Enhancement Of Current Density Research Articles

Thermal-driven gigantic enhancement in critical current density of high-entropy alloy superconductors

The high-entropy alloy (HEA) superconductor, Ta1/6Nb2/6Hf1/6Zr1/6Ti1/6 (Ta–Nb–Hf–Zr–Ti), is systematically studied to examine changes in superconducting critical properties, critical temperature (Tc), critical current density (Jc), and upper critical field (Hc2), concerning thermal treatment conditions. Annealing condition affects Jc more significantly than Tc and Hc2, with a large improvement of flux pinning force density (Fp). The Jc of bare sample is reduced to 10 A cm–2 at an applied magnetic field of approximately 1.5 T, whereas the sample annealed at 550 °C for 12 h exhibits Jc > 100 kA cm–2 up to around 4 T. Furthermore, the Vickers hardness (HVIT) of the Ta–Nb–Hf–Zr–Ti HEA superconductor notably increases from ∼384 to 528 HVIT following a 24-h annealing at 500 °C. These results demonstrate that thermal annealing is a powerful process to optimize both the superconducting and mechanical properties of high-entropy alloy superconductors.

Enhancement of irreversibility field and critical current density of rare earth containing V0.60Ti0.40 alloy superconductor by cold-working and annealing

β-V1−xTix alloy superconductors are considered to be promising materials for high magnetic field applications. So far, attempts to improve the critical current density (JC) of β-V1−xTix alloys have shown limited success. Improving JC requires a controlled generation of defects. Similar to the V0.6Ti0.4-RE (RE = Gd, Y) alloys, RE = Ce, Dy and Nd are also immiscible in the V0.6Ti0.4 matrix. The superconducting transition temperature (TC), upper critical field (HC2), irreversibility field (HIrr), and JC increase with the RE addition. However, the tensile strength of V0.6Ti0.4-Gd alloy is observed to be significantly lower than that of V0.6Ti0.4 alloy. Cold-working is found to further improve the TC, HC2, HIrr, and JC of all the V0.6Ti0.4-RE alloys. Successive cold-working (with 50% reduction of thickness each time) and annealing (SCA) at 450∘C for 5 hrs is found to significantly improve the HIrr, and JC of V0.6Ti0.4-RE (RE = Gd, Ce) alloys. The tensile strength is also found to increase to about 60–70% of the V0.6Ti0.4 alloy after the third annealing. It is observed that α′ and ω phases form at the defect sites at various stages of cold-working and annealing. JC(H = 0) and HIrr are about 840 Amm−2 and 7 T respectively for the as-cast V0.6Ti0.4-RE alloys. Cold-working on the V0.6Ti0.4-RE alloys further improves the JC(H = 0) and HIrr to about 1250 Amm−2 and 8.45 T respectively. SCA increases the JC(H = 0) and HIrr to about 4000 Amm−2 (or more) and 9 T respectively, and the JC(7 T) to about 500 Amm−2 in V0.6Ti0.4-RE alloy at 4 K. We present a detailed description of the defect structure in these alloys and its role in pinning the magnetic flux lines, thereby improving the overall JC.

Local pH Change during CoMo-TiO2 Composite Electrodeposition and Alkaline HER Electrolysis

