Zhiyong Liu
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Zhiyong Liu has a total of 266 co-authors. Here are the top co-authors by number of shared publications:
- Xuhong Guo
East China University of Science and Technology
49 shared publications Jianning Wu
School of Chemistry and Chemical Engineering, Shihezi University/Key Laboratory of Silicon Chemical New Materials, Shihezi, Xinjiang, 832003, P. R. China
42 shared publicationsGuihua Meng
26 shared publicationsYixi Wang
School of Chemistry and Chemical Engineering, Shihezi University, Key Laboratory for Green Processing of Chemical Engineering of Xinjiang Bingtuan, Key Laboratory of Materials-Oriented Chemical Engineering of Xinjiang Uygur Autonomous Region, Engineering Research Center of Materials-Oriented Chemical Engineering of Xinjiang Bingtuan, Shihezi, Xinjiang, China
14 shared publicationsLin Cui
School of Medicine Shihezi University Shihezi 832003 P. R. China
13 shared publicationsShengchao Yang
School of Chemistry and Chemical Engineering, Shihezi University/Key Laboratory of Silicon Chemical New Materials, Shihezi, Xinjiang, 832003, P. R. China
12 shared publications
Latest Publications
- 21 March 2026
- Published by Elsevier in Phytomedicine
- Vol. 155, 158098
Alisol B as a novel inhibitor of TβRs suppresses the growth and metastasis of non-small cell lung cancer by inhibiting TGF-β-induced epithelial-mesenchymal transition
- 21 March 2026
- Published by Elsevier in Phytomedicine
- Vol. 155, 158098
Alisol B as a novel inhibitor of TβRs suppresses the growth and metastasis of non-small cell lung cancer by inhibiting TGF-β-induced epithelial-mesenchymal transition
- 16 March 2026
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry A
- Vol. 14 (27) , 17550-17560
PPy-MOF-303@SA aerogel composite adsorbent with vertical channels for atmospheric water harvesting in arid environments: preparation and performance evaluation
PPy-MOF-303@SA aerogel, fabricated via directional freezing, combines alginate, MOF-303, and polypyrrole. It achieves 0.39 g·g −1 uptake at 25 °C and 30% RH in 60 min, with 96.73% desorption under 1 kW·m −2 solar irradiation.
- 16 March 2026
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry A
- Vol. 14 (27) , 17550-17560
PPy-MOF-303@SA aerogel composite adsorbent with vertical channels for atmospheric water harvesting in arid environments: preparation and performance evaluation
PPy-MOF-303@SA aerogel, fabricated via directional freezing, combines alginate, MOF-303, and polypyrrole. It achieves 0.39 g·g −1 uptake at 25 °C and 30% RH in 60 min, with 96.73% desorption under 1 kW·m −2 solar irradiation.
- 13 March 2026
- Published by Springer Nature in Carbon Letters
- Vol. 36 (2) , 705-719
Electron transport channel-mediated Z-type α-MnO2/Cd1.7In2S4.7 heterojunction for photocatalytic conversion of 5-hydroxymethylfurfural to 2,5-dicarbonylfuran
- 13 March 2026
- Published by Springer Nature in Carbon Letters
- Vol. 36 (2) , 705-719
Electron transport channel-mediated Z-type α-MnO2/Cd1.7In2S4.7 heterojunction for photocatalytic conversion of 5-hydroxymethylfurfural to 2,5-dicarbonylfuran
- Open Access
- 24 February 2026
- Published by Elsevier in SSRN Electronic Journal
Design of an LSPR‑Driven Hollow Cu2-xS@ZnIn2S4 Heterojunction for Synergistic Photothermal‑Photocatalytic Hydrogen Evolution
To address the challenges of insufficient near-infrared light utilization and rapid charge recombination in traditional photocatalysts, this study designed and synthesized a hollow-structured Cu2-xS@ZnIn2S4 S‑scheme heterojunction with synergistic photothermal‑photocatalytic properties. The synergistic mechanism between plasmonic photothermal effects and heterojunction charge‑transfer in broad‑spectrum catalysis was systematically elucidated. Experimental results demonstrated that the composite achieved a hydrogen evolution rate of 32.58 mmol·g⁻1·h⁻1 under AM 1.5G irradiation without cooling water (WCW), which is 3.00 times that of pure ZnIn2S4. Moreover, the solution temperature reached 47.4 ℃ under near‑infrared (NIR) illumination. Theoretical analysis revealed that the localized surface plasmon resonance (LSPR) of Cu2‑xS extends light absorption into the NIR region and generates a photothermal effect. Meanwhile, the S‑scheme band alignment, together with multiple light scattering induced by the hollow structure, synergistically optimizes carrier separation and promotes directional charge migration. The catalyst exhibited excellent stability over 750 min and demonstrated measurable NIR‑driven activity at wavelengths above 800 nm. By coupling band‑engineering with photothermal conversion, this work provides a theoretical foundation and a material prototype for designing efficient full‑spectrum solar‑to‑hydrogen conversion systems, showing clear application potential in photothermal‑assisted artificial photosynthesis.
