Heterojunction Nanoparticles Research Articles

Heterointerfacial engineering of N,P-doped carbon nanosheets supported Co/Co2P nanoparticles for boosting oxygen reduction and oxygen evolution reactions towards rechargeable Zn-air battery

Transition metal phosphides (TMPs) with high electrocatalytic activity for the oxygen evolution reaction (OER) are reckoned as a substitution of precious group metals catalysts in rechargeable Zn-air battery. In this work, Co/Co2P heterojunction nanoparticles supported N,P-doped carbon nanosheets (Co/Co2P@NPCNS) were designed and prepared via a facile one-step molten salt-assisted pyrolysis process. Density function theory calculations reveal that the heterogeneous interactions of Co/Co2P effectively enhance the bifunctional electrocatalytic activity for oxygen reduction reaction (ORR) and OER. The synergistic interaction between the Co/Co2P heterojunction nanoparticles with highly exposed active sites and excellent catalytic activity and the two-dimensional doped carbon nanosheets with high conductivity contributes to Co/Co2P@NPCNS exhibiting preeminent bifunctional ORR/OER activity and stability with a high half-wave potential for ORR (0.87 V), a low overpotential for OER (302 mV at 10 mA cm−2) and a low potential gap (0.66 V). The homemade rechargeable Zn-air battery performs high peak power density (187 mW cm−2) and exceptional endurance. This heterogeneous interface tactic of integrating TMPs with heteroatom-doped carbon materials may shed light on the research and development of non-precious metal electrocatalysts.

Investigation of UV-blocking and photon-down conversion characteristics of PMMA@ CH3NH3PbBr3:WO3 polymer nanocomposites

Herein, methyl ammonium lead bromide: Tungsten trioxide (CH3NH3PbBr3:WO3) nano heterojunction and polymethyl methacrylate (PMMA) polymer composite films of different weight percentage (wt%) proportions of CH3NH3PbBr3:WO3 nanoparticles (0, 0.5, 1.0, 1.5 and 2.0 wt%) were prepared. The structure, morphology and thermal features of CH3NH3PbBr3:WO3 heterojunctions and PMMA@CH3NH3PbBr3:WO3 nanocomposites were investigated using X-ray diffraction (XRD), Fourier Transform-Infrared (FTIR) spectroscopy, Scanning electron microscopy (SEM) and Differential scanning calorimetry (DSC) techniques. The characterization data revealed decrease in crystallinity (up to 7.97%) and glass transition temperature (Tg) with increase in the concentration of CH3NH3PbBr3:WO3 nanoparticles in PMMA nanocomposites. The UV-visible absorbance and transmittance data of PMMA nanocomposites recorded using UV-visible spectroscopy was used to mathematically deduct the optical characteristics such as absorption coefficient, optical band gap, refractive index, extinction coefficient, finesse coefficient, optical conductivity and Urbach energy. The deducted data revealed improved UV-shielding, refractive index and optical conductivity values while the optical band gap and Urbach energy was found to decrease with concentration of dopant. The experimental data of different PMMA@CH3NH3PbBr3:WO3 composite films showed excellent UV- blocking properties in the wider wavelength range of 259-322nm(4.80eV-3.850eV). The PMMA nanocomposites with 2.0 wt% CH3NH3PbBr3:WO3 filler composition exhibited highest UV-shielding behavior with maximum UV-absorption in the wavelength range of 260 to 300nm. The pristine PMMA films showed a PL emission peak at 410nm while the PMMA nanocomposites exhibited strong emissions in the wavelength range of 485-520nm. The observed hydrophobicity, redshift and longer lifetime decay of 34.3 ns for PMMA nanocomposites is attributed to the incorporated CH3NH3PbBr3:WO3 heterojunction nanoparticles. The chromaticity profile suggested that the emission color changed from blue to green as the filler dose of CH3NH3PbBr3:WO3 varied from 0 to 2.0 wt%. Additionally, the findings from the study reveal that incorporation of CH3NH3PbBr3:WO3 into the PMMA matrix enhances UV-absorption, optical conductivity, hydrophobicity, thermal stability, electrical conductivity and photon-down conversion properties of PMMA which make the material suitable for photonic, photovoltaic, optoelectronic and light emitting diode applications.

