Facile Synthesis of Carbon Nanospheres with High Capability to Inhale Selenium Powder for Electrochemical Energy Storage

Carbon–selenium composite positive electrode (CSs@Se) is engineered in this project using a melt diffusion approach with glucose as a precursor, and it demonstrates good electrochemical performance for lithium–selenium batteries. X-ray diffraction (XRD) and scanning electron microscopy (SEM) with EDS analysis are used to characterize the newly designed CSs@Se electrode. To complete the evaluation, electrochemical characterization such as charge–discharge (rate performance and cycle stability), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS) tests are done. The findings show that selenium particles are distributed uniformly in mono-sized carbon spheres with enormous surface areas. Furthermore, the charge–discharge test demonstrates that the CSs@Se cathode has a rate performance of 104 mA h g⁻¹ even at current density of 2500 mA g⁻¹ and can sustain stable cycling for 70 cycles with a specific capacity of 270 mA h g⁻¹ at current density of 25 mA g⁻¹. The homogeneous diffusion of selenium particles in the produced spheres is credited with an improved electrochemical performance.     

The Use of an Acylhydrazone-Based Metal-Organic Framework in Solid-Contact Potassium-Selective Electrode for Water Analysis

A solid-contact ion-selective electrode was developed for detecting potassium in environmental water. Two versions of a stable cadmium acylhydrazone-based metal organic framework, i.e., JUK-13 and JUK-13_H2O, were used for the construction of the mediation layer. The potentiometric and electrochemical characterizations of the proposed electrodes were carried out. The implementation of the JUK-13_H2O interlayer is shown to improve the potentiometric response and stability of measured potential. The electrode exhibits a good Nernstian slope (56.30 mV/decade) in the concentration range from 10⁻⁵ to 10⁻¹ mol L⁻¹ with a detection limit of 2.1 µmol L⁻¹. The long-term potential stability shows a small drift of 0.32 mV h⁻¹ over 67 h. The electrode displays a good selectivity comparable to ion-selective electrodes with the same membrane. The K-JUK-13_H2O-ISE was successfully applied for the determination of potassium in three certified reference materials of environmental water with great precision (RSD < 3.00%) and accuracy (RE < 3.00%).     

Binder-Free Porous 3D-ZnO Hexagonal-Cubes for Electrochemical Energy Storage Applications

Considerable efforts are underway to rationally design and synthesize novel electrode materials for high-performance supercapacitors (SCs). However, the creation of suitable materials with high capacitance remains a big challenge for energy storage devices. Herein, unique three-dimensional (3D) ZnO hexagonal cubes on carbon cloth (ZnO@CC) were synthesized by invoking a facile and economical hydrothermal method. The mesoporous ZnO@CC electrode, by virtue of its high surface area, offers rich electroactive sites for the fast diffusion of electrolyte ions, resulting in the enhancement of the SC’s performance. The ZnO@CC electrode demonstrated a high specific capacitance of 352.5 and 250 F g⁻¹ at 2 and 20 A g⁻¹, respectively. The ZnO@CC electrode revealed a decent stability of 84% over 5000 cycles at 20 A g⁻¹ and an outstanding rate-capability of 71% at a 10-fold high current density with respect to 2 A g⁻¹. Thus, the ZnO@CC electrode demonstrated improved electrochemical performance, signifying that ZnO as is promising candidate for SCs applications.     

