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Verified CAS / Academic Author11 Decoded Studies

Prof. TU Weifeng

Key Laboratory of Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University

Co-Affiliations:School of Materials Science and Engineering, Tianjin UniversityCollege of New Materials and New Energies, Shenzhen Technology University, Shenzhen, Guangdong 518118, ChinaAnhui Agricultural University, College of Resources and EnvironmentHebei UniversitySchool of Aerospace Engineering, Beijing Institute of TechnologyState Key Laboratory of Coking Coal Resources Green Exploitation, Zhengzhou University, Zhengzhou 450001, China

Research Publications & English Decoded Briefs

Showing 11 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-026-4217-y

Incorporating Triphenylamine Chromophores into Covalent Triazine Frameworks for Effective Photocatalytic Aerobic Oxidations

Rational design and construction of effective photocatalysts is a promising way for green and sustainable chemistry, but still a great challenge. Herein, taking triphenylamine-containing aldehydes as reactants, two covalent triazine frameworks (CTFs), tris(4-formylphenyl)amine (TPA)-CTF and tris(4-formylbiphenyl)amine (TBPA)-CTF, were rationally constructed. The strong electron donor property of the triphenylamine moieties derived from the initial reactants and the strong electron acceptor nature of the in-situ formed built-in triazine rings in CTFs endowed these robust triphenylamine-based CTFs with donor-acceptor (D-A) or donor-π-acceptor (D-π-A) structure features. Photocatalytic experiments revealed that, compared with the controlled phenyl analogue CTF, 1,3,5-tri(p-formylphenyl)benzene (TFPB)-CTF, both of the triphenylamine-based CTFs exhibited superior photocatalytic activity not only in photocatalytic hydrogen peroxide generation, but also in photocatalytic aerobic oxidations of diverse organic substrates. Theoretical studies further confirmed that their enhanced photocatalytic performance should be attributed to their unique D-A or D-π-A features in the constructed triphenylamine-based CTFs. This work successfully demonstrated that rational selection of reactants containing electron donor moieties to construct CTFs should be a reliable way for the construction of effective photocatalysts for photocatalytic oxidation reactions.

SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3622-0

High-resilience, anti-freezing, and vacuum-tolerant eutectogel for self-powered pressure sensing in extreme environments

Triboelectric nanogenerators (TENGs) offer promising solutions for self-powered sensors in the Internet of Things, yet traditional materials suffer from limited mechanical durability, environmental stability, and sensing performance under extreme conditions. This study develops a novel eutectogel composed of a deep eutectic solvent (DES) and a poly(itaconic acid-co-2-hydroxyethyl acrylate) (P(IA-co-HEA)) polymer network. Through careful molecular design and microstructural modification, the eutectogel achieves low hysteresis, excellent resilience (97.8%), high conductivity (48.02 mS m−1), and strong adhesive strength. Benefiting from the low freezing point and low volatility of the DES, the eutectogel retains 75.7% tensile and 69.4% compressive resilience at −40 °C, and shows no significant change in resilience after 24 h storage under −0.1 MPa vacuum. A self-powered TENG pressure sensor incorporating the eutectogel exhibits a fast response time of 16 ms and stable signal output over 16,000 contact-separation cycles. The sensor operates reliably at −60 °C and under vacuum (−0.1 MPa). These attributes make the high-resilience flexible sensor suitable for long-term, reliable pressure monitoring in extreme environments, addressing critical bottlenecks in durability and environmental stability for self-powered sensing technologies.

