Nickel Cobalt Research Articles

Regulation of receptor function in NiCo2O4-SnO2 heterojunction for H2S detection at room temperature

In recent years, the World Health Organization has increasingly emphasized air quality in production environments, leading to heightened societal demands for monitoring of pollutant gases at room temperature. Traditional semiconductor gas-sensitive materials, such as tin oxide (SnO2), have their gas-sensing performance largely limited by their receptor functions, resulting in common issues like low response and poor recovery at room temperature. Spinel-type bimetallic oxides, such as nickel cobaltate (NiCo2O4), offer a unique solution due to their rich adsorption sites on the surface, which provide distinctive receptor functions for detecting toxic gases at room temperature. Herein, NiCo2O4 is synthesized via a one-step hydrothermal method, with a porous spherical cluster structure, and combined with SnO2 to form a heterojunction. The NiCo2O4-SnO2 heterojunction film gas sensor exhibits excellent gas-sensing performance for H2S at room temperature, including high response, short response time, good repeatability, and selectivity. Additionally, the unique receptor functions of the NiCo2O4 were analyzed through first-principles calculations, revealing a semiconductor p-n conversion phenomenon in the presence of H2S gas. The composite also demonstrates a conversion from p-n heterojunction to n-n homojunction during the sensing process, enhancing its gas-sensing performance. This work not only addresses the receptor function limitations of traditional gas-sensitive semiconductor but also provides a feasible approach for controlling carrier types in semiconductors.

Catalytically Active Bimetallic Nickel–Cobalt MOF Linked Via Pyridine 2, 6-Dicarboxylate for Electrochemical Water Splitting Applications

Catalytically Active Bimetallic Nickel–Cobalt MOF Linked Via Pyridine 2, 6-Dicarboxylate for Electrochemical Water Splitting Applications

3D-stacked electrospun iron-doped nickel cobalt oxide nanofibers as integrated electrodes for anion exchange membrane water electrolysis

The commercialization of anion-exchange membrane water electrolysis (AEMWE) requires the development of highly active, stable, and cheap anode catalysts for the oxygen evolution reaction (OER). In this study, we proposed electrospun iron-doped NiCo2O4 (NCO) nanofibers on nickel foam (NF) and evaluated the performances of the resulting samples (FeX-NCO/NF; X = iron loading in NCO (0, 5, 10, and 15 at %)) as unitized anodes for the OER. Among the fabricated electrodes, Fe10-NCO/NF exhibited the lowest overpotential of 352 mV at a current density of 50 mA cm−2 in a half-cell test owing to its improved intrinsic activity. In an AEMWE single-cell test, Fe10-NCO/NF as anode showed high current density (932 mA cm-2 at 1.8 V) and long-term stability for 150 h The improved AEMWE performance of Fe10-NCO/NF was attributed to efficient mass transport enabled by superhydrophilic three-dimensional porous structure featuring stacked nanofibers.

Role of synthetic process parameters of nano-sized cobalt/nickel oxide in controlling their structural characteristics and electrochemical energy performance as supercapacitor electrodes

The synthesis of nano-sized bimetallic Cobalt/Nickel oxides (Ni1.5Co1.5O4) with a 1:1 Co/Ni atomic ratio has been achieved using a surfactant-free co-precipitation/hydrothermal process. The growth mechanism of Cobalt/Nickel oxides Ni1.5Co1.5O4 is elucidated by tuning the synthesis process parameters, including co-precipitation pH and hydrothermal time. The formation of Cobalt/Nickel oxides Ni1.5Co1.5O4 oxide began with the nucleation of cobalt nickel hydroxide nanoplates through the co-precipitation process, followed by dissolution-recrystallization, stacked hexagonal nano-flakes, and a flower-like microstructure. The electrochemical performances of the oxides were evaluated, with the largest surface area observed at pH 9 being the main factor for the best super-capacitive performance. As hydrothermal time increased, the structural directing growth forward, resulted in the formation of a nano-flower structure with a larger surface area. The as-prepared cobalt nickel oxide exhibited a maximum specific capacitance value of 525.5 F g-1 at a current density of 1 A g-1 and energy and power densities of 88.2 WhKg-1 and 606 WKg-1, respectively.

