Cocktail Effect Research Articles

Cocktail effect on superconductivity in hexagonal high-entropy alloys

Cocktail effect on superconductivity in hexagonal high-entropy alloys

Research Progress of High-entropy Oxides for Electrocatalytic Oxygen Evolution Reaction.

High-entropy oxides (HEOs), similar to high-entropy materials (HEMs), have "four-core effects", i. e., high-entropy effect, delayed diffusion effect, lattice distortion effect and cocktail effect, which have attracted more and more attention in the scientific field of renewable energy technology due to their unique structural characteristics, variable chemical composition and corresponding functional properties. HEOs have become potential candidates for electrocatalytic oxygen evolution reaction (OER), which is a key half reaction for electrolytic CO2, nitrogen reduction, and water electrolysis. However, the precise synthesis of HEOs with a wide range of components and structures is challenging, not to mention their active and stable operation for OER. In this paper, we review the recent advancements in the electrocatalytic oxygen evolution facilitated by HEOs in water electrolysis. We analyze these developments from the perspectives of activity and stability in acid and alkaline conditions, respectively. Furthermore, we summarize the design from the aspect of element composition, structure, morphology, and catalyst-support interactions, along with related reaction mechanism of HEOs. Additionally, we discuss the current challenges faced by HEOs in the field of OER and suggest potential directions for the future development of HEOs beyond water electrolysis application.

Layered high-entropy sulfides: boosting electrocatalytic performance for hydrogen evolution reaction by cocktail effects

Abstract This study explores high-entropy sulfides (HESs) as potential electrocatalysts for the hydrogen evolution reaction (HER). Novel Pa-3 and Pnma structured HESs containing Fe, Mn, Ni, Co and Mo, were synthesized via a facile mechanochemical method. Structural and chemical properties were extensively characterized using x-ray diffraction, transmission electron microscopy, energy-dispersive x-ray spectroscopy, and x-ray photoelectron spectroscopy. The electrocatalytic performance of four as-prepared HESs in alkaline electrolyte for HER reveals the remarkable outperformance compared to medium-entropy and conventional sulfides. Particularly, (Fe0.2Mn0.2Ni0.2Co0.2Mo0.2)S2 demonstrated outstanding activities, with minimal overpotentials (187 mV at 10 mA cm–2) and outstanding durability under harsh alkaline conditions (a mere polarization increase ΔE = 17 mV after 14 h via chronopotentiometry). The remarkable catalytic activities can be attributed to synergistic effects resulting from the cocktail effects within the high-entropy disulfide. The introduction of Mo contributes to the formation of a layered structure, which leads to an increased surface area and thus to a superior HER performance compared to other HES and conventional sulfides. This work demonstrates the promising potential of HES and underscores that further development for catalytic applications paves the way for innovative routes to new and more efficient active materials for HER catalysis.

How Do the Four Core Factors of High Entropy Affect the Electrochemical Properties of Energy-Storage Materials?

High-entropy materials (HEMs) are extremely popular for electrochemical energy storage nowadays. However, the detailed effects of four core factors of high entropy on the electrochemical properties of HEMs are still unclear. Here, a high-entropy La1/4Ce1/4Pr1/4Nd1/4Nb3O9 (HE-LaNb3O9) oxide is prepared through multiple rare-metal-ion substitution in LaNb3O9, and uses HE-LaNb3O9 as a model material to systematically study the effects of the four core factors of high entropy on electrochemical energy-storage materials. The high-entropy effect lowers the calcination temperature for obtaining pure HE-LaNb3O9. The lattice distortion in HE-LaNb3O9 leads to its decreased unit-cell-volume variations, which benefits its cyclability. Based on the restrained diffusion arising from the lattice distortion, the Li+ diffusivity of HE-LaNb3O9 at room temperature (25°C) is limited, which causes its lowered rate capability. However, the Li+ diffusivity of HE-LaNb3O9 at high temperature (60°C) becomes faster than that of LaNb3O9, which is attributed to the alleviated lattice distortion at the high-temperature, resulting in higher rate capability. The cocktail effects in HE-LaNb3O9 enable its larger electronic conductivity, better electrochemical activity, more intensive Nb5+ ↔ Nb3+ redox reaction, and larger reversible capacity. The insight gained here can provide a guide for the rational design of new HEMs with good energy-storage properties.

