Precious Metals Research Articles

Perception of Women Towards Investment in Different Investment Alternatives

Women are empowered to take active participation in investment activities through financial education and an inclusive investment environment. Several alternatives to investing are available, including mutual funds, real estate, precious metals, savings accounts, and stocks, which offer potential returns through regular income or capital appreciation. Investment alternatives are differentiated by their unique features, risks, returns, and ease of management. Investors, before investing, must take these features into account in relation to their risk tolerance, goals, and time horizon when considering any particular alternative. As women are recognized for making risk-averse investment decisions, their investments are impacted by numerous factors. The primary goal of this study is to understand the investment perception of women towards different investment alternatives. While the main factors influencing investment decisions are return, risk, and liquidity, several other factors specifically influence women investors, such as social and cultural norms, peers, and family members. Primary data was collected through a well-structured questionnaire consisting of Likert scale questions. SPSS software was used for data analysis. The initial results of the survey showed that 70% of the respondents had an average understanding of different investment options, whereas only 5% had high knowledge of different investment alternatives. When it comes to interest in a particular investment, mutual funds are the most preferred alternative. Additionally, 72% of women respondents show a moderate level of risk tolerance among all respondents in the study.

RELATION BETWEEN δ13С, δ18О AND REE CONTENT IN CARBONATITES OF THE TOMTOR COMPLEX, SAKHA REPUBLIC (YAKUTIA)

The paper reports the comprehensive study of phosphorus-rare metal (polymineral) carbonatites (I) and rare metal (ankerite) carbonatites (II) of the Tomtor massif based on ICP-MS, XRF, XRF-SI, SEM methods and isotope determination of C, O and 86Sr/87Sr. With a similar mineral composition, the REE+Y content in carbonatites (I) averages 0.38 wt. %, and in carbonatites (II) it is 1.3 wt. %. The δ18О-δ13С diagram provides the C and O isotopic compositions of carbonatites (I) and (II) as two intersecting trends: (I) carbonates from wells 4041, 6151, 115-117 represent the secondary generation of carbonates derived with the deuterium fluid involved; (II) depicts transformation of carbonate by low-T fluid, with fluid/rock ratio = 5. The study identified an increase in the REE and δ18O contents in carbonatites as the temperature of their formation decreases and enrichment of rocks with REE minerals, associated with REE mobility reduction in the fluid while the temperature is decreasing.

Mechanism Insight into Direct Amidation Catalyzed by Zr Salts: Evidence of Zr Oxo Clusters as Active Species.

The capricious reactivity and speciation of earth-abundant metals (EAM) hinder the mechanistic understanding essential to boost their efficiency and versatility in catalysis. Moreover, metal's solution chemistry and reactivity are conventionally controlled using organic ligands, while their fundamental chemistry in operando conditions is often overlooked. However, in this study, we showcase how a better understanding of in operando conditions may result in improved catalytic reactions. By assessing the composition and structure of active species for Zr-catalyzed direct amide bond formations under operating conditions, we discovered zirconium oxo clusters form quickly and are likely active species in the reactions. Formation of these clusters dismisses the use of additional organic ligands, inert atmosphere, anhydrous solvents, or even water scavenging to provide amides in good to excellent yields. More specifically, dodeca- and hexazirconium oxo clusters (Zr12 and Zr6, respectively) rapidly form from commercial, readily available Zr salts under reaction conditions known to afford amides directly from nonactivated carboxylic acid and amine substrates. Extended X-ray absorption fine structure (EXAFS) experiments confirm the presence of oxo clusters in solution throughout the reaction, while their key role in the mechanism is supported by an in-depth computational study employing density functional theory (DFT) and molecular dynamics (MD) methods. These results underline the value of (earth-abundant) metals' intrinsic solution chemistry to transformative mechanistic understanding and to enhance the sustainability of organic transformations.