One step glow-discharge electrolysis-based preparation of Al doped Ni-Co layered double hydroxide/ graphene oxide as supercapacitor electrode material

Nickel-cobalt layered double hydroxides (LDHs) are promising materials for supercapacitor electrodes; however, they face challenges in terms of cycling stability and rate capability owing to agglomeration and low conductivity. In this study, Ni(III)CoAlx-LDH/GO with an extended layer spacing and excellent electronic conductivity was synthesized by one-step glow discharge electrolysis. A nickel–cobalt alloy was used as the anode, a graphite rod as the cathode, and sodium chloride as the electrolyte. In addition, incorporating an appropriate amount of aluminum chloride into the electrolyte can alter the microstructure of the electrode material, leading to enhanced electrochemical performance. Ni(III)CoAl0.2-LDH/GO, synthesized using 0.2 g AlCl3, demonstrated exceptional electrochemical performance of 1014C g−1 at 2 A/g. At a current density of 5 A/g, the capacitance retention rate was 85.3 % after 10,000 cycles, indicating strong cyclic stability. Moreover, an asymmetric supercapacitor built with Ni(III)CoAl0.2-LDH/GO as the anode and commercial activated carbon as the cathode achieved a specific capacitance of 146.2F/g at a current density of 1 A/g. This device demonstrated outstanding circular stability, retaining 85.07 % of its capacitance after 10,000 cycles. In addition, the device achieves relatively high energy density and power density (energy density of 66.63 Wh kg−1 at a power density of 1022.23 W kg−1). This study introduces a novel synthesis method for the preparation of high-performance electrode materials aimed at advancing energy storage devices.

Mechanisms of Thermal Decomposition in Spent NCM Lithium-Ion Battery Cathode Materials with Carbon Defects and Oxygen Vacancies.

Resource recovery from retired electric vehicle lithium-ion batteries (LIBs) is a key to sustainable supply of technology-critical metals. However, the mainstream pyrometallurgical recycling approach requires high temperature and high energy consumption. Our study proposes a novel mechanochemical processing combined with hydrogen (H2) reduction strategy to accelerate the breakdown of ternary nickel cobalt manganese oxide (NCM) cathode materials at a significantly lower temperature (450 °C). Particle refinement, material amorphization, and internal energy storage are considered critical success factors for the accelerated decomposition of NCM cathode materials. In our proposed approach, NCM cathode materials can develop active sites with carbon defects (Cv) and oxygen vacancies (Ov), which improve the reduction and breakdown of H2. The adsorbed H2 on the surface of NCM decomposes into H* and combines with oxygen to form OH species, which can be facilitated by Ov via the enhanced charge transfer. The introduced Cv can enhance H2 cracking and generate *C-H species to promote the thermal decomposition of NCM. The presence of defects proves to foster the preferential reduction of Mn(IV) by H2, leading to a lower activation energy for the NCM decomposition (from 139 to 110 kJ/mol) with less H2 consumption. Life cycle assessment suggests a reduction of 4.42 kg CO2 eq for the recycling of every 1.0 kg of retired batteries. This study can promote material circularity and minimize the environmental burden of mining technology-critical metals for a low-carbon transition.

Thermal hazard comparison and assessment of Li-ion battery and Na-ion battery

Na-ion batteries are considered a promising next-generation battery alternative to Li-ion batteries, due to the abundant Na resources and low cost. Most efforts focus on developing new materials to enhance energy density and electrochemical performance to enable it comparable to Li-ion batteries, without considering thermal hazard of Na-ion batteries and comparison with Li-ion batteries. To address this issue, our work comprehensively compares commercial prismatic lithium iron phosphate (LFP) battery, lithium nickel cobalt manganese oxide (NCM523) battery and Na-ion battery of the same size from thermal hazard perspective using Accelerating Rate Calorimeter. The thermal hazard of the three cells is then qualitatively assessed from thermal stability, early warning and thermal runaway severity perspectives by integrating eight characteristic parameters. The Na-ion cell displays comparable thermal stability with LFP while LFP exhibits the lowest thermal runaway hazard and severity. However, the Na-ion cell displays the lowest safety venting temperature and the longest time interval between safety venting and thermal runaway, allowing the generated gas to be released as early as possible and detected in a timely manner, providing sufficient time for early warning. Finally, a database of thermal runaway characteristic temperature for Li-ion and Na-ion cells is collected and processed to delineate four thermal hazard levels for quantitative assessment. Overall, LFP cells exhibit the lowest thermal hazard, followed by the Na-ion cells and NCM523 cells. This work clarifies the thermal hazard discrepancy between the Na-ion cell and prevalent Li-ion cells, providing crucial guidance for development and application of Na-ion cell.

