ABSTRACT
ZnCo2 O4 quantum dots anchored on nitrogen-doped carbon nanotubes (N-CNT) retain the high catalytic activity of ZnCo2 O4 to oxidize water while enabling an efficient oxygen reduction performance thereby combining these desirable features. These advantages realize a bifunctional catalytic activity for ZnCo2 O4 /N-CNT that can be used in rechargeable zinc-air batteries.
ABSTRACT
The development of highly efficient and robust photocatalysts has attracted great attention for solving the global energy crisis and environmental problems. Herein, we describe the synthesis of a p-n heterostructured photocatalyst, consisting of ZnO nanorod arrays (NRAs) decorated with BiOI nanoplates (NPs), by a facile solvothermal method. The product thus obtained shows high photoelectrochemical water splitting performance and enhanced photoelectrocatalytic activity for pollutant degradation under visible light irradiation. The p-type BiOI NPs, with a narrow band gap, not only act as a sensitizer to absorb visible light and promote electron transfer to the n-type ZnO NRAs, but also increase the contact area with organic pollutants. Meanwhile, ZnO NRAs provide a fast electron-transfer channel, thus resulting in efficient separation of photoinduced electron-hole pairs. Such a p-n heterojunction nanocomposite could serve as a novel and promising catalyst in energy and environmental applications.
ABSTRACT
The effective separation and transport of photoinduced electron-hole pairs in photoanodes is of great significance to photoelectrochemical and catalytic performance. Here, a facile and effective two-step strategy is developed to fabricate double-shelled ZnO/CdS/CdSe porous nanotube photoanodes from ZnO nanorod arrays (NRAs). Surprisingly, after the process of the deposition of CdS and CdSe, the ZnO nanorod arrays are partially dissolved, resulting in the formation of ZnO/CdS/CdSe porous nanotube arrays (NTAs). By virtue of their unique porous nanotube structure and cosensitization effect, the ZnO/CdS/CdSe porous NTAs show superior photoelectrochemical water-splitting performance and organic-pollutant-degradation ability under visible light irradiation, as well as excellent long-term photostability.
ABSTRACT
Three-dimensional (3D) nanometal films serving as current collectors have attracted much interest recently owing to their promising application in high-performance supercapacitors. In the process of the electrochemical reaction, the 3D structure can provide a short diffusion path for fast ion transport, and the highly conductive nanometal may serve as a backbone for facile electron transfer. In this work, a novel polypyrrole (PPy) shell@3D-Ni-core composite is developed to enhance the electrochemical performance of conventional PPy. With the introduction of a Ni metal core, the as-prepared material exhibits a high specific capacitance (726â F g(-1) at a charge/discharge rate of 1â A g(-1)), good rate capability (a decay of 33% in Csp with charge/discharge rates increasing from 1 to 20â A g(-1)), and high cycle stability (only a small decrease of 4.2% in Csp after 1000â cycles at a scan rate of 100â mV s(-1)). Furthermore, an aqueous symmetric supercapacitor device is fabricated by using the as-prepared composite as electrodes; the device demonstrates a high energy density (≈21.2â Wh kg(-1)) and superior long-term cycle ability (only 4.4% and 18.6% loss in Csp after 2000 and 5000â cycles, respectively).
ABSTRACT
In this paper, three different morphological Co3O4 electrodes for oxygen evolution reaction (OER) have been synthesized. By comparing the three morphologies of Co3O4, the electrocatalytic properties show that the urchin-like spheres of Co3O4 electrode has relative low overpotential and good electrocatalysis stability, indicating that the structure of urchin-like Co3O4 spheres exhibit an easy OER for water splitting.