Narrow Results

This paper reports on the successful deposition of phosphorus (P)-doped n-type (p-C:P) carbon (C) films, and fabrication of n-C:P/p-Si cells by pulsed laser deposition (PLD) using graphite target at room temperature. The cells performances have been given in the dark I–V rectifying curve and I–V working curve under illumination when exposed to AM 1.5 illumination condition (100mW/cm², 25°C). The n-C:P/p-Si cell fabricated using a target with the amount of P by 7 weight percentages (Pwt%) shows the highest energy conversion efficiency η = 1.14% and fill factor FF = 41%. The quantum efficiency (QE) of the n-C:P/p-Si cells are observed to improve with Pwt%. The dependence of P content on the electrical and optical properties of the deposited films and the photovoltaic characteristics of the n-C:P/p-Si heterojunction solar cell are discussed.

The successful deposition of boron (B)-doped p-type (p-C:B) and phosphorous (P)-doped n-type (n-C:P) carbon (C) films, and fabrication of p-C:B on silicon (Si) substrate (p-C:B/n-Si) and n-C:P/p-Si cells by the technique of pulsed laser deposition (PLD) using graphite target is reported. The cells' performances are represented in the dark I–V rectifying curve and I–V working curve under illumination when exposed to AM 1.5 illumination condition (100 mW/cm², 25°C). The open circuit voltage (V_oc) and short circuit current density (J_sc) for p-C:B/n-Si are observed to vary from 230–250 mV and 1.5–2.2 mA/cm², respectively, and to vary from 215–265 mV and 7.5–10.5 mA/cm², respectively, for n-C:P/p-Si cells. The p-C:B/n-Si cell fabricated using the target with the amount of B by 3 Bwt% shows highest energy conversion efficiency, η = 0.20%, and fill factor, FF = 45%, while, the n-C:P/p-Si cell with the amount of P by 7 Pwt% shows highest energy conversion efficiency, η = 1.14%, and fill factor, FF = 41%. The quantum efficiencies (QE) of the p-C:B/n-Si and n-C:P/p-Si cells are observed to improve with Bwt% and Pwt%, respectively. The contributions of QE are suggested to be due to photon absorption by carbon layer in the lower wavelength region (below 750 nm) and Si substrates in the higher wavelength region. The dependence of B and P content on the electrical and optical properties of the deposited films, and the photovoltaic characteristics of the respective p-C:B/n-Si and n-C:P/p-Si heterojunction photovoltaic cells, are discussed.

This paper reports on the successful deposition of boron (B)-doped p-type (p-C:B) and phosphorus (P)-doped n-type (p-C:P) carbon (C) films, and the fabrication of p-C:B on silicon (Si) substrate (p-C:B/n-Si) and n-C:P/p-Si cells by a pulsed laser deposition (PLD) technique using a graphite target at room temperature. The boron and phosphorus atoms incorporated in the films were determined by X-ray photoelectron spectroscopy (XPS) to be in the range of 0.2–1.75 and 0.22–1.77 atomic percentages, respectively. The cells performances have been given in the dark I–V rectifying curve and I–V working curve under illumination when exposed to AM 1.5 illumination conditions (100 mW/cm², 25°C). The open circuit voltage (V_oc) and short circuit current density (J_sc) for p-C:B/n-Si are observed to vary from 230 to 250 mV and from 1.5 to 2.2 mA/cm², respectively; they vary from 215 to 265 mV and from 7.5 to 10.5 mA/cm², respectively, for n-C:P/p-Si cells. The p-C:B/n-Si cell fabricated using the target with the amount of boron by 3 weight percentages (Bwt%) showed the highest energy conversion efficiency, η = 0.20% and fill factor, FF = 45%. The n-C:P/p-Si cell fabricated using the target with the amount of 7 Pwt% showed the highest η = 1.14% and FF = 41%. The quantum efficiency (QE) of the p-C:B/n-Si and n-C:P/p-Si cells were observed to improve with Bwt% and Pwt%, respectively. The contribution of QE in the lower wavelength region (below 750 nm) may be due to photon absorption by the carbon layer, in the higher wavelength region it was due to the Si substrates. In this paper, the dependence of the boron and phosphorus content on the electrical and optical properties of the deposited films and the photovoltaic characteristics of the respective p-C:B/n-Si and n-C:P/p-Si heterojunction solar cells are discussed.

Crystalline cubic silicon carbide (3C-SiC) surface layers have been prepared by carbon-ion implantation into silicon (100) using a MEVVA ion source and subsequent annealing at 1250°C for 2 h. The obtained films have been characterized by SEM, XRD, and micro-Raman analysis. The effect of carbon-ion dose on the surface morphology of the ion-implanted samples has been investigated. Rectangular patterns are observed on the surfaces of carbon-ion-implanted silicon substrates. It is found that the amount of rectangular patterns increases with ion dose, suggesting the dependence of surface morphology on ion dose. The formation of rectangular patterns has been elucidated in this paper.

