One-Pot Synthesis of LiFePO4/N-Doped C Composite Cathodes for Li-ion Batteries

LiFePO₄/N-doped C composites with core–shell structures were synthesized by a convenient solvothermal method. Cetyltrimethylammonium bromide (CTAB) and glucose were used as nitrogen and carbon sources, respectively. The growth of LiFePO₄ nanocrystals was regulated by CTAB, resulting in an average particle size of 143 nm for the LiFePO₄/N-doped C. The N atoms existed in the carbon of LiFePO₄/N-doped C in the form of pyridinic N and graphitic N. The LiFePO₄/N-doped C composites delivered discharge specific capacities of 160.7 mAh·g⁻¹ (0.1 C), 128.4 mAh·g⁻¹ (5 C), and 115.8 mAh·g⁻¹ (10 C). Meanwhile, no capacity attenuation was found after 100 electrochemical cycles at 1 C. N-doping enhanced the capacity performance of the LiFePO₄/C cathode, while the core–shell structure enhanced the cycle performance of the cathode. The electrochemical test data showed a synergistic effect between N-doping and core–shell structure on the enhancement of the electrochemical performance of the LiFePO₄/C cathode.     

Flake (NH4)6Mo7O24/Polydopamine as a High Performance Anode for Lithium Ion Batteries

Ammonium molybdate tetrahydrate ((NH₄)₆Mo₇O₂₄) (AMT) is commonly used as the precursor to synthesize Mo-based oxides or sulfides for lithium ion batteries (LIBs). However, the electrochemical lithium storage ability of AMT itself is unclear so far. In the present work, AMT is directly examined as a promising anode material for Li-ion batteries with good capacity and cycling stability. To further improve the electrochemical performance of AMT, AMT/polydopamine (PDA) composite was simply synthesized via recrystallization and freeze drying methods. Unlike with block shape for AMT, the as-prepared AMT/PDA composite shows flake morphology. The initial discharge capacity of AMT/PDA is reached up to 1471 mAh g⁻¹. It delivers a reversible discharge capacity of 702 mAh g⁻¹ at a current density of 300 mA g⁻¹, and a stable reversible capacity of 383.6 mA h g⁻¹ is retained at a current density of 0.5 A g⁻¹ after 400 cycles. Moreover, the lithium storage mechanism is fully investigated. The results of this work could potentially expand the application of AMT and Mo-based anode for LIBs.     

Effect of Residual Trace Amounts of Fe and Al in Li[Ni1/3Mn1/3Co1/3]O2 Cathode Active Material for the Sustainable Recycling of Lithium-Ion Batteries

As the explosive growth of the electric vehicle market leads to an increase in spent lithium-ion batteries (LIBs), the disposal of LIBs has also made headlines. In this study, we synthesized the cathode active materials Li[Ni_1/3Mn_1/3Co_1/3]O₂ (NMC) and Li[Ni_1/3Mn_1/3Co_1/3Fe_0.0005Al_0.0005]O₂ (NMCFA) via hydroxide co-precipitation and calcination processes, which simulate the resynthesis of NMC in leachate containing trace amounts of iron and aluminum from spent LIBs. The effects of iron and aluminum on the physicochemical and electrochemical properties were investigated and compared with NMC. Trace amounts of iron and aluminum do not affect the morphology, the formation of O3-type layered structures, or the redox peak. On the other hand, the rate capability of NMCFA shows high discharge capacities at 7 C (110 mAh g⁻¹) and 10 C (74 mAh g⁻¹), comparable to the values for NMC at 5 C (111 mAh g⁻¹) and 7 C (79 mAh g⁻¹), respectively, due to the widened interslab thickness of NMCFA which facilitates the movement of lithium ions in a 2D channel. Therefore, iron and aluminum, which are usually considered as impurities in the recycling of LIBs, could be used as doping elements for enhancing the electrochemical performance of resynthesized cathode active materials.     