Desert dust improves the photophysiology of heat-stressed corals beyond iron

Desert dust is an important source of essential metals for marine primary productivity, especially in oligotrophic systems surrounded by deserts, such as the Red Sea. However, there are very few studies on the effects of dust on reef-building corals and none on the response of corals to heat stress. We therefore supplied dust to two coral species (Stylophora pistillata and Turbinaria reniformis) kept under control conditions (26 °C) or heat stress (32 °C). Since dust releases large amounts of iron (Fe) in seawater, among other metals, the direct effect of different forms of Fe enrichment on coral photosynthesis was also tested. First, our results show that the desert dust altered the coral metallome by increasing the content of metals that are important for coral physiology (e.g. lithium (up to 5-fold), manganese (up to 4-fold in S. pistillata), iron (up to 3-fold in S. pistillata), magnesium (up to 1.3-fold), molybdenum (up to 1.5-fold in S. pistillata)). Overall, metal enrichment improved the photosynthetic performance of corals, especially under thermal stress (e.g. Pgross (up to 2-fold), Pnet (up to 10-fold), chlorophyll (up to 1.5-fold), symbionts (up to 1.6-fold)). However, Fe exposure (ferric chloride or ferric citrate) did not directly improve photosynthesis, suggesting that it is the combination of metals released by the dust, the so-called “metal cocktail effect”, that has a positive impact on coral photophysiology. Dust also led to a decrease in Ni uptake (up to 1.4-fold in the symbionts), likely related to the nitrogen metabolism. Finally, we found that the isotopic signature of metals such as iron, zinc and copper is a good indicator of heat stress and dust exposure in corals. In conclusion, desert dust can increase coral resistance to bleaching by supplying corals with essential metals.

3d-orbital overlap modulated d-band center of high-entropy oxyhydroxide for efficient oxygen evolution reaction

As an emerging high entropy material, recently, a few studies have shown that high-entropy oxyhydroxides possess higher catalytic performance due to their multiple active sites and more excellent stability for the oxygen evolution reaction (OER). Although the high-entropy effect, cocktail effects etc. have been proposed for the catalytic mechanism, the electronic interaction mechanisms among multiple metal elements still require further in-depth investigation. Herein, a high-entropy oxyhydroxide (FeCoNiZnOOH) was synthesized. Experimental results and density functional theory (DFT) calculation demonstrate that there are electronic interactions and strong 3d orbital overlap among the four metals. This overlapping effect of the Fe/Co/Ni/Zn 3d orbitals shifts the d-band center downward, thereby reducing the adsorption barrier for oxygen intermediates during the reaction and accelerating the reaction kinetics. The FeCoNiZnOOH shows excellent electrocatalytic performance with a low overpotential of 206 mV at a current density of 20 mA cm−2, and a Tafel slope of 54.3 mV dec–1, which is better than the synthesized monometallic oxyhydroxide, bimetallic oxyhydroxide, medium entropy oxyhydroxides and commercial Ir/C catalyst. This work offers new insight into designing efficient OER catalysts through regulate the electronic structure and optimize electrochemical performance for high-entropy electrocatalysts.

Exposure to food additive mixtures and type 2 diabetes risk in the NutriNet-Santé cohort

Abstract Background So far, the safety evaluation of food additives has been performed substance by substance, while in real life, millions of individuals are exposed to mixtures of food additives daily. According to preliminary experimental data, some of these chemicals, alone and/or in synergy are suspected to impact metabolic health. The objective of this study was to investigate for the first time the associations between exposure to mixtures of food additives and type 2 diabetes (T2D) risk in a large prospective cohort of French adults. Methods Participants (n = 108,783, 79.2% women, mean age=42.4 years, SD = 14.6) from the NutriNet-Santé cohort (2009-2024) completed repeated 24h-dietary records, detailing industrial product brands. Additive exposure was assessed using composition databases and laboratory assays. Five mixtures of additives were identified through non-negative matrix factorisation (NMF). Associations between these mixtures and the risk of T2D were characterised using multivariable proportional hazards Cox models adjusted for known risk factors. Findings 1115 participants were identified with T2D during follow-up. Two additive mixtures were associated with increased T2D risk. The first mixture included higher exposure to modified starches E14xx, pectins E440, guar gum E412, carrageenan E407, and polyphosphates E452 (HRper 1SD increment=1.11 [1.05-1.18]), p < 0.0001). The second mixture comprised citric acid E330, sodium citrates E331, phosphoric acid E338, sulphite ammonia caramel E150d, acesulfame-K E950, aspartame E951, sucralose E955 and arabic gum E414 (HR1SD=1.13 [1.08-1.18]), p < 0.0001). Interpretation This large prospective cohort study revealed direct associations between T2D risk and exposure to two food additive mixtures. Molecular epidemiology and experimental studies will be necessary to depict underlying mechanisms and potential cocktail effects. Key messages • Consumed together, widely used food additives may contribute to T2D aetiology, shedding light on the detrimental impact of highly processed foods on metabolic health. • This study highlights positives associations between T2D risk and exposure to two food additive mixtures.

