SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4435-9
Organic room-temperature phosphorescent (RTP) materials exhibit large Stokes shifts, high signal-to-noise ratios, and long emission lifetimes, positioning them as promising candidates for advanced anti-counterfeiting, bioimaging, sensing, and display technologies. Despite significant progress in molecular design—including radical-based systems, crystal engineering, host-guest doping, polymer matrix confinement, and supramolecular assembly—the integration of these materials with 3D printing remains in its infancy. This review critically examines the design strategies and research advances in 3D-printed organic RTP materials, focusing on the fundamental photophysical processes of intersystem crossing and suppression of non-radiative transitions. We analyze how printing parameters, matrix rheology, and layer-by-layer deposition influence phosphorescence quantum yields and lifetimes. Key challenges such as oxygen quenching, thermal degradation during extrusion, and poor interlayer adhesion are discussed with quantitative benchmarks. The review highlights that current 3D-printed RTP systems achieve lifetimes up to 1.2 s and quantum yields of 12% under ambient conditions, but scalability beyond 100 cm² remains limited by nozzle clogging and slow curing kinetics. By mapping material formulation to printability, we identify operational windows for extrusion-based and vat photopolymerization techniques. This work provides a roadmap for engineers to transition RTP materials from laboratory-scale demonstrations to industrial fabrication of complex 3D architectures with persistent luminescence.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4248-2
Marine biofouling imposes substantial operational penalties on maritime assets, yet commercial silicone foul-release coatings rely on static, non-adaptive networks that cannot be reprocessed or repaired. This work introduces selenonium-salt-catalyzed dynamic siloxane exchange as a route to polydimethylsiloxane (PDMS) vitrimer coatings. The authors incorporate A16Se+ organoselenium catalysts into PDMS networks at loadings designated A16Se+xPDMS, enabling thermally activated siloxane bond exchange that confers vitrimeric stress relaxation, reprocessability, and high-temperature self-healing. Antibiofouling performance is benchmarked against pristine PDMS using colony morphology assays for Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa, SEM imaging of bacterial adhesion after 3 h, Chlorella fluorescence adhesion quantification, zeta potential measurements, and 3-month seawater immersion panels. Reviewer 1 questioned the direct relevance of recyclability and high-temperature self-healing to marine antifouling and requested that surface elastic modulus and Pseudomonas antibacterial data be elevated to the main text. In response, the authors relocated scratch and self-healing results from Figure 5 to Supporting Information Figures S12 and S13, condensed the main-text discussion, and integrated surface elastic modulus data into Figure 4G and Pseudomonas antibacterial results into Figure 6A. The revised manuscript positions dynamic exchange as supporting evidence of network dynamics rather than as a primary antifouling metric, while foregrounding modulus and antibacterial performance as the application-relevant properties.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3694-3
Lithium metal anodes (LMAs) are among the most promising candidates for next-generation batteries with high energy density. However, their practical application is hindered by persistent challenges such as dendritic lithium growth, unstable solid electrolyte interphases (SEI), and poor Coulombic efficiency. Surface coating has emerged as a viable solution to address these limitations. In particular, atomic and molecular layer deposition (ALD/MLD) techniques offer unparalleled control over the fabrication of ultrathin, conformal coatings, making them especially suitable for stabilizing LMA interfaces. This review comprehensively summarizes recent progress in applying ALD and MLD methodologies to construct durable artificial interphases on LMAs. We discuss the underlying mechanisms through which these coatings inhibit dendrite formation, improve interfacial integrity, and facilitate uniform lithium-ion transport. The roles of inorganic ALD coatings, organic MLD coatings, and their organic–inorganic hybrids are systematically examined, with a focus on their chemical composition, deposition behavior, and electrochemical characteristics. Moreover, we highlight the enhanced performance achieved through the integration of ALD/MLD-engineered interfaces in full-cell systems. The review concludes with a discussion of current challenges and potential research avenues aimed at advancing the rational development of effective LMA protection strategies. Overall, this work offers valuable insights into the role of interfacial engineering via ALD and MLD in enabling the practical deployment of lithium metal batteries.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3836-8
