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Polaritons in polar biaxial crystals with extreme anisotropy offer a promising route to manipulate nanoscale light-matter interactions. The dynamical modulation of their dispersion is great significance for future integrated nano-optics but remains challenging. Here, we report a momentum-directed strategy, a coupling between the modes with extra momentum supported by the interface and in-plane hyperbolic polaritons, to tailor topological transitions of anisotropic polaritons in biaxial crystals. We experimentally demonstrate such tailored polaritons at the interface of heterostructures between graphene and {\alpha}-phase molybdenum trioxide ({\alpha}-MoO3). The interlayer coupling can be electrically modulated by changing the Fermi level in graphene, enabling a dynamic topological transition. More interestingly, we found that the topological transition occurs at a constant Fermi level when tuning the thickness of {\alpha}-MoO3. The momentum-directed strategy implemented by interface engineering offers new insights for optical topological transitions, which may shed new light for programmable polaritonics, energy transfer and neuromorphic photonics.

Self-trapped excitons (STEs) have attracted tremendous attention due to their intriguing properties and potential optoelectronic applications. STEs are formed from the lattice distortion induced by the strong electron (exciton)-phonon coupling in soft semiconductors upon photoexcitation, which features in broadband photoluminescence (PL) emission spectra with a large Stokes shift. Recently, significant progress has been achieved in this field but many remain challenges that need to be solved, including the understanding of the underlying physical mechanism, tuning of the performance, and device applications. Along these lines, for the first time, systematic experimental characterizations and advanced theoretical calculations are presented in this review to shed light on the physical mechanism. The possibility of tuning the STEs through multiple degrees of freedom is also presented, along with an overview of the STE-based emerged applications and future research perspectives.

This paper shows a new classification of preparing biomass-based porous carbon materials. The design of high-performance biomass-based porous carbon materials and their recent progress in the field of supercapacitors are reviewed.

Advances in the optoelectronics and information industries have allowed modern electronic devices to undergo a continuous trend toward miniaturization and integration, which poses significant chall...

In this paper, a simple "one-step" route is introduced to prepare a kind of novel honeycomb-like hierarchical porous carbon (h-HPC) by carbonizing and activating garlic seeds. Due to its special microstructure, h-HPC shows excellent electrochemical properties and high supercapacitor performances. The experimental results reveal the following: (1) There exists an optimal condition for synthesizing h-HPC, i.e., 700 °C carbonization temperature and 1:1 mass ratio of KOH and garlic seeds. (2) h-HPC has a three-dimensional interconnected porous structure and exhibits a specific surface area as high as 1417 m2/g with a narrow pore size distribution. (3) When h-HPC is employed as an electrode material in supercapacitors, its specific capacitance reaches a value up to 268 F/g at a current density of 0.5 A/g and excellent rate capability. (4) The h-HPC-based symmetric supercapacitor shows a high energy density of 31.7 Wh/kg at a power density of 500 W/kg and retains 99.2% of the initial capacitance after 10,000 charge/discharge cycles at 200 mV/s. When compared with similar works, these data are competitive, which demonstrates that the garlic-derived h-HPC is a kind of promising electrode material for the next-generation high-energy-density supercapacitors.

Highlights A comprehensive review of the recent development of two-dimensional (2D) PtSe2 synthesis strategies has been extensively surveyed.The applications of 2D PtSe2 materials in areas, including opto/electric devices, photocatalysis, hydrogen evolution reaction, and sensors, have been reviewed.Current challenges in the development of 2D PtSe2 materials are identified, and outlooks toward unexplored research areas are suggested., In recent years, emerging two-dimensional (2D) platinum diselenide (PtSe2) has quickly attracted the attention of the research community due to its novel physical and chemical properties. For the past few years, increasing research achievements on 2D PtSe2 have been reported toward the fundamental science and various potential applications of PtSe2. In this review, the properties and structure characteristics of 2D PtSe2 are discussed at first. Then, the recent advances in synthesis of PtSe2 as well as their applications are reviewed. At last, potential perspectives in exploring the application of 2D PtSe2 are reviewed.

Supercapacitor electrodes based on carbonaceous materials with hierarchical porosity and localized graphitic structure can help supercapacitors to achieve considerable energy capacity. In this work...