Alloys of Co-Mo and Co-Mo-P are of interest for their ability to enhance the hydrogen evolution reaction (HER)1-2 and adding TiO2 to the alloy surface can further enhance HER.3-5 To better understand the influence of TiO2 particles on the electrodeposition of Co-Mo and Co-Mo-P alloys and the resulting HER kinetics, electrodeposition was conducted on a copper mesh electrode in close proximity to a pH probe to measure the local change of pH. The deposit composition and the HER characterized. There was a significant enhancement in the HER exchange current density when TiO2 particles were present in the alloy, taking into account any changes in the surface area. The enhancement was associated with a local pH change. Without TiO2 particles present in the solid state, the local pH change follows an expected increase with time as hydrogen is evolved and the hydroxide ion is generated at the electrode surface. In contrast, when TiO2 particles were present at the surface and in the metal alloy matrix, the local pH initially decreases slightly and remains constant (Fig 1). The results suggest that the enhanced HER performance with TiO2 in the alloy composite electrocatalyst is a consequence of the buffering of the local pH. In contrast, during electrodeposition there is little change in the pH transient with and without having TiO2 particles in the electrolyte. C. C. McCrory, A. Jung, I.M. Ferrer, S.M. Chatman, J.C. Peters, T.F. Jaramillo, J Am Chem Soc, 137 (13) 4347 (2015).A. C. Thenuwara, L. Dheer, N. H. Attanayake, Q. Yan, U. V. Waghmare, D. R. Strongin, ChemCatChem. 10 4832-4837 (2018).A.R. Shetty, A.C. Hegde, Mater. Sci. Energy Technol. 1 (2) 97 (2018).C. Wang, Hubert K. Bilan, E. J. Podlaha, J. Electrochem. Soc. 166 (10) F661 (2019).C. Wang and E. J. Podlaha, J. Electrochem. Soc. 167 (13) 132502 (2020). Figure 1. Change of pH during HER on a Co-Mo electrodeposit at different HER electrolysis current densities. Figure 1

Visible-Light-Enhanced Hydrogen Evolution through Anodic Furfural Electro-Oxidation Using Nickel Atomically Dispersed Copper Nanoparticles.

A novel copper nanoparticle variant, denoted as Cu98Ni2 NPs, which incorporate Ni atoms in an atomically dispersed manner, has been successfully synthesized via a straightforward one-pot electrochemical codeposition process. These nanoparticles were subsequently employed as an anode to facilitate the oxidation of furfural, leading to the production of hydrogen gas. Voltammetric measurements revealed that the inclusion of trace amounts of Ni atoms in the nanoparticles resulted in a pronounced synergistic electronic effect between Cu and Ni. Consequently, a 43% increase in current density at 0.1 V was observed in comparison to pure Cu NPs. Importantly, when the Cu98Ni2 NPs were irradiated with visible light, a remarkable current density enhancement factor of 505% at 0.1 V was achieved relative to that of pure Cu NPs in the absence of light. This enhancement can be attributed to localized surface plasmon resonance induced by visible light, which triggers photothermal and photoelectric effects. These effects collectively contribute to the significant overall improvement in the electrocatalytic oxidation of furfural, leading to enhanced hydrogen evolution.

High-Stability RuNi/C Electrocatalyst for Efficient Hydrogen Oxidation Reaction in Alkaline Condition.

The Ru-based catalyst for hydrogen oxidation reaction (HOR) with remarkable activity and reliability at high potential range remains a formidable challenge. Herein, the RuNi/C nanoparticles are customized, in which NiRu alloy is tightly wrapped with a carbon layer, delivering 2.2-fold and 8.3-fold enhancement in kinetic current density than that of commercial Pt/C and Ru/C, respectively. Notably, the current density maintains 2.93mAcm-2 disk at 0.6 V vsRHE, which effectively improves the stability of Ru-based catalysts at high voltage. The NiRu alloy triggers electron redistribution between two metal elements and regulates the surface adsorption performance, coupled with a tightly wrapped outer carbon layer which is in situ formed with alloy as a good conductor of electronic and protection from the electrolyte. This work not only provides a novel electrocatalyst for efficient HOR with its potential for industrial application but also opens up a new avenue for designing highly active catalytic systems.

