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Highly Stable and Ultrafast Hydrogen Gas Sensor Based on 15 nm Nanogaps Switching in a Palladium-Gold Nanoribbons Array
摘要： Palladium (Pd) nanogap hydrogen gas (H2) sensors based on the large volume expansion of β phase palladium hydride (β-PdH) are highly promising, owing to their fast and accurate sensing capability at room temperature in air. However, such sensors do not work well at H2 concentrations below 1%. At such low H2 concentrations, Pd exists as α-PdH, which has a slow and insufficient volume expansion and cannot completely close nanogaps. Furthermore, the lattice strains induced from the phase transition (α-PdH → β-PdH) behavior degrade the stable and repeatable long-term sensing capability. Here, these issues are resolved by fabricating an array of periodically aligned alloyed palladium–gold nanoribbons (PdAu NRB) with uniform 15 nm nanogaps. The PdAu NRB sensor enables highly stable and ultrafast H2 sensing at the full detection range of H2 concentrations from 0.005% to 10% along with the excellent limit of detection (≈0.0027%), which is sufficiently maintained even after seven months of storage in ambient atmosphere. These breakthrough results will pave the way for developing a practical high-performance H2 sensor chip in the future hydrogen era.
关键词： palladium nanogap,nanoribbon,hydrogen gas sensors,polystyrene thermal shrinkage
更新于2025-09-23 15:22:29
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Hydrogen sensing characteristics of AlGaInP/InGaAs enhancement/depletion-mode co-integrated doping-channel field-effect transistors
摘要： In this article, the hydrogen sensing characteristics of Al0.25Ga0.25In0.5P/In0.1Ga0.9As enhancement/depletion-mode co-integrated pseudomorphic doping-channel field-effect transistors by wet selectively etching process are demonstrated. At drain current of 0.1 mA/mm, the threshold voltages are of (cid:1)0.97 (t0.6) V and (cid:1)1.22 (t0.31) V in air and at hydrogen concentration of 9800 ppm, respectively, for the depletion (enhancement)-mode device. In addition, by employing the co-integrated FETs the transfer characteristics of the direct-coupled FET logic (DCFL) obviously vary under hydrogen ambience. The VOH value reduces and the VOL value increases in the DCFL with the measurement of hydrogen detection.
关键词： Threshold voltage,Hydrogen sense,Doping-channel field-effect transistor,Enhancement/depletion-mode,AlGaInP/InGaAs,Direct-coupled FET logic
更新于2025-09-23 15:22:29
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Fabrication of new metal-free materials for the hydrogen evolution reaction on base of the acridine derivatives immobilized on carbon materials
摘要： The process of adsorption on carbon material (Vulcan XC-72 (VU)) of organic heterocyclic compounds: acridine (I) and its derivatives 9-phenylacridine (II) and N-methyl-9-phenylacridium iodide (III) was studied in detail. Quantitative data on physical adsorption were obtained for all compounds. Based on the adsorption isotherms of Langmuir, the adsorption equilibrium constants K, the parameter A∞ and ΔG0 ad were calculated. It has been shown that the adsorption of compounds I and II is a structurally dependent process that depends on the nature and size of the functional substituents in the molecule, and the adsorption of compound III has a complex mechanism and partially proceeds through the stabilization stage by the functional groups present on the surface (-COOH, -COH, -OH). With the use of quantum chemical calculations, it has been established that the process of adsorption of compounds on the surface of a carbon materials having sections with a graphite-like structure is thermodynamically unprofitable because of the high difference in the energies of the adsorbent's boundary orbitals and the substrate. Using the cyclic voltammetry method, the electrochemical properties of organic compounds immobilized on the surface of a carbon material were studied.