A simple and effective process has been reported to prepare the silver (Ag)/graphene composite with excellent mechanical and electrical properties based on high-quality graphene (HQG). The HQG was fabricated via hot pressing of reduced graphene oxide (RGO) from chemical exfoliation, while the Ag/HQG composite was obtained by using spark plasma sintering (SPS) treatment under high temperature (1500 °C) and moderate pressure (40 MPa). With low oxygen-containing functional groups and defect density, the HQG dispersed homogeneously in the composite after high-energy ball milling. In comparison to pure Ag, the as-prepared Ag/RGO composite exhibited a great enhancement of 11% electrical conductivity and 42% micro-hardness with an optimal RGO adding content (1 wt%). The Ag/HQG composite is expected to open up a new way for the novel Ag-based electrical contact materials, and further to broaden its applications in micro-electronics and switching power. Keywords: Graphene, Silver, Composite, Electrical property, Mechanical property

In this study, a novel brick-like NiCo2O4 material was synthesized via a facile hydrothermal method. The as-prepared NiCo2O4 material possessed high porosity with the BET specific surface area of 58.33 m2/g, and its pore size distribution was in a range of 5–15 nm with a dominant pore diameter of 10.7 nm. The electrochemical performance of the NiCo2O4 was further investigated as anode material for lithium-ion battery. The NiCo2O4 anode possessed a high lithium storage capacity up to 2353.0 mAh/g at the current density of 100 mA/g. Even at the high rate of 1 A/g, a reversible capacity of ∼600 mAh/g was still retained, and an average discharge capacity of ∼1145 mAh/g could be recovered when the current density was reduced back to 150 mA/g. Due to the simple and cost-effective process, the NiCo2O4 bricks anode material shows great potential for further large-scale applications on the area of lithium-ion battery.

The electrochemical performance of lithium ion batteries depend largely on the structural properties of electrode materials. In this work, we propose an approach to synthesize lithium-rich layered oxides (LLOs) materials using a manganese dioxide (MnO2) template strategy, which could control the structure and particle size of final products via choosing different MnO2 templates. Through precisely optimizing, we successfully prepare cross-linked nanorods (CLNs) and agglomerate microrods (AMs) Li1.2Ni0.15Co0.1Mn0.55O2 cathode materials by using carbon-decorated MnO2 nanowires and MnO2 nanorods as templates, respectively. The lithium ion battery based on the CLNs exhibits excellent performance, delivering a high capacity of 286.2 mAh g−1 at 0.1 C and 237.5 mAh g−1 at 1 C. In addition, the device remains 98% and 89% of its initial capacity after 50 cycles at 0.1 C and 100 cycles at 1 C, respectively. The remarkable electrochemical performance can be mainly attributed to the cross-linked nanorods structure which can provide relatively shorter lithium ion diffusion length, larger reaction surface and more internal cavity. This universal structure engineering strategy may shed light on new material structures for high performance lithium-rich layered oxide cathode materials.

Poly(3,4-ethylenedioxythiophene)poly(styrenesulfonate)/carbon nanotube (PEDOT:PSS/CNTs) composite films have been demonstrated to offer an excellent thermoelectric performance. In this work, p-type thermoelectric films prepared by a simple dipping coating process based on the carbon-coated carbon nanotubes (C-CNTs) continuous network are investigated. The highest power factor obtained in this work is 504.8 μW/mK2 (at 300 K) due to the relatively high electrical conductivity and Seebeck coefficient. The excellent TE properties of the C-CNTs/PEDOT:PSS composite film are attributed to the interfacial carrier scattering introduced by the unique structure. Composite materials based on a continuous network would open up new opportunities to develop high performance organic thermoelectric materials.

An inorganic caesium cation was incorporated into perovskite to improve the performance and stability of solar cells with a hole-transport-material free structure in ambient air. A triple cation device with a champion power conversion efficiency of over 15% was achieved, exhibiting superior thermal, long-term and operational stabilities.

Field-effect transistors (FETs) have tremendous applications in the electronics industry due to their outstanding features such as small size, easy fabrication, compatibility with integrated electronics, high sensitivity, rapid detection and easy measuring procedures. However, to meet the increasing demand of the electronics industry, efficient FETs with controlled short channel effects, enhanced surface stability, reduced size, and superior performances based on low-dimensional materials are desirable. In this review, we present the developmental roadmap of FETs from conventional to miniaturized devices and highlight their prospective applications in the field of optoelectronic devices. Initially, a detailed study of the general importance of bulk and low-dimensional materials is presented. Then, recent advances in low-dimensional material heterostructures, classification of FETs, and the applications of low-dimensional materials in field-effect transistors and photodetectors are presented in detail. In addition, we also describe current issues in low-dimensional material-based FETs and propose potential approaches to address these issues, which are crucial for developing electronic and optoelectronic devices. This review will provide guidelines for low-dimensional material-based FETs with high performance and advanced applications in the future.

