Precious Metals Research Articles

Rational Design of Improved Ru Containing Fe-Based Metal-Organic Framework (MOF) Photoanode for Artificial Photosynthesis.

Metal-Organic Frameworks (MOFs) recently emerged as a new platform for the realization of integrated devices for artificial photosynthesis. However, there remain few demonstrations of rational tuning of such devices for improved performance. Here, a fast molecular water oxidation catalyst working via water nucleophilic attack is integrated into the MOF MIL-142, wherein Fe3O nodes absorb visible light, leading to charge separation. Materials are characterized by a range of structural and spectroscopic techniques. New, [Ru(tpy)(Qc)(H2O)]+ (tpy = 2,2':6',2″-terpyridine and Qc = 8-quinolinecarboxylate)-doped Fe MIL-142 achieved a high photocurrent (1.6 × 10-3 A·cm-2) in photo-electrocatalytic water splitting at pH = 1. Unassisted photocatalytic H2 evolution is also reported with Pt as the co-catalyst (4.8 µmol g-1 min-1). The high activity of this new system enables hydrogen gas capture from an easy-to-manufacture, scaled-up prototype utilizing MOF deposited on FTO glass as a photoanode. These findings provide insights for the development of MOF-based light-driven water-splitting assemblies utilizing a minimal amount of precious metals and Fe-based photosensitizers.

Symetric Triplane Complexes Based on Porphyrins and Phtalocyanines with Earth Rare Metals of Type: [(Po) Ln(Pc) Ln (Po)] for Application in Medical Imaging

Symetric Triplane Complexes Based on Porphyrins and Phtalocyanines with Earth Rare Metals of Type: [(Po) Ln(Pc) Ln (Po)] for Application in Medical Imaging

Peculiarities of the chemical enrichment of metal-poor stars in the Milky Way Galaxy

The oldest stars in the Milky Way are metal-poor with Fe/H $<$ -- 1.0, displaying peculiar elemental abundances compared to solar values. The relative variations in the chemical compositions among stars is also increasing with decreasing stellar metallicity, allowing for the pure signature of unique nucleosynthesis processes to be revealed. The study of the $r$-process is, for instance, one of the main goals of stellar archaeology and metal-poor stars exhibit an unexpected complexity in the stellar production of the $r$-process elements in the early Galaxy. In this work, we report the atmospheric parameters, main dynamic properties, and the abundances of four metal-poor stars: HE 1523-–0901, HD 6268, HD 121135, and HD 195636 (--1.5 $>$ Fe/H The abundances were derived from spectra obtained with the HRS echelle spectrograph at the Southern African Large Telescope, using both local and non-local thermodynamic equilibrium (LTE and NLTE) approaches, with the average error between 0.10 and 0.20 dex. Based on their kinematical properties, we show that HE 1523--0901 and HD 195636 are halo stars with typical high velocities. In particular, HD 121135 displays a peculiar kinematical behaviour, making it unclear whether it is a halo or an accreted star. Furthermore, HD 6268 is possibly a rare prototype of very metal-poor thick disk stars. The abundances derived for our stars are compared with theoretical stellar models and with other stars with similar metallicity values from the literature. HD 121135 is Al-poor and Sc-poor, compared to stars observed in the same metallicity range (--1.62 $>$ Fe/H $>$--1.12). The most metal-poor stars in our sample, HE 1523 -- 0901, HD 6268, and HD 195636, exhibit anomalies that are better explained by supernova models from fast-rotating stellar progenitors for elements up to the Fe group. Compared to other stars in the same metallicity range, their common biggest anomaly is represented by the low Sc abundances. If we consider the elements beyond Zn, HE 1523--0901 can be classified as an r-II star, HD 6268 as an r-I candidate, and HD 195636 and HD 121135 exhibiting a borderline $r$-process enrichment between limited-r and r-I star. Significant relative differences are observed between the $r$-process signatures in these stars.

Synergistic growth of nickel and platinum nanoparticles via exsolution and surface reaction

Bimetallic catalysts combining precious and earth-abundant metals in well designed nanoparticle architectures can enable cost efficient and stable heterogeneous catalysis. Here, we present an interaction-driven in-situ approach to engineer finely dispersed Ni decorated Pt nanoparticles (1-6 nm) on perovskite nanofibres via reduction at high temperatures (600-800 oC). Deposition of Pt (0.5 wt%) enhances the reducibility of the perovskite support and promotes the nucleation of Ni cations via metal-support interaction, thereafter the Ni species react with Pt forming alloy nanoparticles, with the combined processes yielding smaller nanoparticles that either of the contributing processes. Tuneable uniform Pt-Ni nanoparticles are produced on the perovskite surface, yielding reactivity and stability surpassing 1 wt.% Pt/γ-Al2O3 catalysts for CO oxidation. This approach heralds the possibility of in-situ fabrication of supported bimetallic nanoparticles with engineered compositional distributions and performance.