Boosting Lithium Storage of a Metal-Organic Framework via Zinc Doping

Lithium-ion batteries (LIBs) as a predominant power source are widely used in large-scale energy storage fields. For the next-generation energy storage LIBs, it is primary to seek the high capacity and long lifespan electrode materials. Nickel and purified terephthalic acid-based MOF (Ni-PTA) with a series amounts of zinc dopant (0, 20, 50%) are successfully synthesized in this work and evaluated as anode materials for lithium-ion batteries. Among them, the 20% atom fraction Zn-doped Ni-PTA (Zn_0.2-Ni-PTA) exhibits a high specific capacity of 921.4 mA h g⁻¹ and 739.6 mA h g⁻¹ at different current densities of 100 and 500 mA g⁻¹ after 100 cycles. The optimized electrochemical performance of Zn_0.2-Ni-PTA can be attributed to its low charge transfer resistance and high lithium-ion diffusion rate resulting from expanded interplanar spacing after moderate Zn doping. Moreover, a full cell is fabricated based on the LiFePO₄ cathode and as-prepared MOF. The Zn_0.2-Ni-PTA shows a reversible specific capacity of 97.9 mA h g⁻¹ with 86.1% capacity retention (0.5 C) after 100 cycles, demonstrating the superior electrochemical performance of Zn_0.2-Ni-PTA anode as a promising candidate for practical lithium-ion batteries.     

Granulation of Silicon Nitride Powders by Spray Drying: A Review

Spray drying is a widely used method of converting liquid material (aqueous or organic solutions, emulsions and suspensions) into a dry powder. Good flowability, narrow size distribution, and controllable morphology are inherent in powders produced by spray drying. This review considers the granulation factors that influence the final properties of the silicon nitride dried powders. The first group includes the types of atomizers, manifolds, and drying chamber configurations. The process parameters fall into the second group and include the following: inlet temperature, atomizing air flow, feed flow rate, drying gas flow rate, outlet temperature, and drying time. Finally, the last group, feedstock parameters, includes many factors such as feed surface tension, feed viscosity, solvent type, solid particle concentration, and additives. Given the large number of factors affecting morphology, particle size and moisture, optimizing the spray drying process is usually achieved by the “trial and error” approach. Nevertheless, some factors such as the effect of a solvent, dispersant, binder, and sintering additives considered in the literature that affect the Si₃N₄ granulation process were reviewed in the work. By summarizing the data available on silicon nitride powder production, the authors attempt to tackle the problem of its emerging demand in science and industry.     

Synthesis and Characterization of Sn/SnO2/C Nano-Composite Structure: High-Performance Negative Electrode for Lithium-Ion Batteries

Tin oxide (SnO₂) and tin-based composites along with carbon have attracted significant interest as negative electrodes for lithium-ion batteries (LIBs). However, tin-based composite electrodes have some critical drawbacks, such as high volume expansion, low capacity at high current density due to low ionic conductivity, and poor cycle stability. Moreover, complex preparation methods and high-cost carbon coating procedures are considered main challenges in the commercialization of tin-based electrodes for LIBs. In this study, we prepared a Sn/SnO₂/C nano-composite structure by employing a low-cost hydrothermal method, where Sn nanoparticles were oxidized in glucose and carboxymethyl cellulose CMC was introduced into the solution. Scanning electron microscope (SEM) and transmission electron microscope revealed the irregular structure of Sn nanoparticles and SnO₂ phases in the conductive carbon matrix. The as-prepared Sn/SnO₂/C nano-composite showed high first-cycle reversible discharge capacity (2248 mAhg⁻¹) at 100 mAg⁻¹ with a first coulombic efficiency of 70%, and also displayed 474.64 mAhg⁻¹ at the relatively high current density of about 500 mAg⁻¹ after 100 cycles. A low-cost Sn/SnO₂/C nano-composite with significant electrochemical performance could be the next generation of high-performance negative electrodes for LIBs.     

Enhanced Switching Reliability of Sol–Gel-Processed Y2O3 RRAM Devices Based on Y2O3 Surface Roughness-Induced Local Electric Field

Sol–gel-processed Y₂O₃ films were used as active channel layers for resistive random access memory (RRAM) devices. The fabricated ITO/Y₂O₃/Ag RRAM devices exhibited the properties of conventional bipolar memory devices. A triethylamine stabilizer with a high vapor pressure and low surface tension was added to realize the local electric field area. During drying and high-temperature post-annealing processes, the large convective flow enhanced the surface elevation, and the increased –OH groups accelerated the hydrolysis reaction and aggregation. These phenomena afforded Y₂O₃ films with an uneven surface morphology and an increased surface roughness. The increased roughness of the Y₂O₃ films attributable to the triethylamine stabilizer enhanced the local electrical field, improved device reliability, and achieved successful repetition of the switching properties over an extended period.     

