Direct Current Pulse Atmospheric Pressure Plasma Jet Treatment on Electrochemically Deposited NiFe/Carbon Paper and Its Potential Application in an Anion-Exchange Membrane Water Electrolyzer.

An atmospheric pressure plasma jet (APPJ) is used to process electrochemically deposited NiFe on carbon paper (NiFe/CP). The reactive oxygen and nitrogen species (RONs) of the APPJ modify the surface properties, chemical bonding types, and oxidation states of the material at the self-sustained temperature of the APPJ. The APPJ treatment further enhances the hydrophilicity and creates a higher disorder level in the carbon material. Moreover, the metal carbide bonds of NiFe/CP formed in the electrochemical deposition (ED) process are converted to metal oxide bonds after APPJ processing. The potential application of APPJ treatment on NiFe/CP in alkaline water electrolysis is demonstrated. With more oxygen-containing species and better hydrophilicity after APPJ treatment, APPJ-treated NiFe/CP is applied as the electrocatalyst for the oxygen evolution reaction (OER) in alkaline water electrolysis. APPJ-treated NiFe/CP is also used in a custom-made anion-exchange membrane water electrolyzer (AEMWE); this should contribute toward realizing the practical large-scale application of AEM for hydrogen production.

Ultrafast Fabrication of H2SO4, LiCl, and Li2SO4 Gel Electrolyte Supercapacitors with Reduced Graphene Oxide (rGO)-LiMnOx Electrodes Processed Using Atmospheric-Pressure Plasma Jet.

Pastes containing reduced graphene oxide (rGO) and LiCl-Mn(NO3)2·4H2O are screen-printed on a carbon cloth substrate and then calcined using a nitrogen atmospheric-pressure plasma jet (APPJ) for conversion into rGO-LiMnOx nanocomposites. The APPJ processing time is within 300 s. RGO-LiMnOx on carbon cloth is used to sandwich H2SO4, LiCl, or Li2SO4 gel electrolytes to form hybrid supercapacitors (HSCs). The areal capacitance, energy density, and cycling stability of the HSCs are evaluated using electrochemical measurement. The HSC utilizing the Li2SO4 gel electrolyte exhibits enhanced electrode-electrolyte interface reactions and increased effective surface area due to its high pseudocapacitance (PC) ratio and lithium ion migration rate. As a result, it demonstrates the highest areal capacitance and energy density. The coupling of charges generated by embedded lithium ions with the electric double-layer capacitance (EDLC) further contributed to the significant overall capacitance enhancement. Conversely, the HSC with the H2SO4 gel electrolyte exhibits better cycling stability. Our findings shed light on the interplay between gel electrolytes and electrode materials, offering insights into the design and optimization of high-performance HSCs.

NiFe2O4 Material on Carbon Paper as an Electrocatalyst for Alkaline Water Electrolysis Module.

NiFe2O4 material is grown on carbon paper (CP) with the hydrothermal method for use as electrocatalysts in an alkaline electrolyzer. NiFe2O4 material is used as the anode and cathode catalysts (named NiFe(+)/NiFe(-) hereafter). The results are compared with those obtained using CP/NiFe as the anode and CP/Ru as the cathode (named NiFe)(+)/Ru(-) hereafter). During cell operation with NiFe(+)/Ru(-), the current density reaches 500 mA/cm2 at a cell voltage of 1.79 V, with a specific energy consumption of 4.9 kWh/m3 and an energy efficiency of 66.2%. In comparison, for NiFe(+)/NiFe(-), the current density reaches 500 mA/cm2 at a cell voltage of 2.23 V, with a specific energy consumption of 5.7 kWh/m3 and an energy efficiency of 56.6%. The Faradaic efficiency is 96-99%. With the current density fixed at 400 mA/cm2, after performing a test for 150 h, the cell voltage with NiFe(+)/Ru(-) increases by 0.167 V, whereas that with NiFe(+)/NiFe(-) decreases by only 0.010 V. Good, long-term stability is demonstrated.