Study on the preparation of SiC–C–t‐ZrO2 composites and its corrosion resistance to crushed after‐used lithium batteries

AbstractIn order to solve the severe erosion of kiln refractories for the high‐temperature treatment used during the process of recovering valuable metal elements from waste lithium batteries, this study investigates the low‐cost, no‐firing preparation technology of erosion‐resistant SiC–C–t‐ZrO2 composites with self‐prepared t‐ZrO2–SiC–C powder, as well as silicon carbide and flake graphite as the main raw materials, and phenolic resin as the binding agent. (1) The effects of different t‐ZrO2–SiC–C powder additions and heat treatment temperatures on the properties of SiC–C–t‐ZrO2 composites were studied in details. (2) The erosion resistance of SiC–C–t‐ZrO2 composites to after‐use lithium battery waste was evaluated using the static crucible method. The mechanical properties of the t‐ZrO2–SiC–C composites was the best that its cold modulus of rupture (CMOR) was 11.37 MPa and cold crush strength (CCS) was 41.96 MPa when heat treatment temperature was 600°C and content of t‐ZrO2–SiC–C powder was 10 wt%. At that condition, the bulk density of samples reached to 3.15 g/cm3 and apparent porosity of it was only at 11.09% which means that the samples designed in this work are compacted enough. In the erosion test, the t‐ZrO2–SiC–C composites had an excellent resistance to erosion of lithium battery waste.

Methane Combustion Kinetics over Palladium-Based Catalysts: Review and Modelling Guidelines

Fugitive methane emissions account for a significant proportion of greenhouse gas emissions, and their elimination by catalytic combustion is a relatively easy way to reduce global warming. New and novel reactor designs are being considered for this purpose, but their correct and efficient design requires kinetic rate expressions. This paper provides a comprehensive review of the current state of the art regarding kinetic models for precious metal catalysts used for the catalytic combustion of lean methane mixtures. The primary emphasis is on relatively low-temperature operation at atmospheric pressure, conditions that are prevalent in the catalytic destruction of low concentrations of methane in emission streams. In addition to a comprehensive literature search, we illustrate a detailed example of the methodology required to determine an appropriate kinetic model and the constants therein. From the wide body of literature, it is seen that the development of a kinetic model is not necessarily a trivial matter, and it is difficult to generalize. The model, especially the dependence on the water concentration, is a function of not only the active ingredients but also the nature of the support. Kinetic modelling is performed for six catalysts, one commercial and five that were manufactured in our laboratory, for illustration purposes.

Bimetallic Ni and Pt single atoms anchored on nitrogen–phosphorus doped porous carbon fibers to achieve significant electrocatalytic hydrogen evolution

The commercial application of water electrolysis for hydrogen production requires the development of low precious metal catalysts with a high crustal abundance. One feasible strategy is to utilize bimetallic catalysts composed of both transition and precious metals. In this study, a novel N/P-doped Ni/Pt bimetallic catalyst is developed (NiPt@C-NP, 3.68 % Ni, 0.2 % Pt) using polyacrylonitrile fibers as an inexpensive carbon source for catalyst support. Due to strong anchoring from the N and P heteroatoms, the nickel and platinum species are mono-atomically dispersed throughout the catalyst. Under acidic conditions, NiPt@C-NP exhibits a hydrogen evolution overpotential of 89 mV (10 mA cm−2), whereas an unsupported platinum catalyst gives an overpotential of 302 mV. The mass activity of Pt in NiPt@C-NP reaches 36.17 A mgPt−1, which is 33 times higher than 20 % Pt/C (1.07 A mgPt−1). Density functional theory (DFT) calculations reveal that synergistic interactions between Ni and Pt significantly increase the density of state near the Fermi level of NiPt@C-NP, resulting in a reduced bandgap and an enhanced charge transfer capability. Furthermore, the Gibbs free energy at the Pt and Ni sites is − 0.25 and − 0.63 eV, respectively, indicating fast reaction kinetics.

