Simultaneous Solar Steam Generation and Catalytic Degradation

AbstractSolar‐driven steam generation has emerged as a sustainable technology for addressing freshwater scarcity. However, significant challenges still exist in developing high‐performance, multifunctional evaporators that are adept at both efficiently evaporating water and degrading pollutants, primarily because of the trade‐offs among functional designs. Here, a self‐floating solar evaporator is reported by functionalizing balsa wood with solar‐thermal conversion material carbon nanotubes and catalytic manganese dioxide (MnO2) nanoflowers for simultaneous solar evaporation and pollutant degradation. MnO2 nanoflowers are rich in oxygen vacancies that can effectively activate peroxymonosulfate to generate reactive oxygen species for efficient organic pollutant degradation. A distinctive non‐wetted porous interior structure and a precisely targeted water pathway are spontaneously established in the multifunctional evaporator, ensuring fast water supply, thermal insulation, efficient mass transfer, and high buoyancy. The resulting evaporators successfully combine an impressive evaporation rate of 2.74 kg m−2 h−1, a high pollutant degradation efficiency (98.3% for 100 mg L−1 tetracycline and 97.4% for 200 mg L−1 Methyl orange), and stable self‐floating and self‐standing capabilities that ensure long‐term operation stability even in complex real‐world environments. This work provides an approach to design multifunctional solar evaporators, ensuring strong alignment with practical requirements while expanding their potential application scenarios.

Boosting the Energy Density of Bowl-Like MnO2@Carbon Through Lithium-Intercalation in a High-Voltage Asymmetric Supercapacitor with "Water-In-Salt" Electrolyte.

Highly concentrated "'water-in-salt"' (WIS) electrolytes are promising for high-performance energy storage devices due to their wide electrochemical stability window. However, the energy storage mechanism of MnO2 in WIS electrolytes-based supercapacitors remains unclear. Herein, MnO2 nanoflowers are successfully grown on mesoporous bowl-like carbon (MBC) particles to generate MnO2/MBC composites, which not only increase electroactive sites and inhibit the pulverization of MnO2 particles during the fast charging/discharging processes, but also facilitate the electron transfer and ion diffusion within the whole electrode, resulting in significant enhancement of the electrochemical performance. An asymmetric supercapacitor, assembled with MnO2/MBC and activated carbon (AC) and using 21m LiTFSI solution as the WIS electrolyte, delivers an ultrahigh energy density of 70.2Whkg-1 at 700W kg-1, and still retains 24.8Whkg-1 when the power density is increased to 28kWkg-1. The ex situ XRD, Raman, and XPS measurements reveal that a reversible reaction of MnO2 + xLi+ + xe-↔LixMnO2 takes place during charging and discharging. Therefore, the asymmetric MnO2/MBC//AC supercapacitor with LiTFSI electrolyte is actually a lithium-ion hybrid supercapacitor, which can greatly boost the energy density of the assembled device and expand the voltage window.

Hydrogel-integrated multimodal biosensor for the detection of glucose and carcinoembryonic antigen

Multimodal biosensors can reduce false negative/positive rates to produce more reliable results. In this study, we report a multimodal biosensor that can achieve the detection of biomarkers by color, temperature and distance signals. The detection of glucose and carcinoembryonic antigen (CEA) is demonstrated as an example. The horseradish peroxidase (HRP), glucose oxidase (GOx) and 3,3′,5,5′-tetramethylbenzidine (TMB) are all entrapped in the gelatin hydrogel. When glucose is present, the final product oxTMB shows the blue signal and photothermal effect that can cause the gel-sol phase transition of the gelatin hydrogel, which enables the detection of glucose based on color, temperature and water flow distance on the pH indicator paper. To further broaden the application of this biosensor, a multimodal immunosensor is constructed to detect CEA using detection antibody-modified MnO2 Nanoflowers (NFs) as detection probe. Based on the oxidase-like activity of MnO2 NFs and the gel-sol transition property of the gelatin hydrogel, the detection of CEA with multiple signals as mentioned above was achieved by the sandwich immunoassay. Additionally, the detection of glucose and CEA is also fulfilled for in real samples. Overall, the hydrogel-integrated multimodal biosensor is simple to operate and the resulting multiple signals can complement each other, providing a versatile method for analysis of biomarkers.

Mn2+-Mediated Modulation of PfAgo Activity for Biosensing.

