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Using a thermal evaporator, various porous Cu films were deposited according to the deposition pressure. CuO films were formed by post heat treatment in the air. Changes in morphological and structural characteristics of films were analyzed using field-emission scanning electron microscopy (FE-SEM) and X-ray diffraction (XRD). Relative density and porosity were quantitatively calculated. CuO films with various pores ranging from 39.4 to 95.2% were successfully manufactured and were applied as gas sensors for H2S detection on interdigitated electrode (IDE) substrate. Resistance change was monitored at 325 °C and an increase in porosity of the film improved the sensor performance. The CuO-10 gas sensor with a high porosity of 95.2% showed a relatively high response (2.7) and a fast recovery time (514 s) for H2S 1.5 ppm. It is confirmed that the porosity of the CuO detection layer had a significant effect on response and recovery time.

Achieving high ionic conductivity, wide voltage window, and good mechanical strength in a single material remains a key challenge for polymer-based electrolytes for use in solid-state supercapacitors (SCs). Herein, we report cross-linked composite gel polymer electrolytes (CGPEs) based on multi-cross-linkable H-shaped poly(ethylene oxide)–poly(propylene oxide) (PEO-PPO) tetrablock copolymer precursors, SiO2 nanoparticles, and 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, an ionic liquid (IL). Self-standing CGPE membranes with a high IL content were prepared using in situ cross-linking reactions between the silane groups present in the precursor and the SiO2 surface. The incorporation of an optimal amount of SiO2 increased the cross-linking density of the resulting CGPE while reducing polymer-chain ordering and, consequently, increasing both ionic conductivity and mechanical strength. As a result, the CGPE with 0.1 wt % SiO2 exhibited a high ionic conductivity (2.22 × 10–3 S cm–1 at 25 °C), good tensile strength (453 kPa), and high thermal stability up to 330 °C. Finally, an all-solid-state SC assembled with the prepared CGPE showed a high operating voltage (3 V), a large specific capacitance (103.9 F g–1 at 1 A g–1), and excellent durability (94% capacitance retention over 10,000 charge/discharge cycles), which highlights its strong potential as a solid-state electrolyte for SCs.

Nanolenses of alkali metal halides can be a unique optical element due to their hygroscopicity, optical transparency, and high mobility of constituent ions. It has been challenging, however, to form and place such lenses in a controlled manner. Here, we report micro/nanolenses of various alkali metal halides arranged as a one-dimensional (1D) array, using the exterior of single-walled carbon nanotubes (SWNTs) as a template for forming the lenses. Applying an electrical bias to an aqueous solution of alkali metal halides placed at the end of an SWNT array causes ionic transport along the exterior of SWNTs and the subsequent formation of salt micro/nanocrystals. The crystals serve as micro/nanolenses that optically visualize individual SWNTs and amplify their Raman scattering by orders of magnitude. Molecules dissolved in the ionic solution can be electrokinetically transported along the nanotubes, captured within the lenses, and analyzed by Raman spectroscopy, which we demonstrate by detecting ∼12 attomoles of glucose and 2 femtomoles of urea. The hygroscopic salt nanolenses are robust under various ambient conditions indefinitely, by transitioning to liquid droplets above their deliquescence relative humidity, yet can be removed nondestructively by water. Our approach could have broad implications in the optical visualization of 1D nanostructures, molecular transport or chemical reactions in 1D space, and molecular spectroscopy in salty environments.

For decades, scholars of religious studies have questioned the anachronism of the category of “religion” for discussing the historical emergence of Judaism, Christianity, Buddhism, and Hinduism. Beginning already with Wilfred Cantwell Smith in the 1960s, however, Manichaeism was heralded as an exception to this pattern, and Mani has been understood as perhaps the first to found a new “religion.” This article considers how this model shaped the interpretation of the Cologne Mani Codex (CMC) and offers a fresh reading of its rhetoric of differentiation and identification. It attends to how the CMC frames Mani as a reformer among the Baptists and in continuity with this Baptist past. It ultimately argues that the creators of the CMC did not think of “Manichaeism” as a distinct “religion.” Finally, it aims to recalibrate the study of the Cologne Mani Codex towards broader attempts at situating it within a Syro-Mesopotamian milieu.

Novel nitrogen-functionalized multimodal porous graphite felt (GF) electrodes for all-vanadium redox flow batteries (VRFB) have been developed using a simple binder-free fabrication method. We synergistically combined a polymer of intrinsic microporosity (PIM), as a carbon and nitrogen precursor, with vapor-induced phase separation. The GF with a carbonized PIM skin layer showed a high surface area and multimodal pore architecture featuring interconnected micro-, meso-, and macropores. The enhanced electrochemical reactivity and wettability , and excellent electronic conductivity of the prepared electrodes successfully improved the overall kinetics of the redox reactions of the vanadium ion species by providing highly active catalytic sites and efficient ion and electron transport pathways. This resulted in the outstanding performance of VRFB single cells using this material as electrodes.