Biopolymers as three-dimensional structural binders for nickel-cobalt sulfide supercapacitor electrodes

Ion diffusion and electron transfer are hindered by commonly used hydrophobic binders, which directly affect the electrochemical performance of the electrodes. Hydrophilic binders are selected to efficaciously solve the problem of relatively low actual specific capacitance and rate performance in the field of nickel cobalt sulfide electrode materials. In the paper, RuCoNiS electrodes were prepared using polytetrafluoroethylene (PTFE), carboxymethyl cellulose (CMC), xanthan gum (XG), and chitosan (CS) as binders. The surface wettability, morphological structure, specific surface area, and electrochemical performance of electrodes with different binders were analyzed by XRD, SEM, BET, CV, GCD, and EIS, etc. It's shown that the synthesis of CoNi2S is confirmed by XRD. The XPS results verify the existence of RuO2 and Ni2+/Ni3+ and Co2+/Co3+ redox couples. A cross-linked network structure is formed on the surface of the RuCoNiS by CS. The CS-RuCoNiS electrode has the largest specific surface area and microporosity. Ion migration in the electrolyte is facilitated by the excellent wettability of the CS-RuCoNiS electrode. The CS-RuCoNiS electrode reachs 1193.52 F g-1, which is 1.74 times higher than that of the PTFE-RuCoNiS electrode at 1 A g-1. The CS binder with its three-dimensional structure has the highest ionic conductivity of 2.29 × 10-4 S cm-1, a lower Rct, good cycling stability with a capacity retention of 84.3% after 5000 cycles at 200 mV s-1, and excellent rate performance of 85.6%. It can provide a practical application in supercapacitors.

Effects of molybdenum and cobalt alloying on corrosion resistance of electrochemical coatings based on the Ni–W system

The paper studies coatings of the Ni–W system alloyed with molybdenum and cobalt obtained by electrodeposition. The effect of the concentration of salts of the alloying element in the electrolyte on the chemical composition of the coatings was studied under various synthesis conditions. All the obtained coatings are nanocrystalline or amorphous solid solutions of tungsten, molybdenum or cobalt in nickel with a FCC crystal lattice. Polarization measurements made it possible to establish that the most resistant to corrosion in a 3.5% NaCl solution is a coating containing 35% W and 8% Mo.

Preparation of NiCo hydroxide by chloride corrosion for electrocatalytic upcycling of polyethylene terephthalate plastic waste

Upcycling plastic waste into value-added chemicals is an innovative strategy that addresses environmental concerns and creates economic value. As one of the polyesters that is widely used, polyethylene terephthalate (PET) plastic waste is employed as the model substrate. Here we report a chloride corrosion method to synthesize bimetallic hydroxide catalysts on nickel foam. By using a nickel–cobalt hydroxide catalyst (NiCo-OH/NF), we demonstrate an electrocatalytic oxidation strategy to transform real-world polyethylene terephthalate (PET) water bottle into potassium formate and terephthalic acid (TPA) with high Faraday efficiency of 92.1 % at 1.40 V vs. RHE. The in situ spectroscopy and theoretical calculations provide insights into the catalytic mechanism especially active sites, pivotal intermediates, and favorable pathways. This work highlights the significant potential of electrochemical conversion as a means of achieving PET upcycling.

The synergistic effects on the magnetic CoNi and Fe3O4 nanoparticles co-embedded porous carbon toward enhanced microwave absorbing performance

Abstract Lightweight and environmentally friendly three-dimensional biomass-derived porous carbon (3D BPC) holds great potential as a highly effective material for microwave absorption (MA) applications. However, the high complex permittivity and lack of magnetic loss in a single 3D BPC lead to impedance mismatching and a limited absorption bandwidth. Developing 3D BPC–based absorbers with multiple loss mechanisms and excellent impedance matching remains a notable yet challenging task. In this study, inspired by a synergistic composition and microstructure design, 3D BPC co-embedded with magnetic cobalt–nickel (CoNi) and iron(III) oxide (Fe3O4) nanoparticles (3D BPC@CoNi@Fe3O4) was developed. 3D BPC@CoNi@Fe3O4 exhibited consistently low complex permittivity, primarily due to the suppression of conductive loss, whereas the introduction of magnetic phases (CoNi and Fe3O4) enhanced the magnetic loss. Optimised impedance matching, achieved through the synergistic regulation of the electromagnetic parameters, emerged as the key mechanism for improving the MA properties. The as-synthesised 3D BPC@CoNi@Fe3O4 composite, with only 20 wt.% loading demonstrated a wide effective absorption bandwidth (reflection loss [RL] < −10 dB) of 6.08 GHz and an impressive minimum RL value of −40.08 dB. These findings offer valuable insights into the development of high-performance 3D BPC–based microwave absorbers through composition and microstructure optimisation.