A Review of the Structure–Property Relationship of Nickel Phosphides in Hydrogen Production

Hydrogen, one of the most promising forms of new energy sources, due to its high energy density, low emissions, and potential to decarbonize various sectors, has attracted significant research attention. It is known that electrocatalytic hydrogen production is one of the most widely investigated research directions due to its high efficiency in the conversion of electricity to H2 gas. However, given the limited reserves and high cost of precious metals, the search for non-precious metal-based catalysts has been widely explored, for example, transition metal phosphides, oxides, and sulfides. Despite this interest, a detailed survey unveils that the surface and internal structures of the alternative catalysts, including their surface reconstruction, composition, and electronic structure, are poorly studied. As a result, a disconnection in the structure–property relationship severely hinders the rational design of efficient and reliable non-precious metal-based catalysts. In this review, by focusing on Ni5P4, a bifunctional catalyst for water splitting, we systematically summarize the material motifs pertaining to the different synthetic methods, surface characteristics, and hydrolysis properties. It is believed that a cascaded correlation may provide insights toward understanding the fundamental catalytic mechanism and design of robust alternative catalysts for hydrogen production.

Improved hydrogen generation via NaBH4 hydrolysis: Synergistic role of sulfur and C4+-Doping unveils (440) high-index facets and modulates Co2+/Co3+ ratios in the Co3O4 lattice

Sodium borohydride (NaBH4) is crucial for eco-friendly “green” hydrogen (H2) storage, employing controlled release through catalyzed NaBH4 hydrolysis, mitigating its inherent sluggish self-hydrolysis. Precious metal catalysts enhance this process, but face scarcity and cost issues hindering widespread use, prompting interest in Co3O4, specifically with (311) orientation for abundant Co2+ sites. However, excess Co2+ on dominant (311) facets limits catalytic efficacy. This study presents a nuanced synthesis of sulfur (S)- and carbon (C4+)-doped Co3O4 that expose high-index (440) facets and optimize Co2+/Co3+ distribution. The catalytic performance of CoSC-0.1-700 on (440) facets demonstrates remarkable hydrogen generation rate of 4.1 L g−1. min−1 within 10.5 min, 1.81×, 2.42×, and 3.83× higher than control samples, and undoped Co3O4 with (311) dominance, and 1.24× higher than (220). An estimated activation energy (Ea) of 33.63 kJ mol−1, comparable to noble metals, indicates high performance and stability over ten (10) cycles. This approach promises sustainable future in "green" H2 production.

Bioinspired Liquid Metal based Soft Humanoid Robots.

The pursuit of constructing humanoid robots to replicate the anatomical structures and capabilities of human beings has been a long-standing significant undertaking and especially garnered tremendous attention in recent years. However, despite the progress made over recent decades, humanoid robots have predominantly been confined to those rigid metallic structures, which however starkly contrast with the inherent flexibility observed in biological systems. To better innovate this area, the present article systematically explores the value and potential of liquid metals and their derivatives in facilitating a crucial transition towards soft humanoid robots. Through a comprehensive interpretation of bionics, we present an overview of liquid metals' multifaceted roles as essential components in constructing advanced humanoid robots - functioning as soft actuators, sensors, power sources, logical devices, circuit systems, and even transformable skeletal structures. We conceived that the integration of these components with flexible structures, facilitated by the unique properties of liquid metals, can create unexpected versatile functionalities and behaviors to better fulfill human needs. Finally, we envision a revolution in humanoid robots, transitioning from metallic frameworks to hybrid soft-rigid structures resembling that of biological tissues. This article is expected to provide fundamental guidance for the coming research, thereby advancing the area. This article is protected by copyright. All rights reserved.

A dynamic kinetic resolution catalyzed by immobilized lipase coupled with a novel grinding immobilized oxovanadium：Kinetic model and performance

A dual immobilized lipase and oxovanadium co-catalyzed dynamic kinetic resolution (DKR) system was established and successfully applied to synthesize (R)-1-(3-Methoxyphenyl) acetate in batch, resulting in a key chiral intermediate of (S)-rivastigmine with highly yield (97.6 %), e.e (99.01 %) and selectivity Sel (99.4 %). Herein, oxovanadium was immobilized onto diatomite via grinding immobilization for the first time to access a novel immobilized oxovanadium (V-D) used to catalyze an in situ racemization of undesired enantiomer substrate. The racemization rate of hydrated vanadyl sulfate was found for the first time to be much higher than that of vanadyl sulfate without crystalline water because water molecules in the former may form ion clusters of solvation membranes to disperses the charge density of positive carbon ions and promote their stability. This grinding immobilization approach may become a promising alternative for the immobilization of metals, especially precious metals due to its low cost, high efficiency, easily separated and large reaction interface. The kinetic model of the kinetic resolution catalyzed by LA-MR was developed, which may obey the sequential mechanism with both substrate and product inhibition, while the in-situ racemization reaction catalyzed by V-D may comply with power law.