Material Optimization Engineering toward xLiFePO4·yLi3V2(PO4)3 Composites in Application-Oriented Li-Ion Batteries

The development of LiFePO₄ (LFP) in high-power energy storage devices is hampered by its slow Li-ion diffusion kinetics. Constructing the composite electrode materials with vanadium substitution is a scientific endeavor to boost LFP’s power capacity. Herein, a series of xLiFePO₄·yLi₃V₂(PO₄)₃ (xLFP·yLVP) composites were fabricated using a simple spray-drying approach. We propose that 5LFP·LVP is the optimal choice for Li-ion battery promotion, owning to its excellent Li-ion storage capacity (material energy density of 413.6 W·h·kg⁻¹), strong machining capability (compacted density of 1.82 g·cm⁻³) and lower raw material cost consumption. Furthermore, the 5LFP·LVP||LTO Li-ion pouch cell also presents prominent energy storage capability. After 300 cycles of a constant current test at 400 mA, 75% of the initial capacity (379.1 mA·h) is achieved, with around 100% of Coulombic efficiency. A capacity retention of 60.3% is displayed for the 300th cycle when discharging at 1200 mA, with the capacity fading by 0.15% per cycle. This prototype provides a valid and scientific attempt to accelerate the development of xLFP·yLVP composites in application-oriented Li-ion batteries.     

The Role of Sintering Temperature and Dual Metal Substitutions (Al3+, Ti4+) in the Development of NASICON-Structured Electrolyte

The aim of this study is to synthesize Li_1+xAl_xTi_xSn_2−2x(PO₄) sodium super ion conductor (NASICON) -based ceramic solid electrolyte and to study the effect of dual metal substitution on the electrical and structural properties of the electrolyte. The performance of the electrolyte is analyzed based on the sintering temperature (550 to 950 °C) as well as the composition. The trend of XRD results reveals the presence of impurities in the sample, and from Rietveld Refinement, the purest sample is achieved at a sintering temperature of 950 °C and when x = 0.6. The electrolytes obey Vegard′s Law as the addition of Al³⁺ and Ti⁴⁺ provide linear relation with cell volume, which signifies a random distribution. The different composition has a different optimum sintering temperature at which the highest conductivity is achieved when the sample is sintered at 650 °C and x = 0.4. Field emission scanning electron microscope (FESEM) analysis showed that higher sintering temperature promotes the increment of grain boundaries and size. Based on energy dispersive X-ray spectroscopy (EDX) analysis, x = 0.4 produced the closest atomic percentage ratio to the theoretical value. Electrode polarization is found to be at maximum when x = 0.4, which is determined from dielectric analysis. The electrolytes follow non-Debye behavior as it shows a variety of relaxation times.     

Effect of Sintering Temperature and Polarization on the Dielectric and Electrical Properties of La0.9Sr0.1MnO3 Manganite in Alternating Current

The electrical characterization ofa La_0.9Sr_0.1MnO₃ compound sintered at 800, 1000 and 1200 °C was investigated by means of the impedance-spectroscopy technique. As the results, the experimental conductivity spectra were explained in terms of the power law. The AC-conductivity study reveals the contributions of different conduction mechanisms. Indeed, the variation in the frequency exponents (‘s₁’ and ‘s₂’) as a function of the temperature confirms the thermal activation of the conduction process in the system. It proves, equally, that the transport properties are governed by the non-small-polaron-tunneling and the correlated-barrier-hopping mechanisms. Moreover, the values of the frequency exponents increase under the sintering-temperature (TS) effect. Such an evolution may be explained energetically. The jump relaxation model was used to explain the electrical conductivity in the dispersive region, as well as the frequency-exponent values by ionic conductivity. Under electrical polarization with applied DC biases of Vp = 0.1 and 2 V at room temperature, the results show the significant enhancement of the electrical conductivity. In addition, the dielectric study reveals the evident presence of dielectric relaxation. Under the sintering-temperature effect, the dielectric constant increases enormously. Indeed, the temperature dependence of the dielectric constant is well fitted by the modified Curie–Weiss law. Thus, the deduced values of the parameter (γ) confirm the relaxor character and prove the diffuse phase transition of our material. Of note is the high dielectric-permittivity magnitude, which indicates that the material is promising for microelectronic devices.     