关键词： Electocatalysis,Acridine derivatives,Immobilization,Adsorption,Carbon materials,Hydrogen evolution reaction
更新于2025-09-23 15:22:29
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In-situ hydrothermal fabrication of CdS/g-C3N4 nanocomposites for enhanced photocatalytic water splitting
摘要： In this work, a series of CdS/g-C3N4 nanocomposites with varying wt% CdS were prepared via an in-situ hydrothermal synthesis method. 10 wt% CdS/g-C3N4 nanocomposites displayed the highest rate of hydrogen evolution via photocatalytic water splitting. The H2 evolution rate of 10 wt% CdS/g-C3N4 is 21 times greater than pure g-C3N4 and 4 times greater than that of pure CdS. Key factors responsible for the enhanced photocatalytic activity can be attributed to the improved charge separation and increased surface area of CdS/g-C3N4 nanocomposites. These findings may serve as a platform for the fabrication of other photocatalytic multi-material nanocomposites in the future.
关键词： Nanocomposite,Photocatalysis,Solar fuels,Electrical properties,Hydrogen production
更新于2025-09-23 15:22:29
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Design, synthesis and structural optimization of two click modified butterfly molecules: Aggregation induced ratiometric fluorescence change and ICT associated hydrogen bonding effect in solvatochromic analysis
摘要： Two click modi?ed butter?y molecules are designed and synthesized having presence and absence of the aggregative moiety to differ between aggregation induced ratiometric emission changes via excimer formation and ICT associated hydrogen bonding effect. These two distinct phenomena can be successfully employed in solvatochromic analysis. This is also supported by the theoretical study through the structural variation of the two butter?y molecules.
关键词： Hydrogen bonding,Butter?y molecules,Ratiometric,AIE,Solvatochromic
更新于2025-09-23 15:22:29
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Comparing postdeposition reactions of electrons and radicals with Pt nanostructures created by focused electron beam induced deposition
摘要： The ability of electrons and atomic hydrogen (AH) to remove residual chlorine from PtCl2 deposits created from cis-Pt(CO)2Cl2 by focused electron beam induced deposition (FEBID) is evaluated. Auger electron spectroscopy (AES) and energy-dispersive X-ray spectroscopy (EDS) measurements as well as thermodynamics calculations support the idea that electrons can remove chlorine from PtCl2 structures via an electron-stimulated desorption (ESD) process. It was found that the effectiveness of electrons to purify deposits greater than a few nanometers in height is compromised by the limited escape depth of the chloride ions generated in the purification step. In contrast, chlorine atoms can be efficiently and completely removed from PtCl2 deposits using AH, regardless of the thickness of the deposit. Although AH was found to be extremely effective at chemically purifying PtCl2 deposits, its viability as a FEBID purification strategy is compromised by the mobility of transient Pt–H species formed during the purification process. Scanning electron microscopy data show that this results in the formation of porous structures and can even cause the deposit to lose structural integrity. However, this phenomenon suggests that the use of AH may be a useful strategy to create high surface area Pt catalysts and may reverse the effects of sintering. In marked contrast to the effect observed with AH, densification of the structure was observed during the postdeposition purification of PtCx deposits created from MeCpPtMe3 using atomic oxygen (AO), although the limited penetration depth of AO restricts its effectiveness as a purification strategy to relatively small nanostructures.
关键词： electron beam processing,focused electron beam induced deposition (FEBID),atomic oxygen,purification,atomic hydrogen
更新于2025-09-23 15:22:29
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Hydrogen Gas Sensing Characterizations Based on Nanocrystalline SnO<sub>2</sub> Thin Films Grown on SiO<sub>2</sub>/Si and Al<sub>2</sub>O<sub>3</sub> Substrates
摘要： High-quality nanocrystalline (NC) SnO2 thin films were grown on SiO2/Si and Al2O3 substrates using sol–gel spin coating method. The structural properties, surface morphologies and gas sensing properties of the NC SnO2 were investigated. XRD measurements showed a tetragonal rutile structure and the diffraction peaks for NC SnO2 thin films grown on Al2O3 substrates outperformed those of NC SnO2 films grown on SiO2/Si substrates. The surface morphology of the annealed SnO2 thin films at 500 oC appeared as polycrystalline with uniform nanoparticle distribution. Hydrogen (H2) gas sensing performance of the NC SnO2 was examined for H2 concentrations ranging from 150 ppm to 1000 ppm at different temperatures (room temperature, 75 and 125 oC) for over 50 min. The room temperature sensitivities for H2 gas sensors based on NC SnO2 thin films grown on Al2O3 and SiO2/Si substrates was 2570% and 600%, respectively upon exposure to 1000 ppm of H2 gas. While the sensitivity values at 125 oC increased to 9200% and 1950%, respectively.