New Carbon Materials2026DOI: 10.1016/S1872-5805(26)61069-4

Discontinuous ablation behavior of four-directional dual-matrix C/C composites under dual-pulse solid rocket motors

Four-directional dual-matrix C/C composites were fabricated from PAN-based carbon fibers using a combined approach of soft-hard hybrid weaving preform molding, chemical vapor infiltration (CVI) of pyrolytic carbon (PyC), and high-pressure impregnation and carbonization of pitch-derived carbon. The ablation resistance was evaluated in a dual-pulse solid rocket motor, and the ablation behavior was investigated. The carbon rods, formed by twisting and carbonizing fiber bundles, exhibited a hexagonal cross-section, surrounded by a dense PyC 'wall' structure. The linear ablation rates after pulse I and pulse II were 0.068 mm/s and 0.113 mm/s, respectively. A cellular-like PyC layer and nanowire structures were deposited on the surface of the throat convergent section during the post-combustion cooling phase, while cracks and delamination occurred on and within the divergent section. The ablation process involved ultra-high temperatures, high-speed gas scouring, oxygen-containing thermochemical ablation, and thermal shock. This work elucidates the ablation behaviors under dual-pulse conditions and provides technical guidance for designing C/C composites for extreme environments.

Chinese Journal of Environmental Engineering2026DOI: 10.12030/j.cjee.202507111

Pulsed Electric Field Enhancement of Nitrogen Removal Performance and Microbial Community Structure Response in Anammox Granular Sludge

This study investigated the effects of a ring-shaped pulsed electric field (PEF) (1.5 V, 4 h on-time per cycle) on nitrogen removal performance and microbial community structure of anammox granular sludge (AnGS). Two anaerobic sequencing batch reactors (R1 control, R2 with PEF) were operated under stepwise increasing nitrogen loading rates (NLR). At NLR below 1,155 mg·(L·d)−1, R2 exhibited total nitrogen removal efficiency (TRE) 7.5%–17.0% higher than R1, with biomass, specific anammox activity (SAA), and extracellular polymeric substances (EPS) increased by 5%–7%, 21%–71%, and 54%–77%, respectively. However, at NLR above 1,320 mg·(L·d)−1, the toxic effect of nitrite dominated, and PEF enhancement diminished or even reversed to inhibition. Microbial community analysis revealed that at low-to-moderate NLR, PEF increased the relative abundance of Planctomycetes and key anammox bacteria (Candidatus Brocadia and Candidatus Jettenia), along with enhanced community richness (Chao1) and diversity (Shannon/Simpson indices). At high NLR, PEF decreased microbial richness compared to R1. Principal component analysis and redundancy analysis indicated that PEF was the key factor driving community differences at low-to-moderate NLR, whereas nitrite concentration became the dominant factor at high NLR. This study provides theoretical support for enhancing the resilience and engineering application of anammox processes.

New Carbon Materials2026DOI: 10.1016/S1872-5805(26)61093-1

A platinum catalyst with hierarchical porosity supported on a honeycomb-like nitrogen-doped carbon for excellent oxygen reduction reaction performance

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.

New Carbon Materials2026DOI: 10.1016/S1872-5805(26)61104-3

Fluorination Regulates Heat Generation in Ah-Level Lithium/Fluorinated Carbon Pouch Cells

Lithium/fluorinated carbon (Li/CFx) batteries are among the most promising high-energy-density primary batteries, yet substantial heat generation during discharge poses safety concerns, particularly for high-mass-loaded pouch cells. This study systematically investigates the effects of fluorination temperature on the structure and kinetics of fluorinated porous carbon (FPC) cathodes and on heat generation in Ah-level Li/FPC pouch cells. FPC samples with varying degrees of fluorination were synthesized by adjusting fluorination temperature, which influenced not only the F/C ratio but also the C–F bonding configuration, pore structure, and electronic transport capability. Pouch cells employing more highly fluorinated cathodes generated the most heat during discharge, with heat generation exhibiting clear stage dependence, predominantly in the 0–20% depth of discharge (DOD) range. Post-discharge structural characterization and kinetic analysis revealed that highly fluorinated FPC cathodes (FPC-250) undergo more concentrated LiF accumulation, leading to higher charge-transfer resistance, stronger polarization, lower Li+ diffusivity, and higher nucleation overpotential. These factors collectively intensify early-stage heat generation. The study establishes a correlation between fluorination temperature and cathode structure, discharge-product evolution, discharge kinetics, and heat generation, demonstrating that regulating fluorination temperature is an effective strategy for improving the thermal safety of Li/CFx batteries.