The Fe–C–H interaction near defects in iron structures was studied using qualitative structure calculations in the framework of the atom superposition and electron delocalization molecular orbital. Calculations were performed using three Fe clusters to simulate an edge dislocation, a divacancy; both in bcc iron and a stacking fault in an fcc iron structure. In all cases, the most stable location for C atom inside the clusters was determined. Therefore, H atom was approximated to a minimum energy region where the C atom resides. The total energy of the cluster decreases when the C atom is located near the defects zone. In addition, the presence of C in the defects zone makes no favorable H accumulation. The C acts as an expeller of H in a way that reduces the hydrogen Fe–Fe bonds weakening.

Recent research has shown that fly ash may catalyze the oxidation of elemental mercury and facilitate its removal. However, the nature of mercury-fly ash interaction is still unknown, and the mechanism of mercury retention in fly ash needs to be investigated more thoroughly. In this work, a fly ash from a coal-fired power plant is used to characterize the inorganic and organic constituents and then evaluate its mercury retention capacities. The as-received fly ash sample is mechanically sieved to obtain five size fractions. Their characteristics are examined by loss on ignition (LOI), scanning electron microscope (SEM), energy dispersive X-ray detector (EDX), X-ray diffraction (XRD), and Raman spectra. The results show that the unburned carbon (UBC) content and UBC structural ordering decrease with a decreasing particle size for the five ashes. The morphologies of different size fractions of as-received fly ash change from the glass microspheres to irregular shapes as the particle size increases, but there is no correlation between particle size and mineralogical compositions in each size fraction. The adsorption experimental studies show that the mercury-retention capacity of fly ash depends on the particle size, UBC, and the type of inorganic constituents. Mercury retention of the types of sp² carbon is similar to that of sp³ carbon.

The solution plasma process (SPP) has attracted considerable attention for the synthesis of carbon nanomaterials; the SPP uses electrical discharges generated directly by a bipolar pulsed power supply for various combinations of the solvents and solutes in the solution. However, the SPP requires high-temperature heat treatment for enhancing conductivity and exhibiting catalyst activity. Furthermore, the metal used as the electrode in the SPP is generally sputtered during discharge. This study presents the feasibility of reducing the heat-treatment step and solving the problem of sputtering of the metal electrodes by simply increasing the repetition frequency of the bipolar pulsed power. During synthesis, the pulse frequency acts as the graphitization catalyst. The enhancement of crystallinity was further confirmed by X-ray diffraction (XRD), Raman spectroscopy, and transmission electron microscopy (TEM). The findings of this study are expected to contribute toward research on improving the properties of carbon for various applications of the SPP synthesis methods.

This study examines the machinability of hybrid fiber metal laminates (HFML), which are made by nickel–chromium alloy (IN-625) metal-cored carbon (Ca)/aramid (Ar) fiber laminate using ultrasonic vibration-coupled microwire electrical discharge machining (UV-$\mu$WEDM). Since UV-$\mu$WEDM parameters significantly impact the erosion rate ($E_R$) and surface undulation ($S_U$), the main objective was to identify the optimal machining parameters. The input variables include the pulse on ($P_{\text{on}}$), pulse off ($P_{\text{off}}$), current ($I_C$), cutting inclination ($C_I$), and servo voltage ($S_V$) coupled with ultrasonic vibration (UV). The empirical findings show that the servo voltage ($S_V$) significantly impacts $E_R$ (73.93%) and $S_U$ (70.02%). The performance categorization order of significant influencing variable is $S_V>P_{\text{off}}>C_I>P_{\text{on}}>I_C$. The desirability interpretation generated the optimum setting for minimizing $S_U$ and maximizing $E_R$ is $P_{\text{on}}=8\mu$s, $P_{\text{off}}=14\mu$s, $S_V=50$V, $I_C=3$A, and $C_I=30^{\circ }$. Scanning electron microscopic (SEM) images were used to perform the micro-interlayer analysis on the machined surface. Moreover, creating an appropriate HFML is necessary to cut various shapes and sizes to satisfy the demands of diverse applications. 60% of components in the aerospace sector are reportedly rejected in real time due to dimension departure, poor surface finish, and damage found in the final assembly. Investigating the viability of cutting-edge machining techniques like UV-$\mu$WEDM is crucial to minimize damage and improve the quality of HFMLs.

A hierarchical carbon material containing nanopores (micropores and mesopores) and micrometric sized capillaries (macropores) is produced using a combination of hard and soft templates. The hard template is a polypropylene (PP) cloth which decomposes during pyrolysis leaving a macroporous structure. The soft template is a cationic polyelectrolyte which stabilizes the resorcinol/formaldehyde (RF) resin porous structure during drying to give a nanoporous RF resin. The method produces a nanocomposite of the porous RF resin with an imbibed PP cloth. The composite is then pyrolyzed in a inert gas atmosphere to render a carbon material having macropores as well as micro/mesopores. The material exhibits both a large surface area (S_BET = 742 ± 2 m²/g) due to nanopores and goof fluid permeability due to micrometric sized pores. The macropores can be oriented during fabrication. The nanoporous surface can be used to support metal nanoparticles for fuel cell while the macropores allow easy flux of gas and liquids through the monolithic material.