Toxicity of pesticide cocktails in amphibian larvae: understanding the impact of agricultural activity on aquatic ecosystems in the Salado River basin, Argentina

Aquatic communities are increasingly exposed to complex mixtures of contaminants, mainly pesticides due to the impact of agricultural activity. The aim of this study was to evaluate the toxicity of an eight-pesticide cocktail on larvae of the South American common toad, Rinella arenarum. The cocktail represents a realistic mixture of insecticides (cypermethrin, chlorpyrifos and lambda-cyhalothrin), herbicides (glyphosate, glufosinate ammonium, prometryn and metolachlor), and a fungicide (pyraclostrobin) previously found in aquatic organisms (Prochilodus lineatus) from the Salado River Basin, an area with strong agricultural pressure. Computational simulations through the Density Functional Tight-Binding method indicated a strong spontaneous trend toward the formation of the cocktail, suggesting that it may act as a novel xenobiotic entity in the environment. The cocktail effects were evaluated in early-developing and premetamorphic larvae, at feasible concentrations found in real scenarios. The mixture led to high mortality and teratogenicity in early-developing larvae. Premetamorphic larvae showed endocrine disruption, oxidative stress, and impairments in detoxification and hepatic functioning. Neurotoxicity, genotoxicity, cardiotoxicity and high mortality under stress conditions were also observed in exposed larvae. This novel evaluation highlights the ecotoxicological risk for aquatic organisms exposed to complex mixtures and underscores the need to consider cocktail effects in studies regarding ecosystems health.

Deciphering the Underlying Mechanism of the Fourth Entity in Medium-Entropy NiCoFeMP toward Boosting Oxygen Evolution Electrocatalysis.

High-/medium-entropy materials have been explored as promising electrocatalysts for water splitting due to their unique physical and chemical properties. Unfortunately, state-of-the-art materials face the dilemma of explaining the enhancement mechanism, which is now limited to theoretical models or an unclear cocktail effect. Herein, a medium-entropy NiCoFeMnP with an advanced hierarchical particle-nanosheet-tumbleweed nanostructure has been synthesized via simple precursor preparation and subsequent phosphorization. Evaluated as the electrocatalyst for oxygen evolution reaction (OER), the medium-entropy NiCoFeMnP displays a lower overpotential of 272 mV at a current density of 10 mA cm-2, and more favorable kinetics than the binary NiFeP, ternary NiCoFeP, quaternary NiCoFeCuP and NiCoFeCrP counterparts, and other reported high-/medium-entropy electrocatalysts. Careful experimental analyses reveal that the incorporation of Mn can significantly regulate the electronic structure of Ni, Co, and Fe sites. More importantly, the Mn introduction and entropy stabilization effect in the reconstructed metal (oxy)hydroxide simultaneously promote the lattice oxygen mechanism, improving the activity. This work sheds new light on the design of high-/medium-entropy materials from an in-depth understanding of the underlying mechanism for improving energy conversion efficiency.

Chip−like high−entropy oxide catalysts enhance fast sulfur evolution reaction for long−life lithium−sulfur batteries

Many catalysts have shown excellent activity for the sulfur reduction reaction (SRR), but sluggish electrochemistry kinetics have hindered the development of lithium–sulfur batteries. It has been found that the activity of catalysts for the sulfur evolution reaction (SER) plays a crucial role in determining the overall reaction kinetics. To address this issue, the rational design of catalysts is crucial. Here, we proposed a popular rule to accelerate SER by using chip–like high–entropy perovskite oxide La0.7Sr0.3(Fe0.2Co0.2Ni0.2Zn0.2Mn0.2)O3-δ (LMO–HEO) as advanced electrocatalysts. The strong interaction between the adjacent metal atoms in different metals of LMO–HEO electrocatalysts could lead to a "cocktail effect", which not only greatly improved the catalytic capacity toward sulfur species, but also accelerated the oxidation reaction kinetics of Li2S. As a result, the S/La0.7Sr0.3(Fe0.2Co0.2Ni0.2Zn0.2Mn0.2)O3-δ cathodes delivered excellent cyclic stability with a capacity decay of only 0.025% after 1200 cycles at 2 C. This work has provided a rational design idea for new multifunctional electrocatalysts with high catalytic capacity.

