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Verified CAS / Academic Author9 Decoded Studies

Prof. ZHOU Weilong

University of Jinan, Institute for Advanced Interdisciplinary Research (iAIR)

Co-Affiliations:Institute for Advanced Interdisciplinary Research, University of JinanMinistry of Education Key Laboratory of Integrated Regulation and Resource Development on Shallow Lakes, Hohai University, Nanjing 210098, ChinaBeijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, ChinaSchool of Materials Science and Engineering, Kunming University of Science and TechnologySouth China University of Technology

Research Publications & English Decoded Briefs

Showing 9 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-026-4275-3

Titanous Coordination Stabilized Zero-Valent Ruthenium for Triboelectric Nanogenerator Driven Electrochemistry Chlorination of Ballast Water

Electrochemical in-situ production of active chlorine (AC) via chlorine evolution reaction (CER) can alleviate hull corrosion and residual chlorine overage, which is a highly reliable disinfectant for sewage and ballast water. Nonetheless, the primarily competitive oxygen evolution reaction and gradual anode passivation hinder its practical application. Herein, we employed the in-situ hydrothermal strategy to synthesize Ru/TiO2-x to realize high activity and selectivity of CER. The robust interaction of Ru sites and TiO2-x achieved via a one-step hydrothermal synthesis strategy, the structural and valence state characterizations confirm that Ti3+ stabilizes Ru solely in the metallic state (Ru0) via structural confinement effects, effectively inhibiting catalyst oxidation. As a result, the Ru/TiO2-x requires only an overpotential of 33 mV to reach 10 mA cm−2, and possess strong catalytic durability, sustaining continuous operation for 100 h with negligible current decay. Further integration with a triboelectric nanogenerators successfully realizes the generation of AC, which demonstrates a >99.9% inactivation efficiency against Escherichia coli in simulated seawater environments, while also effectively degrading ammonia nitrogen and urea contaminants in domestic wastewater.

SCIENCE CHINA Materials2026DOI: 10.1007/s40843-026-4246-5

Efficient green-solvent, additive-free and post-treatment-free organic solar cells enabled by dithiazolobenzotriazole-based polymer donors

Developing organic solar cells (OSCs) processable from green solvents without additives or post-treatments is essential for sustainable manufacturing, yet high power conversion efficiency (PCE) remains difficult due to limited morphology control. Herein, we develop a new electron-deficient building block, dithiazolo[4',5':3,4;5'',4'':5,6]benzo[1,2-d][1,2,3]triazole (DTzBT), which fuses benzo[d][1,2,3]triazole (BTA) with thiazole to leverage S/N-mediated non-covalent interactions, enhance planarity and lower the HOMO. To isolate side-chain effects, two DTzBT-based donors, namely PTzMe-F (N-methyl) and PTzEH-F (N-2-ethylhexyl), have been designed and synthesized. PTzMe-F exhibits poor solubility and miscibility with L8-BO, yielding 2.64% PCE (chloroform). PTzEH-F exhibits excellent processability and favorable morphology, delivering 17.61% PCE (chloroform) and 19.17% as-cast from toluene without any additive or post-treatments. In addition, the ternary LbL device based on PTzEH-F/L8-BO:PC71BM achieved an impressive efficiency of 20.27%. Comprehensive characterization indicates that 2-ethylhexyl side chains afford optimal solubility while preserving strong intermolecular interactions and favorable phase separation. DTzBT mitigates BTA’s HOMO-raising tendency via electron-withdrawing thiazole fusion, reconciling aggregation tunability with energy-level control. These results show that precise backbone and side-chain co-design enables green-solvent, additive-free processing for high-performance OSCs, advancing sustainable photovoltaic manufacturing.

SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3617-x

Magnetoelectric-bioactive dual functions of MXene regulate macrophage M1-M2 sequential polarization to promote healing of infected wound

Macrophages are pivotal in infection resolution and tissue repair via dynamic M1-to-M2 phenotypic polarization. Although various nano-biomaterials can modulate macrophage polarization, achieving sequential M1-to-M2 transition using a single nanoformulation remains challenging. Here, we propose a strategy employing transition metal carbide/nitride (MXene) nanosheets, internalized by macrophages, as the sole regulator to induce sequential polarization. Under a rotating magnetic field, the high electrical conductivity and magnetoelectric activity of endocytosed MXene generate electrical signals and reactive oxygen species (ROS), driving M1 polarization. Upon magnetic field removal, the inherent bioactivity of MXene facilitates repolarization to the M2 phenotype. Mechanistically, this transition involves inhibition of the NF-κB signaling pathway and activation of the JAK-STAT signaling pathway. In vivo, MXene nanosheets under on-off rotating magnetic field stimulation enabled sequential M1-to-M2 polarization, promoting bacterial clearance and tissue regeneration in infected wounds. This two-step sequential strategy targeting macrophages offers a promising therapeutic approach for infected wound healing.