Ultrafast flowing oxidation reactions in the CoTiO3/TiO2 heterojunction assembled on ceramic membranes: Properties and electron shuttle mechanism

In this study, a novel catalytic ceramic membrane (CCM) applied to couple peroxymonosulfate (PMS) to degrade organic pollutants in wastewater were synthesized by sol–gel method. The CCM was surface-loaded by CoTiO3/TiO2 heterojunction nanoparticles as catalytic layer, achieving an instantaneous oxidation efficiency of 90 % for bisphenol A (BPA, 10 mg/L). The electron shuttle process in the CoTiO3/TiO2 heterojunction was confirmed by theoretical calculations, and strong adsorption (Eads = -5.28 eV) was observed between catalysts and PMS. Differential charge density further suggested the trend of electron transfer from the catalytic layer to the vicinity of PMS, causing an elongation of the peroxy bond of PMS from 1.482 Å to 1.794 Å, which led to the generation of SO4•− and ·OH. Typical non-radical featured by 1O2 was also found in the membrane-base catalytic oxidation system. Finally, the degradation pathways of BPA were elucidated, and the toxicities of degradation products were found to be decreased significantly. The CoTiO3/TiO2 heterojunction modified CCMs couple with PMS could form an efficient synergistic coupling system, which has excellent oxidation to various organic pollutants. This research on the properties and mechanism of the CCMs could provide technical and theoretical backing for efficient oxidation treatment of dissolved organic pollutants in wastewater.

Electronic modulation on allotropic Co2P/CoP heterojunctions with N, P co-doped porous carbon matrix through metal-injection toward high-efficiency water splitting

The interfacial electron modulation of electrocatalysts is a useful technique for promoting catalyst performance for the water-related dissociation reactions. Herein, a high-efficient Fe-doped allotropic Co2P/CoP heterojunction nanoparticles embedded in N, P co-doped carbon matrix was constructed. The intense electrical interfacial contacts between the allotropic heterojunction optimized the reaction kinetics by boosting efficient charged active centers, regulating the intermediate adsorption/desorption. The incorporation of Fe atoms further enhancing the heterointerface contact between CoP and Co2P by providing favorable electronic properties and special coordination environment, causing the interfacial coupling enhancement. Therefore, Fe-Co2P/CoP possesses outstanding performance in both hydrogen evolution reaction and oxygen evolution reaction, with small overpotentials of 174 mV and 286 mV at 10 mA·cm−2 in alkaline medium, respectively. And only 1.71 V battery voltage is needed for the Fe-Co2P/CoP (+, −) cell device with satisfactory durability. This finding provides valuable insights into the engineering of electronic structures of well-designed metal phosphides for water electrolysis.

Facile Synthesis of Organic-Inorganic Hybrid Heterojunctions of Glycolated Conjugated Polymer-TiO2-X for Efficient Photocatalytic Hydrogen Evolution.

The utilization of the organic-inorganic hybrid photocatalysts for water splitting has gained significant attention due to their ability to combine the advantages of both materials and generate synergistic effects. However, they are still far from practical application due to the limited understanding of the interactions between these two components and the complexity of their preparation process. Herein, a facial approach by combining a glycolated conjugated polymer with a TiO2-X mesoporous sphere to prepare high-efficiency hybrid photocatalysts is presented. The functionalization of conjugated polymers with hydrophilic oligo (ethylene glycol) side chains can not only facilitate the dispersion of conjugated polymers in water but also promote the interaction with TiO2-X forming stable heterojunction nanoparticles. An apparent quantum yield of 53.3% at 365nm and a hydrogen evolution rate of 35.7mmol h-1 g-1 is achieved by the photocatalyst in the presence of Pt co-catalyst. Advanced photophysical studies based on femtosecond transient absorption spectroscopy and in situ, XPS analyses reveal the charge transfer mechanism at type II heterojunction interfaces. This work shows the promising prospect of glycolated polymers in the construction of hybrid heterojunctions for photocatalytic hydrogen production and offers a deep understanding of high photocatalytic performance by such heterojunction photocatalysts.