PdMoPtCoNi High Entropy Nanoalloy with d Electron Self-Complementation-Induced Multisite Synergistic Effect for Efficient Nanozyme Catalysis.

Engineering multimetallic nanocatalysts with the entropy-mediated strategy to reduce reaction activation energy is regarded as an innovative and effective approach to facilitate efficient heterogeneous catalysis. Accordingly, conformational entropy-driven high-entropy alloys (HEAs) are emerging as a promising candidate to settle the catalytic efficiency limitations of nanozymes, attributed to their versatile active site compositions and synergistic effects. As proof of the high-entropy nanozymes (HEzymes) concept, elaborate PdMoPtCoNi HEA nanowires (NWs) with abundant active sites and tuned electronic structures, exhibiting peroxidase-mimicking activity comparable to that of natural horseradish peroxidase are reported. Density functional theory calculations demonstrate that the enhanced electron abundance of HEA NWs near the Fermi level (EF) is facilitated via the self-complementation effect among the diverse transition metal sites, thereby boosting the electron transfer efficiency at the catalytic interface through the cocktail effect. Subsequently, the HEzymes are integrated with a portable electronic device that utilizes Internet of Things-driven signal conversion and wireless transmission functions for point-of-care diagnosis to validate their applicability in digital biosensing of urinary biomarkers. The proposed HEzymes underscore significant potential in enhancing nanozymes catalysis through tunable electronic structures and synergistic effects, paving the way for reformative advancements in nano-bio analysis.

High-Entropy Materials for Application: Electricity, Magnetism, and Optics.

High-entropy materials (HEMs) have recently emerged as a prominent research focus in materials science, gaining considerable attention because of their complex composition and exceptional properties. These materials typically comprise five or more elements mixed approximately in equal atomic ratios. The resultant high-entropy effects, lattice distortions, slow diffusion, and cocktail effects contribute to their unique physical, chemical, and optical properties. This study reviews the electrical, magnetic, and optical properties of HEMs and explores their potential applications. Additionally, it discusses the theoretical calculation methods and preparation techniques for HEMs, thereby offering insights and prospects for their future development.

Ferromagnetism in High Entropy Cantor alloy triggered and tuned by severe plastic deformation

The process of severe plastic deformation (SPD) introduces unique conditions to materials, leading to the emergence of novel properties. This research specifically investigates the observation of deformation-induced ferromagnetism resulting from SPD processing. High-pressure torsion (HPT) is utilized to process both single-phase and nanocomposite high entropy alloys (HEAs). Vibrating sample magnetometry (VSM) confirms that HPT processing triggers the development of ferromagnetic properties. The distribution and alignment of magnetic domains post-SPD treatment are further examined using differential phase contrast scanning transmission electron microscopy (DPC STEM). Atom probe tomography (APT) analysis suggests that this phenomenon stems from the localized enrichment of ferromagnetic elements, particularly Ni, induced by deformation. This observation underscores the ‘cocktail effect’ in HEAs, whereby interactions between different elements has led to this unique magnetic behavior. Additionally, deliberate mechanical mixing of the CoCrFeMnNi alloy with a HfNbTaTiZr HEA, comprising non-ferromagnetic constituents, introduces a large rotational strain that alters the ferromagnetic properties. This mixing facilitates a transition from a random orientation of magnetic domains, as seen in the HPT-processed single CoCrFeMnNi alloy, to a coordinated alignment within the nanocomposite HEA.

Exploring Dry Reforming of CH4 to Syngas Using High Entropy Materials: A Novel Emerging Approach

The high global warming potential of natural gas methane necessitates its conversion to valuable products, typically achieved through syngas production, with dry reforming of methane and integrating carbon capture followed by dry reforming of methane standing out among different technologies for methane valorization. However, persistent challenges such as the reverse water gas shift reaction, coke formation, and sintering associated with methane dry reforming have redirected scientific focus toward multi‐metallic catalysts with supports or promoters. High entropy materials have gained attention as promising catalysts because their flexible composition allows fine‐tuning of lattice oxygen reactivity and catalytic activity. Entropy plays a key role in catalysis, and recent research focuses on the enthalpy‐entropy relationship that influences reaction pathways. Alongside entropy, core effects like lattice distortion, sluggish diffusion, and cocktail effects improve catalytic performance by synergistic effects, prevent carbon buildup, and maintain stability at high temperatures, enabling efficient methane conversion. These advancements in high entropy materials drive interest in using entropy‐stabilized systems to address the challenges of methane dry reforming. This review summarizes the recent progress in dry reforming of methane and integrating carbon capture followed by dry reforming of methane using high entropy materials.