van der Waals (vdW) transition metal oxides have attracted extensive attention due to their intriguing physical and chemical properties. However, primary drawbacks of these materials are the lack of band structure tunability and substandard optical properties, which severely hinder their implementation in nanophotonic applications. Atomic intercalation is an emerging structural engineering approach for two-dimensional vdW materials to engineer the atomic structure and modify the optical properties, thereby broadening their range of applications. Herein, we synthesized tin-intercalated ultrathin α-MoO3 (Sn-MoO3) nanoribbons via chemical intercalation method and then investigated the broadband nonlinear optics (NLO) of stable few-layer α-MoO3 by performing a Z-scan laser measurement and femtosecond-resolved transient absorption (TA) spectroscopy. Sn-MoO3 showed a stable structure of Mo-O-Sn-O-Mo and a shorter relaxation time than pristine MoO3, indicating the accelerated recombination process of electrons and holes. Furthermore, Sn-MoO3 nanoribbons were used as an optical saturable absorber for ultrafast photonics; a highly stable femtosecond laser with a pulse width of 467 fs was generated from a single-mode fiber in the telecommunication band (1550 nm). These results indicate that atomic intercalation is an effective way to modulate the band structure and nonlinear optical properties of α-MoO3, which hold a great potential in the generation of ultrafast mode-locked laser pulses for optical communication technologies.

The photocatalytic performance of heterostructure photocatalysts is limited in practical use due to the charge accumulation at the interface and its low efficiency in utilizing solar energy during photocatalytic process. In this work, a ternary hierarchical TiO2 nanorod arrays/graphene/ZnO nanocomposite is prepared by using graphene sheets as bridge between TiO2 nanorod arrays (NRAs) and ZnO nanoparticles (NPs) via a facile combination of spin-coating and chemical vapor deposition techniques. The experimental study reveals that the graphene sheets provide a barrier-free access to transport photo-excited electrons from rutile TiO2 NRAs and ZnO NPs. In addition, there generates an interface scattering effect of visible light as the graphene sheets provide appreciable nucleation sites for ZnO NPs. This synergistic effect in the ternary nanocomposite gives rise to a largely enhanced photocurrent density and visible light-driven photocatalytic activity, which is 2.6 times higher than that of regular TiO2 NRAs/ZnO NPs heterostructure. It is expected that this hierarchical nanocomposite will be a promising candidate for applications in environmental remediation and energy fields.

Limited by the Boltzmann distribution of electrons, the sub-threshold swing (SS) of conventional MOSFETs cannot be less than 60 mV dec−1. This limitation hinders the reduction of power dissipation of the devices. Herein, we present high-performance In2O3 nanowire (NW) negative capacitance field-effect transistors (NC-FETs) by introducing a ferroelectric P(VDF-TrFE) layer in a gate dielectric stack. The fabricated devices exhibit excellent gate modulation with a high saturation current density of 550 μA μm−1 and an outstanding SS value less than 60 mV dec−1 for over 4 decades of channel current. The assembled inverter circuit can demonstrate an impressive voltage gain of 25 and a cut-off frequency of over 10 MHz. By utilizing the self-aligned fabrication scheme, the device can be ultimately scaled down to below 100 nm channel length. The devices with 200 nm channel length exhibit the best performances, in which a high on/off current ratio of >107, a large output current density of 960 μA μm−1 and a small SS value of 42 mV dec−1 are obtained at the same time. All these would not only evidently demonstrate the potency of NW NC-FETs to break through the Boltzmann limit in nanoelectronics, but also open up a new avenue to low-power transistors for portable products.

Carbon materials have attracted great attention for their diversified applications in supercapacitors, and different structures of carbon have been reported to exhibit dissimilar electrochemical properties. In the past, activated carbons, carbon nanotubes (CNTs), carbon nanofibers and graphene have been shown to have excellent electrochemical performances, but it still remains a problem on how to improve the capacitance of carbon-based materials effectively from the viewpoint of their giant commercial potential. Noticing that connecting chemical groups to carbon can provide large pseudo-capacitance, we hereby demonstrated that the position of the chemical groups also plays an important role in the pseudo-capacitance. In our work, we synthesized graphene nanoribbon (GNR), graphene oxide (GO) and functional MWCNTs and showed that GNR has larger capacitance (calculated to be 202 F/g at a scan rate of 5 mV/s) and energy density compared to CNTs and GO when using as electrode materials. Furthermore, the supercapacitor device based on as-synthesized GNR exhibits excellent cycle stability and rate capability which evident is potential in high performance supercapacitor. Revealing the source of the capacitance, we found that though GNR has less oxygen-containing groups, it has larger pseudo-capacitance than GO and CNTs due to the remarkable edge-riched structure with high activity in electrochemical reactions. This finding highlights the importance of edge structure in carbon-based pseudo supercapacitor and suggests a new insight for the development of pseudo-capacitance electrode materials.