Electrochemically Activated Screen-Printed Carbon Sensor Modified with Anionic Surfactant (aSPCE/SDS) for Simultaneous Determination of Paracetamol,Diclofenac and Tramadol

In this work, an electrochemically activated screen-printed carbon electrode modified with sodium dodecyl sulfate (aSPCE/SDS) was proposed for the simultaneous determination of paracetamol (PA), diclofenac (DF), and tramadol (TR). Changes of surface morphology and electrochemical behaviour of the electrode after the electrochemical activation with H₂O₂ and SDS surface modification were studied by scanning electron microscopy (SEM), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS). The influence of various parameters on the responses of the aSPCE/SDS such as pH and concentration of the buffer, SDS concentration, and techniques parameters were investigated. Using optimised conditions (E_acc. of −0.4 V, t_acc. of 120 s, ΔE_A of 150 mV, ν of 250 mV s⁻¹, and t_m of 10 ms), the aSPCE/SDS showed a good linear response in the concentration ranges of 5.0 × 10⁻⁸–2.0 × 10⁻⁵ for PA, 1.0 × 10⁻⁹–2.0 × 10⁻⁷ for DF, and 1.0 × 10⁻⁸–2.0 × 10⁻⁷ and 2.0 × 10⁻⁷–2.0 × 10⁻⁶ mol L⁻¹ for TR. The limits of detection obtained during the simultaneous determination of PA, DF, and TR are 1.49 × 10⁻⁸ mol L⁻¹, 2.10 × 10⁻¹⁰ mol L⁻¹, and 1.71 × 10⁻⁹ mol L⁻¹, respectively. The selectivity of the aSPCE/SDS was evaluated by examination of the impact of some inorganic and organic substances that are commonly present in environmental and biological samples on the responses of PA, DF, and TR. Finally, the differential pulse adsorptive stripping voltammetric (DPAdSV) procedure using the aSPCE/SDS was successfully applied for the determination of PA, DF, and TR in river water and serum samples as well as pharmaceuticals.     

First Screen-Printed Sensor (Electrochemically Activated Screen-Printed Boron-Doped Diamond Electrode) for Quantitative Determination of Rifampicin by Adsorptive Stripping Voltammetry

In this paper, a screen-printed boron-doped electrode (aSPBDDE) was subjected to electrochemical activation by cyclic voltammetry (CV) in 0.1 M NaOH and the response to rifampicin (RIF) oxidation was used as a testing probe. Changes in surface morphology and electrochemical behaviour of RIF before and after the electrochemical activation of SPBDDE were studied by scanning electron microscopy (SEM), CV and electrochemical impedance spectroscopy (EIS). The increase in number and size of pores in the modifier layer and reduction of charge transfer residence were likely responsible for electrochemical improvement of the analytical signal from RIF at the SPBDDE. Quantitative analysis of RIF by using differential pulse adsorptive stripping voltammetry in 0.1 mol L⁻¹ solution of PBS of pH 3.0 ± 0.1 at the aSPBDDE was carried out. Using optimized conditions (E_acc of −0.45 V, t_acc of 120 s, ΔE_A of 150 mV, ν of 100 mV s⁻¹ and t_m of 5 ms), the RIF peak current increased linearly with the concentration in the four ranges: 0.002–0.02, 0.02–0.2, 0.2–2.0, and 2.0–20.0 nM. The limits of detection and quantification were calculated at 0.22 and 0.73 pM. The aSPBDDE showed satisfactory repeatability, reproducibility, and selectivity towards potential interferences. The applicability of the aSPBDDE for control analysis of RIF was demonstrated using river water samples and certified reference material of bovine urine.     

Enhanced Structural Stability and Electrochemical Performance of LiNi0.6Co0.2Mn0.2O2 Cathode Materials by Ga Doping

Structural instability during cycling is an important factor affecting the electrochemical performance of nickel-rich ternary cathode materials for Li-ion batteries. In this work, enhanced structural stability and electrochemical performance of LiNi_0.6Co_0.2Mn_0.2O₂ cathode materials are achieved by Ga doping. Compared with the pristine electrode, Li[Ni_0.6Co_0.2Mn_0.2]_0.98Ga_0.02O₂ electrode exhibits remarkably improved electrochemical performance and thermal safety. At 0.5C rate, the discharge capacity increases from 169.3 mAh g⁻¹ to 177 mAh g⁻¹, and the capacity retention also rises from 82.8% to 89.8% after 50 cycles. In the charged state of 4.3 V, its exothermic temperature increases from 245.13 °C to more than 271.24 °C, and the total exothermic heat decreases from 561.7 to 225.6 J·g⁻¹. Both AC impedance spectroscopy and in situ XRD analysis confirmed that Ga doping can improve the stability of the electrode/electrolyte interface structure and bulk structure during cycling, which helps to improve the electrochemical performance of LiNi_0.6Co_0.2Mn_0.2O₂ cathode material.     

