Photoluminescence blinking—random switching between states of high (ON) and low (OFF) emissivities—is a universal property of molecular emitters found in dyes, polymers, biological molecules and artificial nanostructures such as nanocrystal quantum dots, carbon nanotubes and nanowires. For the past 15 years, colloidal nanocrystals have been used as a model system to study this phenomenon. The occurrence of OFF periods in nanocrystal emission has been commonly attributed to the presence of an additional charge, which leads to photoluminescence quenching by non-radiative recombination (the Auger mechanism). However, this ‘charging’ model was recently challenged in several reports. Here we report time-resolved photoluminescence studies of individual nanocrystal quantum dots performed while electrochemically controlling the degree of their charging, with the goal of clarifying the role of charging in blinking. We find that two distinct types of blinking are possible: conventional (A-type) blinking due to charging and discharging of the nanocrystal core, in which lower photoluminescence intensities correlate with shorter photoluminescence lifetimes; and a second sort (B-type), in which large changes in the emission intensity are not accompanied by significant changes in emission dynamics. We attribute B-type blinking to charge fluctuations in the electron-accepting surface sites. When unoccupied, these sites intercept ‘hot’ electrons before they relax into emitting core states. Both blinking mechanisms can be electrochemically controlled and completely suppressed by application of an appropriate potential.

https://absimage.aps.org/image/MAR12/MWS_MAR12-2011-002227.pdf

Two types of luminescence blinking revealed by spectroelectrochemistry of single quantum dots

This review focuses on introducing and explaining electrodepostion mechanisms and electrodeposition-based synthesis strategies used for the production of catalysts and semiconductor electrodes for use in water-splitting photoelectrochemical cells (PECs). It is composed of three main sections: electrochemical synthesis of hydrogen evolution catalysts, oxygen evolution catalysts, and semiconductor electrodes. The semiconductor section is divided into two parts: photoanodes and photocathodes. Photoanodes include n-type semiconductor electrodes that can perform water oxidation to O2 using photogenerated holes, while photocathodes include p-type semiconductor electrodes that can reduce water to H2 using photoexcited electrons. For each material type, deposition mechanisms were reviewed first followed by a brief discussion on its properties relevant to electrochemical and photoelectrochemical water splitting. Electrodeposition or electrochemical synthesis is an ideal method to produce individual components and ...

Electrochemical Synthesis of Photoelectrodes and Catalysts for Use in Solar Water Splitting

Co2P nanostructures with rod-like and flower-like morphologies have been synthesized by controlling the decomposition process of Co(acac)3 in oleylamine system with triphenylphosphine as phosphorus source. Investigations indicate that the final morphologies of the products are determined by their peculiar phosphating processes. Electrochemical measurements manifest that the Co2P nanostructures exhibit excellent morphology-dependent supercapacitor properties. Compared with that of 284 F g–1 at a current density of 1 A g–1 for Co2P nanorods, the capacitance for Co2P nanoflowers reaches 416 F g–1 at the same current density. Furthermore, an optimized asymmetric supercapacitor by using Co2P nanoflowers as anode and graphene as cathode is fabricated. It can deliver a high energy density of 8.8 Wh kg–1 (at a high power density of 6 kW kg–1) and good cycling stability with over 97% specific capacitance remained after 6000 cycles, which makes the Co2P nanostructures potential applications in energy storage/conver...

Shape-Controlled Synthesis of Co2P Nanostructures and Their Application in Supercapacitors

Carbon nanomaterials in tribology

Inspired by the gradient structures of biological materials, researchers have explored compositional and structural gradients for about 40 years as an approach to enhance the properties of engineering materials, including metals and metallic alloys. The synthesis of various gradient nanostructured materials, such as gradient nanograined, nanolaminated nd nanotwinned metals and alloys, has provided new opportunities to understand gradient-related mechanical behaviour. These emerging gradient materials often exhibit unprecedented mechanical properties, such as strength–ductility synergy, extraordinary strain hardening, enhanced fracture and fatigue resistance, and remarkable resistance to wear and corrosion, which are not found in materials with homogeneous or random microstructures. This Review critically assesses the state of the art in the field of gradient nanostructured metallic materials, covering topics ranging from the fabrication and characterization of mechanical properties to underlying deformation mechanisms. We discuss various deformation behaviours induced by structural gradients, including stress and strain gradients, the accumulation and interaction of new dislocation structures, and unique interfacial behaviour, as well as providing insight into future directions for the development of gradient structured materials. Gradient nanostructured metals and alloys are an emerging class of materials that exhibit a combination of excellent mechanical properties that are not possessed by their homogeneous counterparts. This Review assesses the fabrication, characterization and deformation behaviour of these materials, as well as the challenges and future directions of the field.

Mechanical properties and deformation mechanisms of gradient nanostructured metals and alloys

Femtosecond pulsed laser textured titanium surfaces with stable superhydrophilicity and superhydrophobicity

Microstructure evolution and grain refinement of Ti-6Al-4V alloy by laser shock processing

Room temperature photoluminescence properties of CuO nanowire arrays

We demonstrate a broadband visible-light absorber based on excitation of multiple propagating surface plasmon (PSP) resonances. The simple structure is constructed of continuous gold/silica multi-layers covered by a one-dimensional gold grating. The broadening of bandwidth arises from the inter-layer hybridization and spectral superposition of PSPs, which is predicted with the analytical coupled oscillator model and validated using the RCWA simulation. The average absorption increases with the number of gold/silica pairs and exceeds 95% over the whole visible spectrum when only five pairs are included. Moreover, results show that the absorption can be further enhanced by grading the thickness of silica layers. The presented design might enable promising applications in the fields of photovoltaic cells and thermal emitters, owing to its advantages of wideband, near-unity absorption and simple fabrication simultaneously.

Naifei Ren

Papers

Femtosecond pulsed laser textured titanium surfaces with stable superhydrophilicity and superhydrophobicity

Microstructure evolution and grain refinement of Ti-6Al-4V alloy by laser shock processing

Room temperature photoluminescence properties of CuO nanowire arrays

Broadband visible-light absorber via hybridization of propagating surface plasmon

A finite element analysis of thermal relaxation of residual stress in laser shock processing Ni-based alloy GH4169