다중혈관 관상동맥 환자에서 y-문합을 이용하여 양쪽 내흉동맥만을 사용한 우회술의 조기 성적

A composite film of nickel sulfide/platinum/titanium foil (NiS/Pt/Ti) with low cost and high electrocatalytic activity was synthesized by the use of an in situ electropolymerization route and proposed as a counter electrode (CE) catalyst for flexible dye-sensitized solar cells (FDSSCs). The FDSSC with the NiS/Pt/Ti CE exhibited a comparable power conversion efficiency of 7.20% to the FDSSC with the platinum/titanium (Pt/Ti) CE showing 6.07%. The surface morphology of the NiS/Pt/Ti CE with one-dimensional (1D) structure is characterized by using the scanning electron microscopy (SEM). The NiS/Pt/Ti CE also displayed multiple electrochemical functions of excellent conductivity, great electrocatalytic ability for iodine/triiodine, and low charge transfer resistance of 2.61 ± 0.02 Ω cm2, which were characterized by using the cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and Tafel polarization plots. The photocurrent-photovoltage (J-V) character curves were further used to calculate the theoretical optical light performance parameters of the FDSSCs. It may be said that the NiS/Pt/Ti counter electrode is a promising catalytic material to replace the expensive platinum in FDSSCs.

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A highly efficient flexible dye-sensitized solar cell based on nickel sulfide/platinum/titanium counter electrode

During the last few years, transition metal oxides (TMO) such as molybdenum tri-oxide (MoO3), vanadium pent-oxide (V2O5) or tungsten tri-oxide (WO3) have been extensively studied because of their exceptional electronic properties for charge injection and extraction in organic electronic devices. These unique properties have led to the performance enhancement of several types of devices and to a variety of novel applications. TMOs have been used to realize efficient and long-term stable p-type doping of wide band gap organic materials, charge-generation junctions for stacked organic light emitting diodes (OLED), sputtering buffer layers for semi-transparent devices, and organic photovoltaic (OPV) cells with improved charge extraction, enhanced power conversion efficiency and substantially improved long term stability. Energetics in general play a key role in advancing device structure and performance in organic electronics; however, the literature provides a very inconsistent picture of the electronic structure of TMOs and the resulting interpretation of their role as functional constituents in organic electronics. With this review we intend to clarify some of the existing misconceptions. An overview of TMO-based device architectures ranging from transparent OLEDs to tandem OPV cells is also given. Various TMO film deposition methods are reviewed, addressing vacuum evaporation and recent approaches for solution-based processing. The specific properties of the resulting materials and their role as functional layers in organic devices are discussed.

Transition Metal Oxides for Organic Electronics: Energetics, Device Physics and Applications

Dye-sensitized solar cell (DSSC) offers an efficient and easily implemented technology for future energy supply. Compared to conventional silicon solar cells, it provides comparable power conversion efficiency (PCE) at low material and manufacturing costs. DSSC materials such as titanium oxide (TiO 2 ) are inexpensive, abundant and innocuous to the environment. Since DSSC materials are less prone to contamination and processable at ambient temperature, a roll-to-roll process could be utilized to print DSSCs on the mass production line. DSSCs perform better under lower light intensities, which makes them an excellent choice for indoor applications. Due to the advancement of molecular engineering, colored and transparent thin films have been introduced to enhance the aesthetic values. Up to now, such benefits have attracted considerable research interests and commercialization effort. Here, this review examines advanced techniques and research trends of this promising technology from the perspective of device modeling, state-of-art techniques, and novel device structures.