Sensitivity, durability, and multifunction are the essential requirements for a high-performance wearable sensor. Here, we report a novel multifunctional sensor with high sensitivity and durability by using a buckled spider silk-like single-walled carbon nanotubes (SSL-SWNTs) film as the conducting network and a crack-shaped Au film as the sensitive transducer. Its high sensitivity is inspired by the crack-shaped structure of the spider's slit organs, while the high durability is inspired by the mechanical robustness of the spider silk. Similar to the spider's slit organs that can detect slight vibrations, our sensor also exhibits a high sensitivity especially to tiny strain. The proposed quantum tunneling model is consistent with experimental data. In addition, this sensor also responds sensitively to temperature with the sensitivity of 1.2%/°C. Because of the hierarchical structure like spider silk, this sensor possesses combined superiority of fast response (60 ms) and high durability (10 000 cycles). We also fabricate a wearable device for monitoring various human physiological signals. It is expect that this high-performance sensor will have wide potential applications in intelligent devices, fatigue detection, body monitoring, and human-machine interfacing.

Supercapacitor is a newly-developed device for electrochemical energy storage with high power density, long life span, as well as rapid capture and storage of energy. Carbon-based materials, from carbon nanospheres, nanotubes and nanofibers to graphene, are the most commonly used electrode materials for supercapacitors. Our group has engaged in the research of carbon nanomaterials over the past decade. Herein we summarize some typical carbon nanomaterials and their synthetic routes based on our published works, which is expected to provide the theoretical and experimental basis for further applications on carbon-based energy storage devices.

Supercapacitor is a new type of energy-storage device, and has been attracted widely attentions. As a two dimensional (2D) nanomaterials, graphene is considered to be a promising material of supercapacitor because of its excellent properties involving high electrical conductivity and large surface area. In this paper, the large-scale graphene is successfully fabricated via environmental-friendly electrochemical exfoliation of graphite, and then, the three dimensional (3D) graphene foam is prepared by using nickel foam as template and FeCl 3 /HCl solution as etchant. Compared with the regular 2D graphene paper, the 3D graphene foam electrode shows better electrochemical performance, and exhibits the largest specific capacitance of approximately 128 F/g at the current density of 1 A/g in 6 M KOH electrolyte. It is expected that the 3D graphene foam will have a potential application in the supercapacitors.

The amount of graphene (Gr) in a composite plays a key role in enhancing the performance of the composite. In general, an indirect method, that is, by adjusting the concentration of Gr (or GO) in the electrolyte, is used to study the influence of the graphene content on the properties of copper (Cu)–Gr composite foil. In this paper, we firstly propose a direct and accurate approach, that is, by using an instrumental carbon and sulfur analyzer, to determine the amount of Gr in the direct current electrodeposited Cu–Gr composite foil, and also obtain the relationship between the amount of Gr in the composite foils and the concentration of GO in the electrolyte. Further, mechanical property measurements reveal that: (1) the variations in the mechanical properties (involving the elastic modulus, hardness and tensile strength) of the Cu–Gr foils along with the concentration of GO in the electrolyte exhibit similar tendencies to that of the Gr content in the Cu–Gr foils. (2) According to current experimental conditions, the optimal values of the mechanical properties and the amount of Gr in the foils appears at a GO concentration of 0.5 g L−1 in the electrolyte. (3) When the GO concentration is less than 0.5 g L−1, the values of the mechanical properties and the amount of Gr in the foils present an approximately linear relationship; and beyond 0.5 g L−1, the values become unstable and declining, which can be attributed to an agglomeration of excess GO in the electrolyte which makes it difficult to be co-deposited into the foil.