Effect of the Ca2Mg6Zn3 Phase on the Corrosion Behavior of Biodegradable Mg-4.0Zn-0.2Mn-xCa Alloys in Hank’s Solution

The effect of the Ca₂Mg₆Zn₃ phase on the corrosion behavior of biodegradable Mg-4.0Zn-0.2Mn-xCa (ZM-xCa, x = 0.1, 0.3, 0.5 and 1.0 wt.%) alloys in Hank’s solution was investigated with respect to phase spacing, morphology, distribution and volume fraction. With the increase in Ca addition, the volume fraction of the Ca₂Mg₆Zn₃ phase increased from 2.5% to 7.6%, while its spacing declined monotonically from 43 μm to 30 μm. The Volta potentials of secondary phases relative to the Mg matrix were measured by using scanning kelvin probe force microscopy (SKPFM). The results show that the Volta potential of the intragranular spherical Ca₂Mg₆Zn₃ phase (+109 mV) was higher than that of the dendritic Ca₂Mg₆Zn₃ phase (+80 mV). It is suggested that the Ca₂Mg₆Zn₃ acted as a cathode to accelerate the corrosion process due to the micro-galvanic effect. The corrosion preferred to occur around the spherical Ca₂Mg₆Zn₃ phase at the early stage and developed into the intragranular region. The corrosion rate increased slightly with increasing Ca content from 0.1 wt.% to 0.5 wt.% because of the enhanced micro-galvanic corrosion effect. The decrease in the phase spacing and sharp increase in the secondary phase content resulted in a dramatic increase in the corrosion rate of the ZM-1.0Ca alloy.     

Spark Plasma Sintering of LiFePO4: AC Field Suppressing Lithium Migration

Our work proposes a comparison between Spark Plasma Sintering of LiFePO₄ carried out using an Alternating Current (AC) and Direct Current (DC). It quantifies the Li-ion migration using DC, and it validates such hypothesis using impedance spectroscopy, X-ray photoelectron spectroscopy and inductively coupled plasma optical emission spectroscopy. The use of an AC field seems effective to inhibit undesired Li-ion migration and achieve high ionic conductivity as high as 4.5 × 10⁻³ S/cm, which exceeds by one order of magnitude samples processed under a DC field. These results anticipate the possibility of fabricating a high-performance all-solid-state Li-ion battery by preventing undesired Li loss during SPS processing.     

Formation of Li2CO3 Nanostructures for Lithium-Ion Battery Anode Application by Nanotransfer Printing

Various high-performance anode and cathode materials, such as lithium carbonate, lithium titanate, cobalt oxides, silicon, graphite, germanium, and tin, have been widely investigated in an effort to enhance the energy density storage properties of lithium-ion batteries (LIBs). However, the structural manipulation of anode materials to improve the battery performance remains a challenging issue. In LIBs, optimization of the anode material is a key technology affecting not only the power density but also the lifetime of the device. Here, we introduce a novel method by which to obtain nanostructures for LIB anode application on various surfaces via nanotransfer printing (nTP) process. We used a spark plasma sintering (SPS) process to fabricate a sputter target made of Li₂CO₃, which is used as an anode material for LIBs. Using the nTP process, various Li₂CO₃ nanoscale patterns, such as line, wave, and dot patterns on a SiO₂/Si substrate, were successfully obtained. Furthermore, we show highly ordered Li₂CO₃ nanostructures on a variety of substrates, such as Al, Al₂O₃, flexible PET, and 2-Hydroxylethyl Methacrylate (HEMA) contact lens substrates. It is expected that the approach demonstrated here can provide new pathway to generate many other designable structures of various LIB anode materials.     

Effect of CeO2 Size on Microstructure,Synthesis Mechanism and Refining Performance of Al-Ti-C Alloy

The effects of CeO₂ size on the microstructure and synthesis mechanism of Al-Ti-C alloy were investigated using a quenching experiment method. A scanning calorimetry experiment was used to investigate the synthesis mechanism of TiC, the aluminum melt in situ reaction was carried out to synthesize master alloys and its refining performance was estimated. The results show that the Al-Ti-C-Ce system is mainly composed of α-Al, Al₃Ti, TiC and Ti₂Al₂₀Ce. The addition of CeO₂ obviously speeds up the progress of the reaction, reduces the size of Al₃Ti and TiC and lowers the formation temperature of second-phase particles. When the size of CeO₂ is 2–4 μm, the promotion effect on the system is most obvious. The smaller the size of CeO₂, the smaller the size of Al₃Ti and TiC and the lower the formation temperature. Al-Ti-C-Ce master alloy has a significant refinement effect on commercial pure aluminum. When the CeO₂ size is 2–4 μm, the grain size of commercial pure aluminum is refined to 227 μm by Al-Ti-C-Ce master alloy.     