Doped carbon nanostructures with transition metals and nitrogen (N) as doping sources used as promising non-precious metal (NPM) catalysts for oxygen reduction reaction (ORR) have been intensively researched. However, the NPM catalysts, prepared using a mixture of transition metal, nitrogen, and carbon sources, contained both the transition metal-N and N-doped carbon-coated transition metal nanoparticles (NPs) in the surface structure. However, among the transition metal-N and N-doped carbon-coated transition metal NPs, the predominant electrocatalytic active sites for ORR in the NPM catalysts remain uncertain. In this study, we proposed the NPM catalysts for ORR with various active sites such as the doped carbon-coated Fe NPs and/or N- and/or S-doped carbon structures through one- or two-step heating processes. The sample synthesized using a two-step heating process with doped carbon supported Fe NPs and dicyandiamide exhibited significantly improved activity and stability for ORR in O 2-saturated H2SO4, due to a synergistic effect by the co-doping of S and N in the carbon structure and the Fe NPs encapsulated in the doped carbon, comparable to a commercial Pt/C catalyst. In particular, the Fe NPs encapsulated in the N- and S-doped carbon layers with a nanometer scale thickness are found to be an electrocatalytic active site for ORR.

The adenoma detection rate (ADR) does not reflect the complete detection of every adenoma during colonoscopy; thus, many surrogate indicators have been suggested. This study investigated whether the ADR and surrogate quality indicators reflect the adenoma miss rate (AMR) when performing qualified colonoscopy.We performed a prospective, multicenter, cross-sectional study of asymptomatic examinees aged 50 to 75 years who underwent back-to-back screening colonoscopies by eight endoscopists. The ADR and surrogate quality indicators, including polyp detection rate, total number of adenomas per colonoscopy, additional adenomas found after the first adenoma per colonoscopy (ADR-Plus), and total number of adenomas per positive participant, were calculated for the prediction of AMR.A total of 371 back-to-back colonoscopies were performed. There was a significant difference in ADRs (range, 44% to 75.4%; p=0.024), polyp detection rates (range, 56% to 86.9%; p=0.008) and adenomas per positive participants (range, 1.19 to 2.30; p=0.038), and a tendency of a difference in adenomas per colonoscopy (range, 0.62 to 1.31; p=0.051) and ADR-Plus (range, 0.13 to 0.70; p=0.054) among the endoscopists. The overall AMR was 20.1%, and AMRs were not different (range, 13.9 to 28.6; pgt;0.05) among the endoscopists. No quality indicators were significantly correlated with AMR. The number of adenomas found during the first colonoscopy was an independent factor for increased AMR (odds ratio, 1.79; plt;0.001).The colonoscopy quality indicators were significantly different among high-ADR endoscopists, and none of the quality indicators reflected the AMR of good quality colonoscopy performances. The only factor influencing AMR was the number of adenomas detected during colonoscopy.

Demand for the fabrication of high-performance, transparent electronic devices with improved electronic and mechanical properties is significantly increasing for various applications. In this context, it is essential to develop highly transparent and conductive electrodes for the realization of such devices. To this end, in this work, a chemical vapor deposition (CVD)-grown graphene was transferred to both glass and polyethylene terephthalate (PET) substrates that had been pre-coated with an indium tin oxide (ITO) layer and then subsequently patterned by using a laser-ablation method for a low-cost, simple, and high-throughput process. A comparison of the results of the laser ablation of such a graphene/ITO double layer with those of the ITO single-layered films reveals that a larger amount of effective thermal energy of the laser used is transferred in the lateral direction along the graphene upper layer in the graphene/ITO double-layered structure, attributable to the high thermal conductivity of graphene. The transferred thermal energy is expected to melt and evaporate the lower ITO layer at a relatively lower threshold energy of laser ablation. The transient analysis of the temperature profiles indicates that the graphene layers can act as both an effective thermal diffuser and converter for the planar heat transfer. Raman spectroscopy was used to investigate the graphite peak on the ITO layer where the graphene upper layer was selectively removed because of the incomplete heating and removal process for the ITO layer by the laterally transferred effective thermal energy of the laser beam. Our approach could have broad implications for designing highly transparent and conductive electrodes as well as a new way of nanoscale patterning for other optoelectronic-device applications using laser-ablation methods.