Direct Electrochemistry and Electrocatalysis of Horseradish Peroxidase Immobilized in a DNA/Chitosan-Fe3O4 Magnetic Nanoparticle Bio-Complex Film

A DNA/chitosan-Fe₃O₄ magnetic nanoparticle bio-complex film was constructed for the immobilization of horseradish peroxidase (HRP) on a glassy carbon electrode. HRP was simply mixed with DNA, chitosan and Fe₃O₄ nanoparticles, and then applied to the electrode surface to form an enzyme-incorporated polyion complex film. Scanning electron microscopy (SEM) was used to study the surface features of DNA/chitosan/Fe₃O₄/HRP layer. The results of electrochemical impedance spectroscopy (EIS) show that Fe₃O₄ and enzyme were successfully immobilized on the electrode surface by the DNA/chitosan bio-polyion complex membrane. Direct electron transfer (DET) and bioelectrocatalysis of HRP in the DNA/chitosan/Fe₃O₄ film were investigated by cyclic voltammetry (CV) and constant potential amperometry. The HRP-immobilized electrode was found to undergo DET and exhibited a fast electron transfer rate constant of 3.7 s⁻¹. The CV results showed that the modified electrode gave rise to well-defined peaks in phosphate buffer, corresponding to the electrochemical redox reaction between HRP(Fe^(III)) and HRP(Fe^(II)). The obtained electrode also displayed an electrocatalytic reduction behavior towards H₂O₂. The resulting DNA/chitosan/Fe₃O₄/HRP/glassy carbon electrode (GCE) shows a high sensitivity (20.8 A·cm⁻²·M⁻¹) toward H₂O₂. A linear response to H₂O₂ measurement was obtained over the range from 2 μM to 100 μM (R² = 0.99) and an amperometric detection limit of 1 μM (S/N = 3). The apparent Michaelis-Menten constant of HRP immobilized on the electrode was 0.28 mM. Furthermore, the electrode exhibits both good operational stability and storage stability.     

A Study of Methylcellulose Based Polymer Electrolyte Impregnated with Potassium Ion Conducting Carrier: Impedance,EEC Modeling,FTIR, Dielectric,and Device Characteristics

In this research, a biopolymer-based electrolyte system involving methylcellulose (MC) as a host polymeric material and potassium iodide (KI) salt as the ionic source was prepared by solution cast technique. The electrolyte with the highest conductivity was used for device application of electrochemical double-layer capacitor (EDLC) with high specific capacitance. The electrical, structural, and electrochemical characteristics of the electrolyte systems were investigated using various techniques. According to electrochemical impedance spectroscopy (EIS), the bulk resistance (R_b) decreased from 3.3 × 10⁵ to 8 × 10² Ω with the increase of salt concentration from 10 wt % to 40 wt % and the ionic conductivity was found to be 1.93 ×10⁻⁵ S/cm. The dielectric analysis further verified the conductivity trends. Low-frequency regions showed high dielectric constant, ε′ and loss, ε″ values. The polymer-salt complexation between (MC) and (KI) was shown through a Fourier transformed infrared spectroscopy (FTIR) studies. The analysis of transference number measurement (TNM) supported ions were predominantly responsible for the transport process in the MC-KI electrolyte. The highest conducting sample was observed to be electrochemically constant as the potential was swept linearly up to 1.8 V using linear sweep voltammetry (LSV). The cyclic voltammetry (CV) profile reveals the absence of a redox peak, indicating the presence of a charge double-layer between the surface of activated carbon electrodes and electrolytes. The maximum specific capacitance, C_s value was obtained as 118.4 F/g at the sweep rate of 10 mV/s.     