Argonaute (Ago) as a powerful enzyme has provided new insights into biosensing due to its programmability, high sensitivity, and user-friendly operation. However, current strategies mainly rely on phosphorylated guide DNA to modulate the cleavage activity of Ago, which is limited in versatility and simplicity. Herein, the authors report the Mn2+-enhanced cleavage activity of Ago and employ Mn-ions with variable valence to regulate the activity of Pyrococcus furiosus Ago (PfAgo) for biosensing applications. The conversion of Mn ions with different valence states through MnO2 nanoflowers enables the sensitive detection of ascorbic acid, alkaline phosphatase, and arsenic with limits of detection of 2.5 nmol L-1, 0.009 U L-1, and 0.4 ng mL-1, respectively. A PfAgo-based immunoassay is further developed that allows for the detection of diverse targets, thus providing a promising toolbox to broaden PfAgo-based sensors into versatile bioanalytical and biomedical applications.

Oxygen Vacancy-Rich Manganese Nanoflowers as Ferroptosis Inducers for Tumor Radiotherapy.

The combination of ferroptosis and innovative tumor therapy methods offers another promising answer to the problem of tumors. In order to generate effective ferroptosis in tumor cells, iron-based nanomaterials are commonly utilized to introduce foreign iron as a trigger for ferroptosis. However, this usually necessitates the injection of larger doses of iron into the body. These exogenous iron increases are likely to create concealed concerns for symptoms such as liver damage and allergy. Herein, an iron-free radiosensitizer is introduced, oxygen-vacancy-rich MnO2 nanoflowers (ovs-MnO2), that promotes ferroptosis and modifies the tumor microenvironment to assist radiotherapy. ovs-MnO2 with enriched oxygen vacancies on the surface induces the release of intracellular free iron (Fe2+), which functions as an activator of Fenton reaction and enhances the accumulation of intracellular reactive oxygen species. On the other hand, Fe2+ also triggers the ferroptosis and promotes the accumulation of lipid peroxides. Subsequently, the depletion of glutathione and accumulation of lipid peroxidation in tumor cells leads to the inactivation of glutathione peroxidase 4 (GPX4) and ferroptosis, thereby enhancing the therapeutic efficacy of radiotherapy. The nanoplatform provides a novel strategy for generating novel nanomedicines for ferroptosis-assisted radiotherapy.

Multienzyme Active Manganese Oxide Alleviates Acute Liver Injury by Mimicking Redox Regulatory System and Inhibiting Ferroptosis.

Drug-induced liver injury (DILI) is a severe condition characterized by impaired liver function and the excessive activation of ferroptosis. Unfortunately, there are limited options currently available for preventing or treating DILI. In this study, MnO2 nanoflowers (MnO2Nfs) with remarkable capabilities of mimicking essential antioxidant enzymes, including catalase, superoxide dismutase (SOD), and glutathione peroxidase are successfully synthesized, and SOD is the dominant enzyme among them by density functional theory. Notably, MnO2Nfs demonstrate high efficiency in effectively eliminating diverse reactive oxygen species (ROS) such as hydrogen peroxide (H2O2), superoxide anion (O2 •-), and hydroxyl radical (•OH). Through in vitro experiments, it is demonstrated that MnO2Nfs significantly enhance the recovery of intracellular glutathione content, acting as a potent inhibitor of ferroptosis even in the presence of ferroptosis activators. Moreover, MnO2Nfs exhibit excellent liver accumulation properties, providing robust protection against oxidative damage. Specifically, they attenuate acetaminophen-induced ferroptosis by inhibiting ferritinophagy and activating the P62-NRF2-GPX4 antioxidation signaling pathways. These findings highlight the remarkable ROS scavenging ability of MnO2Nfs and hold great promise as an innovative and potential clinical therapy for DILI and other ROS-related liver diseases.

Signal-off nanozyme-based colorimetric aptasensor for sensitive detection of ampicillin using MnO2 nanoflowers and gold nanoparticles

The combination of nanomaterials possessing distinct characteristics and the precision of aptamers facilitates the creation of biosensors that exhibit exceptional selectivity and sensitivity. In this manuscript, we present a highly sensitive aptasensor that utilizes the distinctive characteristics of MnO2 nanoflowers and gold nanoparticles to selectively detect ampicillin (AMP). In this aptasensor, the mechanism of signal change is attributed to the difference in the oxidase-mimicking activity of MnO2 nanoflowers in the presence of a free sequence. The inclusion of AMP hindered the creation of a double-stranded DNA configuration through its binding to the aptamer, resulting in an observable alteration in absorbance. The relative absorbance varied linearly with the concentration of AMP in the range of 70 pM to 10 nM with a detection limit of 21.7 pM. In general, the colorimetric aptasensor that has been developed exhibits exceptional selectivity and remarkable stability. It also demonstrates favorable performance in human serum, making it a highly reliable diagnostic tool. Additionally, its versatility is noteworthy as it holds great potential for detecting various antibiotics present in complex samples by merely replacing the utilized sequences with new ones.