Single-walled carbon nanotubes (SWCNTs) were fabricated using AC dielectrophoresis into chemocapacitive sensors, and molecular receptors were applied for the selective detection of several chemical warfare agents (CWAs). The selective responses toward nerve simulants (G and V), choking and blister agents as well as a pesticide were investigated with specific receptor molecules that were either covalently functionalized or noncovalently coated onto the surfaces of the SWCNTs. The SWCNT-based chemocapacitive sensors showed reproducibility and sensitivity to 200 ppb for several target molecules. The fabricated sensor arrays were assessed for the selective detection of six different CWAs, and the principal component analysis demonstrated their specificity. VX, a real nerve agent, was tested on the fabricated SWCNT-based chemocapacitive sensor coated with a thiourea-functionalized siloxane polymer, and the successful detection of VX at 100 ppb confirmed that our SWCNT-based sensors are suitable for practical a...

To obtain high transparecy conductive films (TCFs), graphene embedded indium tin oxide (ITO) TCFs (ITO-graphene-ITO) were formed (I-G-I), using ITO sputtering, and the exfoliation/transfer ...

We develop a novel approach to improve the robustness of the interface between the hydrocarbon (HC) membrane and the perfluorosulfonic acid (PFSA) ionomer-based catalyst layer (CL) in membrane electrode assemblies (MEAs). This approach involves the creation of a gradient-composition interfacial bonding layer, in which the HC and PFSA contents are gradually varied along the thickness direction. The layer is fabricated using a simple spray-coating method, in which HC and PFSA ionomer mixtures with different compositions are sprayed stepwise onto both sides of the HC membrane surface. The interfacial structure developed in this process minimizes the chemical incompatibility between the HC and PFSA polymers. Owing to the tightly bound sublayers resulting from the intertwined HC and PFSA microdomains, the gradient-composition bonding layer provides a significantly improved interfacial adhesion strength (14 times higher than that of the pristine membrane without bonding layer) between the HC membrane and the PFSA-based CL. Finally, the fabricated MEA exhibits a >433% higher durability in humidity cycling tests compared with the pristine MEA without interfacial bonding layer, together with a better retention of its initial performance.

As direct formation of p-type two-dimensional transition metal dichalcogenides (TMDC) films on substrates, tungsten disulfide (WS2) thin films were deposited onto sapphire glass substrate through shadow mask patterns by radio-frequency (RF) sputtering at different sputtering powers ranging from 60 W to 150 W and annealed by rapid thermal processing (RTP) at various high temperatures ranging from 500 °C to 800 °C. Based on scanning electron microscope (SEM) images and Raman spectra, better surface roughness and mode dominant E12g and A1g peaks were found for WS2 thin films prepared at higher RF sputtering powers. It was also possible to obtain high mobilities and carrier densities for all WS2 thin films based on results of Hall measurements. Process conditions for these WS2 thin films on sapphire substrate were optimized to low RF sputtering power and high temperature annealing.

The exterior of single-walled carbon nanotubes is shown to facilitate preferential migration of cations over a millimeter length scale. Applying an electric field to droplets of NaCl placed at both...

The growing demands of next-generation applications for high power and energy sources necessitate advances in hierarchically porous carbon-based energy storage materials, which improve the overall kinetics of electrolytic reactions by providing efficient ion and electron transport pathways and facilitate electrolyte infiltration into the electrode during charging/discharging. Herein, we fabricate hierarchically structured porous carbon electrodes (cNPIM), prepared by solution casting of a polymer of intrinsic microporosity (PIM-1) followed by nonsolvent-induced phase separation and carbonization. The obtained material exhibits a considerable surface area (∼2100 m2 g−1), high electrical conductivity (150 S cm−1), high specific capacitances (345, 235, and 195 F g−1 in three-, two-electrode aqueous systems, and two-electrode organic systems, respectively) at 1 A g−1, and an exceptional specific energy of 43.2 W h kg−1 at a specific power of 1.25 kW kg−1, featuring a pore size gradient in the surface normal direction.

Semiconducting single-walled carbon nanotubes (SWNTs) show promise as core materials for next-generation solar cells and nanoelectronic devices. However, most commercial SWNT production methods generate mixtures of metallic SWNTs (m-SWNTs) and semiconducting SWNT (sc-SWNTs). Therefore, sc-SWNTs must be separated from their original mixtures before use. In this study, we investigated a polymer-based, noncovalent sc-SWNT separation approach, which is simple to perform and does not disrupt the electrical properties of the SWNTs, thus improving the performance of the corresponding sc-SWNT-based applications. By systematically investigating the effect that different structural features of the semiconductor polymer have on the separation of sc-SWNTs, we discovered that the length and configuration of the alkyl side chains and the rigidity of the backbone structure exert significant effects on the efficiency of sc-SWNT separation. We also found that electron transfer between the semiconductor polymers and sc-SWNTs is strongly affected by their energy-level alignment, which can be tailored by controlling the donor-acceptor configuration in the polymer backbone structures. Among the polymers investigated, the highly planar P8T2Z-C12 semiconductor polymer showed the best sc-SWNT separation efficiency and unprecedentedly strong electronic interaction with the sc-SWNTs, which is important for improving their performance in applications.