SCIENCE CHINA Materials2026DOI: 10.1007/s40843-025-3785-5

Redox dual-cocatalysts modified ZnIn2S4 hollow sphere with spatially separated carrier for photocatalytic H2 production coupled with selective benzyl alcohol oxidation

The effective separation and utilization of photo-generated carriers are critical for advancing photocatalysis, particularly in coupled reactions of H2 production and value-added chemical synthesis. Here, a sandwich-structured MnO2@ZnIn2S4@Ti3C2 hollow sphere was designed, with MnO2 and Ti3C2 loaded on the inner and outer surfaces of ZnIn2S4, respectively. MnO2 acts as an oxidation cocatalyst collecting photo-generated holes, while Ti3C2 serves as a reduction cocatalyst for electrons, promoting spatial separation of carriers and enabling spatially separated redox reactions. The hollow structure enhances light harvesting. The optimal catalyst achieves photocatalytic H2 production rate of 6.29 mmol g−1 h−1 and benzaldehyde production rate of 5.26 mmol g−1 h−1 from benzyl alcohol oxidation, significantly outperforming ZnIn2S4, MnO2@ZnIn2S4, and ZnIn2S4@Ti3C2. In situ irradiated X-ray photoelectron spectroscopy confirms effective carrier separation. In situ electron paramagnetic resonance and diffuse reflectance infrared Fourier transform spectroscopy reveal reaction intermediates. This work provides a strategy for designing efficient photocatalysts for coupled H2 production and selective oxidation.

Journal of Environmental Engineering Technology2026DOI: 10.13205/j.hjgc.202604014

CFD-Based Investigation of Ice Slurry Pigging and Optimization of Cleaning Parameters

Ice slurry pigging is an emerging technology for cleaning water supply pipelines, yet quantitative understanding of its cleaning mechanisms and optimal operating conditions remains limited. This study developed a computational fluid dynamics (CFD) model integrating the kinetic theory of granular flows (KTGF), the Euler-Euler method, and the shear stress transport (SST) model to simulate ice slurry flow and wall shear stress distribution. The model was validated against experimental data, showing a 6.4% error in particle concentration distribution, a 3.3% average error in solid-phase velocity in the mainstream region, and a pressure drop error within 20%. A total of 125 simulations were performed under varying initial concentrations (20%–60%), particle diameters (0.3–1.0 mm), and flow velocities (0.2–1.0 m/s). Results indicate that higher initial concentrations (60%) achieve effective cleaning of both upper and lower pipe walls, with an effective shear stress ratio of 77.39%. Larger particles exhibit pronounced upward movement, increasing non-uniformity in solid distribution. Flow velocity is the dominant factor affecting wall shear stress; at 1.0 m/s, the effective shear stress ratio reaches 83.16%. The optimal parameters for cumulative shear stress were identified as 50% initial concentration, 0.5 mm particle diameter, and 1.0 m/s flow velocity, yielding an average cumulative shear stress of 11.59 Pa·s. For effective cumulative shear stress, the same parameters produced 9.89 Pa·s, while the highest effective shear stress ratio (88.50%) was achieved with 0.3 mm particles at 1.0 m/s and 50% concentration. This research provides theoretical guidance for ice slurry pigging operations in water supply pipelines.

SCIENCE CHINA Materials2025DOI: 10.1007/s40843-025-3366-9

Organic Solar Cells Surpassing 20% Power Conversion Efficiency: Material Innovations, Device Engineering, and Pathways to Flexible Power Suppliers