Environmental Chemistry2026DOI: 10.7524/j.issn.0254-6108.2025012302

Effects of Different Novel Fertilizer Applications on Phosphorus Loss from Surface and Seepage Water in Paddy Fields in the Chaohu Lake Watershed

Phosphorus (P) loss from paddy fields contributes to eutrophication in Chaohu Lake. This study evaluated the effects of novel fertilizers and P reduction on P loss and rice yield. Seven treatments were established: no P (CK), rice-specific fertilizer (ZYF), slow-release blended fertilizer (SRF), Xinjutian compound fertilizer (XJT), enhanced loss-controlled fertilizer (CRF), CRF with 10% P reduction (CRF-10P%), and CRF with 30% P reduction (CRF-30P%). Results showed that novel fertilizers and P reduction significantly reduced concentrations of total phosphorus (TP), dissolved phosphorus (DP), and particulate phosphorus (PP) in surface water and leachate. The first 5 days after basal fertilization and heavy rainfall were high-risk periods for P loss. Rainfall increased TP concentrations by 417.74%–432.86% and 94.85%–351.35% in surface water and leachate, respectively; DP increased by 120.80%–322.44%, and PP by 280.66%–501.77% and 80.23%–297.55%. Compared with ZYF, SRF, XJT, and CRF reduced TP loss by 15.43%–33.95%, with SRF showing the lowest loss. Under P reduction, CRF-10P% and CRF-30P% reduced TP loss by 31.48% and 37.04%, respectively, with CRF-30P% achieving the lowest loss. Notably, CRF-10P% increased rice yield by 22.37% relative to ZYF, indicating that moderate P reduction with enhanced loss-controlled fertilizer can maintain or increase yield while reducing environmental risk. The study concludes that CRF-10P% offers a promising strategy for sustainable rice production in the Chaohu Lake watershed.

SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3817-3

Ultra-robust Y-doped hafnium oxide ferroelectric memristors for intelligent edge computing

The rapid development of artificial intelligence (AI) and big data-driven edge intelligence applications has created an urgent demand for highly efficient computing hardware. Ferroelectric memristors have emerged as promising candidates for edge hardware due to their multi-level conductance tunability and high integration potential. In this work, we fabricated yttrium-doped hafnium oxide (YHO) memristors with a remanent polarization of ~30 μC/cm2, a multi-level resistive state retention time of approximately 10^5 s, and an endurance of up to 10^9 cycles. Based on this device, we constructed a real-time path-tracking system for intelligent vehicles—which achieves 100% path recognition accuracy—and a traffic sign denoising network optimized for hardware mapping via a hierarchical mixed-precision quantization strategy; this network yields denoised images with a peak signal-to-noise ratio (PSNR) of 27.04 and a structural similarity index measure (SSIM) of 0.80. This work paves an innovative pathway for the practical application of hafnium-based ferroelectric memristors, accelerating the development of highly efficient hardware for edge intelligence.

SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3963-5

Review on in-situ active modulation technology in metal additive manufacturing processes

Metal additive manufacturing (MAM) enables integrated one-piece fabrication of parts, high material utilization efficiency, and unparalleled design freedom. However, problems such as low production efficiency, difficulties in ensuring quality stability and defect control limit the large-scale industrial application of AM. In-situ active modulation for AM enables dynamic regulation of parts during the fabrication process, thereby enhancing the quality of the final fabricated parts without introducing extra processing steps. In-situ active regulation enables direct intervention during defect nucleation, providing better effectiveness than post-printing repairs while avoiding performance degradation risks associated with post-processing. Based on the difference of core factors directly affected during regulation, in-situ active regulation is categorized into the following. (1) Process and path parameter optimization, where regulation directly impacts manufacturing-related procedural rules. It is the simplest method of control and the preferred approach, with widespread attention focused on its effects on microstructure and mechanical properties. (2) Laser beam shaping, where regulation directly influences the energy carrier morphology. To address issues such as edge over-melting and localized energy deficiency caused by non-uniform energy distribution, laser beam shaping should be employed. (3) Additional physical field modulation achieved by superimposing supplementary physical fields. When optimal process and path parameters still fail to obtain the desired microstructure and mechanical properties, additional physical field control may be considered. Meanwhile, this work summarized the effects of different additional physical fields on the mechanical properties of various metallic base materials. The future trends of in-situ modulation in additive manufacturing are also discussed.

