Shilei Xie

H-TiO2@MnO2//H-TiO2@C Core–Shell Nanowires for High Performance and Flexible Asymmetric Supercapacitors

A flexible solid-state asymmetric supercapacitor device with H-TiO(2) @MnO(2) core-shell NWs as the positive electrode and H-TiO(2) @C core-shell NWs as the negative electrode is developed. This device operates in a 1.8 V voltage window and is able to deliver a high specific capacitance of 139.6 F g(-1) and maximum volumetric energy density of 0.30 mWh cm(-3) with excellent cycling performance and good flexibility.

High energy density asymmetric quasi-solid-state supercapacitor based on porous vanadium nitride nanowire anode.

To push the energy density limit of asymmetric supercapacitors (ASCs), a new class of anode materials is needed. Vanadium nitride (VN) holds great promise as anode material for ASCs due to its large specific capacitance, high electrical conductivity, and wide operation windows in negative potential. However, its poor electrochemical stability severely limits its application in SCs. In this work, we demonstrated high energy density, stable, quasi-solid-state ASC device based on porous VN nanowire anode and VOx nanowire cathode for the first time. The VOx//VN-ASC device exhibited a stable electrochemical window of 1.8 V and excellent cycling stability with only 12.5% decrease of capacitance after 10,000 cycles. More importantly, the VOx//VN-ASC device achieved a high energy density of 0.61 mWh cm(-3) at current density of 0.5 mA cm(-2) and a high power density of 0.85 W cm(-3) at current density of 5 mA cm(-2). These values are substantially enhanced compared to most of the reported quasi/all-solid-state SC devices. This work constitutes the first demonstration of using VN nanowires as high energy anode, which could potentially improve the performance of energy storage devices.

Stabilized TiN Nanowire Arrays for High-Performance and Flexible Supercapacitors

Metal nitrides have received increasing attention as electrode materials for high-performance supercapacitors (SCs). However, most of them are suffered from poor cycling stability. Here we use TiN as an example to elucidate the mechanism causing the capacitance loss. X-ray photoelectron spectroscopy analyses revealed that the instability is due to the irreversible electrochemical oxidation of TiN during the charging/discharging process. Significantly, we demonstrate for the first time that TiN can be stabilized without sacrificing its electrochemical performance by using poly(vinyl alcohol) (PVA)/KOH gel as the electrolyte. The polymer electrolyte suppresses the oxidation reaction on electrode surface. Electrochemical studies showed that the TiN solid-state SCs exhibit extraordinary stability up to 15,000 cycles and achieved a high volumetric energy density of 0.05 mWh/cm(3). The capability of effectively stabilizing nitride materials could open up new opportunities in developing high-performance and flexible SCs.

Oxygen‐Deficient Hematite Nanorods as High‐Performance and Novel Negative Electrodes for Flexible Asymmetric Supercapacitors

Oxygen-deficient α-Fe2 O3 nanorods with outstanding capacitive performance are developed and demonstrated as novel negative electrodes for flexible asymmetric supercapacitors. The asymmetric-supercapacitor device based on the oxygen-deficient α-Fe2 O3 nanorod negative electrode and a MnO2 positive electrode achieves a maximum energy density of 0.41 mW·h/cm(3) ; it is also capable of charging a mobile phone and powering a light-emitting diode indicator.

Facile synthesis of large-area manganese oxide nanorod arrays as a high-performance electrochemical supercapacitor

Large-area manganese oxide nanorod arrays (MONRAs) and herringbones (MOHBs) were successfully synthesized on F-doped SnO2 coated glass (FTO) substrates by a simple electrochemical method. Cyclic voltammetry (CV) and galvanostatic charge/discharge measurements demonstrated that the MONRAs and MOHBs exhibited excellent specific capacitance and good cycling stability in 0.5 M Na2SO4 aqueous solution. For example, the specific capacitance of the MONRAs achieves as high as 660.7 F g−1 at a scan rate of 10 mV s−1 and 485.2 F g−1 at a current density of 3 A g−1, respectively. Furthermore, the presented method may be extended to allow similar MONRs with a specific capacitance of 583.6 F g−1 to grow on flexible Ti foil, which may have great potential application in fabricating flexible supercapacitors.

Oxygen vacancies promoting photoelectrochemical performance of In 2 O 3 nanocubes

This work reports a facile method for preparing the new photoactive In2O3 films as well as their implementation in photoelectrochemical (PEC) application. We firstly investigated the relationship between oxygen vacancies (VO) and PEC performance and revealed a rule between them. We found that the optimized In2O3−n sample yielded a photocurrent density up to 3.83 mA/cm2 in 1 M Na2SO4 solution under the solar illumination. It also gave efficiency as high as 75% over 400 nm in the incident-photon-to-current-conversion efficiency (IPCE) spectrum, which is the best value for an In2O3 photoanode reported. Moreover, the PEC performance of these films is enhanced as the VO increased and then decreased with further increasing VO. This two-side effect means VO can favor the photoelectron activation, or act as recombination centers to prohibit the generation of photocurrent. Making highly photoactive In2O3 nanostructures in this work will open up new opportunities in various areas.

Controllable synthesis of porous nickel-cobalt oxide nanosheets for supercapacitors†

Vertically aligned nickel–cobalt oxide (NCO) nanosheets with porous structure were successfully synthesized on FTO substrates by a simple electrochemical method without any templates. Cyclic voltammetry (CV) and galvanostatic charge/discharge measurements show that the porous NCO nanosheets have an ideal capacitive performance and long-term stability. With an optimum amount of Ni, the specific capacitance for the NCOs could reach as high as 453 F g−1 at a scan rate of 5 mV s−1 and 506 F g−1 at a current density of 1 A g−1, showing an improvement of around 50% compared with cobalt oxide. Furthermore, a symmetric supercapacitor based on two NCO electrodes exhibits a maximum specific capacitance of 89.2 F g−1 at 0.17 A g−1.

TiO2@C core–shell nanowires for high-performance and flexible solid-state supercapacitors

A flexible and solid-state supercapacitor device based on TiO2@C core–shell nanowires has been developed and exhibited excellent flexibility—it can even be folded and twisted without sacrificing electrochemical properties—and good electrochemical performance with a maximum energy density of 0.011 mW h cm−3.

Facile electrochemical synthesis of single crystalline CeO2 octahedrons and their optical properties.

We developed a simple electrochemical process for the large-scale fabrication of single crystalline CeO(2) octahedrons and nanospheres from DMSO aqueous solution. The octahedrons with some structural defects have a size ranging from 200 to 300 nm. Moreover, highly crystalline CeO(2) nanospheres were also obtained via this electrochemical process based on the oriented attachment mechanism. The absorption edge of octahedrons and spheres shows a red-shift, and that of the octahedrons was near the visible region.

Redox cycles promoting photocatalytic hydrogen evolution of CeO2 nanorods

Oriented hexagonal CeO2 NRs were directly grown on Ti substrates via a simple template-free electrochemical method. These CeO2 NRs with {110} planes as the main exposed surfaces show significant photocatalytic activity for hydrogen evolution with Na2S–Na2SO3 as sacrificial agents due to their special redox capacity.