Shift from legacy to emerging per- and polyfluoroalkyl substances for watershed management along the coast of China

Per- and polyfluoroalkyl substances and their short-chain alternatives have attracted world-wide attention due to their widespread presence and persistence in the environment. However, the sources, environmental fate, and driving forces of PFAS in coastal ecosystems remain poorly understood. In this study, the spatial distribution, source apportionment, and driving mechanisms of PFAS were investigated through a comprehensive analysis of water samples collected along the China's coastline. The concentrations of Σ25PFAS in water samples followed a general pattern, with higher levels observed in northern coastal zones of China than the south, ranging from 0.72 to 1872.21 ng L−1. PFOA and PFBA were dominant. Emerging short-chain PFAS, such as PFBS, PFBA, F-53B and GenX, were frequently detected, with detection rates of 97%, 99%, 95% and 77%, respectively. This indicated a shift in coastal PFAS contamination from legacy compounds to emerging short-chain alternatives. Source apportionment using the Positive Matrix Factorization model identified key contributors to PFAS pollution, including textile production, volatile precursors, precious metal industries, aqueous film-forming foam, metal-plating, electrochemical fluorination, and fluoropolymer manufacturing. Additionally, PFAS concentrations were significantly positively correlated with cultivated land, urban area, and wastewater discharge, while negatively correlated with annual precipitation and woodland coverage (p < 0.05). Socio-economic development was identified as a major driver of PFAS emissions, while the hydrological factors and vegetation coverage can significantly enhance watershed resilience against PFAS pollution.

Exploring the Potential of Bimetallic PtPd/C Cathode Catalysts to Enhance the Performance of PEM Fuel Cells.

Bimetallic platinum-containing catalysts are deemed promising for electrolyzers and proton-exchange membrane fuel cells (PEMFCs). A significant number of laboratory studies and commercial offers are related to PtNi/C and PtCo/C electrocatalysts. The behavior of PtPd/C catalysts has been studied much less, although palladium itself is the metal closest to platinum in its properties. Using a series of characterization methods, this paper presents a comparative study of structural characteristics of the commercial PtPd/C catalysts containing 38% wt. of precious metals and the well-known HiSpec4000 Pt/C catalyst. The electrochemical behavior of the catalysts was studied both in a three-electrode electrochemical cell and in the membrane electrode assemblies (MEAs) of hydrogen-air PEMFCs. Both PtPd/C samples demonstrated higher values of the electrochemically active surface area, as well as greater specific and mass activity in the oxygen reduction reaction in comparison with conventional Pt/C, while not being inferior to the latter in durability. The MEA based on the best of the PtPd/C catalysts also exhibited higher performance in single tests and long-term durability testing. The results of this study conducted indicate the prospects of using bimetallic PtPd/C materials for cathode catalysts in PEMFCs.

Aging Retardation of Lead-Acid Batteries by Adjusting Charge Controller Threshold Values in Off-grid Photovoltaic System

Hybrid systems or coupled power plants with energy storage are becoming more and more popular due to the rising need for energy. Researchers have been conducting several experiments to assure longer-lasting battery use due to the increasing widespread use of energy storage and the depletion of resources such as silicon and precious metals. In this study, a simulation study is carried out in PVSyst software on lead-acid batteries, which have a low cycle and a very traditional electrochemical structure. The simulation is realized by scaling Spain’s consumption curve in 2023, taken from the European Network of Transmission System Operators for Electricity (ENTSO-E), together with lead acid batteries and off-grid photovoltaic (PV) modules. After the off-grid system design is created and consumption data is imported, it is aimed to extend battery life by changing the charge-discharge threshold values of the charge controllers. Threshold values are in two categories, high and low, and seventeen different cases are simulated. According to the results of the simulation, the state of charge (SOC) levels of the batteries decreases significantly due to radiation and cloudiness in the winter months and remain high in the spring and summer months. When charge controllers are set to high thresholds levels, they cause gassing currents that rise to an average of 20 amps, while battery life extends up to 5.3 years. When low threshold values are used, negligible levels of oxygen and hydrogen gasses are formed in the battery, but battery life decreases to 4.1 years.

Porous N-Doped Carbon-encapsulated Iron as Novel Catalyst Architecture for the Electrocatalytic Hydrogenation of Benzaldehyde.

Carbon porous materials containing nitrogen functionalities and encapsulated iron-based active sites have been suggested as electrocatalysts for energy conversion, however their applications to the hydrogenation of organic substrates via electrocatalytic hydrogenation (ECH) remain unexplored. Herein, we report on a Fe@C:N material synthesized with an adapted annealing procedure and tested as electrocatalyst for the hydrogenation of benzaldehyde. Using different concentrations of the organic, and electrolysis coupled to gas chromatography experiments, we demonstrate that it is possible to use such architectures for the ECH of unsaturated organics. Potential control experiments show that ECH faradaic efficiencies >70 % are possible in acid electrolytes, while maintaining selectivity for the alcohol over the pinacol dimerization product. Estimates of product formation rates and turnover frequency (TOF) values suggest that these carbon-encapsulated architectures can achieve competitive performance in acid electrolytes relative to both base and precious metal electrodes.