关键词： Sensing,Room Temperature,Hydrogen,Nanocrystalline SnO2,Thin Films,Sol-Gel
更新于2025-09-23 15:22:29
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Enantioselective Visible Light-mediated Formation of 3-Cyclopropylquinolones via Triplet-sensitized Deracemization
摘要： 3-Allyl-substituted quinolones undergo a triplet-sensitized di-π-methane rearrangement to the corresponding 3-cyclopropylquinolones upon irradiation with visible light (λ = 420 nm). A chiral hydrogen bonding sensitizer (10 mol%) was shown to promote the reaction enantioselectively (88-96% yield, 32-55% ee). Surprisingly, it was found that the enantiodifferentiation does not occur at the state of initial product formation but that it is the result of a deracemization event. The individual parameters that control the distribution of enantiomers in the photostationary state have been identified.
关键词： enantioselectivity,small ring systems,photochemistry,hydrogen bonds,sensitizers,chiral resolution
更新于2025-09-23 15:22:29
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In-situ Platinum Plasmon Resonance Effect Prompt Titanium Dioxide Nanocube Photocatalytic Hydrogen Evolution
摘要： In-situ photodeposition Pt nanoparticles (Pt NPs) on TiO2 on account of the surface plasmonic resonance (SPR) effect and strong interaction of two components, which exhibits an elevated solar-driven photocatalytic hydrogen evolution performance. Herein, Pt-decorated TiO2 nanocube hierarchy structure (Pt-TNCB) was in-situ fabricated via a facile solvothermal synthesis and photodeposition strategy. The Pt-TNCB exhibits an excellent solar-driven photocatalytic hydrogen evolution rate (337.84 μmol h-1), which is about 37 times higher than that of TNCB (9.19 μmol h-1). Interestingly, its photocatalytic property is still superior to TNCB with post modification Pt (1 wt %) (208.11 μmol h-1). The introduction of Pt efficiently extends the photoresponse of composite material from UV to visible light region, simultaneously boost their solar-driven photocatalytic performance, which attribute to the porous structure, the subsize TNCB, the SPR effect of Pt NPs and strong interaction of two components. In fact, Pt NPs can enhance collective oscillations on delocalized electrons, which is conducive to capture electrons and hinder the recombination of photogenerated electron-hole pairs, leading to the longer lifetime of photogenerated charges. The fabrication of Pt-TNCB photocatalyst with SPR effect may provide a promising method to improve visible-light photocatalytic activities for traditional photocatalysts.
关键词： hydrogen evolution,titanium dioxide,surface plasmonic resonance,photodeposition,photocatalyst
更新于2025-09-23 15:22:29
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Integrating non-precious-metal cocatalyst Ni3N with g-C3N4 for enhanced photocatalytic H2 production in water under visible-light irradiation
摘要： Photocatalytic H2 production via water splitting in a noble-metal-free photocatalytic system has attracted much attention in recent years. In this study, noble-metal-free Ni3N was used as an active cocatalyst to enhance the activity of g-C3N4 for photocatalytic H2 production under visible-light irradiation (λ > 420 nm). The characterization results indicated that Ni3N nanoparticles were successfully loaded onto the g-C3N4, which accelerated the separation and transfer of photogenerated electrons and resulted in enhanced photocatalytic H2 evolution under visible-light irradiation. The hydrogen evolution rate reached ~305.4 μmol h?1 g?1, which is about three times higher than that of pristine g-C3N4, and the apparent quantum yield (AQY) was ~0.45% at λ = 420 nm. Furthermore, the Ni3N/g-C3N4 photocatalyst showed no obvious decrease in the hydrogen production rate, even after five cycles under visible-light irradiation. Finally, a possible photocatalytic hydrogen evolution mechanism for the Ni3N/g-C3N4 system is proposed.
关键词： Hydrogen evolution,g-C3N4,Cocatalyst,Ni3N,Photocatalysis
更新于2025-09-23 15:22:29