Constructing heterojunction on N-doped porous carbon nanofibers for Li-S batteries: Effect of built-in electric field on efficient catalytic transformation kinetics

In this study, the CoP-Co2P heterojunction nanoparticles embedded in N-doping porous carbon nanofibers (CoP-Co2P/NPCNFs) are designed and prepared. The highly conductive grid of NPCNFs can physically confining lithium polysulfide (LiPS) and provide facilitated channels for Li+ transport. Furthermore, due to the spontaneous built-in electric field (BIEF) based on at the formed heterogeneous interfaces of CoP-Co2P, the heterojunction can significantly catalyze bi-directional conversion of LiPS and chemically adsorb LiPS which confirmed by the DFT calculations, suppressing the “shuttle effect” of LiPS. Thus, the Li-S batteries with the CoP-Co2P/NPCNFs modified separators exhibit a high initial specific capacity of 1322.86 mAh g−1 at 1 mA cm−2 and stable 695 cycles with a low decay rate (0.069 %). More importantly, the assembled pouch cell also can run with ultra-low specific capacity decay rate. Additionally, the pouch battery can also be applied to the operation of fans, temperature and humidity meters, mobile phone charging, etc.

Delocalizing Excitation for Highly‐Active Organic Photovoltaic Catalysts

AbstractLocalized excitation in traditional organic photocatalysts typically prevents the generation and extraction of photo‐induced free charge carriers, limiting their activity enhancement under illumination. Here, we enhance delocalized photoexcitation of small molecular photovoltaic catalysts by weakening their electron‐phonon coupling via rational fluoro‐substitution. The optimized 2FBP‐4F catalyst we develop here exhibits a minimized Huang–Rhys factor of 0.35 in solution, high dielectric constant and strong crystallization in the solid state. As a result, the energy barrier for exciton dissociation is decreased, and more importantly, polarons are unusually observed in 2FBP‐4F nanoparticles (NPs). With the increased hole transfer efficiency and prolonged charge carrier lifetime highly related to enhanced exciton delocalization, the PM6 : 2FBP‐4F heterojunction NPs at varied concentration exhibit much higher optimized photocatalytic activity (207.6–561.8 mmol h−1 g−1) for hydrogen evolution than the control PM6 : BP‐4F and PM6 : 2FBP‐6F NPs, as well as other reported photocatalysts under simulated solar light (AM 1.5G, 100 mW cm−2).

Interfacial Electronic Interactions Between Ultrathin NiFe-MOF Nanosheets and Ir Nanoparticles Heterojunctions Leading to Efficient Overall Water Splitting.

Creating specific noble metal/metal-organic framework (MOF) heterojunction nanostructures represents an effective strategy to promote water electrolysis but remains rather challenging. Herein, a heterojunction electrocatalyst is developed by growing Ir nanoparticles on ultrathin NiFe-MOF nanosheets supported by nickel foam (NF) via a readily accessible solvothermal approach and subsequent redox strategy. Because of the electronic interactions between Ir nanoparticles and NiFe-MOF nanosheets, the optimized Ir@NiFe-MOF/NF catalyst exhibits exceptional bifunctional performance for the hydrogen evolution reaction (HER) (η10 = 15mV, η denotes the overpotential) and oxygen evolution reaction (OER) (η10 = 213mV) in 1.0m KOH solution, superior to commercial and recently reported electrocatalysts. Density functional theory calculations are used to further investigate the electronic interactions between Ir nanoparticles and NiFe-MOF nanosheets, shedding light on the mechanisms behind the enhanced HER and OER performance. This work details a promising approach for the design and development of efficient electrocatalysts for overall water splitting.

In Situ injectable photo-crosslinking hydrogel with heterojunction nanoparticles for dual-channel synergistic disinfection and cutaneous regeneration in diabetic chronic wound healing

Recurrent inflammation, intense bacterial infections, and inadequate blood vessel growth make diabetic wounds non-healing. Under pathological environment, cellular functions are also inhibited. In this paper, we developed a novel in situ injectable photo-crosslinking hydrogel embedded with heterojunction Ag@ZnO nanoparticles (NPs) which exhibit dual-channel synergistic ion release and reactive oxygen species (ROS) production for anti-bacteria and cutaneous regeneration. This novel hydrogel platform can be introduced onto any irregular wound and form gelation with 395 nm UV light irradiation in only 5 s. After being affixed to the wound, Ag+ and Zn2+ can be released as the first interaction for wound healing. Foremost, the heterojunction formed on interface of Ag and ZnO has the ability to capture oxygen and water to instigate the generation of a “ROS storm”, which can disrupt the structural integrity of bacteria, trigger the leakage of bacterial cytoplasmic content, enhance angiogenesis by activating VEGF and CD31 expression, and stimulate the steps of wound healing. The continuous release of Ag+, Zn2+ and “ROS storm” collaboratively drive bacterial deactivation, suppress inflammation, promote cellular proliferation, collagen deposition and angiogenesis. These effects significantly accelerate diabetic chronic wounds healing. Therefore, such dual-channel synergistic hydrogel platform might provide a promising new insight to diabetic chronic wound treatment.