Cocktail effects of clothianidin and imidacloprid in zebrafish embryonic development, with high and low concentrations of mixtures.

There is growing concern that sprayed neonicotinoid pesticides (neonics) persist in mixed forms in the environmental soil and water systems, and these concerns stem from reports of increase in both the detection frequency and concentration of these pollutants. To confirm the toxic effects of neonics, we conducted toxicity tests on two neonics, clothianidin (CLO) and imidacloprid (IMD), in embryos of zebrafish. Toxicity tests were performed with two different types of mixtures: potential mixture compounds and realistic mixture compounds. Potential mixtures of CLO and IMD exhibited synergistic effects, in a dose-dependent manner, in zebrafish embryonic toxicity. Realistic mixture toxicity tests that are reflecting the toxic effects of mixture in the aquatic environment were conducted with zebrafish embryos. The toxicity of the CLO and IMD mixture at environmentally-relevant concentrations was confirmed by the alteration of the transcriptional levels of target genes, such as cell damage linked to oxidative stress response and thyroid hormone synthesis related to zebrafish embryonic development. Consequently, the findings of this study can be considered a strategy for examining mixture toxicity in the range of detected environmental concentrations. In particular, our results will be useful in explaining the mode of toxic action of chemical mixtures following short-term exposure. Finally, the toxicity information of CLO and IMD mixtures will be applied for the agricultural environment, as a part of chemical regulation guideline for the use and production of pesticides.

Simultaneous Tailoring of Chemical Composition and Morphology Configuration in Metal Hexacyanoferrate for Ultrafast and Durable Sodium-Ion Storage.

Metal hexacyanoferrates (MHCFs) with adjustable composition and open framework structures have been considered as intriguing cathode materials for sodium-ion batteries (SIBs). Exploiting MHCFs with ultrafast and durable sodium storage capability as well as comparable capacity is always a goal that many investigators pursue, but remains challenging. Herein, simultaneous tailoring of chemical composition and morphology configuration is carried out to design a hollow monoclinic high-entropy MHCF (HMHE-HCF) assembled by nanocubes for the first time to realize the objective. The "cocktail effect" of high-entropy construction, rich sodium content of monoclinic phase, and unique hollow structure endow HMHE-HCF cathode with fast reaction kinetics and energetically stable performance during continuous charging/discharging processes. As a result, the HMHE-HCF cathode demonstrates superior rate performance up to an ultra-high rate of 100 C (71.1 % retention to 0.1 C), and remarkable cycling stability with a capacity retention of 77.8 % over 25,000 cycles at 100 C, outperforming most reported sodium-ion cathodes. Further, the HMHE-HCF//hard carbon full-cell delivers capacities of 99.0 and 82.3 mAh g-1 at 0.1 C and 10 C, respectively, and retains 98.1 % of the initial capacity after 1,600 cycles at 5 C, demonstrating its potential application for sodium-ion storage.

Simultaneous Tailoring of Chemical Composition and Morphology Configuration in Metal Hexacyanoferrate for Ultrafast and Durable Sodium‐ion Storage

Metal hexacyanoferrates (MHCFs) with adjustable composition and open framework structures have been considered as intriguing cathode materials for sodium‐ion batteries (SIBs). Exploiting MHCFs with ultrafast and durable sodium storage capability as well as comparable capacity is always a goal that many investigators pursue, but remains challenging. Herein, simultaneous tailoring of chemical composition and morphology configuration is carried out to design a hollow monoclinic high‐entropy MHCF (HMHE‐HCF) assembled by nanocubes for the first time to realize the objective. The “cocktail effect” of high‐entropy construction, rich sodium content of monoclinic phase, and unique hollow structure endow HMHE‐HCF cathode with fast reaction kinetics and energetically stable performance during continuous charging/discharging processes. As a result, the HMHE‐HCF cathode demonstrates superior rate performance up to an ultra‐high rate of 100 C (71.1% retention to 0.1 C), and remarkable cycling stability with a capacity retention of 77.8% over 25,000 cycles at 100 C, outperforming most reported sodium‐ion cathodes. Further, the HMHE‐HCF//hard carbon full‐cell delivers capacities of 99.0 and 82.3 mAh g–1 at 0.1 C and 10 C, respectively, and retains 98.1% of the initial capacity after 1,600 cycles at 5C, demonstrating its potential application for sodium‐ion storage.