Fe-Catalyzed α-C(sp3)-H Amination of N-Heterocycles.

Nitrogen-heterocycles are privileged structures in both marketed drugs and natural products. On the other hand, C-H amination reactions furnish unconventional and straightforward approaches for the construction of C-N bonds. Yet, most of the known methods rely on precious metal catalysts. Herein we report a site-selective intermolecular C(sp3)-H amination of N-heterocycles, catalyzed by inexpensive FeCl2,which allows the functionalization of a wide range of pharmaceutically relevant cyclic amines. The C-H amination occurs site-selectively in α-position to the nitrogen atom, even when weaker C-H bonds are present, and furnishes Troc-protected aminals or amidines. The method employs the N-heterocycle as limiting reagent and is applicable to the late-stage functionalization of complex molecules. Its synthetic potential was further illustrated through the derivatization of α-aminated products and the application to a concise total synthesis of the reported structure for senobtusin. Mechanistic studies allowed to propose a plausible reaction mechanism involving a turnover-limiting Fe-nitrene generation followed by fast H atom transfer and radical rebound.

Fe‐Catalyzed α‐C(sp3)–H Amination of N‐Heterocycles

Nitrogen‐heterocycles are privileged structures in both marketed drugs and natural products. On the other hand, C–H amination reactions furnish unconventional and straightforward approaches for the construction of C–N bonds. Yet, most of the known methods rely on precious metal catalysts. Herein we report a site‐selective intermolecular C(sp3)–H amination of N‐heterocycles, catalyzed by inexpensive FeCl2, which allows the functionalization of a wide range of pharmaceutically relevant cyclic amines. The C–H amination occurs site‐selectively in α‐position to the nitrogen atom, even when weaker C–H bonds are present, and furnishes Troc‐protected aminals or amidines. The method employs the N‐heterocycle as limiting reagent and is applicable to the late‐stage functionalization of complex molecules. Its synthetic potential was further illustrated through the derivatization of α‐aminated products and the application to a concise total synthesis of the reported structure for senobtusin. Mechanistic studies allowed to propose a plausible reaction mechanism involving a turnover‐limiting Fe‐nitrene generation followed by fast H atom transfer and radical rebound.

One-pot synthesis of porous carbon nanospheres supported CuPd alloy catalysts for the hydrogenation-dechlorination of 2,3,6-trichloropyridine

Hydrogenation-dechlorination to produce 2,3-dichloropyridine is important for the next-generation pesticides. In this work, we successfully synthesized porous carbon nanospheres supported CuPd alloy nanoparticles via a simple and efficient one-pot strategy. Furthermore, by adjusting the Cu/Pd ratio and carbonization temperature, the obtained Cu2Pd1@PCNs-500-H2O2 showed the highly catalytic activity for the hydrogenation-dechlorination of 2,3,6-trichloropyridine with a conversion rate of 70.1 % and selectivity of 71.2 %. The catalyst showed outstanding catalysis performance even after five cycles. This simple and rapid one-pot strategy provides a new approach for the large-scale synthesis of efficient heterogeneous catalysts and offers an effective solution for reducing the high costs associated with precious metals.

Late devonian calc-alkaline high-k fractionated “Ferroan” I-type leucogranites (Rudny Altai)

The paper presents the geological, geochemical and isotope-geochronological studies of the Rudny Altai granitoids in the west of Central Asian Orogenic Belt (CAOB) – the front part of the Altai convergent margin of the Siberian continent. Isotopic U–Pb dating of zircons showed an age range from 367 to 363 Ma. Geochemical characteristics indicate the relevance of leucogranites to calc-alkaline high-K series (SiO2 73 wt.%, Na2O+K2O = 6.9–9 wt.%, Na2O/K2O = 0.7–1.2), with calc-alkaline and alkaline-calcic affinities (MALI = 6.32–8.41). They bear meta- to weakly-peraluminous values (A/CNK = 0.9–1.2), high Fe* index (0.84–0.97) and high fluorine (0.04–0.17 wt.%) content. Variations of HFSEs, LILEs contents, Ga/Al ratios and strong negative A/CNK-P2O5 correlation indicate their affinity with fractionated I-type granitoids. Rare metal (beryllium) mineralization is spatially and genetically related to leucogranites. It is assumed that the formation of granitoids was associated with shearing setting at the convergent margin of the Siberian continent, as a result of oblique subduction of the Irtysh-Zaisan ocean plate.