Enhancement of Critical Current Density of Nb3Al Superconductors by B Doping

Boron (B)‐doped Nb3Al superconductors are prepared by mechanical alloying and subsequent sintering process in this work. Then, the critical current density (Jc) of Nb3Al with different amounts of B doping is studied. In the results, it is shown that Jc performance of Nb3Al is improved obviously after B doping. The best Jc value obtained in this work is 2.2 × 104 A cm−2 (4.2 K, 5 T) for Nb3(Al0.9B0.1) sample. Furthermore, the mechanism of enhanced Jc performance for Nb3(Al0.9B0.1) sample is comprehensively explored. It is found that B doping can significantly enhance the grain connectivity of Nb3Al superconductor, and the active cross‐sectional area fraction values increase from 0.11 for the undoped sample to 0.34 for Nb3(Al0.9B0.1) sample. In addition, the lattice distortion caused by the interstitially dissolved B may also serve as flux pinning centers, which strengthens the flux pinning force of Nb3(Al0.9B0.1).

Synergistic lattice regulation of additive and interface engineering to realize high efficiency CsPbI2Br perovskite solar cell

The CsPbI2Br material has gained recognition as an exceptional candidate for both single- and multi- junction solar cells due to its remarkable thermal and light stability, along with its suitable band gap. However, despite these inherent advantages, CsPbI2Br perovskite solar cells (PSCs) still encounter significant energy losses, which impede the further enhancement of their efficiency. Although various approaches involving additives and interface engineering techniques improved device performance, the influence of these methods on the perovskite lattice is frequently overlooked. Herein, synergistic lattice regulation through the combination of potassium acetate (KAc) as electron interface layer and methylammonium chloride (MACl) as perovskite additive, was proposed. The MACl dopant effectively increases the crystallinity and grain size of CsPbI2Br film by retarding the crystallization rate of perovskite, resulting in the enhancement in short-circuit current density (Jsc) of PSCs. Unfortunately, unlike the behavior observed in inorganic–organic perovskites, the introduction of Cl‾ from MACl into the interstitial positions leads to lattice expansion in CsPbI2Br, resulting in reduced open-circuit voltage (Voc) and fill factor (FF). However, the incorporation of K+ replacing Cs+ effectively mitigates lattice distortion phenomena. Consequently, the CsPbI2Br PSCs, benefiting from the complementary effects of the MACl additive and KAc interfacial layer, exhibit an outstanding champion power conversion efficiency of 17.11 %. This research offers profound insights into the impact of ions introduced through additive and interface engineering on perovskite lattice stress.

Enhancement of critical current density and critical magnetic field of superconducting medium entropy alloy Nb2/5Hf1/5Zr1/5Ti1/5

We investigated the superconducting properties of medium entropy alloys (MEA) Nb2/5Hf1/5Zr1/5Ti1/5, synthesized by arc melting (AM) and powder metallurgical spark plasma sintering (SPS) methods. The samples exhibit superconducting transitions at Tc=7.99 K (AM) and 6.63 K (SPS) from the electrical resistivity measurements. The upper critical field at zero-temperature limit μoHc2(0) gives a relatively high value of 14.63 T (AM) and 11.68 T (SPS). The isothermal magnetic hysteresis of the SPS-MEA shows significantly enhanced vortex pinning, resulting in the enhancement of critical current density (Jc= 39,000 A/cm2) compared with the AM-MEA (Jc= 5,500 A/cm2) at 2 K (about seven times enhancement). The SPS-MEA shows a significant suppression of vortex avalanches compared with the previously reported SPS-HEA Ta1/6Nb2/6Hf1/6Zr1/6Ti1/6 superconductor. The SPS-MEA showed the secondary fishtail effect at a high magnetic field. There was a sizable specific heat jump ΔC(Tc)/γTc (3.3 for AM and 3.9 for SPS), significantly higher than the value of BCS prediction (1.43). Superconducting properties of MEA suggest the intermediate coupling of the electron-phonon coupling constant λ∼1 (λel−ph≃0.89 for AM and λel−ph≃0.78 for SPS) and the intermediate to strong coupling regime. The Kadowaki-Woods plot of the compounds is located on the line of the heavy fermion system. The Uemura plot indicates that the compounds are close to the conventional BCS superconductor. The contradictory property of strongly correlated and conventional BCS-type metallic superconductivity may come from the dirty superconducting regime with high Fermi velocity. Enhancing critical current density with significantly suppressed vortex avalanches on the SPS-MEA Nb2/5Hf1/5Zr1/5Ti1/5 compound suggests possible practical applications on the bulk superconductivity.