Co/CoO heterojunction rich in oxygen vacancies introduced by O2 plasma embedded in mesoporous walls of carbon nanoboxes covered with carbon nanotubes for rechargeable zinc–air battery

AbstractHerein, Co/CoO heterojunction nanoparticles (NPs) rich in oxygen vacancies embedded in mesoporous walls of nitrogen‐doped hollow carbon nanoboxes coupled with nitrogen‐doped carbon nanotubes (P–Co/CoOV@NHCNB@NCNT) are well designed through zeolite‐imidazole framework (ZIF‐67) carbonization, chemical vapor deposition, and O2 plasma treatment. As a result, the three‐dimensional NHCNBs coupled with NCNTs and unique heterojunction with rich oxygen vacancies reduce the charge transport resistance and accelerate the catalytic reaction rate of the P–Co/CoOV@NHCNB@NCNT, and they display exceedingly good electrocatalytic performance for oxygen reduction reaction (ORR, halfwave potential [EORR, 1/2 = 0.855 V vs. reversible hydrogen electrode]) and oxygen evolution reaction (OER, overpotential (ηOER, 10 = 377 mV@10 mA cm−2), which exceeds that of the commercial Pt/C + RuO2 and most of the formerly reported electrocatalysts. Impressively, both the aqueous and flexible foldable all‐solid‐state rechargeable zinc–air batteries (ZABs) assembled with the P–Co/CoOV@NHCNB@NCNT catalyst reveal a large maximum power density and outstanding long‐term cycling stability. First‐principles density functional theory calculations show that the formation of heterojunctions and oxygen vacancies enhances conductivity, reduces reaction energy barriers, and accelerates reaction kinetics rates. This work opens up a new avenue for the facile construction of highly active, structurally stable, and cost‐effective bifunctional catalysts for ZABs.

Surface oxygen vacancy engineering of Cr-doped FeNi3/NiFe2O4 Mott-Schottky heterojunction as efficient electrocatalyst for high current density water oxidation

The defect engineering at the surface by filling of oxygen vacancies during OER causing surface reconstruction is considered to be a unique way to boost up intrinsic electrocatalytic activity, especially towards oxygen evolution reaction (OER) mechanism. The present study aimed creation of large number of oxygen vacancies by Cr-doping into FeNi3/NiFe2O4 Mott-Schottky heterojunction electrocatalyst causing much desirable surface engineering and electronic modulation in favour of OER activity. The optimized heterojunction nanoparticles exhibited an excellent catalytic activity with low overpotential of 246 mV at the current density of 20 mA cm−2 with low Tafel slope value of 55 mV dec−1 for OER. Such oxygen vacancy-aided surface reconstruction during OER demonstrated an outstanding durability over 200 h even at high current density of 1000 mA cm−2 in 1 M KOH electrolyte. The surface oxygen vacancy engineering with the help of ex-situ Raman spectroscopy at different anodic potentials reveals the filling of vacancies and generation of MOOH as surface reconstruction of electrocatalyst during OER, also supported by XPS, TEM and EELS analyses.

A photocatalyst with an enhanced Schottky effect and an efficient electron-transfer channel fabricated by assembling Ni–WC heterojunction nanoparticles on g-C3N4 for highly efficient removal of chlorophenols

An enhanced Schottky effect and efficient electron-transfer channel in Ni–WC/CN enable the efficient separation and transfer of photoexcited electrons, which boosts efficient photocatalytic degradation of toxic 4-chlorophenol.

Impact of water solvation on the charge carrier dynamics of organic heterojunction photocatalyst nanoparticle dispersions.