Cross-linked K0.5MnO2 nanoflower composites for high rate and low overpotential Li–CO2 batteries

The synergistic effect between ultra-thin K0.5MnO2 nanoflowers and CNTs effectively promotes the nucleation and charging decomposition of Li2CO3, achieving low overpotential and high average energy efficiency as a Li–CO2 cathode.

Hydrogen-bond chemistry inhibits Jahn–Teller distortion caused by Mn 3d orbitals for long-lifespan aqueous Zn//MnO2 batteries

By introducing NH4+, hydrogen-bond-modulated MnO2 nanoflowers inhibit the stretching of the [MnO6] octahedra along the z axis, reduce the occurrence of Jahn–Teller distortion, and achieve long-lifespan aqueous Zn//MnO2 batteries.

Construction of a colorimetric sensor array for the identification of phenolic compounds by the laccase-like activity of N-doped manganese oxide

Phenolic compounds, widely distributed in nature, encompass a diverse array of bioactive and antioxidant properties. The detection of different phenolic compound types holds paramount importance in elucidating their bioactivity and health effects, ensuring the quality and safety of food and drugs. Consequently, the development of simple, rapid, and cost-effective colorimetric sensing arrays capable of simultaneous phenolic compound detection has emerged as a prominent research pursuit. In this study, we present a one-step hydrothermal synthesis of N-doped MnO2 nanoflowers (NMF). NMF possess an extensive specific surface area and abundant oxygen vacancies, effectively mimicking the activity of natural laccase. Leveraging this laccase-like activity, NMF demonstrates the ability to catalyze various phenolic compounds, generating distinctive fingerprint signals. Notably, the developed colorimetric sensing array exhibits remarkable efficacy in effectively identifying and differentiating phenolic compounds within complex mixtures. Furthermore, the NMF colorimetric sensing array demonstrates successful identification of phenolic compounds in diverse environments, including food and urine samples. Overall, this study provides new insights into the design of transition metal materials for the simulation of laccase and colorimetric sensing arrays. It provides a promising avenue for the development of advanced detection platforms for phenolic compounds.

Near-infrared light activated and hybridization chain reaction cascaded CRISPR/Cas12a system under the enhancement of Mn2+ for intracellular biosensing

While CRISPR/Cas12a system is a potent in vitro fluorescence biosensing toolbox, several difficulties including collective biological delivery, potential pre-activation and inadequate sensitivity make it challenging to further perform intracellular application. Herein, we raise a series of solving strategies. First, MnO2 nanoflower is used to conjointly carry the biomolecular modules comprising CRISPR/Cas12a system through a simple physisorption to actualize an efficient endocytosis, after which the MnO2 matrix will be reduced by the widespread intracellular biothiols to not only release the surface attached biomolecules but also produce abundant Mn2+ to enhance trans-cleavage activity. Besides, a light activation conception realized by inserting the biosensing frame with a facile photocleave group is applied to achieve a controllable spatiotemporal behavior, for which the target recognition process will be manually initiated by illuminating with an ultraviolet upconversion luminescence converted from 808 nm near-infrared photons. By making usage of hybridization chain reaction to construct a final cascaded CRISPR/Cas12a system, the additional signal amplification design renders this newly-raised CRISPR/Cas12a system-mediated fluorescent biosensor has an ultra-sensitive detection ability for microRNA-21. Moreover, this special CRISPR/Cas12a system is also equipped with a high-efficiency imaging performance in live cells and even bodies, impelling the development of CRISPR system based biosensing techniques.