Enhancing Stability of Surface Au under Oxidizing Conditions through Reduced Bulk Au Content.

Contrary to the common assumption that a higher bulk content of precious metals facilitates the preservation of more surface noble metal by serving as a reservoir for surface enrichment, we demonstrate that a lower bulk content of Au results in a more stable arrangement of Au atoms at the surface of Cu-Au nanoparticles when exposed to an O2 atmosphere. Using ambient pressure X-ray photoelectron spectroscopy, we investigate the surface segregation and oxidation behavior of Cu-Au nanoparticles across various compositions. Our results reveal that in Au-rich nanoparticles exposed to an H2 atmosphere, surface segregation prompts the formation of a continuous Au-enriched shell, which subsequently oxidizes into a complete CuOx shell upon transitioning to an O2 atmosphere. Conversely, in Au-poor nanoparticles during H2 treatment, segregation results in the emergence of Au clusters embedded within the surface layer, persisting upon exposure to O2. This unexpected phenomenon shows that reducing the bulk content of precious metals can enhance the surface stability of noble atoms under oxidizing conditions, as further demonstrated by comparing the catalytic performance of Cu-Au nanoparticles with varying Au bulk contents in CO oxidation.

Efficiency of Penicillium sp. and Aspergillus sp. for bioleaching lithium cobalt oxide from battery wastes in potato dextrose broth and sucrose medium

Lithium-ion batteries, a primary power source, generate electronic hazardous waste at the end of their lifespan, which is a richer source of highly concentrated metals such as cobalt and lithium than those in natural resources. The waste is a potential renewable resource for the extraction of metals. Bioleaching, a process utilizing microbial activity, was used in this study to investigate the cobalt and lithium leaching efficiency from battery wastes. Two fungal strains, Aspergillus sp. strain JMET 15 and Penicillium sp. strain JMET 24 were used with different organic carbon sources (sucrose medium and potato dextrose broth) at 1 % pulp density. The sucrose medium derived a higher acid quantity and leached higher concentration of cobalt and lithium than in potato dextrose broth. Leaching efficiency by JMET 24 was higher than JMET 15. Cobalt (32.57 % and 27.19 %) and lithium (65.07 % and 40.58 %) were bioleached by JMET 24 and JMET 15, respectively, after 30 d cultivation in the sucrose medium. Lower pulp density was conducted to achieved higher leaching efficiency by JMET24, cobalt (77.87 % and 74.5 %) and lithium (99.88 % and 78.4 %) were bioleached at 0.1 % and 0.5 % pulp density, respectively. Cobalt oxide (Co3O4) was the product of the one-step recovery (leaching and precipitation) process. Cobalt was transformed from lithium cobalt oxide to cobalt phosphate-oxalate by JMET 24 in the sucrose medium. Thus, the potential of bioleaching as an effective method for recovering valuable metals from lithium-ion battery waste is demonstrated, presenting a promising approach for both waste management and resource recovery.

Anion Selectivities in Zwitterion Grafted Nanopores: Effect of Zwitterion Architecture.

The separation of ions of similar charge is a crucial challenge in many applications, from water treatment to precious metal recovery. Membranes with cross-linked zwitterionic amphiphilic copolymer (ZAC-X) selective layers, which feature self-assembled, zwitterion-lined nanodomains for permeation, offer unique permselectivity between monovalent anions (e.g., Cl-/F-). This has motivated studies on the mechanisms of transport and selectivity in this family of materials. In this study, we conducted molecular dynamics simulations of aqueous salt solutions within zwitterion-functionalized nanopores to elucidate the influence of dipole orientation of the ZI ligands on anion diffusivities, partitioning, and permeabilities. Our model compares systems with contrasting ZI organization: surface-cation-anion (S-ZI+-ZI-, Motif A) and surface-anion-cation (S-ZI--ZI+, Motif B). Our results reveal that Motif A exhibits less pronounced ion pairing due to a spatial separation in the radial profiles of cations and anions. Motif B demonstrates prominent ion pairing for smaller anions owing to their overlap with cation distributions. Further, our potential of mean force profiles reveals that anion partitioning increases with anion size in both ligand motifs, whereas Motif B exhibits significantly higher partitioning selectivity toward larger anions compared to Motif A. Our results for ion diffusivities show that the self-diffusivities of both anions and cations are lower for Motif B compared to Motif A. Such trends in anion partitioning and diffusivities can be explained by differences in the interactions and steric hindrance experienced by the anionic species in Motifs A and B. Finally, our results for anion permselectivity, obtained by combining partitioning and diffusivity, indicate that partitioning trends dominate over diffusivity trends. Consequently, anion permeability increases with anion size, and ligand Motif B yields much higher permselectivity toward larger anions compared to ligand Motif A.