Direct One-Step Growth of Bimetallic Ni2Mo3N on Ni Foam as an Efficient Oxygen Evolution Electrocatalyst

A simple and economical synthetic route for direct one-step growth of bimetallic Ni₂Mo₃N nanoparticles on Ni foam substrate (Ni₂Mo₃N/NF) and its catalytic performance during an oxygen evolution reaction (OER) are reported. The Ni₂Mo₃N/NF catalyst was obtained by annealing a mixture of a Mo precursor, Ni foam, and urea at 600 °C under N₂ flow using one-pot synthesis. Moreover, the Ni₂Mo₃N/NF exhibited high OER activity with low overpotential values (336.38 mV at 50 mA cm⁻² and 392.49 mV at 100 mA cm⁻²) and good stability for 5 h in Fe-purified alkaline electrolyte. The Ni₂Mo₃N nanoparticle surfaces converted into amorphous surface oxide species during the OER, which might be attributed to the OER activity.     

Effect of Sintering Process on Ionic Conductivity of Li7-xLa3Zr2-xNbxO12 (x = 0, 0.2, 0.4, 0.6) Solid Electrolytes

Garnet-type Li₇La₃Zr₂O₁₂ (LLZO) is considered as a promising solid electrolyte. Nb-doped LLZO ceramics exhibit significantly improved ion conductivity. However, how to prepare the Nb-doped LLZO ceramics in a simple and economical way, meanwhile to investigate the relationship between process conditions and properties in Li_7-xLa₃Zr_2-xNb_xO₁₂ ceramics, is particularly important. In this study, Li_7-xLa₃Zr_2-xNb_xO₁₂ (LLZN_xO, x = 0, 0.2, 0.4, 0.6) ceramics were prepared by conventional solid-state reaction. The effect of sintering process on the structure, microstructure, and ionic conductivity of LLZN_xO (x = 0, 0.2, 0.4, 0.6) ceramics was investigated. Due to the more contractive Nb-O bonds in LLZN_xO ceramics, the cubic structures are much easier to form and stabilize, which could induce the decreased preparation time. High-performance garnet LLZN_xO ceramics can be obtained by optimizing the sintering process with lower calcining temperature and shorter holding time. The garnet samples with x = 0.4 calcined at 850 °C for 10 h and sintered at 1250 °C for 4 h exhibit the highest ionic conductivity of 3.86 × 10⁻⁴ S·cm⁻¹ at room temperature and an activation energy of 0.32 eV, which can be correlated to the highest relative density of 96.1%, and good crystallinity of the grains.     

Effect of Heat Treatment on Structural,Magnetic and Electrical Properties of La2FeMnO6

In this study, the effect of heat treatment on the structural, magnetic and electrical properties of La₂FeMnO₆ prepared via the sol–gel and sintering method were investigated. The heat-treatment conditions, i.e., the calcination temperature (1023 K and 1173 K), sintering temperature and time (1273 K for 1 and 3 h) were carried out. X-ray diffraction (XRD) revealed orthorhombic pnma (62) symmetry without any impurity phase for all samples. X-ray photoelectron spectroscopy confirmed the presence of Fe²⁺–Fe³⁺–Fe⁴⁺ and Mn³⁺–Mn⁴⁺ mixed states, and lanthanum and oxygen vacancies resulting in various magnetic exchange interactions. Furthermore, the magnetisation hysteresis showed enhanced hysteresis loops accompanied by an increase in magnetisation parameters with calcination temperature. The Raman phonon parameters induced a redshift in the phonon modes, alongside an increase in the intensity and compression of the linewidth, reflecting a decrease in lattice distortion, which was confirmed by XRD. The temperature-dependent conductivity showed that the conduction mechanism is dominated by p-type polaron hopping, and the lowest activation energy was approximately 0.237 ± 0.003 eV for the minimum heat-treatment conditions. These results show that varying heat-treatment conditions can significantly affect the structural, magnetic and electrical properties of the La₂FeMnO₆ system.     

Performance Enhancement in N2 Plasma Modified AlGaN/AlN/GaN MOS-HEMT Using HfAlOX Gate Dielectric with Γ-Shaped Gate Engineering