Review on dye-sensitized solar cells (DSSCs): Advanced techniques and research trends

Electrochromics for smart windows: Oxide-based thin films and devices

Ultrathin transition-metal-based nanomeshes can perfectly combine the advantages of two-dimensional (2D) ultrathin nanosheets and porous nanostructures, which have wide applications in energy storage and conversion. In this work, we present an etch-free one-step approach to directly synthesize the ultrathin Co3O4 nanomeshes (Co-UNMs) by employing a CoCl2/K3Co(CN)6 cyanogel as the reaction precursor. The 2D planar structural unit and solid properties of the cyanogel result in the preferential assembly of generated crystal nuclei at the solid–liquid interface (i.e., cyanogel–solution interface) in the 2D direction, which plays a key role in the formation of nanomeshes. The as-prepared Co-UNMs with 1.5 nm thickness and abundant pores have high surface area and numerous defect atoms, resulting in enhanced activity for the oxygen evolution reaction (OER) in alkaline media, such as a low overpotential of 307 mV at 10 mA cm–2, a small Tafel slope of 76 mV dec–1, and attractive durability in 1 M KOH electrolyte.

Ultrathin Co3O4 Nanomeshes for the Oxygen Evolution Reaction

The 2D conductive metal-organic frameworks (MOFs) are expected to be an ideal electrocatalyst due to their high utilization of metal atoms. Exploring a new conjugated ligand with extra active metallic center can further boost the structural advantages of conductive MOFs. In this work, hexaiminohexaazatrinaphthalene (HAHATN) is employed as a conjugated ligand to construct bimetallic sited conductive MOFs (M23(M13∙HAHATN)2) with an extra M-N2 moiety. Density functional theory (DFT) calculations demonstrate that the 2D conjugated framework renders M23(M13∙HAHATN)2 a high electric conductivity with narrow bandgap (0.19 eV) for electron transfer and a favorable in-plane porous structure (2.7 nm) for mass transfer. Moreover, the metal atom at the extra M-N2 moiety has a higher unsaturation degree than that at M-N4 linkage, resulting in a stronger ability to donate electrons for enhancing electroactivity. These characteristics endow the new conductive MOFs with an enhanced electroactivity for hydrogen evolution reaction (HER) electrocatalysis. Among the series of M23(M13∙HAHATN)2 MOF, Ni3(Ni3∙HAHATN)2 nanosheets with the optimal structure exhibit a small overpotential of 115 mV at 10 mA cm-2, low Tafel slope of (45.6 mV dec-1), and promising electrocatalytic stability for HER. This work provides an effective strategy for designing conductive MOFs with a favorable structure for electrocatalysis.

https://onlinelibrary.wiley.com/doi/epdf/10.1002/advs.202000012

Conductive Metal-Organic Frameworks with Extra Metallic Sites as an Efficient Electrocatalyst for the Hydrogen Evolution Reaction.

Optimizing component and morphology of precious metal nanomaterials can effectively promote their electrocatalytic performance and expand their application area. In this work, Rh2P ultrathin nanosheets (Rh2P uNSs) with atomic thickness and big surface area are successfully synthesized by phosphating treatment of Rh ultrathin nanosheets (Rh uNSs). Benefiting from special morphology, component, and electronic structure, Rh2P uNSs simultaneously display enhanced electrocatalytic activity for anodic hydrazine oxidation reaction (HzOR) as well as cathodic hydrogen evolution reaction (HER) compared to Rh uNSs in acidic media, which only require at −10 mV and 300 mV potential to obtain 10 mA cm−2 current density for HzOR and HER in three electrode system, respectively. In two electrode system, the symmetric Rh2P uNSs||Rh2P uNSs electrolyzer only requires electrolysis voltage of 0.377 V to achieve 10 mA cm−2 current density for HzOR boosted water splitting in strong acidic media, highlighting an energy-saving electrochemical hydrogen production method.

Fumin Li

Papers

A highly efficient flexible dye-sensitized solar cell based on nickel sulfide/platinum/titanium counter electrode

Ultrathin Co3O4 Nanomeshes for the Oxygen Evolution Reaction

Conductive Metal-Organic Frameworks with Extra Metallic Sites as an Efficient Electrocatalyst for the Hydrogen Evolution Reaction.

Rhodium phosphide ultrathin nanosheets for hydrazine oxidation boosted electrochemical water splitting

Porous Pd‐PdO Nanotubes for Methanol Electrooxidation