Flotation of Copper Sulfide Ore Using Ultra-Low Dosage of Combined Collectors

Copper sulfide ores frequently co-occur with pyrite, presenting a significant challenge for their selective separation during beneficiation processes. Despite advancements in flotation technology, there remains a critical need for efficient methods to enhance copper recovery while suppressing pyrite interference, particularly without compromising the associated precious metals such as gold and silver. Current practices often struggle with achieving high selectivity and recovery while maintaining environmental sustainability. Here, we investigate the efficacy of a ternary collector mixture consisting of ammonium dibutyl dithiophosphate (ADD), butyl xanthate (BX), and ethyl xanthate (EX) for the selective flotation of copper sulfide from a complex ore containing 0.79% Cu and associated precious metals (0.233 g/t Au and 5.83 g/t Ag). A combination of lime and hydrogen peroxide as inhibitors was employed to suppress pyrite effectively under alkaline conditions (pH = 11.33). The results demonstrate that the optimized ternary collector system (ADD:BX:EX at a ratio of 1:0.5:0.5) significantly improves the copper grade and recovery at an ultra-low dosage of 10 g/t. The optimized flotation method using the combined collectors and inhibitors effectively separated chalcopyrite from pyrite, achieving a copper concentrate with 20.08% Cu content and a recovery of 87.73%. Additionally, the process yielded notable recoveries of gold (9.22%) and silver (26.66%). These findings advance the field by providing a viable and environmentally conscious approach to the beneficiation of sulfide ores, potentially serving as a blueprint for processing similar mineral deposits while minimizing reagent usage and costs.

Hierarchically Structured CuNiP/CuOx‐VP Nanoarrays Construction by Heteroatom Doping Boosting Glycerol Valorization at Industrial‐Level Current Density

AbstractElectrocatalytic valorization of glycerol to formate is considered to be a promising sustainable approach; however, it holds great challenges to increase catalyst activity and deliver market‐demanded chemicals with high Faradaic efficiency (FE) and selectivity under industrial‐level current density. Herein, hierarchically structured phosphorus vacancy‐enriched nickel phosphide porous nanoarrays by copper doping, denoted as CuNiP/CuOx‐VP, are constructed via a facile glycol‐mediated solvothermal approach. The CuNiP/CuOx‐VP yields an industry‐level 1 A cm−2 at the ultralow potential of 1.75 V, while showing notable FE (96.94%) and selectivity (96.76%) to formate over a wide range of potentials. Impressively, a two‐electrode electrolyzer linked to H2 evolution possesses exceptional activity that merely requires a cell voltage of 1.45 V to deliver 40 mA cm−2, exhibiting a high FE (97.53%) for formate production and surpassing the vast majority of previously reported precious metal electrocatalysts. Microscopic and electrochemical characterizations manifest that the CuNiP/CuOx‐VP composed of porous NiP nanosheets attached to aggregated CuOx particles featuring superaerophobic‐hydrophilic morphology enables increased active sites, favorable electronic redistribution, and thus boosted electrocatalytic performance. This study demonstrates an effective nanoarrays electrode for catalyst discovery, going from facile catalyst synthesis to structure‐activity relationship and subsequently developing more highly active electrocatalysts for energy‐saving coproduction of valuable chemicals.