The Effect of Hydrothermal Temperature and Sample Thickness on the Synthesis of BaFe<sub>12</sub>O<sub>19</sub>@MnO<sub>2</sub> Core-Shell Composites

Advances in radar technology today are experiencing rapid development based on the latest findings that complement each other. BaFe12O19 is a type M hexagonal ferrite material as the best candidate for absorber material applications. Manganese dioxide (MnO2) is a transition metal that has a high dielectric loss and has the opportunity to increase the absorption of electromagnetic waves. The BaFe12O19@MnO2 core-shell composite produces the combined characteristics of BaFe12O19 and MnO2, which can improve performance as radar-absorbing material. The BaFe12O19@MnO2 core-shell composite is synthesized in two stages: molten salt synthesis in manufacturing BaFe12O19 as a core and hydrothermal synthesisto grow MnO2 nanoflowers as a shell. The research objective was to produce BaFe12O19@MnO2 core-shell composite for radar absorbing applications in the x-band with absorption of ~99%. In molten salt synthesis, using two calcination operations at 1000 °C for two hours to create BaFe12O19 as a template, then combining BaFe12O19 template with Fe2O3 and BaCl2.2H2O for eight hours at 1100 °C prepared for MnO2 pathways on the BaFe12O19 surface. Hydrothermal synthesis occurs by dissolving BaFe12O19 and KMnO4 in deionized water with a mass ratio of BaFe12O19 to KMnO4 is 1:1, followed by hydrothermal synthesisat a holding time of 12 hours with a temperature of 150 °C; 170 °C; 190 °C. Characterization of vector network analysis on a variation of sample thickness (1; 1.5; 2; 2.5; 3) mm were analyzed in the x-band frequency on 8-12 GHz. BaFe12O19@MnO2 core-shell composite was hydrothermally produced at 170 °C with a particle size of 197.1 nm, a thickness of 2.5 mm, and a reflection loss of -20.31 dB at 8.7 GHz. The absorber material from the combined synthesis of molten salt and hydrothermal synthesis to make BaFe12O19@MnO2 core-shell composite successfully produced microwave absorption up to 99.06%.

MnO2 nanoflowers based colorimetric and fluorescent dual-mode aptasensor for sensitive detection of aflatoxin B1 in milk

Aflatoxin B1 (AFB1) with tremendous toxic effects has caused a serious threat to food security. Accurate quantification of AFB1 in food can effectively prevent the risk of human intake of AFB1. Herein, a colorimetric and fluorescent dual-mode aptasensor for accurate and sensitive detection of AFB1 has been developed based on MnO2 nanoflowers (MnO2NFs) for the first time. MnO2NFs could catalyze the oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) into blue oxidation product (TMBox) by H2O2, which would be used for visible detection of AFB1. Simultaneously, MnO2NFs can be served as a signal amplifier and reduced by ascorbic acid to generate lots of Mn2+ which would quench the fluorescence of calcein for fluorescent detection of AFB1. Both colorimetric and fluorescent methods have been successfully applied for determination of AFB1 in milk samples with satisfactory results. The proposed dual-mode detection method with high detection sensitivity and accuracy showed great promise for monitoring AFB1 in food.

A braided flexible Zn–MnO2 yarn battery based on cobweb-like carbonized polypyrrole modified carbon fiber electrodes

Flexible zinc ion batteries (ZIBs) are promising candidates for energy storage devices because of high safety and low cost. Carbon fibers (CFs) are ideal current collectors for ZIBs due to their good flexibility, electrical conductivity and corrosion resistance. Herein, a novel CFs-based current collector is proposed. At first, the inertness and non-polarity of CFs were significantly modified by activating and etching to obtain a multi-layered porous structure. Thereafter, carbonized polypyrrole (CPPy) nanowire conductive networks were built up on etched carbon fibers (ECFs) by electrochemical in situ growth and carbonization. Based on the CPPy network, MnO2 nanoflowers were grown firmly by the hydrothermal method to construct multi-layer MnO2@CPPy@ECFs composite electrode. The multi-layered 3D CPPy conductive network is rooted in MnO2, providing a dedicated transmission path for both electrons and ions during electrochemical redox reactions. The MnO2@CPPy@ECFs electrode had an initial capacity of 346.1 mA h·g−1 at 0.1 A g−1 and 252.8 mA h·g−1 after 800 cycles. In addition, the integrated flexible Zn–MnO2 2D fabric battery with MnO2@CPPy@ECFs fabric cathode shows a specific capacity of 254.7 mA h·g−1 at 0.1 A g−1. Finally, a flexible Zn–MnO2 yarn battery with high flexibility, shape adaptability, structural integrity and good mechanical stability was fabricated by the 2D braid method. The initial specific capacity of the flexible Zn–MnO2 yarn battery is 111.7 mA h·g−1 at 0.1C, which also presents a remarkable volumetric energy density of 30.5 mW h cm−3. This work opens up a new pathway for the rational design of flexible electrodes for wearable ZIBs.