SinoGreenTech Academic Portal
LC
Verified CAS / Academic Author4 Decoded Studies

Prof. LI Chengtao

State Key Laboratory of Flexible Electronics (LoFE), Institute of Advanced Materials (IAM), School of Chemistry and Life Sciences, Nanjing University of Posts and Telecommunications, Nanjing 210023, China

Co-Affiliations:Shaanxi University Key Laboratory of Industrial Pollution Control and Environmental Health, School of Environmental Science and Engineering, Shaanxi University of Science & Technology, Xi'an, 710021, China

Research Publications & English Decoded Briefs

Showing 4 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-026-4279-0

Inkjet Printing Organic Light-Emitting Diodes

Inkjet printing has emerged as a viable additive manufacturing route for organic light-emitting diodes (OLEDs), offering drop-on-demand patterning, high material utilization, and compatibility with large-area flexible substrates. This review critically examines the formulation science, printhead physics, and drying kinetics that govern the quality of inkjet-printed organic layers. We analyze the rheological window required for stable jetting, typically 1–20 mPa·s viscosity and 25–45 mN/m surface tension, and the dimensionless Ohnesorge number (0.1 < Z < 1) that defines satellite-free droplet formation. The coffee-ring effect, driven by capillary flow and solvent evaporation gradients, remains the dominant failure mode for pixel non-uniformity; binary solvent systems and substrate temperature control (40–60 °C) mitigate this. We survey recent progress in printed hole-transport, emissive, and electron-transport layers, with particular attention to cross-linkable hole-transport materials that resist interlayer dissolution. Device performance metrics from printed OLEDs now reach external quantum efficiencies of 15–20% for fluorescent emitters and >25% for phosphorescent systems, with operating lifetimes (T95) exceeding 1,000 hours at 1,000 cd/m². We identify remaining bottlenecks: nozzle clogging from aggregated nanoparticles, film thickness variation across large panels, and the absence of standardized ink formulations. The review concludes with a roadmap for industrial adoption, emphasizing in-line metrology and closed-loop process control as prerequisites for yield parity with vacuum-deposited OLEDs.

Journal of Fuel Chemistry and Technology2026DOI: 10.1016/S1872-5813(26)60636-6

Direct Oxidation of Methanol to Polyoxymethylene Dimethyl Ethers over Sulfuric Acid-Modified Molybdenum-Doped NASICON Catalysts

Polyoxymethylene dimethyl ethers (DMMx) are promising clean diesel additives. Compared to the traditional aldol condensation route, the one-step oxidative method for producing DMMx directly from methanol is a green synthesis route offering significant advantages. However, due to the complexity of the reaction, a balance must be struck between oxidation depth and C–O chain growth efficiency. This imposes specific requirements on the design of catalysts with multifunctional active sites: the catalyst should possess appropriate oxidative activity, suitable acid strength distribution, and effective synergy between these two functions. To address these challenges, this study designed a sulfuric acid-modified molybdenum-doped NASICON catalyst, which demonstrated favorable catalytic performance in the one-step oxidative synthesis of DMMx from methanol. Over the NSC-Mo-0.5-30% catalyst, methanol conversion rate of 81.3% and the DMMx selectivity of 58.7% were achieved, along with the formation of heavier molecules, as evidenced by the DMM2–6 selectivity of 11.3%. The NH3-TPD, Py-IR and XPS results indicate that the introduction of molybdenum increases the number of weak Lewis acid sites, while sulfuric acid impregnation not only generates gradient-distributed Brønsted acid sites but also promotes the formation of Mo5+/Mo6+ redox pairs. The cooperation of the two types of active sites significantly enhances catalyst performance.

Environmental Chemistry2026DOI: 10.7524/j.issn.0254-6108.2025031001

Bioavailability and Desorption Kinetics of Sulfonamide Antibiotics in Soil Assessed by Diffusive Gradients in Thin-Films

The diffusive gradients in thin-films (DGT) technique has emerged as a promising tool for assessing the desorption kinetics and bioavailability of organic contaminants in soil. This study compared DGT, soil solution, and organic solvent extraction methods for evaluating the bioavailability of four sulfonamide antibiotics (SAs) in soil using pot experiments with Brassica rapa subsp. chinensis and Lactuca sativa. Results demonstrated that plant uptake of SAs depended on compound properties and plant species, with roots as the primary accumulation site. DGT-measured concentrations (CDGT) showed significant linear correlations with SA concentrations in both roots and leaves, and effective concentrations (CE) were positively correlated with plant tissue levels (P < 0.05). The soil solution method also showed predictive ability but with lower stability. The mass of SAs adsorbed by DGT increased non-linearly with deployment time, indicating that solid-phase resupply sustained long-term DGT uptake. DIFS model-derived soil-water partition coefficients (Kdl) ranged from 0.23 to 1.25 mL·g−1, with higher Kdl values corresponding to greater bioavailability. Response times (Tc) ranged from 2307 to 7523 seconds, with sulfamethoxazole (SMZ) exhibiting the highest Tc, indicating its release was most constrained. Meta-analysis of desorption parameters for other organic contaminants revealed that soil pH and particle size were key determinants of Kdl, while molecular volume and hydrophobicity influenced resupply rates. This study confirms the reliability of DGT for assessing antibiotic bioavailability in soil and provides fundamental data on their migration and fate.

Journal of Environmental Engineering Technology2026DOI: 10.13205/j.hjgc.202606020

Operational Efficiency and Fouling Mechanism of a Novel Swinging Ultra-Fine Screen

Municipal wastewater treatment plants in China face excessive influent grit loads and carbon source deficiencies, while conventional pretreatment (screening, grit chambers, primary sedimentation) exhibits low fine grit removal and poor carbon retention. A novel swinging ultra-fine screen with a screening precision of 0.1 mm was developed and tested at a pilot scale of 1000 m³/d. Systematic evaluation of screens with apertures from 0.05 to 0.4 mm was conducted, with mechanisms analyzed via particle size distribution, COD fractionation, and fouling layer characterization. The 0.1 mm screen achieved an SS removal efficiency of 89.3%, significantly higher than 57.4% for conventional processes, while COD removal was only 9.5% versus 28.6%, corresponding to a carbon source retention of 93%. The device nearly completely retained particles >0.1 mm and achieved >98% removal for particles in the 0.075–0.1 mm range. Performance remained stable under fluctuating COD and SS conditions. A three-stage fouling theory for micro-screens was proposed. This work represents the first application of 0.1 mm screening precision in pretreatment, markedly improving fine grit retention and carbon source preservation, with strong resilience to water quality variations.