Nanostructure-induced inhibition of oxygen evolution and enhancement of methanol electrooxidation on engineered anodized brass

To capitalize the improved electrical contact feature, a self-supported hybrid binary/ternary copper and zinc oxides (i.e., ZnO–Cu2O and Cu2O–ZnO–CuO) nanostructures have been generated via a simple potentiostatic mode of anodaization on alpha brass in an alkaline medium. The catalyst nanostructuring i.e., wheat-grain-like to nanograss type structure has improved the mass transport, sluggish kinetics of methanol electrooxidation reaction process, and hindered the competitive oxygen evolution reaction (OER) of direct methanol fuel cell. The catalytic poisoning phenomenon has not been noticed due to two different reaction processes in two potential regions. Interestingly, a significant reduction in overpotential (η10mAcm−2OER−CH3OH) has been noticed for S125@A1 and S125@A2 samples i.e., 236 mV and 350 mV, respectively. The enhancement of current density has been explained through inductive circuit perspective. So, the present study provides a better insights to design and utilize non-precious metal/alloy based catalyst with hindered OER and enhanced methanol electrooxidation reaction activity.

Enhancement of Short-Circuit Current Density in Superlattice-Based InGaN/GaN Solar Cells

In this paper, the mechanism of short-circuit current density (JSC) enhancement in InGaN/GaN superlattices(SLs)-structured solar cells (SCs) is investigated theoretically and experimentally, and compared with conventional InGaN/GaN multiple quantum wells (MQWs) SCs. Due to the ultrathin structure of the X-ray diffraction SLs, a tunneling model is introduced in Silvaco software. The simulation results show that the trend of the simulation results is consistent with the experimental values. Due to the contribution of the tunneling effect, the JSC of SCs with SLs structure is greatly improved, but the open circuit voltage (VOC) is also reduced due to defects in the growth process of epitaxial wafers with SLs structure. These observations suggest that tunneling effects increase the JSC of the SCs, thus improving the photovoltaic conversion efficiency (PCE) of SCs. This study provides evidence for the fabrication of highly efficient InGaN SCs.

Electrochemically-mediated reactive separation of nitric oxide into nitrate using iron chelate

Valorization of nitric oxide is a promising solution for addressing the environmental and resource issues related to the nitrogen cycle. However, low concentrations of nitric oxide combined with impurities in exhaust streams limit its potential, and it requires extensive energy to produce high-purity nitric oxide. Here, we propose a synergistic reactive separation system that combines iron-chelate selective absorption with an electrochemical reaction to convert nitric oxide to nitrate. Among the iron-based chelates tested, EDTA was found to be the most effective in capturing gas-phase nitric oxide. Direct electrochemical oxidation of Fe-EDTA-NO solution exhibited Faradaic efficiency and a partial current density toward nitrate of 70% and 30.1 mA cm−2 at 2.2 V vs RHE and pH 7, resulting in a 43-fold enhancement of nitrate partial current density and a 2-fold improvement in Faradaic efficiency compared to simple purging without selective absorbent. Nitrate was then selectively recovered from the Fe-EDTA system using simple polarity reversal following electrooxidation with a separation factor of 13 over background sulfate. This study offers a new approach to gas-phase NO remediation and valorization using an electrified means.

