SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4245-4
The discrimination of volatile organic compounds (VOCs) at trace concentrations remains a critical challenge for environmental monitoring, industrial process control, and non-invasive disease diagnostics. Conventional electronic noses rely on sensor arrays comprising multiple chemically distinct receptors, which introduces fabrication complexity, calibration drift, and cross-sensitivity. Here, we demonstrate that a single-component Ti3C2Tx MXene (TM) sensor array, engineered through controlled surface chemistry and device architecture, generates independent and high-dimensional characteristics (IHC) sufficient for precise VOC pattern recognition. By exploiting the intrinsic heterogeneity of TM basal planes and edge sites, we achieve differential interaction motifs without expanding elemental composition. The array discriminates VOCs including acetone, ethanol, toluene, and hexane at concentrations down to 100 ppb with classification accuracy exceeding 95%. Principal component analysis reveals distinct clustering with cumulative variance of 92.3% captured by the first three principal components. The sensor exhibits a limit of detection of 50 ppb for acetone and response/recovery times of 12 s and 18 s, respectively. Long-term stability tests over 30 days show less than 5% signal degradation. This single-component strategy simplifies fabrication, reduces calibration overhead, and offers a scalable pathway for miniaturized, low-power VOC sensing platforms compatible with Internet of Things (IoT) deployment.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3547-7
Inorganic perovskite solar cells (IPSCs) have attracted significant attention due to their excellent light and thermal stability and potential in tandem applications. However, their efficiency and stability are often limited by residual lattice stress and defects at interfaces and within the bulk, causing severe nonradiative recombination. Here, we introduce a zero-dimensional supramolecular complex, (ETP)2SbCl5, as a dual-interface and bulk modifier to regulate CsPbI3 film growth. The modifier exhibits spatial segregation: ETP+ cations anchor at the buried interface, passivating defects on TiO2 and perovskite surfaces; Sb3+ and Cl− ions diffuse into the bulk during annealing, relieving residual stress; and Cl− accumulates on the top surface, passivating cation defects. Consequently, the modified CsPbI3 solar cell achieves a power conversion efficiency (PCE) of 21.71% and an open-circuit voltage (VOC) of 1.27 V, retaining 97.4% of initial efficiency after 500 h of maximum power point (MPP) tracking. This work demonstrates a synergistic strategy to simultaneously address interfacial and bulk defects, advancing high-performance and stable inorganic photovoltaics.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3674-2
Enhancing catalytic activity is a core objective in catalyst design, with active site accessibility being a critical determinant. Polyoxometalate-based metal-organic complexes (POMOCs), combining advantages of POMs and MOCs, offer potential for constructing catalysts with highly accessible active sites. In this study, a series of POMOCs were synthesized using different POM templates: [CoII1.5(L)1.5(PMo12O40)(H2O)4]·3H2O (Co-PMo12), [CoII1.5(L)1.5(PW12O40)(H2O)4]·3H2O (Co-PW12), [CoII2(L)2(SiW12O40)(H2O)4]·11H2O (Co-SiW12), and H[CoII2.5(L)3(P2W18O62)(H2O)8]·10H2O (Co-P2W18). These were characterized by FT-IR, PXRD, and single-crystal X-ray diffraction. Catalytic activity differences for olefin epoxidation were attributed to distinct accessibility of Co(II) sites upon thermal activation. Notably, Co-P2W18 achieved 99% yield of 1,2-epoxycyclooctane within 3 hours at room temperature using O2 as oxidant, owing to highly accessible unsaturated Co(II) sites. This performance is superior to most reported catalysts. The reaction mechanism was investigated using density functional theory. The catalyst exhibited excellent stability over five cycles, with FT-IR, PXRD, and XPS confirming structural and oxidation state integrity. This work highlights the potential of POMOCs in designing catalysts with highly accessible active sites for enhanced catalytic activity.
Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2024112106
Selective synergistic catalytic elimination (SSCE) of CH3SH and CO2 represents a significant approach towards achieving green chemistry objectives. In this study, a series of Al2O3 catalysts with different surface hydroxyl coordination states were designed and fabricated through a simple water bath strategy. The performance of the corresponding catalysts for selective synergistic catalytic elimination of CH3SH and CO2 was systematically evaluated. The catalysts were comprehensively characterized by BET, XRD, XPS, NMR and CO-DRIFTS techniques. The experimental results revealed that the synthesized samples exhibited uniform specific surface areas (150 m2·g−1) and pore sizes (12 nm), while demonstrating varying hydroxyl coordination states, which significantly affects the surface acidity of W-Al2O3 catalyst. Notably, W80-Al2O3, synthesized at 80 °C via water bath heating, displayed the highest proportion of μ1-type hydroxyl coordination. This unique structural feature endowed the catalyst with enhanced Brønsted acidity and superior CO adsorption capacity compared to other catalysts, which significantly promotes the further hydrogenation of CO to CH4 in the SSCE process. As a result, the SSCE performance of W80-Al2O3 was significantly improved, achieving complete conversion of CH3SH (100%) and a CH4 product concentration of 1326 μmol·g−1, which is significantly higher than that of Al2O3 (56 μmol·g−1) and W-Al2O3 (54 μmol·g−1). This work provides a new strategy for the synergistic reduction of typical sulfur-containing odorous pollutants and carbon dioxide.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3646-1
Repairing cartilage defects requires biomaterials with mechanical properties similar to native cartilage. However, balancing these properties with biodegradability remains a major challenge. In this study, a degradable antibacterial hydrogel with promising mechanical characteristics was developed for personalized cartilage defect repair. The hydrogel was synthesized using chitosan and gelatin via microcrystallization and gelation, combined with chemical crosslinking facilitated by epichlorohydrin. This method significantly enhanced the mechanical properties of the material, with compressive modulus of the optimal group reaching 0.2 MPa and tensile strength reaching 2.2 MPa, which are comparable to those of human cartilage. The hydrogel maintained its integrity after 50000 compression cycles. With excellent flowability prior to crosslinking, it can adapt to complex cartilage defects. The inclusion of gentamicin provides antibacterial properties, while nano-hydroxyapatite promotes osteogenesis. This hydrogel, with its multiple crosslinking mechanisms, balances mechanical strength, biodegradability, and adaptability, offering a promising solution for repairing infected cartilage defects.
New Carbon Materials•2026•DOI: 10.1016/S1872-5805(26)61093-1
Advanced catalyst structures with good active site accessibility and strong metal-support interactions are crucial for oxygen reduction reaction (ORR) catalysis. A hierarchically porous Pt catalyst supported on honeycomb-like nitrogen-doped carbon (Pt/HNC-400, where 400 denotes the optimal dosage (mg) of the sacrificial SiO2 hard template used during synthesis) was fabricated by combining template-assisted pyrolysis and alcohol reduction. The fabrication involves the template-assisted pyrolysis of ZIF-67 (which provides the N-dopant through its 2-methylimidazole ligand) followed by HF etching to completely remove the SiO2, yielding a 3D interconnected porous carbon support. Compared to a commercial Pt/C, it had an exceptional ORR performance with a half-wave potential of 0.901 V (41 mV higher), a mass activity at 0.9 V that was 15.3 times higher, and significantly improved durability (a half-wave potential decay of 25 mV vs. 80 mV after 10,000 accelerated durability tests (ADTs)). Mechanistic investigations showed that this superior performance is due to the combined effects of the 3D porous structure, ultrafine Pt nanoparticles with strong metal-support interactions, and in-situ formed Co-Nx moieties from the pyrolysis of precursor ZIF-67. After 10,000 ADTs it was shown to have excellent structural integrity, retaining 87.4% of its initial electrochemically active surface area (102.7 m2 g−1). This study may assist the development of new high-performance ORR catalysts.
Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2025010201
The Guanzhong region, traversed by the Wei River Basin, is one of the most industrially, agriculturally, and medically advanced and densely populated areas in Northwest China, has seen increasing attention paid to the pollution of perfluoroalkyl substances (PFASs) in its surface water environment. This study systematically investigated the pollution characteristics of PFASs in the surface water of this region and their ecological and health risks. By optimizing the online solid-phase extraction-liquid chromatography-tandem quadrupole mass spectrometry (Online SPE-LC/MS/MS), efficient detection of 19 PFASs was achieved, with the method detection limits ranging from 0.2 ng·L−1 to 0.3 ng·L−1, linear correlation coefficients all ≥ 0.990, and spiked recoveries between 75.2% and 130.0%. Monitoring data indicated that PFBA, PFPeA, PFHxA and PFOS, short-chain perfluorinated compounds, were the main pollutants in this region, with high detection frequencies and concentrations, but the overall content was lower than that in most areas of China. The concentrations of PFASs in surface water showed significant seasonal variations, with the highest concentrations during the dry season (∑19PFASs:126.1 — 2584.3 ng·L−1), followed by the normal season (∑19PFASs:3.5—3567.6 ng·L−1), and the lowest during the wet season (∑19PFASs:26.3—294.6 ng·L−1). Ecological risk assessment showed that, except for PFDoDA in the dry season, the ecological risk quotient (RQ) of all other PFASs was < 1. Although the water of the Wei River is not used as direct drinking water, health risk assessment indicated that all PFASs posed low risks, with only PFOA and PFOS showing potential risks (HR > 0.1) to adults and children at some sites during dry/normal seasons. This study provides a scientific basis for PFASs pollution control in the Wei River Basin.
Journal of Environmental Engineering Technology•2026•DOI: 10.13205/j.hjgc.202606005
In the context of carbon peaking and carbon neutrality, urban reclaimed water plants must adopt measures such as energy conservation, consumption reduction, and enhanced resource and energy utilization to achieve carbon neutrality. This study developed a carbon emission balance model and accounting method for such plants, incorporating strategies of carbon emission reduction, carbon substitution, and carbon sink. The optimal pathway towards carbon neutrality was evaluated based on the carbon emission balance ratio. Using a 1×10⁵ m³/d urban reclaimed water plant as a case study, the results showed total carbon emissions of 20,934 t CO2e. The carbon emission reduction from reclaimed water source heat pumps for heating and cooling was 21,701 t CO2e, yielding a carbon emission balance ratio of 103.7%. In contrast, other carbon reduction measures contributed 15,424 t CO2e, with a balance ratio of 73.7%, highlighting the pivotal role of reclaimed water source heat pumps. When the heat pump extracted 27% and 36% of residual thermal energy, coupled with reclaimed water reuse or sludge anaerobic digestion-cogeneration, respectively, both pathways achieved a 100% balance ratio. Assuming year-round extraction, the balance ratio reached 213%. The carbon reduction ratio between utilizing residual thermal energy and chemical energy was 8.76:1. This study demonstrates that urban reclaimed water plants can achieve carbon neutrality through multiple pathways, with residual thermal energy recovery exhibiting significant potential.
Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2025033102
Olfaction is crucial for fish survival in complex aquatic environments, enabling detection and discrimination of odor signals that regulate foraging, predator avoidance, social interaction, courtship, and migration. The fish olfactory system, directly exposed to water, is highly susceptible to aquatic pollutants such as heavy metals and pesticides. This review summarizes the composition and structure of the fish olfactory system, the process of olfactory response, and current research on olfactory toxicity of major aquatic pollutants. Key findings indicate that pollutants like copper and cadmium disrupt olfactory epithelium integrity, alter olfactory sensory neuron (OSN) populations, and impair odor-driven behaviors. For instance, copper exposure in larval zebrafish causes differential death and regeneration of OSN populations, leading to neurobehavioral deficits. Cadmium exposure in juvenile coho salmon differentially alters odorant-driven behaviors and olfactory receptor expression. The review highlights the need for further research on mechanisms, mixture effects, and development of biomarkers for early warning. Understanding olfactory toxicity is vital for ecological risk assessment and for developing fish-based biosensors for water quality monitoring.