Electrochemical recycling of lithium‐ion batteries: Advancements and future directions

AbstractLithium‐ion batteries (LIBs) are at the forefront of technological innovation in the current global energy‐transition paradigm, driving surging demand for electric vehicles and renewable energy‐storage solutions. Despite their widespread use and superior energy densities, the environmental footprint and resource scarcity associated with LIBs necessitate sustainable recycling strategies. This comprehensive review critically examines the existing landscape of battery recycling methodologies, including pyrometallurgical, hydrometallurgical, and direct recycling techniques, along with emerging approaches such as bioleaching and electrochemical separation. Our analysis not only underscores the environmental and efficiency challenges posed by conventional recycling methods but also highlights the promising potential of electrochemical techniques for enhancing selectivity, reducing energy consumption, and mitigating secondary waste production. By delving into recent advancements and juxtaposing various recycling methodologies, we pinpoint electrochemical recycling as a pivotal technology for efficiently recovering valuable metals, such as Li, Ni, Co, and Mn, from spent LIBs in an environmentally benign manner. Our discussion extends to the scalability, economic viability, and future directions of electrochemical recycling, and advocates for their integration into global battery‐recycling infrastructure to address the dual challenges of resource depletion and environmental sustainability.image

Optimizing Ni-Zr-Ti metallic glasses: Cluster design and molecular dynamics evaluation of glass forming ability

Ni-based metallic glasses have garnered significant attention due to their excellent mechanical properties and wide application prospects. However, their low glass forming ability (GFA) limits broader applications. This study explores the Ni-Zr-Ti ternary system, which excludes precious metals, using clusters and mixing entropy composition design method to develop a series of Ni-based metallic glasses with improved GFA. The study found that the composition Ni60.91Zr24.97Ti14.12 (NZT3) had the best GFA, with its cluster expression Ni-Ni8Ti4 + 1.17838 Ni-Ni6Zr6. To gain a deeper understanding of the GFA of metallic glasses, molecular dynamics (MD) simulations were conducted on the designed compositions. The simulation results indicated a significant correlation between the average local five-fold symmetry (ALFFS) and the GFA of the compositions. Ni60.91Zr24.97Ti14.12 exhibited the highest ALFFS value and the best GFA. The research demonstrates that by combining clusters and mixing entropy composition design method with the simulated ALFFS, metallic glasses with excellent GFA in the Ni-Zr-Ti system can be rapidly screened. The successful application of this innovative approach in this system not only deepens the understanding of metallic glass formation mechanisms but also provides significant guidance for future materials design.

Ultralow Ru-doped NiFe catalyst on stainless-steel fibers for enhanced oxygen evolution reaction in anion-exchange membrane water electrolysis

Designing high-performance, stable electrodes for the oxygen evolution reaction (OER) is essential for anion-exchange membrane water electrolysis (AEMWE) in industrial-scale hydrogen production. AEMWE has not yet been commercialized due to the high cost of precious metal catalysts and unsatisfactory performance of non-precious metal catalysts. Although various anodes are being developed to replace expensive Ir-based catalysts, low-cost catalysts that demonstrate a balance of performance and stability remain limited. In the present study, we fabricated a NiFe catalyst on a corrosion-resistant stainless-steel fiber paper substrate using a simple electrodeposition method and introduced small amounts of Ru via galvanic displacement. In half-cell tests, an enhanced overpotential of 229 mV was observed for the Ru-NiFe/SS anode at 10 mA/cm2. Using Ru-NiFe/SS as an anode for OER in AEMWE assembled with a commercial Pt/C cathode exhibited high performance with a current density of 8.73 A cm−2 (at 2.05 Vcell and 80℃). Long-term stability tests also showed that the Ru-NiFe/SS anode had higher stability than commercial IrO2 electrodes at 1 A cm−2 and 80℃ for 50 h. Therefore, Ru-NiFe/SS can be considered an alternative to conventional Ir-based electrodes to reduce hydrogen production costs.

Flash Joule heating technology in two-dimensional materials and beyond

In recent decades, ongoing exploration on material synthesis, coupled with advancements in science and technology, has led to the invention and application of numerous specialized devices. To fulfill the demand for high-performance materials in modern society, flash Joule heating (FJH) has been invented and applied in this context to achieve high efficiency, low cost, and environmental sustainability in material synthesis. This technology offers fast heating and cooling rates, high energy utilization, and promising results in material synthesis. FJH finds its applications in synthesizing two-dimensional materials, recycling battery metals, graphite, cathode, and recovery of precious metals from mines. This review presents an overview of FJH technology and its applications and prospects.