In this work, we established a one-step strategy to synthesize three-dimensional porous graphitic biomass carbon (PGBC) from bamboo char (BC), and studied its electrochemical performance as electrode materials for supercapacitors. Using potassium ferrate (K2FeO4) to fulfil the synchronous carbonization and graphitization of bamboo carbon, this method is less time-demanding, highly efficient and pollution-free, when compared with a conventional two-step strategy. The as-prepared PGBC sample possessed a porous structure with a large specific surface area (1732 m2 g−1) and abundant micropores, as well as a high graphitization degree demonstrated by XRD and Raman. Further electrochemical measurements revealed that the PGBC electrode exhibited a high specific capacitance of 222.0 F g−1 at 0.5 A g−1, and the solid-state symmetric supercapacitor in an aqueous electrolyte (KOH/PVA) presented considerable synergetic energy–power output properties with an energy density of 6.68 W h kg−1 at a power density of 100.2 W kg−1, and 3.33 W h kg−1 at 10 kW kg−1. Moreover, the coin-type symmetric supercapacitor in an ionic liquid electrolyte (EMIM TFSI) delivered a higher energy density of 20.6 W h kg−1 at a power density of 12 kW kg−1. This approach holds great promise to achieve low-cost, green and industrial-grade production of renewable biomass-derived carbon materials for advanced energy storage applications in the future.

Highlights A comprehensive review on the recent development of two-dimensional (2D) nanomaterials for bulk or thin-film thermoelectric materials, as well as composite filler, has been extensively presented.Development of micro-device platform and its application to study the inherent thermoelectric properties of individual single- and few-layer 2D nanomaterials., Thermoelectric generators have attracted a wide research interest owing to their ability to directly convert heat into electrical power. Moreover, the thermoelectric properties of traditional inorganic and organic materials have been significantly improved over the past few decades. Among these compounds, layered two-dimensional (2D) materials, such as graphene, black phosphorus, transition metal dichalcogenides, IVA–VIA compounds, and MXenes, have generated a large research attention as a group of potentially high-performance thermoelectric materials. Due to their unique electronic, mechanical, thermal, and optoelectronic properties, thermoelectric devices based on such materials can be applied in a variety of applications. Herein, a comprehensive review on the development of 2D materials for thermoelectric applications, as well as theoretical simulations and experimental preparation, is presented. In addition, nanodevice and new applications of 2D thermoelectric materials are also introduced. At last, current challenges are discussed and several prospects in this field are proposed.

A simple and effective approach based on the liquid phase exfoliation (LPE) method has been put forward for synthesizing boron quantum dots (BQDs). By adjusting the interactions between bulk boron and various solvents, the average diameter of produced BQDs is about 7 nm. The nonlinear absorption (NLA) responses of as-prepared BQDs have been systematically studied at 515 nm and 1030 nm. Experimental results prove that BQDs possess broadband saturable absorption (SA) and good third-order nonlinear optical susceptibility, which are comparable to graphene. The fast relaxation time and slow relaxation time of BQDs at 515 nm and 1030 nm are about 0.394–5.34 ps and 4.45–115 ps, respectively. The significant ultrafast nonlinear optical properties can be used in optical devices. Here, we successfully demonstrate all-optical diode application based on BQDs/ReS2 tandem structure. The findings are essential for understanding the nonlinear optical properties in BQDs and open a new pathway for their applications in optical devices.

All-optical devices without external electronic components have drawn extraordinary attentions in all-optical communication. In this work, boron quantum dots (BQDs) were synthesized by a facile liquid-phase exfoliation method. The as-prepared BQDs showed good structural homogeneity and crystallinity, broadband optical absorption as well as excellent photothermal properties. Femtosecond-resolved transient absorption further revealed the short carrier relaxation time of BQDs. Inspired by the outstanding photothermal properties and ultrafast carrier dynamic of BQDs, we fabricated BQDs-based all-optical modulator. The phase shift with a slope efficiency of 0.032 π/mW and response time of 0.97 ms can be achieved. The modulator was used in laser resonance cavity to achieve all-optical actively Q-switched laser operation with control repetition rate. This prototypical BQDs-based all-optical modulator shows a great potential to be applied in all-optical information processing and communication.

A facile approach to fabricate low-cost hole-transport-material (HTM)-free perovskite solar cell(PSC) based on commercial P25 nanoparticles and bilayer hybrid carbon electrode under ambient condition is reported. The performance of such HTM-free PSCs are highly dependent on the thickness and morphology of the P25 based TiO 2 electron-transport layer(ETL), which can be adjusted by the amount of ethanol and ethyl cellulose in the paste. After optimization, a power conversion efficiency of 12.48% is obtained, which is enhanced by 20.46% compared with solar cells employing hydrothermal TiO 2 ETL. In addition, PSCs with P25 ETL also exhibit excellent long-term stability together with reduced hysteresis. With advantages of low-cost, high efficiency and facile fabrication process, commercial P25 nanoparticles based PSC is highly potential for future commercialization.

