Porous unsupported CuO nanoplates for efficient photothermal CO oxidation.

It is a significant issue for environmental protection and industrial production to eliminate CO, a gas harmful to life and some important reaction sites. Real environmental conditions require catalytic CO oxidation to occur at relatively low temperature. Nowadays, photothermal catalysis has been exploited as a new way to achieve CO elimination, different from thermal catalysis. CuO, as cheap and abundant substitute for precious metals, is considered to have potential in photothermal catalysis. Oxygen vacancies (OV) and lattice oxygen (OL) activity are considered extremely crucial for oxide catalysts in CO oxidation, according to Mars-van Krevelen mechanism. Herein, porous CuO nanoplates with adjustable OVand OLactivity were prepared by a facile method via controlling the morphology and phase composition of precursors. The light-off temperature (50% conversion) of the best sample obtained under the optimal conditions was ∼110 °C and an almost complete conversion was reached at ∼150 °C. It also achieved nearly 70% conversion under 6 standard Suns (6 kW cm-2irradiation) and could work in infrared radiation (IR) regions, which could be attributed to the photo-induced thermal effect and activation effect. The simple synthesis and characterization provide a good example for the future photothermal catalysis.

Hollowsphere Nanoheterojunction of g-C3N4@TiO2 with High Visible Light Photocatalytic Property.

In this work, g-C3N4@TiO2 nanostructures with hollow sphere morphology, small grain size, high crystalline quality, and high surface area are successfully synthesized by the annealing method using melamine and hollowsphere precursor, which could be a universal method to synthesis hollow sphere nanoheterojunction. Excellent photocatalytic property was observed from the as-prepared g-C3N4@TiO2 nanostructure with 466.43 µmol·g-1·h-1 hydrogen generation rate under visible light irradiation (>420 nm), which was 5.5 times as much as the control couple, nanoparticle nanoheterojunction g-C3N4@TiO2. No apparent deactivation was found during the follow-up cycle performance test. The special morphology and the heterojunction construction contribute to both visible light absorption and photogenerated electron-hole pair separation efficiency and finally to the photocatalytic property. The content of g-C3N4 was proved to be an important parameter for the promotion of the photocatalytic property. Overlarge content may lead to lower photogenerated electron-hole pair separation efficiency.

Cu2O photocathodes for unassisted solar water-splitting devices enabled by noble-metal cocatalysts simultaneously as hydrogen evolution catalysts and protection layers.

Here, we report a Cu2O-based photocathode applied with pulsed-laser-deposited overlayers with the structure of Ga2O3/AZO/TiO2 and 60 nm dense Pt simultaneously as a hydrogen evolution catalyst and protective layer under backside illumination from ITO substrate. And by depositing thin Au nanoparticles on the bottom of Cu2O, we observe the increase of light harvesting and the production of hot electrons from the surface plasmon resonance effect. The modified photocathode presents a photocurrent density of -4 mA cm-2 at 0 V versus reversible hydrogen electrode and a thermodynamically-based energy conversion efficiency of 0.27% in a weak acidic electrolyte. The stability is tremendously improved compared with other structures without the dense Pt layer. This enhancement is attributed to the formation of a p-n junction at the Cu2O and Ga2O3 interface and surface stabilization by TiO2 and Pt. To demonstrate the impact on the practical application of the photocathode, we fabricate the bias-free solar water-splitting tandem device using a transparent BiVO4 photoanode, which exhibits a stabilized peak photocurrent density of 0.1 mA cm-2 under continuous illumination.

Optimization of photoelectrochemical performance in Pt-modified p-Cu2O/n-Cu2O nanocomposite.

As it is expected to be one of the most promising materials for utilizing solar energy, Cu2O has attracted considerable attention with respect to the achievement of solar energy conversion. Until now, the photocurrent densities of all planar structure of the Cu2O photocathode have not even come close to the theoretical value of -14.7 mA cm-2 due to the incompatible light absorption and charge carrier diffusion lengths. Here, we have fabricated p-n Cu2O homojunction nanocomposite by multiple steps of electrochemical deposition processing with the optimization of deposition periods. The p-Cu2O/n-Cu2O nanocomposite fabricated by optimized pH (4.9) and deposition time (4 min) exhibited double the photocurrent density of that of the bare p-Cu2O photocathode. And the highest photocurrent density of nanostructured p-n Cu2O nanorod homojunction photocathode with a p-Cu2O blocking layer reached -10.0 mA cm-2 at 0 V versus the reversible hydrogen electrode under simulated AM 1.5G illumination (100 mW cm-2).

Improving the photovoltaic performance of the all-solid-state TiO2 NR/CuInS2 solar cell by hydrogen plasma treatment.

The interfacial properties of the heterojunction between p-type and n-type materials play an important role in the performance of the solar cell. In this paper, a p-type CuInS2 film was deposited on TiO2 nanorod arrays by spin coating to fabricate an all-solid-state solar cell and the TiO2 nanorod arrays were treated with hydrogen plasma(H:TiO2) to ameliorate the interfacial properties. The influence of the hydrogen plasma treatment on the performance of the solar cell was investigated. The short-circuit current density was obviously raised and the power conversion efficiency of the solar cell improved to 0.30%, which is three times that of solar cells without hydrogen plasma treatment. The enhancement of the performance is attributed to not only the enhancement of carrier separation and transport, but the reduction of the recombination of electrons and holes, which is caused by hydrogen plasma treatment.

A full compositional range for a (Ga1-x Zn x )(N1-x O x ) nanostructure: high efficiency for overall water splitting and optical properties.