Low-Pressure Plasma-Processed Ruthenium/Nickel Foam Electrocatalysts for Hydrogen Evolution Reaction.

In this paper, low-pressure 95%Ar-5%H2, pure Ar, and 95%Ar-5%O2 plasmas were used for post-treatment of ruthenium (Ru) deposited on nickel foam (NF) (Ru/NF). Ru/NF was then tested as a catalyst for a hydrogen evolution reaction. Significant improvement in electrocatalytic activity with the lowest overpotential and Tafel slope was observed in an alkaline electrolyte (1 M KOH) with 95%Ar-5%O2 plasma processing on Ru/NF. Linear scanning electrical impedance spectroscopy (EIS) and cyclic voltammetry (CV) also indicate the lowest interfacial impedance and largest electrical double layer capacitance. Experimental results with 0.1 M phosphate buffered saline (PBS) and 0.5 M H2SO4 electrolytes were also demonstrated and compared.

The Influence of Helium Dielectric Barrier Discharge Jet (DBDjet) Plasma Treatment on Bathocuproine (BCP) in p-i-n-Structure Perovskite Solar Cells.

A bathocuproine (BCP) layer is typically used as the hole-blocking layer in p-i-n-structure perovskite solar cells (PSCs) between PC61BM and Ag electrodes. Before evaporating the Ag, we used a low-temperature (<40 °C) atmospheric-pressure dielectric barrier discharge jet (DBDjet) to treat the BCP with different scan rates. The main purpose of this was to change the contact resistance between the BCP layer and the Ag electrodes through surface modification using a DBDjet. The best power conversion efficiency (PCE) of 13.11% was achieved at a DBDjet scan rate of 2 cm/s. The He DBDjet treatment introduced nitrogen to form C-N bonds and create pits on the BCP layer. This deteriorated the interface between the BCP and the follow-up deposited-Ag top electrode. Compared to the device without the plasma treatment on the BCP layer, the He DBDjet treatment on the BCP layer reduced photocurrent hysteresis but deteriorated the fill factor and the efficiency of the PSCs.

Dielectric Barrier Discharge Plasma Jet (DBDjet) Processed Reduced Graphene Oxide/Polypyrrole/Chitosan Nanocomposite Supercapacitors.

Reduced graphene oxide (rGO) and/or polypyrrole (PPy) are mixed with chitosan (CS) binder materials for screen-printing supercapacitors (SCs) on arc atmospheric-pressure plasma jet (APPJ)-treated carbon cloth. The performance of gel-electrolyte rGO/CS, PPy/CS, and rGO/PPy/CS SCs processed by a dielectric barrier discharge plasma jet (DBDjet) was assessed and compared. DBDjet processing improved the hydrophilicity of these three nanocomposite electrode materials. Electrochemical measurements including electrical impedance spectroscopy (EIS), cyclic voltammetry (CV), and galvanostatic charging-discharging (GCD) were used to evaluate the performance of the three types of SCs. The Trasatti method was used to evaluate the electric-double layer capacitance (EDLC) and pseudocapacitance (PC) of the capacitance. The energy and power density of the three types of SCs were illustrated and compared using Ragone plots. Our experiments verify that, with the same weight of active materials, the combined use of rGO and PPy in SCs can significantly increase the capacitance and improve the operation stability.

Electropolymerized Poly(3,4-ethylenedioxythiophene)/Screen-Printed Reduced Graphene Oxide-Chitosan Bilayer Electrodes for Flexible Supercapacitors.