Two dimensional materials have promising benefits in photoelectronic devices, including facilitating charge transport and reducing defects in perovskite solar cells (PSCs) and photodetectors (PDs) through interface engineering. Herein, a two dimension polymeric material of graphitic carbon nitride quantum dots (g-CNQDs) interlayer is used to modify the SnO2/perovskite interface in both ambient PSCs and PDs to improve the overall performance. The introduction of g-CNQD layer improves the crystalline quality of sequential perovskite absorber with high phase purity, less grain boundaries, low trap states and suppressed carrier recombination due to the intrinsic cross-linkable feature and relatively smooth surface of g-CNQD. As a result, with optimal modification, fully air-processed PSC reached a champion power conversion efficiency of 21.23% with negligible hysteresis, and the PDs had remarkable performance enhancement. Moreover, our PSCs have good stability in ambient air, keeping over 90% of the initial efficiency after 30 days’ exposure.

The influence of variant graphenes on electrochemical performance for supercapacitors was studied comparatively and systematically by using SEM, FTIR and Raman spectroscopy, cyclic voltammetry (CV), galvanostatic charge/discharge and electrochemical impedance spectroscopy (EIS). The results revealed that: 1) the nitrogen-doped graphene (N-G) electrode exhibited the highest specific capacitance at the same voltage scan rate; 2) the specific capacitance of the N-G reached up to 243.5 F/g at 1 A/g, while regular graphite oxide (GO) was 43.5 F/g and reduced graphene oxide (rGO) was 67.9 F/g; 3) N-G exhibited the best supercapacitance performance and the superior electrochemical properties, which made it an ideal electrode material for supercapacitors.

In this work, a novel carbon nanotubes (CNTs)/NiCo2S4 composite for high performance supercapacitors was prepared via a simple chemical bath deposition combined with a post-anion exchange reaction. The morphologies and phase structures of the composites were characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), Raman spectroscopy (Raman), X-ray photoelectron spectroscopy (XPS) and low-temperature sorption of nitrogen (BET). The electro-chemical tests revealed that the CNT/NiCo2S4 composite exhibited high electrochemical performance, because the CNTs were used as a conductive network for the NiCo2S4 hexagonal nanoplates. Compared with pure NiCo2S4 and the mechanically mixed CNTs/NiCo2S4 composite, the CNTs/NiCo2S4 composite electrode material exhibited excellent supercapacitive performance, such as a high specific capacitance up to 1537 F/g (discharge current density of 1 A/g) and an outstanding rate capability of 78.1% retention as the discharge current density increased to 100 A/g. It is therefore expected to be a promising alternative material in the area of energy storage.

This paper introduced a process to prepare the carbon nanosphere (CNS)/NiCo2O4 core-shell sub-microspheres. That is: 1) CNSs were firstly prepared via a simple hydrothermal method; 2) a layer of NiCo2O4 precursor was coated on the CNS surface; 3) finally the composite was annealed at 350 °C for 2 hours in the air and the CNS/NiCo2O4 core-shell sub-microspheres were obtained. This core-shell sub-microsphere was prepared with a simple, economical and environmental-friendly hydrothermal method and was suitable for large-scale production, which expects a promising electrode candidate for high performance energy storage applications. Electrochemical experiments revealed that the composite exhibited remarkable electrochemical performances with high capacitance and desirable cycle life at high rates, such as: 1) the maximum specific capacitance was up to 1420 F/g at 1 A/g; 2) about 98.5% of the capacitance retained after 3000 charge-discharge cycles; 3) the capacitance retention was about 72% as the current density increase from 1 A/g to 10 A/g.

A kind of sandwich-like NiCo2O4/rGO/NiO heterostructure composite has been successfully anchored on nickel foam substrate via a three-step hydrothermal method with successive annealing treatment. The smart combination of NiCo2O4, reduced graphene oxide (rGO), and NiO nanostructure in the sandwich-like nano architecture shows a promising synergistic effect for supercapacitors with greatly enhanced electrochemical performance. For serving as supercapacitor electrode, the NiCo2O4/rGO/NiO heterostructure materials exhibit remarkable specific capacitance of 2644 mF cm−2 at current density of 1 mA cm−2, and excellent capacitance retentions of 97.5% after 3000 cycles. It is expected that the present heterostructure will be a promising electrode material for high-performance supercapacitors. Graphical Abstract