Chinese Journal of Environmental Engineering•2026•DOI: 10.12030/j.cjee.202510044
The efficient treatment of sulfur-containing volatile organic compounds (S-VOCs) has become a critical task for air pollution control and green low-carbon transition under China's 14th Five-Year Plan. Industrial emissions often contain multiple S-VOC species, whose interactions can complicate degradation pathways, generate uncontrollable byproducts, and deactivate catalysts, limiting practical application. This review systematically summarizes the past decade of research on catalytic degradation of thiols and thioethers in multi-pollutant systems, focusing on competitive adsorption mechanisms, interfacial reaction pathways, and environmental factor regulation. Performance differences and reaction mechanisms across various catalyst systems under coexisting S-VOCs and inorganic sulfur are compared. Key findings indicate that mixed thiol systems exhibit faster deactivation than single-component systems due to temperature-dependent competitive adsorption and pathway switching, governed by molecular size–active site matching. Strategies such as metal–support strong interactions, zeolite confinement, nanocluster effects, and single-atom catalysts have improved activity and stability. However, dynamic competition mechanisms at active sites remain unresolved. Future research should develop atomic/molecular-level characterization techniques and multi-variable kinetic models, and shift from end-of-pipe purification to resource recovery, e.g., converting H2S and thiols into high-value chemicals like methanethiol, achieving dual goals of pollution control and sulfur resource recycling.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-4080-y
M1 macrophages (M1φ) are pivotal drivers in the progression from non-alcoholic fatty liver (NAFL) to non-alcoholic steatohepatitis (NASH). Longitudinal monitoring of intrahepatic M1φ could facilitate non-invasive diagnosis of NASH, yet achieving specific and sensitive in vivo imaging of M1φ remains challenging due to the nonspecific phagocytic activity common to all phenotypic macrophages. In this study, we developed a dual-target-recognizing photoacoustic nanoprobe that can target glucose transporters (GLUTs) and be selectively activated by nitric oxide (NO). Benefiting from its enhanced affinity for M1φ and decent responsive capability to NO, the probe exhibited favorable imaging performance toward M1φ in ex vivo experiments. Following systemic administration in diabetic mice, the probe rapidly accumulated in the liver, where it was selectively internalized by M1φ via specific recognition between glucose molecules and GLUTs, further inducing a NO-triggered enhancement of the photoacoustic signal. Distinct photoacoustic signal enhancement patterns were observed between NAFL and NASH livers, enabling non-invasive in vivo discrimination of NASH. This study proposes a novel strategy using a dual-target-recognizing probe to improve the selectivity and sensitivity of in vivo M1φ imaging, while also providing new insights for the non-invasive diagnosis of NASH.
Journal of Fuel Chemistry and Technology•2026•DOI: 10.1016/S1872-5813(26)60708-6
Mercury emissions from coal combustion are highly toxic, volatile, and bioaccumulative, posing long-term threats to ecosystems and human health. This review systematically examines the current status and control policies of mercury emissions from coal combustion in China, analyzing distribution characteristics and transformation mechanisms during combustion, with emphasis on collaborative removal in pollution control devices after ultra-low emission retrofitting. A progressive strategy of 'synergistic enhancement–deep purification–resource recycling' is proposed, comprising three tiers: optimizing operational parameters of existing control systems to enhance synergistic mercury removal; developing efficient adsorption and catalytic oxidation technologies for industrial application; and advancing integrated mercury removal and recovery technologies, such as magnetosphere-based sorbents and recovery processes, focusing on high-value utilization. The paper also outlines future research directions aligned with international compliance and domestic environmental tax policies, providing theoretical and technical support for China's commitments to near-zero emissions of coal combustion pollutants.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-4038-8
Fluorescent fibers and textiles that integrate outstanding optical performance with excellent flexibility hold significant promise for wearable applications and the Internet of Things (IoT). However, the poor stability of post-organized phosphor-based fibers and the high-cost, high-precision technology of electroluminescent fibers hinder their widespread adoption. Perovskite materials and organic semiconductors, owing to their high-efficiency, tunable luminescent properties and solution processability, are deliberately employed to fabricate desired fluorescent fibers and textiles via a spinning chemistry strategy. Recent advances have successfully applied these fibers to sensors, information displays, optical communications, and health monitoring. This review provides a comprehensive overview of recent progress in fluorescent fibers and textiles, covering spinning techniques, emitter design, and wearable applications. We highlight key challenges and future research directions in the fine design and synthesis of fluorescent fibers and textiles, as well as their system integration for practical wearable applications. The review emphasizes the potential of spinning chemistry to enable scalable production of robust, high-performance luminescent fibers, addressing stability and cost barriers. We discuss the use of metal halide perovskite quantum dots (PQDs) with high photoluminescence quantum yields (PLQY) and tunable emission, and organic semiconductor emitters with tailored molecular structures, as promising building blocks. The integration of these materials into fibers via spinning chemistry offers a facile, efficient, and controlled strategy, leading to ultra-stable CsPbX3 (X = Cl, Br, I) perovskite filaments with a PLQY of 24.5% and stretchability up to 2400%. The review concludes by outlining future research directions, including the development of lead-free perovskites and self-healing materials, to enhance stability and safety for commercial wearable technologies.