An electropolymerized poly(3,4-ethylenedioxythiophene) (PEDOT)/screen-printed reduced graphene oxide (rGO)-chitosan (CS) bilayer material was coated on carbon cloth to form electrodes for gel-electrolyte flexible supercapacitors. The conductive polymer and carbon-based materials mainly contribute pseudocapacitance (PC) and electrical double-layer capacitance (EDLC), respectively. The high porosity and hydrophilicity of the PEDOT/rGO-CS bilayer material offers a large contact area and improves the contact quality for the gel electrolyte, thereby enhancing the capacitive performance. Cyclic voltammetry (CV) under a potential scan rate of 2 mV/s revealed that a maximum areal capacitance of 1073.67 mF/cm2 was achieved. The capacitance contribution ratio PC/EDLC was evaluated to be ∼67/33 by the Trasatti method. A 10,000-cycle CV test showed a capacitance retention rate of 99.3% under a potential scan rate of 200 mV/s, indicating good stability. The areal capacitance remains similar under bending with a bending curvature of up to 1.5 cm-1.

Improved efficiency and air stability of two-dimensional p-i-n inverted perovskite solar cells by Cs doping.

Two-dimensional perovskite solar cells (2-D PSCs) have attracted much research attention in recent years because they are more stable in a regular environment than three-dimensional (3-D) ones are. In this study, we doped Cs into 2D perovskite (BA2(MA)2Pb3I10) films as the absorbing layers of the 2-D p-i-n inverted PSCs to investigate the influence of the Cs doping concentration on the properties of the 2-D perovskite films and the fabricated solar cells. Cs doping clearly improves the power conversion efficiency (PCE) and air stability of the PSCs. Doping perovskite with 10% Cs (the best doping concentration in this study) can increase the PSC efficiency from 7.98% to 10.11%. Scanning electron microscopy indicates the improved surface quality and crystallinity by Cs doping. However, excess Cs doping degrades the PCE of the PSCs. Furthermore, 10% Cs doped PSCs show air stability superior to that of undoped ones in unpackaged humidity environments. After exposure to 55% relative humidity (RH) in 19 °C air for 300 h, the PCE of the PSC decreased by only 39%, in contrast to 84% for the undoped PSC.

Low-Temperature (<40 °C) Atmospheric-Pressure Dielectric-Barrier-Discharge-Jet Treatment on Nickel Oxide for p-i-n Structure Perovskite Solar Cells.

A scan-mode low-temperature (<40 °C) atmospheric-pressure helium (He) dielectric-barrier discharge jet (DBDjet) is applied to treat nickel oxide (NiO) thin films for p-i-n perovskite solar cells (PSCs). Reactive plasma species help reduce the trap density, improve the transmittance and wettability, and deepen the valence band maximum (VBM) level. A NiO surface with the lower trap density surface of NiO allows better interfacial contact with the MAPbI3 layer and increases the carrier extraction capability. MAPbI3 can better crystallize on a more hydrophilic NiO surface, thereby suppressing charge recombination from the grain boundary and the interface. Further, the deeper VBM allows better band alignment and reduces the probability of nonradiative recombination. NiO treatment using He DBDjet with a scan rate of 0.3 cm/s can improve PSC efficiency from 13.63 to 14.88%.

Atmospheric Pressure Plasma Jet-Assisted Synthesis of Zeolite-Based Low-k Thin Films.

Zeolites are ideal low-dielectric constant (low-k) materials. This paper reports on a novel plasma-assisted approach to the synthesis of low-k thin films comprising pure-silica zeolite MFI. The proposed method involves treating the aged solution using an atmospheric pressure plasma jet (APPJ). The high reactivity of the resulting nitrogen plasma helps to produce zeolite crystals with high crystallinity and uniform crystal size distribution. The APPJ treatment also remarkably reduces the time for hydrothermal reaction. The zeolite MFI suspensions synthesized with the APPJ treatment are used for the wet deposition to form thin films. The deposited zeolite thin films possessed dense morphology and high crystallinity, which overcome the trade-off between crystallinity and film quality. Zeolite thin films synthesized using the proposed APPJ treatment achieve low leakage current (on the order of 10-8 A/cm2) and high Young's modulus (12 GPa), outperforming the control sample synthesized without plasma treatment. The dielectric constant of our zeolite thin films was as low as 1.41. The overall performance of the low-k thin films synthesized with the APPJ treatment far exceed existing low-k films comprising pure-silica MFI.