Environmental Chemistry2026DOI: 10.7524/j.issn.0254-6108.2025031905

Assessment and Source Analysis of Soil Heavy Metal Pollution under Different Land Use Types in the Yixun River Basin

Land use types profoundly influence the accumulation, speciation, and ecological risk of heavy metals through differences in human activity intensity, pollution input pathways, and soil self-regulation capacity. This study investigated soils of different land use types in Longhua County, downstream of the Yixun River Basin, central Chengde City, Hebei Province. Using the Nemerow Index and Potential Ecological Risk Index, the overall regional pollution was mild (Pn=1.65) with low ecological risk (RI=121.17). Main pollutants were Cd, Pb, Zn, and Hg, with Cd and Hg as primary ecological risk factors. Construction land exhibited moderate pollution and medium risk, with a Nemerow Index of 2.37 and average RI of 190.78, significantly exceeding other land use types. PMF model identified four pollution sources: pedogenic parent material natural source (43.54% contribution) dominating Cr, Cu, Ni, Zn enrichment; metallogenic parent material natural source (19.88%) controlling Cd spatial differentiation; agricultural-transportation mixed source (24.79%) driving As and Pb accumulation; and industrial source (11.93%) causing local Hg enrichment. Natural sources contributed 63.42% of total heavy metals, being the primary contributor. As was generally below background values, not constituting pollution; Pb exceeded standards but posed low ecological risk; industrial Hg enrichment in construction land presented high pollution and ecological risk, requiring priority control.

Journal of Fuel Chemistry and Technology2026DOI: 10.1016/S1872-5813(26)60664-0

Switching Hydrogenation Pathways of Furfural via Reduction-Degree Engineering of Ni-Based Catalysts

The selective hydrogenation of biomass-derived furfural (FAL) to high-value chemicals such as furfuryl alcohol (FOL) or tetrahydrofurfuryl alcohol (HFOL) is pivotal yet challenging due to the need for precise control over reaction pathways. In this study, a Ni2Al-LDO (layered double oxide) catalyst with highly dispersed surface NiO was synthesized via structural topological transformation of layered double hydroxides. The catalyst exhibited excellent performance in furfural hydrogenation, achieving a 91.42% yield of FOL at 160 °C and 1.4 MPa H2. Gradual reduction of Ni2Al-LDO produced Ni/NiO mixtures, enabling a tunable shift from FOL to HFOL as NiO content decreased and metallic Ni content increased. After reduction at 700 °C for 2 hours, the HFOL yield reached 93.95% under identical conditions. CO2-TPD, NH3-TPD, and FT-IR analyses revealed that variations in reduction degree influenced furfural adsorption behavior. NiO species selectively adsorb the C=O group of furfural, with isopropanol serving as the hydrogen source via the Meerwein-Ponndorf-Verley (MPV) pathway, yielding FOL. In contrast, metallic Ni0 surfaces facilitate flat adsorption, enabling simultaneous activation of both the furan ring and carbonyl group, and can activate both H2 and isopropanol, with H2 as the primary hydrogen source, leading to complete hydrogenation to HFOL. This work elucidates a clear structure-activity relationship centered on the metal oxidation state and provides a practical reduction-engineering approach for designing adaptable catalysts in biomass upgrading.