Efficient recovery and recycling/upcycling of precious metals using hydrazide-functionalized star-shaped polymers

There is a growing demand for adsorption technologies for recovering and recycling precious metals (PMs) in various industries. Unfortunately, amine-functionalized polymers widely used as metal adsorbents are ineffective at recovering PMs owing to their unsatisfactory PM adsorption performance. Herein, a star-shaped, hydrazide-functionalized polymer (S-PAcH) is proposed as a readily recoverable standalone adsorbent with high PM adsorption performance. The compact chain structure of S-PAcH containing numerous hydrazide groups with strong reducibility promotes PM adsorption by enhancing PM reduction while forming large, collectable precipitates. Compared with previously reported PM adsorbents, commercial amine polymers, and reducing agents, S-PAcH exhibited significantly higher adsorption capacity, selectivity, and kinetics toward three PMs (gold, palladium, and platinum) with model, simulated, and real-world feed solutions. The superior PM recovery performance of S-PAcH was attributed to its strong reduction capability combined with its chemisorption mechanism. Moreover, PM-adsorbed S-PAcH could be refined into high-purity PMs via calcination, directly utilized (upcycled) as catalysts for dye reduction, or regenerated for reuse, demonstrating its high practical feasibility. Our proposed PM adsorbents would have a tremendous impact on various industrial sectors from the perspectives of environmental protection and sustainable development.

Extreme Events Cause Market Efficiency or Inefficiency? Evidence from Precious Metals and Green Stock Indices

Background: Green investments offer a promising market-based approach to tackling global climate change but are susceptible to risk transmission from multiple assets. Purpose: To examine the multifractality between precious metals (Gold, Silver, Platinum) and green stock indices, such as Clean Energy Fuels, Nasdaq Clean Edge Green Energy, S&P Global Clean Energy and WilderHill Clean Energy, over the period from 1 January 2018 to 23 November 2023. The study aims to answer the following question: Did the events of 2020 and 2022 cause efficiency or inefficiency in the markets analysed? Methods: The Detrended Fluctuation Analysis (DFA) econophysics model will be used to answer the research question. Results: During the period of stability, there was a clear division between the markets, with Gold and green energy indices demonstrating market efficiency, while Platinum, Silver and some green indices exhibited price persistence, suggesting opportunities for above-average gains. However, the 2020 global pandemic led to widespread inefficiencies in all the markets analysed, with precious metals and green energy indices showing price persistence, indicating patterns that could lead to arbitrage opportunities. The persistence in returns suggested a tendency for asset prices to continue in the same direction for an extended period, offering opportunities to identify ongoing market trends for investment. In the pre-conflict period, the random walk hypothesis was rejected in all markets, with precious metals exhibiting anti-persistence in returns, while green energy indices showed significant persistence. During the conflict period, precious metals and green energy indices converged towards persistence in returns, except Platinum, which showed anti-persistence. Conclusion: This study provides valuable insights for investors and financial market professionals, highlighting the importance of understanding asset price behaviour patterns in different economic contexts.

Interfacial self-assembled of covalent organic framework onto MXenes for efficient enrichment and recovery of Au(III) and Pd(II) from aqueous solution

Recovery of precious metal ions in wastewater could not only improve resource utilization, but also could reduce environmental pollution. Herein, a composite of TpPa@Nb2C was constructed by an interfacial self-assembled method and explored the synergistic adsorption effects for precious metals. The structure and morphology of the composites were analyzed by advanced characterization techniques, followed by parametric analysis of Au(III)/Pd(II) adsorption from the simulated wastewater. The results showed that the grafting of COFs with abundant reducing active sites on the MXenes could significantly improve the selectivity and adsorption capacity. Meanwhile, the interaction was found as monolayer way and controlled by chemistry process, and the maximum equilibrium Au(III) and Pd(II) uptake reached up to 910.1 and 386.2 mg/g, respectively. The competitive adsorption study showed that the co-existence of impurities had little effect on the removal rate. The mechanism analysis demonstrated that the precious metal ions were reduced to elemental gold/palladium on the network of TpPa@Nb2C, and they got three electrons or two electrons from the hydroxyl groups through redox reaction, respectively. Thus, this study provided an excellent material for enrichment and recovery of precious metals in waste liquid and the treatment of e-waste.