Investigation of the corrosion behavior of 29NC alloy in LiCl-KCl melt at 500 oC depending on the content of Li2O and LiOH from 0 to 2 mol. %

Molten chloride salt electrolytes are promising for use as a working medium for the implementation of high-temperature technologies. Alkali metal chlorides are an aggressive environment in relation to structural materials. One of the possible methods of reducing the corrosion damage of a structural material is the method of oxygen passivation of the surface of a metal or alloy by introducing a certain amount of oxygen-containing additives into the melt. The article considers the effect of oxygen-containing impurities (lithium oxide and lithium hydroxide) on the corrosive behavior of a metal material — an alloy of the composition iron–cobalt–nickel. To assess the corrosion resistance of materials, gravimetric analysis, micro-X-ray spectral analysis (XRSA) of the surface and cross-section sections, and X-ray phase analysis (XRF) of the sample surface were used. The dependences of the corrosion rate of the material on the concentration of oxygen-containing additives Li2O and LiOH are presented. Based on the data set of gravimetric, MRSA and XRF data, it was found that 29NC alloy samples in the LiCl–KCl–nLi2O salt melt are not susceptible to corrosion, but in the LiCl–KCl–nLiOH melt, the speed of the 29NC alloy increases significantly due to the interaction of the LiOH additive with the most electronegative component of the alloy — iron.

Substrate and Step Rate Dependence Electrodeposition of Nickel–Cobalt–Molybdenum–Phosphorous Alloy for Efficient Hydrogen Evolution Reaction

Understanding the hydrogen economy involves recognizing the crucial role of water‐splitting in producing green, clean, and carbon‐free hydrogen. In that respect, the role of catalyst is very important as it enhances the reaction rate and efficiency, making hydrogen production more viable and sustainable. Herein, nickel–cobalt–molybdenum–phosphorous (Ni–Co–Mo–P) alloy has shown efficient catalysis properties for hydrogen evolution reaction (HER) in an alkaline medium. The quaternary alloys are directly grown on different substrates like nickel sheet, copper sheet, and stainless‐steel sheet by employing a simple pulse electrodeposition method. The method is conducted with a pulse interval time of 15 s at various pulse rates while maintaining the pH of 4 at room temperature. The alloy deposition is performed at a potential range from −1.5 V to −0.15 V (vs Ag/AgCl). The electrodeposition of the alloy in different substrates is first established with X‐Ray diffraction (XRD), field‐emission scanning electron microscopy (FESEM), and Raman spectroscopy. The deposited quaternary alloy exhibits the lowest overpotential of −163 mV at 10 mA cm−2 for copper substrate with a Tafel slope of 154 mV dec−1. The microcrystalline structure or amorphous nature and the rough grain surface of Ni‐Co‐Mo‐P alloys have characterized by XRD and scanning electron microscopy micrograph, respectively.

Rapid and controllable microwave synthesis of nickel cobalt sulfide electrodes for high-performance asymmetric supercapacitors

The efficient and controllable synthesis method of high-performance energy storage electrode materials is crucial for advancing the development of energy storage technologies. Herein, by leveraging microwave heating technology in the sulfidation of nickel cobalt MOF, we effectively enhanced the efficiency of the synthesis process. Notably, sulfidation time emerged as a pivotal factor in tuning the crystalline phase structure and conductive properties of the material, leading to the successful development of NCS2 electrode material with a unique structure through optimized sulfidation conditions. Electrochemical performance tests of the NCS2 material revealed exceptional results; it exhibited a specific capacity of 1311 Fg[Formula: see text] at a current density of 1 Ag[Formula: see text] and retained 73.4% of its initial capacity when the current density increased to 10 Ag[Formula: see text], demonstrating outstanding rate performance. The composite NCS2//AC supercapacitor exhibits an energy density of 24.2 Whkg[Formula: see text] at power density of 800 Wkg[Formula: see text], even though after 1000 consecutive charge-discharge cycles, the capacity retention rate remained high at 77.1%, validating the exceptional stability and reliability of the NCS2 material during cycling. This work employs microwave sulfidation for the rapid and controlled synthesis of nickel cobalt sulfides, providing a green and efficient synthetic strategy for metal sulfide active materials.