Superior energy storage performance and excellent multiferroic properties of BaTi1-xGdxO3 (0 ≤ x ≤ 0.06) ceramics

Ceramic based capacitors with superior energy storage performance and high storage energy density play an important role in modern electronic devices. Several ferroelectric materials with high dielectric constant and relaxor behavior become the most promising systems for realizing higher energy storage performance. In the present work, environmentally lead-free BaTi1-xGdxO3 (0 ≤ x ≤ 0.06) nanostructures were synthesized using the sol-gel auto-combustion process. The doping of Gd at the Ti site causes the transformation of the ferroelectric behavior to the relaxor ceramics, which is important for finding the large energy storage efficiency of the material. The surface morphology of undoped and doped samples was examined through the SEM studies. Ferroelectric study evidence that the system is going to a more symmetric phase due to a reduction in the polarization parameters and enhancement in the leakage current density. Moreover, the energy discharge density and energy storage efficiency were boosted in x = 0.02 and x = 0.04 samples with energy storage efficiencies reaching ∼81% and 83%, respectively. The linear enhancement in the magnetic moment and the dielectric constant in the doped sample make the system favorable for multifunctional applications. The samples' piezoelectric constant (d33) remains preserved under Gd doping. Hence, the present study opens a propagable and feasible route to synthesize novel lead-free ferroelectric material for energy storage applications.

Effects of the oxygen source configuration on the superconducting properties of internally-oxidized internal-Sn Nb3Sn wires

We successfully manufactured 12-filament rod-in-tube Nb3Sn wires with oxide nanoparticles formed by the internal oxidation method. We employed Nb-7.5 wt%Ta-1 wt%Zr and Nb-7.5 wt%Ta-2 wt% Hf alloys along with oxygen sources (OSs) in two different configurations—in the core of Nb filaments (coreOS) and at the boundary between the filaments and the Cu tube (annularOS)—to assess the influence of the OS layout on the superconducting properties and grain size. The simultaneous presence of the OS and of Hf or Zr reduced the average Nb3Sn grain size to around 50 nm, leading to an enhancement of the layer critical current density (Jc ) up to 3000 A mm−2 at 4.2 K and 16 T for the Hf-annularOS wire. Samples manufactured with an OS show a shift toward higher reduced magnetic fields of the position of the maximum in pinning-force density, this shift being more pronounced when SnO2 is added in the annularOS configuration, and for the Hf-containing samples. This enhanced pinning at higher magnetic field is beneficial for high-field magnet applications. Moreover, we measured a very high upper critical field, reaching 29.3 T at 4.2 K in the Hf-annularOS samples.

Fluorescent Waveguide Lattices for Enhanced Light Harvesting and Solar Cell Performance.

We present the properties and performance of fluorescent waveguide lattices as coatings for solar cells, designed to address the significant mismatch between the solar cell's spectral response range and the solar spectrum. Using arrays of microscale visible light optical beams transmitted through photoreactive polymer resins comprising acrylate and silicone monomers and fluorescein o,o'-dimethacrylate comonomer, we photopolymerize well-structured films with single and multiple waveguide lattices. The materials exhibited bright green-yellow fluorescence emission through down-conversion of blue-UV excitation and light redirection from the dye emission and waveguide lattice structure. This enables the films to collect a broader spectrum of light, spanning UV-vis-NIR over an exceptionally wide angular range of ±70°. When employed as encapsulant coatings on commercial silicon solar cells, the polymer waveguide lattices exhibited significant enhancements in solar cell current density. Below 400 nm, the primary mode of enhancement is through down-conversion and light redirection from the dye emission and collection by the waveguides. Above 400 nm, the primary modes of enhancement were a combination of down-conversion, wide-angle light collection, and light redirection from the dye emission and collection by the waveguides. Waveguide lattices with higher dye concentrations produced more well-defined structures better suited for current generation in encapsulated solar cells. Under standard AM 1.5 G irradiation, we observed nominal average current density increases of 0.7 and 1.87 mA/cm2 for single waveguide lattices and two intersecting lattices, respectively, across the full ±70° range and reveal optimal dye concentrations and suitable lattice structures for solar cell performance. Our findings demonstrate the significant potential of incorporating down-converting fluorescent dyes in polymer waveguide lattices for improving the current spectral and angular response of solar cell technologies toward increasing clean energy in the energy grid.