Organic solar cells (OSCs) have transitioned from <1% initial power conversion efficiency (PCE) to a benchmark exceeding 20% in single-junction and tandem architectures, marking a critical milestone for solution-processable photovoltaics. This review consolidates recent reports (2022–2025) on OSCs with PCE >20%, analyzing key strategies: photoactive material innovation (wide-bandgap polymer donors, narrow-bandgap non-fullerene acceptors), multi-component system construction, deposition protocol optimization, solid/solvent additive engineering, and hole/electron transport layer development. Empirical data from 15 high-impact studies reveal PCEs of 20.0–20.6% in single-junction devices and 20.2–26% in perovskite/organic tandem cells, with interfacial engineering (e.g., yttrium phosphotungstate, carbazole-modified 2PACz, naphthalene diimide interlayers) suppressing bimolecular recombination and enabling scalable large-area fabrication. Operational stability remains a bottleneck: amide-based cathode interlayers achieve 20% PCE with dual-modification mechanisms, while self-assembled monolayers enable hole transport layer-free devices with 18% efficiency and improved stability. The review identifies next-stage challenges: reducing voltage losses (to <0.5 V), scaling deposition uniformity beyond 100 cm², and achieving cost parity with silicon (<$0.30/Wp). These issues are critical for flexible and wearable power suppliers, where mechanical durability (<5% PCE degradation after 1000 bending cycles) and low-temperature processing (<150°C) are mandatory. The analysis provides a roadmap for industrial translation, emphasizing that material–device co-optimization, rather than isolated breakthroughs, will determine commercial viability.

SCIENCE CHINA Materials2025DOI: 10.1007/s40843-025-3423-6

Realizing high thermoelectric performance in copper sulfide via intermediate doping

Copper sulfide (Cu2−xS) is a low-cost, eco-friendly thermoelectric material, but its performance is limited by the trade-off between electrical conductivity and thermal conductivity. This study introduces an intermediate doping strategy using copper alloys (bronze, cupronickel, brass) to partially replace the copper source in Cu1.8S, addressing excessive Cu vacancies. The approach enhances the solubility limits of Zn, Sn, Pb, and Ni, optimizing carrier concentration, and generates in situ nanoscale second phases that scatter phonons. The optimal composition, Cu1.8S + 5 wt.% bronze + 3 wt.% cupronickel + 2 wt.% brass, achieves a ZT of 1.7 at 673 K, a 247% improvement over pristine Cu1.8S and the highest reported for this system. This work establishes intermediate doping as a viable paradigm for optimizing thermoelectric properties in alloy-based systems.

SCIENCE CHINA Materials2025DOI: 10.1007/s40843-025-3380-6

Enhancement of anomalous Hall effect in SrIrO3/NiCo2O4 heterostructures induced by interfacial charge transfer

The anomalous Hall effect (AHE) in strongly correlated transition metal oxide (TMO) systems provides a platform for investigating coupled spin, charge, orbital, and lattice degrees of freedom, and enables spin current-driven magnetization switching. However, enhancing the AHE in such systems remains a critical challenge. This work systematically investigates the electronic transport properties of SrIrO3/NiCo2O4 (SIO/NCO) heterostructures. The AHE of SIO/NCO heterostructures is enhanced by an order of magnitude compared to ferrimagnetic NCO single films. The enhancement becomes more pronounced as the SIO sublayer thickness decreases, which is attributed to large strain exacerbating interfacial charge transfer. X-ray photoelectron spectroscopy reveals variations in binding energies and concentrations of electronic states, confirming the charge transfer mechanism. The AHE in SIO/NCO heterostructures arises from the synergistic effect of the intrinsic mechanism dominated by Berry curvature and the extrinsic mechanism caused by impurity scattering. These findings advance the reliability of TMO-based spintronic devices.

SCIENCE CHINA Materials2025DOI: 10.1007/s40843-025-3529-7

Economical Approach to Thermoelectric Cooling: Development of Conductive Polyethylene/Polypyrrole@Constantan Composite Using Extensional Rheological Technology

Thermoelectric cooling offers a fluoride-free alternative to vapor compression refrigeration, yet commercial adoption is constrained by low figures of merit (ZT) and high material costs. This study reports an economical fabrication route for conductive polyethylene/polypyrrole@constantan (PE/[email protected]) composites via a self-created extensional rheological technology. Pyrrole monomers are polymerized on Ni0.49Cu0.59 particles and subsequently dispersed within a polyethylene matrix under an extensional flow field, forming a continuous conductive network. The resulting composite exhibits an electrical conductivity of 1699.8 S cm−2, a thermal conductivity of 13.9 W m−1 K−1, and a ZT of 0.16 at 25 °C. A thermoelectric device integrating PE/Ppy@iron achieved a temperature reduction of 0.4 °C under 30 V/0.3 A direct current. Square-wave pulsed current excitation stabilized the cooling efficiency at its optimum level, while a custom thermal insulation system mitigated parasitic heat loss, collectively yielding a total temperature reduction of 1.6 °C. These results demonstrate a scalable, low-cost pathway for thermoelectric cooling materials, with potential for large-scale commercialization.