Comparison of pesticide contamination between captive-reared and wild grey partridges: insights into environmental exposure disparities.

Pesticide contamination is often cited as a key factor in the global decline of farmland birds. However, the majority of studies on pesticide exposure in non-target fauna are not representative of what happens in nature because they are limited to artificial conditions. The aim of this study was to define and compare, for the first time, pesticide contamination in grey partridges (Perdix perdix) from two different contexts, i.e., captivity vs. the wild. Blood samples taken from 35 captive and 54 wild partridges in 2021-2022 were analysed for 94 pesticides most commonly used in French agriculture. Captive partridges had 29 molecules detected in their blood (12 herbicides, 14 fungicides, and three insecticides) compared to wild partridges, which had 50 molecules (13 herbicides, 23 fungicides, and 14 insecticides). Of these pesticide compounds found in individuals, 26 were banned. Captive partridges had significantly fewer pesticide molecules than wild partridges, with one to 14 pesticides per captive individual and 8 to 20 pesticides per wild individual. Nineteen molecules were common to both groups, with concentrations up to three times higher in wild partridges than in captive partridges. Our results thus show multiple exposures for most of our individuals, especially in wild partridges, which can lead to cocktail effects, which are never considered. Furthermore, the difference in contamination between the wild and captive partridges reflects the multiple routes of contamination in nature, in particular, due to the use of a wide range of habitats by wild partridges.

Achieving excellent strength-ductility balance in the lightweight refractory high-entropy alloy by incorporating aluminum

Refractory high-entropy alloys (RHEAs) have garnered widespread attention as a novel class of alloys with promising applications in high-temperature environments. However, their limited ductility has constrained their engineering application. In this study, a Ti40Zr40Nb10Ta10 base alloy with enhanced ductility was chosen, and various amounts of Al were added to investigate the microstructure and mechanical behavior of these alloys. The addition of Al aimed to trigger the cocktail effect while simultaneously enhancing the specific strength of alloys. Scanning electron microscopy and transmission electron microscopy were employed to investigate the phase composition and microstructure, revealing that the addition of Al promoted the formation of a B2 structure. With the incorporation of Al, both the yield strength and hardness of alloys increased. When the Al content reached to 8 at.%, the alloy achieved an optimal strength-ductility balance (yield strength 1030 MPa, elongation 13.4 %). The strengthening contribution was calculated and indicated that solid solution strengthening and precipitation strengthening are the two main methods. While the excellent ductility is contributed by the cross-slip of dislocations, the presence of kink bands accommodated dislocation slip and reduced stress concentration, enhancing the elongation. This study reports a system of RHEAs with excellent room-temperature strength-ductility balance, shedding light on its potential engineering applications.

Recent progress in high‐entropy nanocatalysts

AbstractHigh‐entropy alloys (HEAs) are a promising group of materials composed of multiple elements (≥5) in nearly equal proportions (5 at%–35 at%), which exhibit uniformly mixed compositions and highly stable crystal structures and offer a wide range of design possibilities, making them exceptionally stable, multifunctional, and suitable for various applications. Recent research studies have identified the potential of HEAs as catalysts for electrocatalytic reactions, focusing on adjustable stress environments, optimizable d‐band centers, and high conformational entropy. Understanding the interactions among constituent elements, alloy formation, and catalytic reaction mechanisms is essential for optimizing HEAs' catalytic performance. This comprehensive review delves into the historical context, defining characteristics, and underlying significance of HEAs development. It also examines four primary effects of HEAs (high‐entropy effect, lattice distortion, sluggish diffusion, and cocktail effect) and their relevance to catalyst design criteria (selectivity, activity, stability, and cost). Additionally, it summarizes recent advances in nanostructured HEA catalyst synthesis, highlighting their advantages and challenges and explores the use of HEAs in electrocatalytic redox reactions involving small molecules (H, C, O, N). The paper underscores the importance of integrating experimental methods and theoretical calculations to design, synthesize, and understand alloy–property relationships of HEAs, emphasizing their vast potential for catalytic applications.