Heterogeneous Structure of Ni-Mo Nanoalloys Decorated on MoO for an Efficient Hydrogen Evolution Reaction Using Hydrogen Spillover.

Herein, a heterogeneous structure of Ni-Mo catalyst comprising NiMo nanoalloys decorated on a MoO matrix via electrodeposition is introduced. This catalyst exhibits remarkable hydrogen evolution reaction (HER) activity across a range of pH conditions. The heterogeneous Ni-Mo catalyst showed low overpotentials only of 24 and 86, 21 and 60, and 37 and 168 mV to produce a current density of 10 and 100 mA cm (η and η) in alkaline, acidic, and neutral media, respectively, which represents one of the most active catalysts for the HER.

Development of Hybrid Pseudohalide Tin Perovskites for Highly Stable Carbon-Electrode Solar Cells.

Tin-based perovskites degrade rapidly upon interaction with water and oxygen in air because Sn-I bonds are weak. To address this issue, we developed novel tin perovskites, FASnI(SCN) ( = 0, 1, 2, or 3), by employing a pseudohalide, thiocyanate (SCN), as a replacement for halides and as an inhibitor to suppress the Sn/Sn oxidation. The structural and electronic properties of pseudohalide tin perovskites in this series were explored with quantum-chemical calculations by employing the plane-wave density functional theory (DFT) method; the corresponding results are consistent with the experimental results.

Freestanding Ion Gels for Flexible, Printed, Multifunctional Microsupercapacitors.

Freestanding ion gels (FIGs) provide unique opportunities for scalable, low-cost fabrication of flexible microsupercapacitors (MSCs). While conventional MSCs employ a distinct electrolyte and substrate, FIGs perform both functions, offering new possibilities for device integration and multifunctionality while maintaining high performance. Here, a capillarity-driven printing method is demonstrated to manufacture high-precision graphene electrodes on FIGs for MSCs.

Transfer Printing of Sub-5 μm Graphene Electrodes for Flexible Microsupercapacitors.

Printed graphene microsupercapacitors (MSCs) are attractive for scalable and low-cost on-chip energy storage for distributed electronic devices. Although electronic devices have experienced significant scaling to smaller formats, the corresponding miniaturization of energy storage components has been limited, with a typical resolution of ∼30 μm for printed graphene patterns to date. Transfer printing is demonstrated here for patterning graphene electrodes with fine line and spacing resolution less than 5 μm.

All-Printed, Self-Aligned Carbon Nanotube Thin-Film Transistors on Imprinted Plastic Substrates.

We present a self-aligned process for printing thin-film transistors (TFTs) on plastic with single-walled carbon nanotube (SWCNT) networks as the channel material. The SCALE (self-aligned capillarity-assisted lithography for electronics) process combines imprint lithography with inkjet printing. Specifically, inks are jetted into imprinted reservoirs, where they then flow into narrow device cavities due to capillarity.

Ga-Doped Pt-Ni Octahedral Nanoparticles as a Highly Active and Durable Electrocatalyst for Oxygen Reduction Reaction.

Bimetallic PtNi nanoparticles have been considered as a promising electrocatalyst for oxygen reduction reaction (ORR) in polymer electrolyte membrane fuel cells (PEMFCs) owing to their high catalytic activity. However, under typical fuel cell operating conditions, Ni atoms easily dissolve into the electrolyte, resulting in degradation of the catalyst and the membrane-electrode assembly (MEA). Here, we report gallium-doped PtNi octahedral nanoparticles on a carbon support (Ga-PtNi/C).

High-Resolution Transfer Printing of Graphene Lines for Fully Printed, Flexible Electronics.

Pristine graphene inks show great promise for flexible printed electronics due to their high electrical conductivity and robust mechanical, chemical, and environmental stability. While traditional liquid-phase printing methods can produce graphene patterns with a resolution of ∼30 μm, more precise techniques are required for improved device performance and integration density. A high-resolution transfer printing method is developed here capable of printing conductive graphene patterns on plastic with line width and spacing as small as 3.

Surface Modification of TiO2 Photoanodes with Fluorinated Self-Assembled Monolayers for Highly Efficient Dye-Sensitized Solar Cells.

Dye aggregation and electron recombination in TiO2 photoanodes are the two major phenomena lowering the energy conversion efficiency of dye-sensitized solar cells (DSCs). Herein, we introduce a novel surface modification strategy of TiO2 photoanodes by the fluorinated self-assembled monolayer (F-SAM) formation with 1H,1H,2H,2H-perfluorooctyltriethoxysilane (PFTS), blocking the vacant sites of the TiO2 surface after dye adsorption. The F-SAM helps to efficiently lower the surface tension, resulting in efficient repelling ions, e.

Densely packed siloxane barrier for blocking electron recombination in dye-sensitized solar cells.

A challenge in developing photovoltaic devices is to minimize the loss of electrons, which can seriously deteriorate energy conversion efficiency. In particular, minimizing this negative process in dye-sensitized solar cells (DSCs) is imperative. Herein, we use three different kinds of siloxanes, which are adsorbable to titania surfaces and polymerizable in forming a surface passivation layer, to reduce the electron loss.

Toward Higher Energy Conversion Efficiency for Solid Polymer Electrolyte Dye-Sensitized Solar Cells: Ionic Conductivity and TiO2 Pore-Filling.

Even though the solid polymer electrolyte has many intrinsic advantages over the liquid electrolyte, its ionic conductivity and mesopore-filling are much poorer than those of the liquid electrolyte, limiting its practical application to electrochemical devices such as dye-sensitized solar cells (DSCs). Two major shortcomings associated with utilizing solid polymer electrolytes in DSCs are first discussed, low ionic conductivity and poor pore-filling in mesoporous photoanodes for DSCs. In addition, future directions for the successful utilization of solid polymer electrolytes toward improving the performance of DSCs are proposed.

Tetrathiafulvalene as an electron acceptor for positive charge induction on the surface of silver nanoparticles for facilitated olefin transport.

Tetrathiafulvalene (TTF), a well-known electron donor, can also behave as an electron acceptor after being adsorbed on the surface of silver nanoparticles (Ag NPs), thereby inducing a partial positive charge on the Ag NPs surface. The Ag NPs activated by TTF help propylene transport much faster than propane, i.e.

Successful demonstration of an efficient I(-)/(SeCN)2 redox mediator for dye-sensitized solar cells.

A new I(-)/(SeCN)(2) redox mediator has favorable properties for dye-sensitized solar cells (DSCs) such as less visible light absorption, higher ionic conductivity, and downward shift of redox potential than I(-)/I(3)(-). It was then applied for DSCs towards increasing energy conversion efficiency, giving a new potential for improving performance.

Synergistic catalytic effect of a composite (CoS/PEDOT:PSS) counter electrode on triiodide reduction in dye-sensitized solar cells.

Inorganic/organic nanocomposite counter electrodes comprised of sheetlike CoS nanoparticles dispersed in polystyrenesulfonate-doped poly(3,4-ethylenedioxythiophene (CoS/PEDOT:PSS) offer a synergistic effect on catalytic performance toward the reduction of triiodide for dye-sensitized solar cells (DSSCs), yielding 5.4% power conversion efficiency, which is comparable to that of the conventional platinum counter electrode (6.1%).