Bimetallic Co-Based (CoM,M = Mo,Fe, Mn) Coatings for High-Efficiency Water Splitting

Bimetallic cobalt (Co)-based coatings were prepared by a facile, fast, and low-cost electroless deposition on a copper substrate (CoFe, CoMn, CoMo) and characterized by scanning electron microscopy with energy dispersive X-ray spectroscopy and X-ray diffraction analysis. Prepared coatings were thoroughly examined for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in alkaline solution (1 M potassium hydroxide, KOH) and their activity compared to that of Co and Ni coatings. All five coatings showed activity for both reactions, where CoMo and Co showed the highest activity for HER and OER, respectively. Namely, the highest HER current density was recorded at CoMo coating with low overpotential (61 mV) to reach a current density of 10 mA·cm⁻². The highest OER current density was recorded at Co coating with a low Tafel slope of 60 mV·dec⁻¹. Furthermore, these coatings proved to be stable under HER and OER polarization conditions.     

Hazardous Petroleum Sludge-Derived Nitrogen and Oxygen Co-Doped Carbon Material with Hierarchical Porous Structure for High-Performance All-Solid-State Supercapacitors

Rational design and sustainable preparation of high-performance carbonaceous electrode materials are important to the practical application of supercapacitors. In this work, a cost-effective synthesis strategy for nitrogen and oxygen co-doped porous carbon (NOC) from petroleum sludge waste was developed. The hierarchical porous structure and ultra-high surface area (2514.7 m² g⁻¹) of NOC electrode materials could provide an efficient transport path and capacitance active site for electrolyte ions. The uniform co-doping of N and O heteroatoms brought enhanced wettability, electrical conductivity and probably additional pseudo-capacitance. The as-obtained NOC electrodes exhibited a high specific capacitance (441.2 F g⁻¹ at 0.5 A g⁻¹), outstanding rate capability, and cycling performance with inconspicuous capacitance loss after 10,000 cycles. Further, the assembled all-solid-state MnO₂/NOC asymmetrical supercapacitor device (ASC) could deliver an excellent capacitance of 119.3 F g⁻¹ at 0.2 A g⁻¹ under a wide potential operation window of 0–1.8 V with flexible mechanical stability. This ASC device yielded a superior energy density of 53.7 W h kg⁻¹ at a power density of 180 W kg⁻¹ and a reasonable cycling life. Overall, this sustainable, low-cost and waste-derived porous carbon electrode material might be widely used in the field of energy storage, now and into the foreseeable future.     

Electrocatalytic Properties of Ni(II) Schiff Base Complex Polymer Films

Platinum electrodes were modified with polymers of the (±)-trans-N,N′-bis(salicylidene)-1,2-cyclohexanediaminenickel(II) ([Ni(salcn)]) and (±)-trans-N,N′-bis(3,3′-tert-Bu-salicylidene)-1,2-cyclohexanediaminenickel(II) ([Ni(salcn(Bu))]) complexes to study their electrocatalytic and electroanalytical properties. Poly[Ni(salcn)] and poly[Ni(salcn(Bu))]) modified electrodes catalyze the oxidation of catechol, aspartic acid and NO₂⁻. In the case of poly[Ni(salcn)] modified electrodes, the electrocatalysis process depends on the electroactive surface coverage. The films with low electroactive surface coverage are only a barrier in the path of the reducer to the electrode surface. The films with more electroactive surface coverage ensure both electrocatalysis inside the film and oxidation of the reducer directly on the electrode surface. In the films with the most electroactive surface coverage, electrocatalysis occurs only at the polymer–solution interface. The analysis was based on cyclic voltammetry, EQCM (electrochemical quartz crystal microbalance) and rotating disc electrode method.     