Predictive pretrained transformer (PPT) for real-time battery health diagnostics

Modeling and forecasting the evolution of battery systems involve complex interactions across physical, chemical, and electrochemical processes, influenced by diverse usage demands and dynamic operational patterns. In this study, we developed a predictive pre-trained Transformer (PPT) model equipped with 1,871,114 parameters that enhance identification of both short-term and long-term patterns in time-series data. This is achieved through the integration of convolutional layers and probabilistic sparse self-attention mechanisms, which collectively enhance prediction accuracy and efficiency in diagnosing battery health. Moreover, the customized hybrid-model fusion supports parallel computing and employs transfer learning, reducing computational costs while enhancing scalability and adaptability. Consequently, this allows for precise real-time health estimations across various battery cycles. We validated this method using a public dataset of 203 commercial lithium iron phosphate (LFP)/graphite batteries charged at rates ranging from 1C to 8C. By using only partial charge data—from an 80 % state of charge to the maximum charging voltage (3.6 V for LFP batteries, 4.2 V for ternary batteries)—and avoiding complex feature engineering, error metrics were achieved below 0.3 % for root mean square error (RMSE), weighted mean absolute percentage error (WMAPE), and mean absolute error (MAE), with an R2 of 98.9 %. The generalization capabilities were further demonstrated across 36 different testing protocols, encompassing 23,480 cycles throughout the entire life cycle, with a total inference time of 9.88 s during the testing phases. Further experiments on 30 nickel cobalt aluminum (NCA) batteries and 36 nickel cobalt manganese (NCM) batteries, across different battery types and operational scenarios, resulted in RMSE, WMAPE, and MAE all below 0.9 %, with R2 values of 94.1 % and 94.4 %, respectively. These findings highlight the potential of our customized deep transfer neural networks to enhance diagnostic accuracy, accelerate training, and improve generalization in real-time applications.

Nanostructured Ni–Co catalysts: Effect of impregnation sequence and complexing agent

This paper explores the synthesis by the impregnation method using citric acid and the characterization of bimetallic Nickel–Cobalt (Ni–Co) catalysts, focusing on their application in ethanol steam reforming leveraging the demonstrated improved stability and catalytic activity observed in previous works when Co is introduced into Ni catalysts. The study aims to investigate the effects of the sequence of incorporation of Ni and Co in the catalyst support in order to optimize the catalytic performance. The results indicate that the optimal sequence for introducing Co and Ni significantly enhanced the catalytic performance in ethanol steam reforming and it was associated to a higher Ce+3/Ce+4 ratio and a stronger active site-support interactions that modified the CNT growth mechanism, preventing increasing pressure drop through the reactors. The best catalytic performance corresponded to the system, Co/Ni/MgAl2O4–CeO2, in which Co was incorporated after Ni.

Enhanced energy storage efficiency of an innovative three-dimensional nickel cobalt metal organic framework nanocubes with molybdenum disulphide electrode material as a battery-like supercapacitor

Recently, metal-organic frameworks (MOFs) with transition metal sulfides have gained much attention as electrode materials for supercapacitors (SCs). In this work, 3D-NCMOF@MS NCs, incorporating two-dimensional molybdenum disulphide (2D-MS) nanosheets and three-dimensional nickel cobalt-MOF nanocubes (3D-NCMOF NCs) are synthesized by a solvothermal and precipitation process. Owing to their enhanced electrical conductivity and huge surface area, the 3D-NCMOF@MS NCs produce superior electrochemical responses in SCs compared to 2D-MS and 3D-NCMOF NCs. The results demonstrate that the synergistic 3D-NCMOF@MS NCs increased specific capacitance up to 1048 Fg−1 at 1 Ag−1, revealing outstanding cycle stability with a capacitance retention of 99.06 %. Besides, the exposed high-power density of 3D-NCMOF@MS NCs reached 400 W kg−1 as well as an outstanding maximum energy density of 188.64 Wh kg−1. Such synergistic effects of the multivalent states of Ni, Co, and Mo promote electrochemical characteristics, implying that the 3D-NCMOF@MS NCs could potentially be used in energy storage systems, boosting electrochemical performance.