Carbon-modified Ti${}^{3+}$ self-doped hierarchical porous titanium dioxides were synthesized by one-step soft chemical method. The contents of carbon and Ti${}^{3+}$ of the catalysts were tuned through a facile heat treatment. The prepared photocatalysts possess well-packed uniform macropores with the size of $\sim 200$nm, mesoporous structure with the pore size of 5.9–6.8nm, and the specific surface area of 50–200m²/g. The results illustrate the carbon combined with TiO₂ via the interfacial C$-$O$-$Ti bonds and the rich existence of Ti${}^{3+}$. The catalyst with 18wt.% carbon content exhibits a degradation ratio of crystal violet up to 97.5%. The enhanced photocatalysis is ascribed to the synergistic effect of carbon and Ti${}^{3+}$. The interfacial C$-$O$-$Ti bonds act as the pathway to transfer excited electrons and the Ti${}^{3+}$ can trap the electrons to hinder the recombination of electrons and holes.

In rechargeable lithium-sulfur (Li-S) batteries, the conductive carbon materials with high surface areas can greatly enhance the electrical conductivity of sulfur cathode, and metal oxides can restrain the dissolution of lithium polysulfides within the electrolyte through strong chemical bindings. The rational design of carbon-metal oxide nanocomposite cathodes has been considered as an effective solution to increase the sulfur utilization and improve cycling performance of Li-S batteries. Here, we summarize the recent progresses in the carbon-metal oxide composites for Li-S battery cathodes. Some insights are also offered on the future directions of carbon-metal oxide hybrid cathodes for high performance Li-S batteries.

In this paper, carbon particles with micro- and nano-particle size were synthesized through a hydrothermal reaction of glucose, namely C-1(123.1 nm), C-2(229.2 nm), C-3(335.1 nm), C-4(456.2 nm) and C-5(534.0 nm) with distinct sizes. We utilized five size carbon particles as individual fillers into the EHS matrix materials to prepare composite eutectic phase change materials (C/EHS PCMs) by melt blending technique. The impact of carbon particle size on the dispersion stability and thermal properties of Na₂SO₄⋅10H₂O–Na₂HPO₄⋅12H₂O (EHS) phase change materials was investigated. Scanning electron microscopy (SEM) and dynamic light scattering (DLS) analysis were done to analyze the diameters of carbon particles. The cryogenic-scanning electron microscopy (Cryo-SEM) analysis indicated that the carbon particles resulted in modification in the morphology of the EHS. The results of in situ X-ray diffraction (XRD) and Fourier-transformed infrared (FTIR) analysis showed only simple physical mixing between carbon particles and EHS. It is shown that adding 0.2 wt.% C-2 can decrease the supercooling degree of EHS to 1.5${}^{\circ }$C. The cyclic stability of C/EHS varies significantly depending on the size of carbon particles. The thermal conductivity of EHS increased by 42.1%, 39.9%, 14.4%, 19.5%, and 18.8% with the addition of C-1, C-2, C-3, C-4, and C-5, respectively, at a mass fraction of 0.2%. The results of differential scanning calorimetry reveal that the incorporation of C-1, C-2, C-3, and C-4 into EHS leads to an enhancement of latent heat. The latent heat capacity of EHS with 0.2 wt.% C-2 is 243.4 J⋅g${}^{-1}$, and after undergoing 500 cycles of solid-liquid phase transition, the latent heat remained above 200 J⋅g${}^{-1}$. Through the comprehensive analysis, the C-2/EHS composite phase change material holds significant potential for advancing building insulation and solar energy storage technologies.

As green anode materials with wide distribution, controllable cost, and diversified structure, carbon materials have received more attention. In this paper, iodine- and nitrogen-co-doped carbon flower materials were prepared. The flower-like structure of the material ensures the rapid diffusion of lithium ions, and the synergistic effect of iodine and nitrogen atoms improves the pore size distribution, the conductivity and the active sites of carbon materials realizing the high ion storage and the fast charge diffusion. As the anode material of lithium-ion batteries, the iodine- and nitrogen-co-doped carbon flower could have the capacitance of 410 mAh g${}^{-1}$ at the current density of 0.1 A g${}^{-1}$ after 150 cycles and 181 mAh g${}^{-1}$ at the high current density of 2.0 A g${}^{-1}$ after 1000 cycles. The results of electrochemical impedance spectroscopy, kinetics, and GITT show this material has fast charge transport kinetics and excellent rate performance.