Organic heterojunction nanoparticles (NP) have recently gained significant interest as photocatalysts for visible light-driven hydrogen production. Whilst promising photocatalytic efficiencies have been reported for aqueous NP dispersions, the underlying dynamics of photogenerated charges in such organic heterojunction photocatalysts and how these might differ from more widely studied dry heterojunction films remain relatively unexplored. In this study, we combine transient optical spectroscopies over twelve orders of magnitude in time, using pulsed and continuous light illumination, to elucidate the differences in the charge carrier dynamics of heterojunction NP dispersions, dried NP films, and bulk heterojunction films prepared by spin coating. The ultrafast fast (ps to ns) transient absorption results show efficient charge generation and indistinguishable nanosecond charge recombination decay kinetics of separated charges in all three samples. In contrast, on the slower μs to ms time range, the decay kinetics of heterojunction NP dispersion exhibited up to 15-fold larger amplitude and more than one order of magnitude slower decay of the photogenerated charges than those in films. The analysis of the nanomorphology, NP surfactant, polymer residual metal content and local polar environment suggest that the longer lifetime differences (in ms) in the charge recombination in NP dispersion are mostly associated with a charge carrier stabilisation on a shallow density of states on the NP surface of ∼350 meV by interaction with local water environment, resulting in suppressed charge recombination. The lengthening of NP dispersion charge carrier lifetime is discussed regarding the energetic loss for function and their implications in photocatalysis.

Synthesis and characterization of lamellar-like Cu2(OH)3NO3 nanosheets integrated with Mg(OH)2 nanoparticles heterojunction for photocatalytic activity

Synthesis and characterization of lamellar-like Cu2(OH)3NO3 nanosheets integrated with Mg(OH)2 nanoparticles heterojunction for photocatalytic activity

Oleyl Phosphate-Modified Crystalline-Amorphous TiO2/Ce2O3 heterojunction nanoparticles with significantly reduced photocatalytic activity as stable UV-Shielding fillers

As a stable and inexpensive UV-absorber, TiO2 is widely used in UV-shielding products. However, its poor compatibility with matrix polymers and photocatalytic degradation hazard still limit its performance. Herein, we construct the crystalline-amorphous TiO2/Ce2O3 heterojunctions with an average size of 15 nm via an in-situ solvothermal process, significantly reducing the photocatalytic activity through the carrier redistribution between TiO2 and Ce2O3. In the photocatalytic experiments for the degradation of three dyes (RhB, MB, and RR-120), the apparent reaction rate constants (k) of the optimal sample TiO2/Ce2O3-3 % are 33.92, 28.54, and 24.78 times lower than those of pure TiO2, respectively. The characterizations and theoretical calculations together reveal that the photogenerated carriers accumulate on the amorphous Ce2O3 with rich defects, promoting the recombination of electron-hole pairs and reducing the carriers’ redox potential. Additionally, oleyl phosphate (OP) is used for surface modification to achieve TiO2/Ce2O3 organic solvent-dispersible and improve its compatibility with matrix polymers, thus the UV-shielding OP-TiO2/Ce2O3/fluorocarbon hybrid coating is prepared with high transparency.

Bioinspired supramolecular arrayed heterojunction-based room-temperature sensor for high-performance gas detection

Nitrogen dioxide (NO2) has been severely polluting the atmosphere and deteriorating human beings’ sustainable lives. Therefore, development of gas sensors for high-selectivity and high-sensitivity detection of NO2 has been attracting increasing attention. The state-of-the-art inorganic NO2 gas sensors require harsh fabrication conditions or toxic materials, making the devices intrinsically eco-unfriendly. Furthermore, in most cases the sensors work at high temperatures. These disadvantages severely impede their practical applications. Herein, we report a room-temperature and highly-integrated NO2 sensor composed of p-type self-assembled peptide fibrillar nanoforests (SPNFs) scaffolded with n-type SnO2 nanoparticles (NPs) heterojunctions. The p-n conformations provide efficient access to target gases and allow reliable electron transformations, while the SPNFs afford a large specific surface area and multiporous structures for gas adsorption and SnO2 NPs dispersion, resulting in an ultrahigh selectivity for NO2 detection. Especially, the sensing performance can be optimized by modulating the thickness and density of the SPNFs, showing a high response, short response and recovery times, along with a low detection limitation. Our strategy demonstrates the development of a bioinspired platform by utilizing peptide self-assemblies to fabricate integrated sensors for polluting gas detections.