Enhancements of critical current density in Bi1.6Pb0.4Sr2Ca2Cu3O10+δ superconductors by additions of SnO2 nanoparticles

The impact of adding SnO2 nanoparticles on the enhancements of critical current density (Jc) of the Bi1.6Pb0.4Sr2Ca2Cu3O10+δ superconductors was studied. Polycrystalline superconductors with stoichiometry of (Bi1.6Pb0.4Sr2Ca2Cu3O10+δ)1−x(SnO2)x where was x was ranged from 0.000, 0.002, 0.004, 0.006, 0.008 to 0.010 were made through traditional solid state reaction technique. X-ray diffraction data revealed that all fabricated samples consisted of Bi-2223 and Bi-2212 superconducting phases. The volume fraction of the Bi-2223 phase decreased with SnO2 addition. Analyses of textural structure using scanning electron microscopy data evidenced a clear decrease in grain orientation and porosity with increased doping levels. SnO2 presence in connection to Bi-2223 deceleration reduced the critical temperature. Values of Jc deduced from the magnetization hysteresis loops measured at different temperatures of 35 K, 45 K, 55 K, 65 K were found to enhance for the SnO2 added samples. In the x = 0.002 samples, the field dependent Jc achieved its maximum values. In order to have a deeper understanding in the improvements of flux pinning properties, small and large bundle fields were determined by using the collective pinning theory. The obtained values indicate the expansion of the two corresponding regimes with appropriate. By analyzing the dependence of normalized Jc versus normalized critical temperature, the dominant flux pinning mechanisms in all samples were consistent with δl pinning. Besides, the addition of SnO2 nanoparticles was likely to produce pinning centers in form of core point as evidenced by using the Dew–Hughes model.

High-field critical current density enhancement in GdBCO coated conductors by cooperative defects

Irradiation can precisely control defects in, and improve the superconducting properties of, REBa2Cu3O7−δ (REBCO, RE: rare earth) coated conductors (CCs). Here we report an effective approach for enhancing the in-field performance of GdBCO CCs. The critical current density (J c) of GdBCO films was significantly improved through cooperative defects created by co-irradiation with O ions and protons, especially at low temperatures and high magnetic fields. Surprisingly, the in-field J c of commercial CCs can be nearly doubled. The cooperative irradiation-induced defects are uniformly distributed throughout the GdBCO layer, which promotes the overall performance of the CC. Moreover, the dimensions of these irradiation-induced defects closely match the coherence length of REBCO. This simple and efficient method is a practical post-production solution to improve the in-field performance of commercial REBCO CCs.

Self‐Formed Fluorinated Interphase with Fe Valence Gradient for Dendrite‐Free Solid‐State Sodium‐Metal Batteries

AbstractThe poor anode/electrolyte compatibility and dendrite growth have discouraged the development of solid‐state sodium‐metal batteries (SSSMBs). Here, a self‐formed interphase with a unique Fe valence gradient is designed to stabilize the anode interface of Na3Zr2Si2PO12 solid electrolyte. This interphase consists of a Fe‐ and NaF‐containing outer layer near the Na anode and a Fe2+/Fe3+‐rich inner layer, which are in situ formed upon contacting Na with a sodiophilic α‐Fe2O3‐xFx interlayer specially coated on Na3Zr2Si2PO12. The NaF and Fe prevents continuous reduction reactions and homogenize the electric filed, while the iron oxide gradient layer offers buffering Na storage during plating, further suppressing dendrite growth. Benefiting from the dynamically stable, low‐impedance and dendrite‐free interface, the symmetric cells achieve a 20‐fold reduction in interfacial resistance and a fourfold enhancement in critical current density (CCD) at 25 °C, and powered a high CCD of 1.9 mA cm‐2 and a 1000‐h cycle life at 1 mA cm‐2 at 80 °C. The corresponding SSSMBs based on Na3V2(PO4)3 cathodes deliver a capacity retention rate of 96% over 120 cycles at 1 C. This robust interface design supports one of the best electrochemical performances ever reported and offers a comprehensive solution to stabilize the Na3Zr2Si2PO12/Na interface toward practical SSSMBs.