Modified Activation Process for Supercapacitor Electrode Materials from African Maize Cob

In this work, African maize cobs (AMC) were used as a rich biomass precursor to synthesize carbon material through a chemical activation process for application in electrochemical energy storage devices. The carbonization and activation were carried out with concentrated Sulphuric acid at three different temperatures of 600, 700 and 800 °C, respectively. The activated carbon exhibited excellent microporous and mesoporous structure with a specific surface area that ranges between 30 and 254 m²·g⁻¹ as measured by BET analysis. The morphology and structure of the produced materials are analyzed through Field Emission Scanning Electron Microscopy (FESEM), Fourier Transform Infrared Spectroscopy (FTIR), X-Ray Diffraction (XRD), Boehm titration, X-ray Photoelectron Spectroscopy (XPS) and Raman Spectroscopy. X-ray photoelectron spectroscopy indicates that a considerable amount of oxygen is present in the materials. The functional groups in the activated carbon enhanced the electrochemical performance and improved the material’s double-layer capacitance. The carbonized composite activated at 700 °C exhibited excellent capacitance of 456 F g⁻¹ at a specific current of 0.25 A g⁻¹ in 6 M KOH electrolyte and showed excellent stability after 10,000 cycles. Besides being a low cost, the produced materials offer good stability and electrochemical properties, making them suitable for supercapacitor applications.     

Silver Nanoparticles Embedded on Reduced Graphene Oxide@Copper Oxide Nanocomposite for High Performance Supercapacitor Applications

In this work, silver (Ag) decorated reduced graphene oxide (rGO) coated with ultrafine CuO nanosheets (Ag-rGO@CuO) was prepared by the combination of a microwave-assisted hydrothermal route and a chemical methodology. The prepared Ag-rGO@CuO was characterized for its morphological features by field emission scanning electron microscopy and transmission electron microscopy while the structural characterization was performed by X-ray diffraction and Raman spectroscopy. Energy-dispersive X-ray analysis was undertaken to confirm the elemental composition. The electrochemical performance of prepared samples was studied by cyclic voltammetry and galvanostatic charge-discharge in a 2M KOH electrolyte solution. The CuO nanosheets provided excellent electrical conductivity and the rGO sheets provided a large surface area with good mesoporosity that increases electron and ion mobility during the redox process. Furthermore, the highly conductive Ag nanoparticles upon the rGO@CuO surface further enhanced electrochemical performance by providing extra channels for charge conduction. The ternary Ag-rGO@CuO nanocomposite shows a very high specific capacitance of 612.5 to 210 Fg⁻¹ compared against rGO@CuO which has a specific capacitance of 375 to 87.5 Fg⁻¹ and the CuO nanosheets with a specific capacitance of 113.75 to 87.5 Fg⁻¹ at current densities 0.5 and 7 Ag⁻¹, respectively.     

Bismuth/Porous Graphene Heterostructures for Ultrasensitive Detection of Cd (II)

Heavy metals pollution is one of the key problems of environment protection. Electrochemical methods, particularly anodic stripping voltammetry, have been proven a powerful tool for rapid detection of heavy metal ions. In the present work, a bismuth modified porous graphene (Bi@PG) electrode as an electrochemical sensor was adopted for the detection of heavy metal Cd²⁺ in an aqueous solution. Combining excellent electronic properties in sensitivity, peak resolution, and high hydrogen over-potential of bi-continuous porous Bi with the large surface-area and high conductivity on PG, the Bi@PG electrode exhibited excellent sensing ability. The square wave anodic stripping voltammetry response showed a perfect liner range of 10⁻⁹–10⁻⁸ M with a correlation coefficient of 0.9969. The limit of detection (LOD) and the limit of quantitation (LOQ) are calculated to be 0.1 and 0.34 nM with a sensitivity of 19.05 μA·nM⁻¹, which is relatively excellent compared to other carbon-based electrodes. Meanwhile, the Bi@PG electrode showed tremendous potential in composite detection of multifold heavy metals (such as Pb²⁺ and Cd²⁺) and wider linear range.     

