Single-crystalline Zn(2)GeO(4) nanobelts with lengths of hundreds of micrometers, thicknesses as small as ∼7 nm, and aspect ratios of up to 10,000 were synthesized in a binary ethylenediamine/water solvent system using a solvothermal route. The ultralong and ultrathin geometry of the Zn(2)GeO(4) nanoribbon proves to greatly promote the photocatalytic activity toward reduction of CO(2) into renewable hydrocarbon fuel (CH(4)) in the presence of water vapor.
Photocatalysis has been invariably considered as an unselective process (especially in water) for a fairly long period of time, and the investigation on selective photocatalysis has been largely neglected. In recent years, the field of selective photocatalysis is developing rapidly and now extended to several newer applications. This review focuses on the overall strategies which can improve the selectivity of photocatalysis encompassing a wide variety of photocatalysts, and modifications thereof, as well as the related vital processes of industrial significance such as reduction and oxidation of organics, inorganics, and CO transformation. Comprehensive and successful strategies for enhancing the selectivity in photocatalysis are abridged to reinvigorate and stimulate future investigations. In addition, nonsemiconductor type photocatalysts, such as Ti-Si molecular sieves and carbon quantum dots (CQDs), are also briefly appraised in view of their special role in special selective photocatalysis, namely epoxidation reactions, among others. In the end, a summary and outlook on the challenges and future directions in the research field are included in the comprehensive review.
Visible light-induced degradation of rhodamine B (RhB) and eosin Y (EO) in a heterogeneous TiO(2) P-25/EO/RhB system was investigated in the present work. The results showed that the photodegradation of RhB is enhanced significantly when EO is introduced into the P-25/RhB system. Under optimal conditions (50 mg P-25, 20 mg L(-1) EO), RhB (4 mg L(-1)) almost decomposed completely after 35 min of visible light irradiation, though EO was photodegraded simultaneously. The possible photodegradation mechanism was studied by the examination of active species HO*, O(2)(*-) anions, or dye radical cations through adding their scavengers such as methanol, t-butanol, benzoquinone, EDTA, and the I(-) anion. In addition, the electron paramagnetic resonance (EPR) spin trapping technique was also used to monitor the active oxygen species formed in the photocatalytic process. Combined with the contrastive experiments under different atmospheres (N(2)-purged or air) and in different systems, it can be deduced that dissolved O(2) plays a crucial role in dye photodegradation and the O(2)(*-) anion is possibly the major active oxygen species. The low degradation rate with the introduction of EDTA or I(-) indicated that dye radical cations also play a part in photodegradation. Furthermore, except for the dye-sensitized photodegradation on the P-25 surface, reaction in bulk solution also occurs in this system, leading to effective photodegradation of RhB.
Ultrathin and uniform Bi(2)WO(6) square nanoplates of ∼9.5 nm thickness corresponding to six repeating cell units were prepared in the presence of oleylamine using a hydrothermal route. The Bi(2)WO(6) nanoplates show great potential in the utilization of visible light energy to the highly efficient reduction of CO(2) into a renewable hydrocarbon fuel. On the one hand, the ultrathin geometry of the nanoplates promotes charge carriers to move rapidly from the interior to the surface to participate in the photoreduction reaction. This should also favor the improved separation of photogenerated electron and hole and a lower electron-hole recombination rate; on the other hand, the Bi(2)WO(6) square nanoplate is proven to provide the well-defined {001} facet for two dominantly exposed surfaces, which is a prerequisite for the high level of photocatalytic activity of CO(2) fixation.
Element doping has been extensively attempted to develop visible-light-driven photocatalysts, which introduces impurity levels and enhances light absorption. However, the dopants can also become recombination centers for photogenerated electrons and holes. To address the recombination challenge, we report a gradient phosphorus-doped CdS (CdS-P) homojunction nanostructure, creating an oriented built-in electric-field for efficient extraction of carriers from inside to surface of the photocatalyst. The apparent quantum efficiency (AQY) based on the cocatalyst-free photocatalyst is up to 8.2% at 420 nm while the H evolution rate boosts to 194.3 μmol·h·mg, which is 58.3 times higher than that of pristine CdS. This concept of oriented built-in electric field introduced by surface gradient diffusion doping should provide a new approach to design other types of semiconductor photocatalysts for efficient solar-to-chemical conversion.
A simple, green, and fast approach (complete within 5 min) was explored for the fabrication of hybrid AgCl/Ag plasmonic nanoparticles under microwave (MW) irradiation. In this method, beet juice served as a reducing reagent, which is an abundant sugar-rich agricultural produce. Interestingly, the obtained AgCl/Ag samples have a smaller size than the AgCl reaction precursor. This makes it an unusual top-down hydrothermal synthesis. The as-prepared material displayed good photocatalytic activity for the degradation of methyl orange (MO) dye.
Graphene is a promising candidate in analog electronics with projected operation frequency well into the terahertz range. In contrast to the intrinsic cutoff frequency (f) of 427 GHz, the maximum oscillation frequency (f) of graphene device still remains at low level, which severely limits its application in radio frequency amplifiers. Here, we develop a novel transfer method for chemical vapor deposition graphene, which can prevent graphene from organic contamination during the fabrication process of the devices. Using a self-aligned gate deposition process, the graphene transistor with 60 nm gate length exhibits a record high f of 106 and 200 GHz before and after de-embedding, respectively. This work defines a unique pathway to large-scale fabrication of high-performance graphene transistors, and holds significant potential for future application of graphene-based devices in ultra high frequency circuits.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.