In this paper, we have demonstrated the optimized device performance in the Γ-shaped gate AlGaN/AlN/GaN metal oxide semiconductor high electron mobility transistor (MOS-HEMT) by incorporating aluminum into atomic layer deposited (ALD) HfO₂ and comparing it with the commonly used HfO₂ gate dielectric with the N₂ surface plasma treatment. The inclusion of Al in the HfO₂ increased the crystalline temperature (~1000 °C) of hafnium aluminate (HfAlO_X) and kept the material in the amorphous stage even at very high annealing temperature (>800 °C), which subsequently improved the device performance. The gate leakage current (I_G) was significantly reduced with the increasing post deposition annealing (PDA) temperature from 300 to 600 °C in HfAlO_X-based MOS-HEMT, compared to the HfO₂-based device. In comparison with HfO₂ gate dielectric, the interface state density (D_it) can be reduced significantly using HfAlO_X due to the effective passivation of the dangling bond. The greater band offset of the HfAlO_X than HfO₂ reduces the tunneling current through the gate dielectric at room temperature (RT), which resulted in the lower I_G in Γ-gate HfAlO_X MOS-HEMT. Moreover, I_G was reduced more than one order of magnitude in HfAlO_X MOS-HEMT by the N₂ surface plasma treatment, due to reduction of N₂ vacancies which were created by ICP dry etching. The N₂ plasma treated Γ-shaped gate HfAlO_X-based MOS-HEMT exhibited a decent performance with I_DMAX of 870 mA/mm, G_MMAX of 118 mS/mm, threshold voltage (V_TH) of −3.55 V, higher I_ON/I_OFF ratio of approximately 1.8 × 10⁹, subthreshold slope (SS) of 90 mV/dec, and a high V_BR of 195 V with reduced gate leakage current of 1.3 × 10⁻¹⁰ A/mm.     

Preparation and Characterization of Mg–Al–B Alloy (Mg0.5Al0.5B2) Via High-Temperature Sintering

Boron and its alloys have long been explored as potential fuel and increasingly replace pure aluminum powder in high-energy formulations. The ignition and burning properties of boron can be improved by making boron alloys. In this study, an Mg–Al–B alloy was synthesized from magnesium, aluminum and boron powders in a 1:1:4 molar ratio by preheating to 600 °C for 30 min, followed by high-temperature sintering in a tube furnace. The effects of sintering temperature (700–1000 °C) and holding time (0.5–10 h) on the phase composition of mixed powders were studied. After the samples were cooled to room temperature, they were ground into powder. The phase composition, micromorphology and the bonding forms of elements of the synthesized samples were studied using XRD, SEM and XPS. The results show that each element exists in the form of simple substance in the alloy. The influence of the sintering temperature on the synthesis reaction of Mg_0.5Al_0.5B₂ is very important, but holding time has little effect on it. With the increase of sintering temperature, the content of the Mg_0.5Al_0.5B₂ phase gradually increases, and the phase content of residual metal gradually decreases. The phase and morphology analyses show that the optimum sintering temperature is 1000 °C with a minimum holding time of 0.5 h. It is expected to be used in gunpowder, propellant, explosives and pyrotechnics with improved characteristics.     

Dynamics of O2 consumption in rat pancreatic islets

Summary The O₂ consumption of rat pancreatic islets was determined by monitoring pO₂ in the perifusate from groups of 200–300 islets. Basal respiration was maintained for up to 2 h. The insulin secretagogues, glucose and 4-methyl-2-oxopentanoate, provoked an immediate (<5 s) increase in islet respiration which attained a new steady-state within 10–40 min. The respiratory changes were immediately reversible upon removal of the substrate and were parallelled by changes in insulin release and substrate oxidation. The concentration dependence of glucose-induced respiratory changes was sigmoidal with a threshold at 3 mmol/l. The concentration dependence with 4-methyl-2-oxopentanoate was characterised by a hyperbolic relationship. The weak insulin secretagogues 3-methyl-2-oxobutyrate and d,1-3-methyl-2-oxopentanoate, although stimulating islet respiration were not more effective than 4-methyl-2-oxopentanoate at non-insulinotropic concentrations. Rotenone, antimycin and oligomycin inhibited both basal O₂ consumption and the ability of glucose and 4-methyl-2-oxopentanoate to increase islet respiration. 2,4-Dinitrophenol increased islet O₂ consumption. The omission of Ca²⁺ and Mg²⁺ from the perifusing media, or the addition of the ionophore A23187, had little effect on respiration. The omission of K⁺ inhibited glucose-induced changes but had a lesser effect in the absence of substrate or in the presence of 4-methyl-2-oxopentanoate. The omission of HCO₃ ^- reduced both basal and secretagogue-induced changes in islet respiration. It is concluded that mitochondrial O₂ consumption linked to oxidative phosphorylation is a major component in the respiratory response, and that some energy consuming process in the islets depends on the availability of HCO₃ ^-. Mitochondrial reactions may generate a signal initiating the secretory process.