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Wide bandgap semiconductor-based photocatalysts are usually limited by their low solar energy conversion efficiency due to their limited absorption solar wavelength, their rapid surface recombination of the photogenerated electron–hole pairs, and their low charge-carrier mobility. Here, we report a novel stepwise solution synthesis for achieving a new photocatalytic core–shell consisting of a titanate nanowire/reduced graphene oxide shell (or titanate/rGO) 1D-nanocomposite. The new core–shell nanocomposite maximized the specific surface area, largely reduced the charge transfer resistance and reaction energy barrier, and significantly improved the absorption of visible light. The core–shell nanocomposites' large on/off current ratio and rapid photo-responses boosted the photocurrent by 30.0%, the photocatalysis rate by 50.0%, and the specific surface area by 16.4% when compared with the results for the pure titanate nanowire core. Our numerical simulations support the effective charge separation on the new core–shell nanostructure, which can help further advance the novel photocatalysis. [ABSTRACT FROM AUTHOR]

Undersea optical communication (UOC) has been considered as the most potential next‐generation underwater wireless communication technology for ocean exploration. Photodetector is the essential component in UOC system, however, the harsh undersea environment like light attenuation and seawater corrosivity restricts the applications of conventional photodetectors. Herein, a novel natural‐electrolyte self‐powered photoelectrochemical (PEC) photodetector based on core‐shell structured Cu@GaN nanowires (NWs) network is demonstrated and direct utilization of seawater. High quality GaN shell is encapsulated on the Cu NWs network through Ga‐coating and high temperature nitridation processes. A Schottky junction along radial direction has formed at the Cu/GaN interface due to the outward diffusion of Cu into the GaN layer. Such a structure provides narrowed band detection on blue light as well as efficient carrier separation. A self‐powered undersea PEC photodetector is designed with a mini‐pipes connected device chamber, which allows direct indrawing of seawater and blue channel light communication (458 nm). This photodetector works stably for UOC in both shallow and deep‐sea conditions in Pacific Ocean area. It shows a high responsivity up to 5.04 mA W−1 and rapid response time of 0.68 ms. This photodetector can be easily integrated to marine equipment without waterproof packaging for the future energy‐saving UOC. [ABSTRACT FROM AUTHOR]

Structure has been considered to play an important role in photocatalytic performance of the semiconductors, but the intrinsic factors were rarely revealed. Herein, ZnO nanomaterials in the structures of thin film, nanowire array and nanosheet array were synthesized, and their structural characteristics, optical properties, photocurrent response and photocatalytic efficiency were compared with each other for illustrating the issue. The photoluminescence intensity decreased in the order of nanosheets, thin film and nanowires for improved lifetime of the photoexcited charges. The absorption of the nanosheets and nanowires improved obviously in the visible range with a redshift of the absorption edge than that of the thin film. The nanowires possessed the highest response current of 82.65 μA at a response time of 2.0 ms in a sensitivity of 87.93 at the light frequency of 1 Hz, and gained the largest catalytic efficiency of 2.45 μg/cm2 h for the methylene blue degradation in UV light. Nevertheless, the improvement of catalytic efficiency of the nanosheets (up to 42.4%) was much larger than that of nanowires (5.7%) and thin film (2.6%) for the Au coating. The analysis revealed that the photocatalytic efficiency of the ZnO nanomaterials was modulated by the structure as it contained different surface area, roughness, defect and doping states, vacancies, polar and non-polar crystalline faces, which would provide structural design of semiconductor nanomaterials for the photoelectric and photocatalytic applications. [ABSTRACT FROM AUTHOR]

With a precise control of temperature, gas flow, and pressure and with sequentially increased durations for reactions, the detailed processes of catalyzing, nucleation, and growth of the SiOx nanowires were successfully traced. Especially a stepwise nonuniformity in diameter of nanowire during the growth was for the first time detected. With analysis of these detailed processes via nanocurvature and nano ripening effects, a further understanding of the vapor-liquid-solid mechanism was achieved and a novel mechanism for formation of the stepwise nonuniformity in diameter of nanowire was particularly proposed. All these will be the crucial basis for the further, accurately controlled growth of SiOx nanowires and the relevant applications. [ABSTRACT FROM AUTHOR]

Hierarchical arrays of ZnO/Si nanowires were prepared through very convenient two-step solution method on silicon substrates. The tree-like nanowire structures showed high crystal quality, where well aligned Si nanowires were grown vertical to the substrate surface, whereas uniform assembly of branched ZnO nanowires was grown normal to the Si nanowires (backbones). Raman analysis indicated that among all the specimens having identical chemical compositions and dimensions but different forms (thin films or nanowires), Ag-decorated hierarchical arrays of ZnO/Si nanowires possessed the highest intensity peak in surface enhanced Raman scattering spectra. Such arrays demonstrated exceptional ability of detecting Rhodamine 6 G, limiting to a value as low as 1×10 −8 mol/L and an enhancement factor up to 1.5 × 10 4 . Both, experimental designing and band structure analysis indicated that electromagnetic effect of the localized surface plasmon resonance of Ag nanoparticles caused eight times enhancement, whereas chemical effect of hierarchical arrays of ZnO/Si nanowires played a more critical role in the high Raman sensitivity. Our results would be helpful to better understand the enhancement mechanisms and meanwhile, could be extended for further potential applications of hierarchical semiconducting nanowires. [ABSTRACT FROM AUTHOR]

ZnO/Si nanowire arrays with hierarchical architecture were synthesized by solution method with ZnO seed layer grown by atomic layer deposition and magnetron sputtering, respectively. The photocatalytic activity of the as-grown tree-like arrays was evaluated by the degradation of methylene blue under ultraviolet light at ambient temperature. The comparison of morphology, crystal structure, optical properties, and photocatalysis efficiency of the two samples in different seeding processes was conducted. It was found that the ZnO/Si nanowire arrays presented a larger surface area with better crystalline and more uniform ZnO branches on the whole sidewall of Si backbones for the seed layer by atomic layer deposition, which gained a strong light absorption as high as 98% in the ultraviolet and visible range. The samples were proven to have a potential use in photocatalyst, but suffered from photodissolution and memory effect. The mechanism of the photocatalysis was analyzed, and the stability and recycling ability were also evaluated and enhanced. [ABSTRACT FROM AUTHOR]

[Display omitted] • Core-shell Si/TiO 2 nanowires were synthesized vertically on silicon substrate. • The heterostructure owned a wide spectral absorption with large photocurrent. • The catalytic efficiency of the sample was 86.82% in 1 h with good stability. • The excited charges were effectively separated by the internal electric field. Semiconductor photocatalysts can eliminate organic pollutants completely, but the poor utilization of solar energy and rapid recombination of photogenerated electron-hole pairs have become a vital obstacle for their widespread application. Herein Si/TiO 2 nanowire arrays with core–shell structures were fabricated by metal-assisted chemical etching and atomic-layered deposition. The physical properties and photocatalytic performance of the specimens were tested and compared with pristine Si nanowire arrays. The specimens showed perfect light absorption. The photoluminescence was generally depressed by the shell layer, and the photocurrent and photocatalytic efficiency of Si/TiO 2 were improved by 297 and 2 times respectively in contrast to Si. The magnitude of the photocurrent and photocatalytic activity could be modulated by the etching period, in which an ideal etching time of 2 h produced the highest photocatalytic performance. The high efficient photocatalysis of the heterostructure was well illustrated by the Z-scheme band alignment and large specific surface area. [ABSTRACT FROM AUTHOR]