Atmospheric-pressure-plasma-jet processed carbon nanotube (CNT)-reduced graphene oxide (rGO) nanocomposites for gel-electrolyte supercapacitors.

This study evaluates DC-pulse nitrogen atmospheric-pressure-plasma-jet processed carbon nanotube (CNT)-reduced graphene oxide (rGO) nanocomposites for gel-electrolyte supercapacitor applications. X-ray photoelectron spectroscopy (XPS) indicates decreased oxygen content (mainly, C-O bonding content) after nitrogen APPJ processing owing to the oxidation and vaporization of ethyl cellulose. Nitrogen APPJ processing introduces nitrogen doping and improves the hydrophilicity of the CNT-rGO nanocomposites. Raman analysis indicates that nitrogen APPJ processing introduces defects and/or surface functional groups on the nanocomposites. The processed CNT-rGO nanocomposites on carbon cloth are applied to the electrodes of H2SO4-polyvinyl alcohol (PVA) gel-electrolyte supercapacitors. The best achieved specific (areal) capacitance is 93.1 F g-1 (9.1 mF cm-2) with 15 s APPJ-processed CNT-rGO nanocomposite electrodes, as evaluated by cyclic voltammetry under a potential scan rate of 2 mV s-1. The addition of rGOs in CNTs in the nanoporous electrodes improves the supercapacitor performance.

A Photoactivated Gas Detector for Toluene Sensing at Room Temperature Based on New Coral-Like ZnO Nanostructure Arrays.

A photoactivated gas detector operated at room temperature was microfabricated using a simple hydrothermal method. We report that the photoactivated gas detector can detect toluene using a UV illumination of 2 µW/cm². By ultraviolet (UV) illumination, gas detectors sense toluene at room temperature without heating. A significant enhancement of detector sensitivity is achieved because of the high surface-area-to-volume ratio of the morphology of the coral-like ZnO nanorods arrays (NRAs) and the increased number of photo-induced oxygen ions under UV illumination. The corresponding sensitivity (ΔR/R0) of the detector based on coral-like ZnO NRAs is enhanced by approximately 1022% compared to that of thin-film detectors. The proposed detector greatly extends the dynamic range of detection of metal-oxide-based detectors for gas sensing applications. We report the first-ever detection of toluene with a novel coral-like NRAs gas detector at room temperature. A sensing mechanism model is also proposed to explain the sensing responses of gas detectors based on coral-like ZnO NRAs.

Solution-processed ultra-low-k thin films comprising single-walled aluminosilicate nanotubes.

Nanotube-based ultra-low-k thin films with high Young's modulus composed of single-walled aluminosilicate nanotubes (AlSiNTs) and a trace amount of poly(vinyl alcohol) (PVA) have been developed. The dehydrated AlSiNT film possesses a relative permittivity of 1.05, and a Young's modulus of 25 GPa, which exceed those of most existing ultra-low-k materials.

Rapid atmospheric pressure plasma jet processed reduced graphene oxide counter electrodes for dye-sensitized solar cells.