Cr-doped tri-metallic nano prism catalyst for efficient alkaline and seawater splitting

Electrochemical water splitting is one of the most promising methods for sustainable production of green hydrogen. The oxygen evolution reaction (OER) is a crucial step in the process of water splitting. However, it exhibits sluggish kinetics and requires a significant overpotential for functioning at reasonable reactionrates. The efficiency of the reaction can be enhanced by reducing the overpotential, lowering the energy barrier, and using an effective electrocatalyst. Transition metal-basedcatalysts are well studied for this purpose. Specially, nickel–cobalt (Ni-Co) based catalysts have been regarded as the best OER electrocatalysts. Therefore, several studies have been carried out to enhance the electrocatalytic efficiency of Ni-Co catalysts. While mixing other transition metals with Ni-Co is a straightforward and reliable method to improve the OER activity of Ni-Co catalysts, there is still a need for a thorough examination of the design of Ni-Co catalysts with various additional elements. Seawater electrolysis, which utilizes abundant water resources that constitute over 97% of the world’s water, is highly appealing for sustainable energy production. To achieve commercial feasibility, scientists are striving to solve challenges, such as corrosion resistance, highoverpotential, and the need for efficient and durable electrocatalysts.In this study, we fabricated a transition metal-based trimetallic catalyst (CNF), consisting of cobalt (Co), nickel (Ni), and iron (Fe). Furthermore, CNF was doped with chromium (Cr-doped CNF) and tested for the OER in alkaline freshwater and alkaline seawater. Our Cr-doped trimetallic CNF catalyst demonstrates exceptional performance in both seawater and freshwater, with overpotential of 320 mV and 280 mV at 10 mA cm−2 current density, making it a promising candidate for large-scale, sustainable hydrogen production.

Prediction of metal recovery potential of end-of-life NEV batteries in China based on GRA-BiLSTM

As Chinese new energy vehicle (NEV) sales continue to grow, end-of-life batteries have great potential for recycling in the future. In this study, a combined model based on Gray Relation Analysis and Bi-directional Long Short-Term Memory (GRA-BiLSTM) is proposed for predicting NEV sales, and the NEV battery life is modeled using the Weibull distribution. Then, the amount of end-of-life batteries, secondary utilization and metal recycling are calculated. The impact of end-of-life battery recycling on the supply and demand of key metals is studied. The results show that in 2040, the secondary utilization of end-of-life batteries in the Standard Growth Rate-Lithium Iron Phosphate Battery Dominated-High Secondary Utilization rate scenario (SGR-LFPH) is 391.76 GWh. The recycling volumes of lithium, nickel and cobalt are 45,900 tons, 92,900 tons and 22,100 tons, respectively. In the Standard Growth Rate-lithium nickel cobalt manganese oxide Battery Dominated-Low Secondary Utilization rate scenario (SGR-NCML), the recycling of lithium, nickel and cobalt is even greater, at 62,600 tons, 372,200 tons and 71,700 tons, respectively. End-of-life batteries recycling can reduce the demand for metals. However, as NEV sales continue to grow, the gap between metal supply and demand remains significant. The findings urge the Chinese government develop appropriate battery management strategies to increase the recycling rate of end-of-life batteries; and to encourage enterprises to research new types of batteries to resolve the conflict between supply and demand for metals.

Comparison of patch testing Brazilian (Green) propolis and Chinese (poplar-type) propolis: Clinical epidemiological study using data from the Information Network of Departments of Dermatology (IVDK).

Propolis types differ regarding their chemical composition. To compare patch test results based on Brazilian (Green) propolis with data based on Chinese (poplar-type) propolis, and to evaluate the specifications of raw materials used for the PT preparations. In the Information Network of Departments of Dermatology (IVDK), 1290 consecutive patients were patch tested with Brazilian (Green) propolis (NH400, SmartPractice Europe). Patch test reactivity was compared with results obtained with Chinese (poplar-type) propolis (NA71, SmartPractice Europe) by calculating frequencies and corresponding 95% confidence intervals. Data on the specifications of raw materials used for NH400 and NA71 were obtained from the manufacturer. Positive reactions to NH400 were found in 303 (23.5%) patients with unclear clinical relevance in most cases. Patients reacting to NH400 were less often sensitised to fragrances and colophony, but more often to nickel sulphate and cobalt chloride than patients reacting to NA71. The NH400 batch used contained high levels of aerobic bacteria, and was not purified by ethanolic extraction. Pattern of concomitant reactivity along with raw material properties suggests that the high frequency of positive reactions to NH400 may primarily result from bacterial contamination or impurities in the PT preparation rather than from propolis constituents.