From the viewpoint of the device performance, the fabrication and patterning of oxide–metal–oxide (OMO) multilayers (MLs) as transparent conductive oxide electrodes with a high figure of merit have been extensively investigated for diverse optoelectronic and energy device applications, although the issues of their general concerns about possible shortcomings, such as a more complicated fabrication process with increasing cost, still remain. However, the underlying mechanism by which a thin metal mid-layer affects the overall performance of prepatterned OMO ML electrodes has not been fully elucidated. In this study, indium tin oxide (ITO)/silver (Ag)/ITO MLs are fabricated using an in-line sputtering method for different Ag thicknesses on glass substrates. Subsequently, a Q-switched diode-pumped neodymium-doped yttrium vanadate (Nd:YVO4, λ = 1064 nm) laser is employed for the direct ablation of the ITO/Ag/ITO ML films to pattern ITO/Ag/ITO ML electrodes. Analysis of the laser-patterned results indicate that the ITO/Ag/ITO ML films exhibit wider ablation widths and lower ablation thresholds than ITO single layer (SL) films. However, the dependence of Ag thickness on the laser patterning results of the ITO/Ag/ITO MLs is not observed, despite the difference in their absorption coefficients. The results show that the laser direct patterning of ITO/Ag/ITO MLs is primarily affected by rapid thermal heating, melting, and vaporization of the inserted Ag mid-layer, which has considerably higher thermal conductivity and absorption coefficients than the ITO layers. Simulation reveals the importance of the Ag mid-layer in the effective absorption and focusing of photothermal energy, thereby supporting the experimental observations. The laser-patterned ITO/Ag/ITO ML electrodes indicate a comparable optical transmittance, a higher electrical current density, and a lower resistance compared with the ITO SL electrode.

Mesoporous reduced graphene oxide ( m -rGO) was synthesized by mixing Zn and graphene oxide in acidic conditions followed by ultrasonication and was investigated as a supercapacitor electrode in a 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (EMIM-TFSI) electrolyte. m -rGO shows a specific capacitance of 104.3 F g −1 at 1 A g −1 and a decrease in capacitance of 3% after 5000 cycles. The high performance is attributed to the significant mesopores, facilitating mass transport of the electrolyte. Thus, we report the facile synthesis of m -rGO with enhanced capacitance and durability in an ionic liquid electrolyte that has great potential for electrochemical energy storage applications.

In this work, a study on a semi-floating-gate synaptic transistor (SFGST) is performed to verify its feasibility in the more energy-efficient hardware-driven neuromorphic system. To realize short- and long-term potentiation (STP/LTP) in the SFGST, a poly-Si semi-floating gate (SFG) and a SiN charge-trap layer are utilized, respectively. When an adequate number of holes are accumulated in the SFG, they are injected into the nitride charge-trap layer by the Fowler&ndash, Nordheim tunneling mechanism. Moreover, since the SFG is charged by an embedded tunneling field-effect transistor existing between the channel and the drain junction when the post-synaptic spike occurs after the pre-synaptic spike, and vice versa, the SFG is discharged by the diode when the post-synaptic spike takes place before the pre-synaptic spike. This indicates that the SFGST can attain STP/LTP and spike-timing-dependent plasticity behaviors. These characteristics of the SFGST in the highly miniaturized transistor structure can contribute to the neuromorphic chip such that the total system may operate as fast as the human brain with low power consumption and high integration density.

A poly (ethylene-co-vinyl acetate) (EVA)/polyimide (PI)/EVA (PIE) tri-layer separator with thermal stability and a shutdown function is fabricated for use in sodium-ion battery (SIB) applications. Porous EVA layers are coated on both sides of an electrospun-PI, acting as a supporting layer, through a dip-coating process accompanying a thermally induced phase separation in which polyethylene-block-poly (ethylene glycol) is used as a polymeric pore generator to obtain an open porous morphology. Excellent thermal stability of the PIE tri-layer separator is demonstrated, with two simultaneous incompatible thermal behaviors, i.e., a negligible thermal shrinkage of up to 200 °C, and a rapid thermal shutdown at approximately 100 °C. In addition, the PIE tri-layer separator shows a higher ionic conductivity and larger electrolyte uptake of the sodium liquid electrolyte than a commercial olefin separator, leading to better cycling performance when assembled into SIB coin cells. All these outstanding properties of PIE tri-layer separator demonstrate that its promise as a candidate separator for use in SIBs.