Graphite sheet-supported bimetallic RhNi thin film alloys for enhanced and durable hydrogen evolution in acidic environments

Noble metal-based materials are excellent catalysts for hydrogen production from water electrolysis, but their high cost and limited availability hinder widespread use. However, precious metals can be effectively utilized in catalysts by forming alloys with low-cost 3d transition metals, thereby reducing the need for precious metals, while enhancing the performance. In this study, aerosol-assisted chemical vapor deposition was employed to deposit bimetallic rhodium-nickel (RhNi) alloy thin films on a graphite sheet for hydrogen evolution reaction (HER) catalysis in a 0.5 M H2SO4 solution. Thin-film morphological patterns were significantly changed as the deposition time varied from 45 to 135 min. The RhNi alloy fabricated for 90 min outperformed its counterparts, displaying lower overpotential of 40 and 197 mV at 10 and 1000 mA cm−2, small Tafel kinetics (54 mV dec−1), high conductivity (0.57 Ω) and large electrochemical surface area (3312 cm2), and extended stability (48 h) compared to pure Rh metal and other reported catalysts. The superior HER performance arises from the synergistic effects between Rh and Ni metals, coupled with a uniform layer of spherical particles that enhance conductive properties and reaction rates by providing maximized active sites on graphite surface. This work provides valuable guidelines for efficiently preparing highly active and durable thin-film electrocatalyst within short time span and applying directly in fuel cell for hydrogen production.

Cellular absorption and cytotoxic mitigation of heavy metals in mining vegetables in southwest China: Mechanistic insights and health implications

The existing health risk assessment models often rely on total concentrations of contaminants, neglecting cellular absorption, leading to an overestimation of risks due to a lack of toxicological verification. In this study, the content, bioaccessibility, and health risk evaluation of Cr, Ni, Cu, and As in vegetables from mining areas in Southwest China were examined. The cytotoxicity and gastric absorption of heavy metals and underlying mechanisms as well as the toxic mitigation approach after consumption of risky vegetables were explored. Our results showed that the heavy metals in cabbage, celery, and garlic seedlings were within the safety limit, even though grown in contaminated soils. The bioaccessibility of As, Cu, Ni, and Cr in vegetables in the gastric phase is from 6.92% to 81.15%, with mint having the highest bioaccessible concentrations of Cr (32.7 μg/kg), Cu (540.1 μg/kg), and As (103.9 μg/kg). The Hazard Quotient and Hazard Index values of the bioaccessible metals suggested an unacceptable cancer risk. Besides, the vegetable extracts increased cell apoptosis and tight junction disruption. Unexpectedly, the high-risk mint extract with the greatest bioaccessibility didn't cause cytotoxicity but inhibited cell apoptosis and enhanced cellular tight junction, evidenced by the upregulation of Zonula Occludens-1, Occludin, and Claudin 3, and a decrease in cellular heavy metal uptake. Furthermore, the mint extract could alleviate garlic seedling extract-induced cytotoxicity, indicating that the special substance in mint has protective effects. Taken together, special components in vegetables, cellular uptake, and toxicity of heavy metals should be considered in the accurate assessment of health risks.

Evaluation of heavy metal accumulation and associated human health risks in three commercial marine fish species from the Aegean Sea, Türkiye

This study investigates the presence and concentrations of ten specific heavy metals in the muscle tissues and gonads of three commercially important marine fish species: Garfish (Belone belone), European barracuda (Sphyraena sphyraena), and Anglerfish (Lophius piscatorius) collected from the Aegean Sea in Türkiye. The results indicate variations in metal accumulation, both between genders and among species. The fish species tend to accumulate higher levels of heavy metals in their gonads than in muscle tissues (p<0.05). While Cr, Cd, and Pb were not detected, Zn, Cu, and Fe are the predominant metals in muscle tissues due to their essential biological roles. However, within toxic elements, Hg was predominant, and L. piscatorius, a benthic fish, exceeded its recommended safety limits. A health risk assessment suggests that except for L. piscatorius, consuming these fish species from the Aegean Sea is generally safe, with estimated weekly intake (EWI) values below permissible limits. Total Hazard Quotient (THQ) values for most metals are below 1, indicating no significant non-carcinogenic health risks for consumers. This study emphasizes the critical need for regularly monitoring heavy metal levels in marine fish from the Aegean Sea, Turkiye. While overall safety in consuming these fish is highlighted, exceptions exist, notably concerning Hg levels in L. piscatorius. Therefore, persistent monitoring of heavy metal concentrations, especially in L. piscatorius, is advised to ensure ongoing safety and mitigate potential risks of metal accumulation.