Dendritic Iron(III) Carbazole Complexes: Structural,Optical, and Magnetic Characteristics

This paper focuses on the synthesis, structural characterization, and study of the optical, magnetic, and thermal properties of novel architectures combining metal ions as magnetoactive centers and photoactive blocks formed by carbazole units. For this purpose, a series of azomethine complexes of the composition [Fe(L)₂]X (L = 3,6-bis[(3′,6′-di-tert-butyl-9-carbazol)-9-carbazol]benzoyloxy-4-salicylidene-N′-ethyl-N-ethylenediamine, X = NO₃⁻, Cl⁻, PF₆⁻) were synthesized by the reaction of metal salts with Schiff bases in a mixture of solvents. The UV–Vis absorption properties were studied in dichloromethane and rationalized via time-dependent density functional theory (DFT) calculations. Upon excitation at 350 nm, the compounds exhibited an intense dual fluorescence with two emission bands centered at ~445 and ~485 nm, which were assigned to π_carb–π* intraligand and π_carb–d_Fe ligand-to-metal charge-transfer excited states. EPR spectroscopy and SQUID magnetometry revealed solid-state partial spin crossover in some compounds, and antiferromagnetic interactions between the neighboring Fe(III) ions.     

Study of Overprotective-Polarization of Steel Subjected to Cathodic Protection in Unsaturated Soil

Various electrochemical methods were used to understand the behavior of steel buried in unsaturated artificial soil in the presence of cathodic protection (CP) applied at polarization levels corresponding to correct CP or overprotection. Carbon steel coupons were buried for 90 days, and the steel/electrolyte interface was studied at various exposure times. The coupons remained at open circuit potential (OCP) for the first seven days before CP was applied at potentials of −1.0 and −1.2 V vs. Cu/CuSO₄ for the remaining 83 days. Voltammetry revealed that the corrosion rate decreased from ~330 µm yr⁻¹ at OCP to ~7 µm yr⁻¹ for an applied potential of −1.0 V vs. Cu/CuSO₄. CP effectiveness increased with time due to the formation of a protective layer on the steel surface. Raman spectroscopy revealed that this layer mainly consisted of magnetite. EIS confirmed the progressive increase of the protective ability of the magnetite-rich layer. At −1.2 V vs. Cu/CuSO₄, the residual corrosion rate of steel fluctuated between 8 and 15 µm yr⁻¹. EIS indicated that the protective ability of the magnetite-rich layer deteriorated after day 63. As water reduction proved significant at this potential, it is proposed that the released H₂ bubbles damage the protective layer.     

Electrodeposition of Manganese-Nickel Oxide Films on a Graphite Sheet for Electrochemical Capacitor Applications

Manganese-nickel (Mn-Ni) oxide films were electrodeposited on a graphite sheet in a bath consisting of manganese acetate and nickel chloride, and the structural, morphological, and electrochemical properties of these films were investigated. The electrodeposited Mn-Ni oxide films had porous structures covered with nanofibers. The X-ray diffractometer pattern revealed the presence of separate manganese oxide (γ-MnO₂) and nickel oxide (NiO) in the films. The electrodeposited Mn-Ni oxide electrode exhibited a specific capacitance of 424 F/g in Na₂SO₄ electrolyte. This electrode maintained 86% of its initial specific capacitance over 2000 cycles of the charge-discharge operation, showing good cycling stability.     

Study on the Behavior of Electrochemical Extraction of Cobalt from Spent Lithium Cobalt Oxide Cathode Materials

The molten salt electrochemical method was used to reduce the Co in spent LiCoO₂. The reduction mechanism of Co (III) in LiCoO₂ was analyzed by cyclic voltammetry, square wave voltammetry, and open circuit potential. The reduction process of Co (III) on Fe electrode was studied in NaCl-CaCl₂-LiCoO₂ molten salt system at 750 °C. The results show that the reduction process of Co (III) is a two-step reduction: Co (III) → Co (II) → Co (0) and they are all quasi-reversible processes controlled by diffusion. Phase analysis (XRD) shows that Li⁺ and Cl²⁻ in the molten salt form LiCl electrolysis experiments with different voltages were carried out, which proved the stepwise reduction of Co in LiCoO₂.     