Molecular Structure Engineering toward Enhanced Photocatalytic Hydrogen Evolution and Stability of Organic Heterojunction Nanoparticles

Molecular Structure Engineering toward Enhanced Photocatalytic Hydrogen Evolution and Stability of Organic Heterojunction Nanoparticles

Supercritical carbon dioxide-assisted TiO2/g-C3N4 heterostructures tuning for efficient interfacial charge transfer and formaldehyde photo-degradation

Long exposure to formaldehyde has been a concern for causing respiratory problems and TiO2/g-C3N4 composite is a potential choice to address this issue. This study developed a supercritical carbon dioxide (ScCO2)-assisted method to fabricate TiO2/g-C3N4 composites with two distinct heterostructures. The g-C3N4 nanosheet/TiO2 nanoparticle (denoted as type 1 heterostructure) heterojunction could accelerate electron migration because of its large interfacial surface contact. The ternary TiO2{101}/g-C3N4/TiO2{001} heterojunction (denoted as type 2 heterostructure) was synthesized for the first time, further promoting the separation of photogenerated electron/hole pairs under full-spectrum irradiation because it provided an additional migration channel for photocarriers. By loading different amounts of TiO2, the heterostructures were modulated, thereby influencing the photoactivity of the composites. The TiO2/g-C3N4 composite with 58% TiO2 loading possessed the best photocatalytic performance, achieving the highest rate constant for formaldehyde degradation, approximately 7 times higher than pure bulk g-C3N4 under either visible or full-spectrum light. Under full-spectrum irradiation, the maximum decomposition rate approached nearly 100% within 90 min. The tuned heterostructures facilitated the generation of O2·− and·OH, which were dominant active oxygen radicals responsible for formaldehyde removal under light irradiation. Thus, this study developed a green route to synthesize composites with tunable heterojunctions and enhanced photocatalytic activity that can be used for indoor air pollutant degradation.

DNA Damage of Iron-Gold Nanoparticle Heterojunction Irradiated by kV Photon Beams: A Monte Carlo Study

This study aims to evaluate the dependence of DNA damage on the proportion of iron and gold in iron-gold nanoparticle heterojunctions using Monte Carlo simulations. The simulation setup included a spherical nanoparticle with varying percentages of iron and gold, irradiated by photon beams of different energies (50–150 keV). The Geant4-DNA Monte Carlo code was utilized for the accurate tracking of radiation transport. The results reveal that DNA damage increases with a higher percentage of gold volume in the heterojunction, primarily due to photoelectric enhancement. Furthermore, a lower photon beam energy of 50 keV induces greater DNA damage compared to energies of 100 keV and 150 keV. The findings suggest that for effective cancer cell eradication through DNA damage, the gold volume should be equal to or greater than 50% in the iron-gold nanoparticle heterojunction. In conclusion, the findings from this study will shed light on the potential of iron-gold nanoparticle heterojunctions in enhancing radiotherapy outcomes. The investigation of DNA damage resulting from the combination of contrast agents and radiosensitizers is crucial for advancing cancer research and treatment. The knowledge gained from this research will aid in the development of personalized and effective radiotherapy approaches, ultimately improving patient outcomes in cancer treatment.

Constructing bimetallic heterostructure as anodes for sodium storage with superior stability and high capacity

Heterostructure materials hold promise as future-generation anodes for sodium-based energy storage. However, the complexity and time-intensity of heterojunction fabrication processes limit their large-scale application. This study utilizes an ultrafast, one-step microwave process to successfully design and fabricate bimetallic selenides heterojunction nanoparticles, anchored on a three-dimensional porous carbon substrate (NiSe2–SnSe2/C). The in-situ formation of NiSe2–SnSe2 heterostructure optimizes sodium ion adsorption and transfer, which facilitates reaction kinetics and subsequently improves both the rate capability and cycle life. The NiSe2–SnSe2/C electrodes demonstrate a high-rate capability (719.8 mAh g−1 at 0.1 A g−1, and 667.9 mAh g−1 after a 50-fold increase in current density to 5 A g−1), maintaining high stability even after 10,000 cycles at 5 A g−1. The impact of the NiSe2–SnSe2 heterostructure on reaction kinetics was examined using density functional theory. The NiSe2–SnSe2/C anode, when coupled with the Na3V2(PO4)3 cathode in a full battery, demonstrated an impressive energy density of 155 Wh kg−1. This work exemplifies an ultrafast synthetic method for constructing heterostructure materials having great rate, high capacity and strong stability for sodium storage, making them promising candidates for large-scale energy storage applications.