Exciton Manipulation for Enhancing Photoelectrochemical Hydrogen Evolution Reaction in Wrinkled 2D Heterostructures.

2D materials' junctions have demonstrated capabilities as metal-free alternatives for the hydrogen evolution reaction (HER). To date, the HER has been limited to heterojunctions of different compositions or band structures. Here, the potential of local strain modulation based on wrinkled 2D heterostructures is demonstrated, whichhelpsto realize photoelectrocatalytically active junctions. By forming regions of high and low tensile strain in wrinkled WS2 monolayers, local modification of their band structure and internal electric field due to piezoelectricity is realized in the lateral direction. This structure produces efficient electron-hole pair generation due to light trapping and exciton funneling toward the crest of the WS2 wrinkles and enhances exciton separation. Additionally, the formation of wrinkles induces an air gap in-between the 2D layer and substrate, which reduces the interfacial scattering effect and consequently improves the charge-carrier mobility. A detailed study of the strain-dependence of the photocatalytic HER process demonstratesa 2-fold decrease in the Tafel slope and a 30-fold enhancement in exchange current density. Finally, optimization of the light absorption through functionalization with quantum dots produces unprecedented photoelectrocatalytic performance and provides a route toward the scalable formation of strain-modulated WS2 nanojunctions for future green energy generation.

Critical current density enhancement of Nb3Sn superconducting wires by incorporating oxygen through rapid-heating method

The critical current density (Jc) still has much room for improvement for Nb3Sn superconductors. In this paper, SnO2 is doped into powder-in-tube (PIT) Nb3Sn superconducting wires as the oxygen source through rapid heating, quenching and annealing (RHQA) process. The results show that the 1.5 wt% SnO2-doped Nb3Sn has much higher Jc@4.2 K,10 T than the pure sample after RHQ at 2150 °C in 2 s. This is not the case when the Nb3Sn wires RHQ at 1700 °C. The increase in Jc is related to a decrease in grain size and an enhancement of inter-grain connectivity.

Electric-Field Emission Mechanism in Q-Carbon Field Emitters.

In this paper, we report the excellent field emission properties of Q-carbon and analyze its field emission characteristics through structural, morphological, and electronic property correlations, supported by density functional theory (DFT) simulation studies. The Q-carbon field emitters show impressive and stable field emission properties, such as a low turn-on electric field of ∼2.38 V/μm, a high emission current density of ∼33 μA/cm2, and a critical field of ∼2.44 V/μm for the transition from a linear region to the saturation region in the F-N plot. The outstanding field emission properties of Q-carbon are attributed to (i) a unique sp2/sp3 mixture in Q-carbon, (ii) sp2-bonded highly conductive amorphous carbon-rich channels inside the Q-carbon cluster, (iii) a large local field enhancement due to the local geometry and microstructure of Q-carbon, and (iv) the presence of sp2-bonded amorphous carbon regions in the composite film. The temperature-dependent field emission properties, such as extreme sensitivity and an enhancement in the emission current density with temperature, can be explained by the local density of states near the Fermi level and the excellent thermal stability of the Q-carbon field emitters. From DFT simulation studies, the computed work function and the field-enhancement factor were determined to be 3.62 eV and ∼2300, respectively, which explains the excellent field emission characteristics of Q-carbon. The obtained field emission properties, in most cases, were superior to those from other carbon/diamond-based field emitters, which will open new frontiers in field emission-based electronic applications.