Weight Goals,Disordered Eating Behaviors,and BMI Trajectories in US Young Adults

BackgroundCommunity sample data indicate that weight control efforts in young adulthood may have associations with greater increases in body mass index (BMI) over time.ObjectiveTo determine the prospective associations between weight goals and behaviors in young adults and BMI trajectories over 15-year follow-up using a nationally representative sample.DesignLongitudinal cohort data collected from 2001 to 2018 of the National Longitudinal Study of Adolescent to Adult Health.ParticipantsYoung adults aged 18–26 years old at baseline stratified by gender and BMI category.Main MeasuresPredictors: weight goals, any weight loss/maintenance behaviors, dieting, exercise, disordered eating behaviors. Outcomes: BMI at 7- and 15-year follow-up.Key ResultsOf the 12,155 young adults in the sample (54% female, 32% non-White), 33.2% reported a goal to lose weight, 15.7% to gain weight, and 14.6% to maintain weight. In unadjusted models, all groups have higher mean BMI at 7- and 15-year follow-up. In mixed effect models, goals to lose weight in men with BMI < 18.5 (5.94 kg/m²; 95% CI 2.58, 9.30) and goals to maintain weight in men with BMI ≥ 25 (0.44; 95% CI 0.15, 0.72) were associated with greater BMI increase compared to no weight goal. Engaging in disordered eating behaviors was associated with greater BMI increase in men with BMI < 18.5 (5.91; 2.96, 8.86) and women with 18.5 ≤ BMI < 25 (0.40; 0.16, 0.63). Dieting (− 0.24; − 0.41, − 0.06) and exercise (− 0.31; − 0.45, − 0.17) were associated with lower BMI increase in women with 18.5 ≤ BMI < 25. In women with BMI < 18.5, dieting was associated with greater BMI increase (1.35; 0.33, 2.37).ConclusionsWeight control efforts may have variable effects on BMI over time by gender and BMI category. These findings underscore the need to counsel patients on the effectiveness of weight control efforts and long-term weight management.KEY WORDS: BMI, weight goals, disordered eating behaviors, young adult, weight trajectories     

Performance Comparison of CdTe:Na,CdTe:As,and CdTe:P Single Crystals for Solar Cell Applications

We compared thermal stability, open-circuit voltage, short-circuit current, and fill factor values of single-crystal Cadmium telluride (CdTe) grown using the vertical Bridgman (VB) technique and doped with group V elements (phosphorus and arsenic), and group Ⅰ element (sodium), followed by an annealing process. The sodium-doped CdTe maintained a hole density of 10¹⁶ cm⁻³ or higher; after annealing for a long time, this decreased to 10¹⁵ cm⁻³ or less. The arsenic-doped CdTe maintained a hole density of approximately 10¹⁶ cm⁻³ even after the annealing process; however its bulk minority carrier lifetime decreased by approximately 10%. The phosphorus-doped CdTe maintained its properties after the annealing process, ultimately achieving a hole density of ~10¹⁶ cm⁻³ and a minority carrier lifetime of ~40 ns. The characteristics of a single-crystal solar cell were evaluated using a solar cell device that contained single-crystal CdTe with various dopants. The sodium-doped sample exhibited poor interfacial properties, and its performance decreased rapidly during annealing. The samples doped with group V elements exhibited stable characteristics even during long-term annealing. We concluded, therefore, that group V elements dopants are more suitable for CdTe single-crystal-based solar cell applications involving thermal stress conditions, such as space missions or extreme fabrication temperature environments.