Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2025011101
This study investigates the adsorption characteristics and mechanisms of Cd, Ni, and Pb on yellow soils collected from multiple sites in Guizhou Province, China. Soil physicochemical properties, potentiometric titration, adsorption edge experiments, and a 1-site/2-pKa surface complexation model (SCM) were integrated to derive acid-base parameters and metal adsorption constants. Linear regression models established quantitative relationships between SCM parameters and soil properties, enabling prediction of adsorption behavior for new soil samples. Results showed that adsorption capacities increased with pH and followed the order Pb > Ni > Cd, influenced by hydrated radius, hydrolysis constant, and electronegativity. Soils with higher surface site concentration (Hs) and lower point of zero charge (pHpzc) exhibited greater metal adsorption. The SCM fitted adsorption edges with R ≥ 0.94, confirming its validity. pH was the dominant factor controlling metal complexation constants (lgKSOMe), acid-base equilibrium constants, and surface site density (Ds), with influence order Pb > Ni > Cd. Free iron oxide correlated negatively with deprotonation constant (pKa2). Ds was also affected by cation exchange capacity and specific surface area. Validation using a separate set of soil samples yielded good agreement between predicted and measured adsorption (R² = 0.75–0.82, RMSE = 0.1–0.51). This combined modeling approach simplifies experimental procedures and offers a robust tool for assessing heavy metal environmental risks and remediation strategies.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3892-2
Single-atom co-catalysts on semiconductor substrates offer a cost-efficient route to enhance photocatalytic performance with minimal precious metal loading. However, precise tuning of local coordination environments and construction of efficient single-atom co-catalysts remain challenging for overall water splitting. Here, we employ an icing-assisted photochemical reduction strategy to anchor atomically dispersed Pt species as hydrogen evolution co-catalysts on Al3+-doped SrTiO3 (Pt SA-STO). The optimized Pt SA-STO exhibits remarkable activity, with hydrogen and oxygen evolution rates of 13.62 and 6.71 mmol h−1 g−1, respectively, and a turnover frequency (TOF) of 2114.5 h−1. We pioneer the use of nuclear magnetic resonance (NMR) spectroscopy to quantitatively track the temporal evolution of Pt4+ to Pt2+ under continuous irradiation during the icing-assisted photoreduction. Advanced characterizations and theoretical calculations confirm that single-atom Pt co-catalysts facilitate directional transfer and extraction of photogenerated charge carriers, effectively suppressing surface recombination. This work provides insights into designing novel single-atom co-catalysts by deepening understanding of electronic configurations and active sites in photocatalytic overall water splitting.
Journal of Environmental Engineering Technology•2026•DOI: 10.13205/j.hjgc.202608023
Zinc-containing steel dust sludge, a by-product of steelmaking, contains high levels of chlorine (Cl) along with valuable metals such as Fe, Zn, K, and Na. When recycled into the steel production process, Cl accumulates, causing sintering instability and severe corrosion of blast furnace linings. This study investigated water leaching for Cl removal from zinc-containing steel dust sludge. Under optimal conditions (liquid-to-solid ratio 5 mL/g, temperature 70 °C, time 60 min, rotation speed 160 r/min), the Cl leaching rate reached 87%. Furthermore, a three-stage countercurrent water washing process at a liquid-to-solid ratio of 6 mL/g and room temperature for 45 min achieved a Cl leaching rate exceeding 90%. The water washing also reduced the leaching toxicity of metals in the sludge to a certain extent. Characterization via XRD, SEM, FT-IR, and XPS revealed that water washing primarily dissolved soluble chlorides (NaCl, KCl, etc.), increasing the specific surface area from 2.71 to 10.11 m²/g and average pore size from 12.83 to 16.29 nm. These findings provide theoretical and technical support for efficient Cl removal from zinc-containing steel dust sludge, facilitating its safe resource utilization.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4123-0
Aqueous aluminum-ion batteries (AAIBs) are promising for large-scale energy storage due to safety, sustainability, and theoretical high capacity. However, sluggish electron/ion transport in conventional cathodes limits rate capability. Here, we first propose high-entropy engineering of metal oxides (HEOs) as cathodes in AAIBs, leveraging the 'cocktail effect' and abundant electron transport pathways to enhance rate-capacity. Atomic-level interactions between different metal atoms broaden the d-band with reduced electronic level degeneracy, facilitating rapid electron transport, achieving one of the best rate capabilities (119.4 mAh g−1 at 10.0 A g−1) among metal-oxide cathodes. The disordered layered oxides formed with a high-entropy framework alleviate electrostatic repulsion between aluminum ions and the fixed lattice, mitigating structural degradation and imparting excellent cycling stability (over 95.1 mAh g−1 after 500 cycles at 2.0 A g−1). The optimized HEO-Cr cathode (Fe0.6Co0.6Ni0.6Mn0.6Cr0.6O4) exhibits outstanding rate performance and cycling stability. DFT simulations and electrochemical tests reveal that multi-transition metal incorporation, bandgap narrowing, and unique lattice structure drastically enhance electron transport efficiency. The layered phase formed after cycling, based on a high-entropy framework, overcomes challenges from high charge density aluminum ions, significantly enhancing cycling stability. This work paves the way for high-performance AAIBs and other aqueous multivalent metal ion batteries by rationally designing high-entropy engineering.