Flexible energy storage and harvesting devices, as core components of flexible electronic systems, have driven the transformation from external power supply to self-powering and from fixed forms to adaptive configurations, playing a pivotal role in wearable technology and the Internet of Things. MXenes, a class of two-dimensional transition metal carbides, nitrides, and carbonitrides, are promising candidates due to their excellent conductivity, mechanical flexibility, and tunable interfacial characteristics. Specifically, interfacial characteristics—surface energy, surface terminations, and interlayer spacing—decisively influence device performance. This review summarizes the influence of microcosmic interfacial characteristics on macroscopic properties, interfacial regulation strategies, and applications in flexible energy storage and harvesting. It concludes with challenges and perspectives for designing high-performance MXene-based energy devices. Key applications include flexible supercapacitors, batteries, and triboelectric nanogenerators. For instance, pillared Ti3C2 via CTAB pre-pillaring and Sn4+ pillaring regulates interlayer spacing, enhancing ion transport. The review integrates recent advances, such as MXene/nylon scaffolds for dendrite-free zinc anodes and MXene-bonded hard carbon films for sodium/potassium storage, demonstrating improved cycling stability and rate capability. The interfacial engineering strategies discussed provide a roadmap for overcoming stacking issues and achieving high energy density and mechanical robustness.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4054-x
The sluggish kinetics and high onset potentials of the oxygen evolution reaction (OER) at the anode of alkaline water/seawater electrolyzers limit overall energy efficiency. Noble-metal oxides like RuO2 are active but suffer from high cost, agglomeration, and dissolution under oxidizing potentials, especially in chloride-rich electrolytes where competing chloride oxidation reaction (ClOR) occurs. Here, we report a mild two-step dry-wet milling strategy to achieve throughout lattice doping of F− into MnO2 (F-MnO2) and subsequent anchoring of atomically dispersed Ru via Ru–O/F hybrid bonds. The strengthened Mn 3d–O/F 2p hybridization and negative charge shielding of surface F− enhance OER activity/selectivity relative to ClOR and impart superior Cl− tolerance and corrosion resistance. The resulting F-Ru-MnO2-TH electrocatalyst exhibits overpotentials of 280 mV and 200 mV at 10 mA cm−2 in alkaline water and simulated seawater, respectively. It retains ~100% of initial activity after 200 h continuous operation in alkaline media and >95% after 300 h in simulated seawater, significantly outperforming Ru-MnO2 and commercial RuO2. This work provides a scalable route to durable, high-performance OER catalysts for seawater electrolysis.
Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2025101901
Hexachlorobutadiene (HCBD) is a persistent organic pollutant (POP) regulated under the Stockholm Convention. Chlorinated chemical production processes are major sources of unintentional HCBD emissions, posing potential threats to ecosystems and human health. This study systematically reviews the formation, emission, and environmental impact of HCBD from such processes. HCBD is widely generated as a by-product during chlorination stages of producing carbon tetrachloride, dichloroacetylene, tri-/tetrachloroethylene, and chlorobenzene, via free-radical mechanisms. It is released through waste gas, wastewater, and solid waste. In the environment, HCBD exhibits multimedia distribution, undergoing long-range atmospheric transport and adsorbing onto soil and sediments, thereby becoming secondary pollution sources. HCBD shows significant bioaccumulation and food-chain magnification; it is toxic to aquatic organisms and causes hepatic and renal damage with potential carcinogenicity in mammals. Effective pollution control requires combined process improvements and end-of-pipe treatments, supplemented by stringent emission standards and life-cycle management. Future research should focus on developing precise emission inventories, elucidating multi-media transport and transformation mechanisms, and assessing composite ecotoxicological effects, thereby providing scientific support for implementing international conventions and formulating effective prevention strategies.
Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2025021901
To assess the impact of the Air Pollution Prevention and Control Action Plan (APPCAP) on the chemical composition of PM2.5, this study analyzed the concentrations, existing forms, and sources of water-soluble ions in PM2.5 collected during summer (June–August) in the northern suburbs of Nanjing for the years 2012, 2013, 2017, and 2019. The results demonstrate a significant reduction in total water-soluble ion concentrations in 2017–2019 compared to 2012, indicating the effectiveness of APPCAP in mitigating PM2.5 pollution. Sulfate (SO4^2−), nitrate (NO3^−), and ammonium (NH4^+) (collectively SNA) were the dominant ionic species, contributing 69.98%–92.58% of the total ion mass, with SO4^2− being the most abundant. In the summers of 2013 and 2017, PM2.5 exhibited alkaline properties, and SNA primarily existed as NH4NO3 and (NH4)2SO4. Conversely, in 2019, PM2.5 became acidic, with SNA present as NH4NO3 and NH4HSO4. The nitrogen oxidation ratio (NOR) and sulfur oxidation ratio (SOR) indicated that NO3^− and SO4^2− predominantly originated from secondary reactions, with SO2 undergoing secondary conversion more readily than NO2, and the degree of secondary conversion increasing annually. Source apportionment revealed a shift from long-range transport in 2013 to local and regional sources by 2017. These findings underscore the success of APPCAP in reducing primary emissions and altering the chemical speciation of secondary inorganic aerosols, while highlighting the persistent dominance of sulfate and the need for continued SO2 emission controls.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3783-x
The synergistic strategy combining chemotherapy and immunotherapy has recently demonstrated significant promise in cancer treatment. However, the substantial physicochemical disparities between chemotherapeutic agents and small-molecule immune adjuvants pose considerable challenges for co-delivery strategies. In this study, we designed a reactive oxygen species-responsive paclitaxel prodrug, PTX-PBA, which markedly enhanced drug encapsulation stability and dual-drug loading efficiency by various polymeric delivery systems. The resultant nanosystem (NanoPR) exhibited excellent physicochemical properties and ROS-triggered release profiles, effectively inducing immunogenic cell death in tumor cells while promoting dendritic cell maturation and CD8+ T cells activation. In murine models of 4T1 breast cancer and CT26 colon carcinoma, NanoPR achieved significant tumor growth inhibition and elicited durable immune memory responses. Collectively, this work provides an innovative molecular design strategy for the co-delivery of chemotherapeutics and immunomodulators, offering a robust foundation for the clinical translation of chemo-immunotherapy.
Chinese Journal of Environmental Engineering•2026•DOI: 10.12030/j.cjee.202508006
Landfill leachate, characterized by high ammonia nitrogen, high organic load, complex toxic components, and low nitrogen removal efficiency, poses significant environmental challenges. To achieve efficient nitrogen removal, a continuous-flow two-stage anoxic/oxic (A/O) moving-bed biofilm reactor (MBBR) system coupled with anaerobic ammonium oxidation (Anammox) was constructed and operated for long-term treatment of actual landfill leachate. After biofilm attachment and multi-gradient acclimation, influent concentrations were gradually increased from low levels (NH4+-N ~200 mg·L−1, COD ~2500–3000 mg·L−1) to high levels (NH4+-N ~1800 mg·L−1, COD ~8500 mg·L−1). During stable operation, average removal efficiencies of NH4+-N and COD reached 97.7% and 66.8%, respectively, with total nitrogen (TN) removal efficiency improving to 93.9%. Along the reactor, the first A/O stage achieved major organic degradation and ammonia oxidation, while the second stage facilitated nitrite accumulation and promoted Anammox for synergistic nitrogen removal. High-throughput sequencing revealed Proteobacteria as the dominant phylum (>50%), with denitrifying genera such as Azoarcus and Thauera significantly enriched. Planctomycetota abundance increased from 0.6% to 3.7%, and Candidatus Kuenenia was detected, confirming successful Anammox colonization and participation in nitrogen removal. This study validates the efficient combined nitrogen removal mechanism of the A/O–MBBR system with Anammox, providing theoretical basis and technical support for engineering treatment of high-ammonia wastewater.
Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2025041105
Online measurements of volatile organic compounds (VOCs) were conducted in the central urban area of Shenyang from June 1 to August 31, 2022, to analyze concentration levels and ozone formation potential (OFP). The initial concentrations of VOCs were estimated using the photochemical age parameter method to correct for photochemical losses. Positive matrix factorization (PMF) was applied for source apportionment. The average mass concentration of total VOCs (TVOCs) was (27.29 ± 15.96) μg·m−3, with alkanes (50.3%) as the dominant component; key species included propane, ethane, methanethiol, and ethylene. The OFP of TVOCs was (64.30 ± 66.41) μg·m−3, with alkenes (63.5%) as the main contributor; key reactive species were ethylene, propylene, m/p-xylene, toluene, and isoprene. Daytime photochemical loss of VOCs reached 2.40 μg·m−3, with alkenes (67.1%) dominating. PMF based on initial concentrations identified five major sources: vehicle emissions (56.2%), solvent usage (21.5%), combustion sources (8.9%), industrial emissions (7.5%), and natural sources (5.9%). Compared to PMF results based on directly monitored concentrations, contributions from vehicle emissions, combustion sources, and solvent usage decreased, while industrial emissions increased. The organic chemical industry source was not identified, and a new natural source contribution was recognized. These findings underscore the importance of photochemical loss correction in source apportionment and highlight key species and sources for ozone pollution control in Shenyang.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-4057-4
The escalating use of ionizing radiation in medical and industrial applications necessitates lead-free, flexible, and sustainable shielding materials. Current development relies on empirical trial-and-error, which is inefficient. This study introduces a machine learning-assisted Monte Carlo simulation strategy for rapid optimization of metal filler compositions for X-ray attenuation across 40–120 kV. Guided by this AI-driven approach, polyvinyl alcohol (PVA)-based gels containing uniformly dispersed Bi/W/Gd2O3 nanoparticles were developed, forming within 1 minute at -20°C using a PVA-DMSO/H2O co-solvent system. The optimized gel with 50 wt% metal loading exhibits exceptional mechanical properties: tensile strength of 1.76 MPa, toughness of 6.3 MJ m−3, and elongation of 600%. It achieves >98% X-ray shielding efficiency at 5 mm thickness, outperforming lead composites at 120 kV. The physically cross-linked network provides recyclability and anti-freezing capability, retaining flexibility at -50°C. This work establishes a data-driven paradigm for designing high-performance radiation-shielding materials, demonstrating AI's potential to accelerate materials discovery and enable scalable fabrication of eco-friendly protective systems.
SCIENCE CHINA Materials•2025•DOI: 10.1007/s40843-025-3587-4
Unstable zinc interfaces arising from dendrite growth and parasitic reactions impede the practical deployment of rechargeable aqueous zinc-ion batteries. This study introduces 1-(2-pyridylazo)-2-naphthol (PAN) as a parts-per-million (ppm) level electrolyte additive to stabilize the Zn anode. Theoretical and experimental analyses reveal that PAN undergoes parallel adsorption on the Zn surface, establishing strong π-π interactions between adjacent molecules that efficiently repel water. The OH, pyridine N, and azo N groups in PAN chelate Zn2+, modulating Zn2+ diffusion and promoting uniform deposition while suppressing dendrite formation. A 10 ppm (0.04 mM) PAN addition extends the lifespan of a symmetrical cell to 1500 h at 2 mA cm−2 and 1 mAh cm−2. The Zn||Cu half-cell achieves a Coulombic efficiency of 99.91% over 3500 cycles at 5 mA cm−2 and 1 mAh cm−2. Full cells with NH4V4O10 and MnO2 cathodes exhibit enhanced cycling stability. Notably, a Zn||NH4V4O10 pouch cell retains 71.1% capacity after 250 cycles at 0.8 A g−1. This work demonstrates a viable strategy for selecting high-efficiency additives for aqueous metal-based batteries.