Innovative green intense tetra-eutectic solvent (ITES) for recovery via occlusion co-precipitation at room temperature

Lithium iron phosphate (LiFePO4) is the widely used cathode material for safe and high-power lithium-ion batteries (LIBs) for electric vehicles (EVs). Therefore, numerous challenges to re-manufacturing, re-use, and recovery from spent LiFePO4/C are tolerated if evaluated early in the innovation process. Herein, innovative green intense tetra-eutectic solvent (ITES) has been used to recover a new Li-metal co-intercalation compound from spent LiFePO4/C cathode material, which is simple and cost-effective. The ITES leaching concerning organic solution with active hydrogen donor-acceptor salts creates a coordination environment through occlusion co-precipitate new co-intercalation compound at room temperature. Innovative green ITES-10 solution has successfully recovered a new Li-metal co-intercalation regarding the active hydrogen donor-acceptor bonding coordination environment of ITES adequate leaching solution and proposed recovery mechanism. The ICP-MS value of recovery metal (7Li) efficiency (%) of ITES-10 leaching for spent LiFePO₄/C cathode materials reaches approximately 0.452% at room temperature for recovery of new co-intercalation compound, besides the fresh LiFePO₄/C cathode materials (as reference), approximately 0.805%, respectively. Therefore, innovative ITES is considered to recover spent Li-based cathode materials in our future works concerning high leaching recovery rates below 100 °C in experimental conditions.

A 2D Acridine-Based Covalent Organic Framework for Selective Detection and Efficient Extraction of Gold from Complex Aqueous-Based Matrices.

Developing candidate materials which possess the ability of both selective detection and efficient capture of precious metal gold is highly desirable for environment and economy. However, most of reported materials only focus on single function, which seriously restricts their practical application as probes or adsorbents. Herein, a two dimensional (2D) acridine-based covalent organic framework (TpDa-COF) is prepared via the linkage of imine bonds for gold detection and adsorption. The synthesized COF can achieve both fluorescence and colorimetric dual sensing for Au3+ in a low concentration range (0.1-1.5 ppm) with the limit of detection (LOD) of 0.036 ppm. Impressively, the selectivity of TpDa-COF for the detection of Au3+ is admirable (Fe3+, Fe2+ and Cu2+ for negligible influence on its fluorescence). In addition, TpDa-COF exhibits ultrahigh adsorption capacity of 982.5 mg ⋅ g-1 for gold at pH=4, which is attributed the synergistic effect of both selective coordination and reductive process of Au(III) to Au(0). Meanwhile, both positive entropy change (ΔS=76.07 J ⋅ mol-1 ⋅ K-1) and high distribution coefficient (Kd=12484.8 mL ⋅ g-1) confirm the good affinity between TpDa-COF framework and gold. This work gives us a new insight to prepare COF with pyridine nitrogen sites for gold detection and adsorption.

Volatility Transmission and Market Connectivity of Metals and Energy Commodities: Insights from the Spillover Index

This paper explores the interconnections between metal and energy commodities by assessing the transmission of volatility within their futures markets. Achieved through the spillover index, the analysis reveals the impact of shocks on asset pairs—highlighting which assets absorb and transmit volatility, thereby explaining market connectivity. The dataset covers a period of twenty years of daily closing prices from the London Metals Exchange for a range of commodities. The Diebold and Yilmaz (2012) index, enriched by Baruník and Krehlík (2018) was used to reflect the changes in trends. The results obtained provide insights into market connectivity and the propagation of volatility during periods of economic distress. In this context, following the 2008 crisis, precious metals exhibited significant interconnectivity, with the emergence of Silver's vulnerability along with Gold's volatility tied to pre-crisis returns. Furthermore, copper's volatility reflects conditional correlations with market stock prices and other commodities particularly during economic downturns.