In this work, we present the use of reduced graphene oxide (rGO) as the counter electrode materials in dye-sensitized solar cells (DSSCs). rGO was first deposited on a fluorine-doped tin oxide glass substrate by screen-printing, followed by post-treatment to remove excessive organic additives. We investigated the effect of atmospheric pressure plasma jet (APPJ) treatment on the DSSC performance. A power conversion efficiency of 5.19% was reached when DSSCs with an rGO counter electrode were treated by APPJs in the ambient air for a few seconds. For comparison, it requires a conventional calcination process at 400 °C for 15 min to obtain comparable efficiency. Scanning electron micrographs show that the APPJ treatment modifies the rGO structure, which may reduce its conductivity in part but simultaneously greatly enhances its catalytic activity. Combined with the rapid removal of organic additives by the highly reactive APPJ, DSSCs with APPJ-treated rGO counter electrode show comparable efficiencies to furnace-calcined rGO counter electrodes with greatly reduced process time. This ultrashort process time renders an estimated energy consumption per unit area of 1.1 kJ/cm(2), which is only one-third of that consumed in a conventional furnace calcination process. This new methodology thus saves energy, cost, and time, which is greatly beneficial to future mass production.

Periodic anti-ring back reflectors for hydrogenated amorphous silicon thin-film solar cells.

Large and periodic anti-ring arrays are fabricated by using a monolayer of polymer/nanosphere hybrid technique and applied as back reflectors in substrate-type hydrogenated amorphous silicon (a-Si:H) thin-film solar cells. The structure of each anti-ring comprises a nanodome centered inside a nanohole. The excitation of Bloch wave surface plasmon polaritons is observed in the Ag-coated anti-ring arrays. The nanodomes of the anti-ring arrays turn out to enhance large-angle light scattering and increase the effective optical path in the solar cell. The resulting efficiency of an ultrathin a-Si:H (thickness: 150 nm) solar cell is enhanced by 39% compared to that with a flat back reflector and by 13% compared to that with a nanohole back reflector.

Multi-layer thermoelectric-temperature-mapping microbial incubator designed for geo-biochemistry applications.

We demonstrate a novel, vertical temperature-mapping incubator utilizing eight layers of thermoelectric (TE) modules mounted around a test tube. The temperature at each layer of the TE module is individually controlled to simulate the vertical temperature profile of geo-temperature variations with depth. Owing to the constraint of non-intrusion to the filled geo-samples, the temperature on the tube wall is adopted for measurement feedback. The design considerations for the incubator include spatial arrangement of the energy transfer mechanism, heating capacity of the TE modules, minimum required sample amount for follow-up instrumental or chemical analysis, and the constraint of non-intrusion to the geo-samples during incubation. The performance of the incubator is experimentally evaluated with two tube conditions and under four preset temperature profiles. Test tubes are either empty or filled with quartz sand, which has comparable thermal properties to the materials in the geo-environment. The applied temperature profiles include uniform, constant temperature gradient, monotonic-increasing parabolic, and parabolic. The temperature on the tube wall can be controlled between 20 °C and 90 °C with an averaged root mean squared error of 1 °C.

Enhanced optical absorption of dye-sensitized solar cells with microcavity-embedded TiO2 photoanodes.

This paper reports the enhanced performance of dye-sensitized solar cells (DSSCs) with microcavity-embedded nanoporous TiO2 photoanodes. For DSSCs with photoanodes composed of a stack TiO2 sublayers with microcavity concentrations arranged from low to high on the light illumination path, the short-circuit current density and the conversion efficiency were improved. A pronounced increase in optical absorption and incident monochromatic photon-to-current conversion efficiency in the long-wavelength region indicated that the enhancement of cell performance was due to the multiple scattering of light by the microcavities and the light confinement by the stack of TiO2 sublayers with a high-to-low effective index of refraction.

Enhanced thermoelectric power in dual-gated bilayer graphene.

The thermoelectric power of a material, typically governed by its band structure and carrier density, can be varied by chemical doping that is often restricted by solubility of the dopant. Materials showing large thermoelectric power are useful for many industrial applications, such as the heat-to-electricity conversion and the thermoelectric cooling device. Here we show a full electric-field tuning of thermoelectric power in a dual-gated bilayer graphene device resulting from the opening of a band gap by applying a perpendicular electric field on bilayer graphene. We uncover a large enhancement in thermoelectric power at a low temperature, which may open up a new possibility in low temperature thermoelectric application using graphene-based device.