Bulk (Ga1-x Zn x )(N1-x O x ) as a photocatalyst has received increasing attention as a potential solution for the energy shortage challenge; however, its catalytic performance is highly limited by its bulk form. To improve the photochemical potential, the nanoscale form of this multiple-metal oxynitrides is desirable. In this work, a new type of (Ga1-x Zn x )(N1-x O x ) nanostructure is obtained. Its composition can tuned to the full range (0.18 < x < 0.95). The (Ga1-x Zn x )(N1-x O x ) nanostructure exhibits excellent photocatalytic activity for overall water splitting, and the highest quantum efficiency of (Ga1-x Zn x )(N1-x O x ) is as high as 17.3% under visible light irradiation. Using this new type of (Ga1-x Zn x )(N1-x O x ) nanostructure, the narrowing of the bandgap for (Ga1-x Zn x )(N1-x O x ) is not only due to an increase in the valence band maximum, but it is also related to a decrease in the conduction band minimum.

Ultrathin Hydrogel Films toward Breathable Skin-Integrated Electronics.

On-skin electronics that offer revolutionary capabilities in personalized diagnosis, therapeutics, and human-machine interfaces require seamless integration between the skin and electronics. A common question remains whether an ideal interface can be introduced to directly bridge thin-film electronics with the soft skin, allowing the skin to breathe freely and the skin-integrated electronics to function stably. Here, an ever-thinnest hydrogel is reported that is compliant to the glyphic lines and subtle minutiae on the skin without forming air gaps, produced by a facile cold-lamination method. The hydrogels exhibit high water-vapor permeability, allowing nearly unimpeded transepidermal water loss and free breathing of the skin underneath. Hydrogel-interfaced flexible (opto)electronics without causing skin irritation or accelerated device performance deterioration are demonstrated. The long-term applicability is recorded for over one week. With combined features of extreme mechanical compliance, high permeability, and biocompatibility, the ultrathin hydrogel interface promotes the general applicability of skin-integrated electronics.

Near-Infrared Organic Photodetectors toward Skin-Integrated Photoplethysmography-Electrocardiography Multimodal Sensing System.

In the fast-evolving landscape of decentralized and personalized healthcare, the need for multimodal biosensing systems that integrate seamlessly with the human body is growing rapidly. This presents a significant challenge in devising ultraflexible configurations that can accommodate multiple sensors and designing high-performance sensing components that remain stable over long periods. To overcome these challenges, ultraflexible organic photodetectors (OPDs) that exhibit exceptional performance under near-infrared illumination while maintaining long-term stability are developed. These ultraflexible OPDs demonstrate a photoresponsivity of 0.53 A W-1 under 940 nm, shot-noise-limited specific detectivity of 3.4 × 1013 Jones, and cut-off response frequency beyond 1 MHz at -3 dB. As a result, the flexible photoplethysmography sensor boasts a high signal-to-noise ratio and stable peak-to-peak amplitude under hypoxic and hypoperfusion conditions, outperforming commercial finger pulse oximeters. This ensures precise extraction of blood oxygen saturation in dynamic working conditions. Ultraflexible OPDs are further integrated with conductive polymer electrodes on an ultrathin hydrogel substrate, allowing for direct interface with soft and dynamic skin. This skin-integrated sensing platform provides accurate measurement of photoelectric and biopotential signals in a time-synchronized manner, reproducing the functionality of conventional technologies without their inherent limitations.

Carbon Sphere Template Derived Hollow Nanostructure for Photocatalysis and Gas Sensing.

As a green and preferred technology for energy crisis and environmental issues, continuous research on photocatalysis and gas sensing has come forth at an explosive rate. Thus far, promising synthetic methods have enabled various designs and preparations of semiconductor-based nanostructure which have shown superior activity. This review summarized various synthetic routines toward carbon sphere template derived hollow nanostructures and their successful attempts in synthesize doping, solid solution, heterostructure, and surface modified nanostructures for heterogeneous photocatalysis and gas sensing. Moreover, the challenges and future prospects are briefly discussed. It is eagerly anticipated that this review may broaden the view and in-depth understanding of carbon sphere template derived hollow nanostructures while expected to have further progresses in heterogeneous photocatalysis, gas sensing and other related fields which will make great contributions to their application.

A two-step synthesis of nanosheet-covered fibers based on α-Fe2O3/NiO composites towards enhanced acetone sensing.

A novel hierarchical heterostructures based on α-Fe2O3/NiO nanosheet-covered fibers were synthesized using a simple two-step process named the electrospinning and hydrothermal techniques. A high density of α-Fe2O3 nanosheets were uniformly and epitaxially deposited on a NiO nanofibers. The crystallinity, morphological structure and surface composition of nanostructured based on α-Fe2O3/NiO composites were investigated by XRD, SEM, TEM, EDX, XPS and BET analysis. The extremely branched α-Fe2O3/NiO nanosheet-covered fibers delivered an extremely porous atmosphere with huge specific surface area essential for superior gas sensors. Different nanostructured based on α-Fe2O3/NiO composites were also explored by adjusting the volume ratio of the precursors. The as-prepared samples based on α-Fe2O3/NiO nanocomposite sensors display apparently enhanced sensing characteristics, including higher sensing response, quick response with recovery speed and better selectivity towards acetone gas at lower operating temperature as compared to bare NiO nanofibers. The sensing response of S-2 based α-Fe2O3/NiO nanosheet-covered fibers were 18.24 to 100 ppm acetone gas at 169 °C, which was about 6.9 times higher than that of bare NiO nanofibers. The upgraded gas sensing performance of composites based on α-Fe2O3/NiO nanosheet-covered fibers might be ascribed to the exclusive morphologies with large surface area, p-n heterojunctions and the synergetic performance of α-Fe2O3 and NiO.