- 24 February 2026
- Published by Elsevier in SSRN Electronic Journal
Open AccessDesign of an LSPR‑Driven Hollow Cu2-xS@ZnIn2S4 Heterojunction for Synergistic Photothermal‑Photocatalytic Hydrogen Evolution
To address the challenges of insufficient near-infrared light utilization and rapid charge recombination in traditional photocatalysts, this study designed and synthesized a hollow-structured Cu2-xS@ZnIn2S4 S‑scheme heterojunction with synergistic photothermal‑photocatalytic properties. The synergistic mechanism between plasmonic photothermal effects and heterojunction charge‑transfer in broad‑spectrum catalysis was systematically elucidated. Experimental results demonstrated that the composite achieved a hydrogen evolution rate of 32.58 mmol·g⁻1·h⁻1 under AM 1.5G irradiation without cooling water (WCW), which is 3.00 times that of pure ZnIn2S4. Moreover, the solution temperature reached 47.4 ℃ under near‑infrared (NIR) illumination. Theoretical analysis revealed that the localized surface plasmon resonance (LSPR) of Cu2‑xS extends light absorption into the NIR region and generates a photothermal effect. Meanwhile, the S‑scheme band alignment, together with multiple light scattering induced by the hollow structure, synergistically optimizes carrier separation and promotes directional charge migration. The catalyst exhibited excellent stability over 750 min and demonstrated measurable NIR‑driven activity at wavelengths above 800 nm. By coupling band‑engineering with photothermal conversion, this work provides a theoretical foundation and a material prototype for designing efficient full‑spectrum solar‑to‑hydrogen conversion systems, showing clear application potential in photothermal‑assisted artificial photosynthesis.
- 4 February 2026
- Published by Springer Nature in Carbon Letters
- Vol. 36 (1) , 423-440
Synthesis and antitumor efficacy of biodegradable hollow mesoporous carbon nanocarriers
- 4 February 2026
- Published by Springer Nature in Carbon Letters
- Vol. 36 (1) , 423-440
Synthesis and antitumor efficacy of biodegradable hollow mesoporous carbon nanocarriers
- 16 January 2026
- Published by Elsevier in Journal of Colloid and Interface Science
- Vol. 709, 139920
Bimetallic plasmonic thermo-cycling driven by strong interfacial coupling in dual-hollow structure for enhanced photothermal hydrogen production
- 16 January 2026
- Published by Elsevier in Journal of Colloid and Interface Science
- Vol. 709, 139920
Bimetallic plasmonic thermo-cycling driven by strong interfacial coupling in dual-hollow structure for enhanced photothermal hydrogen production
- 1 December 2025
- Published by Pleiades Publishing Ltd in Polymer Science, Series B
- Vol. 67 (6) , 31
Chain Extension of PDLLA with 4,4'-Methylene diphenyl diisocyanate and Its Degradation Performance
In this paper, PDLLA was end-capped with 1,4-butanediol to control hydroxyl groups, ensuring a 1 : 1 NCO/OH ratio for MDI chain extension.The chemical degradation, hydrolytic stability, and thermal and mechanical properties of poly(D,L-lactic acid) (PDLLA), as well as its extended polymer obtained by reacting with 4,4'-methylene diphenyl diisocyanate (MDI), were improved. The resulting samples were characteriяed by Fourier transform infrared spectroscopy (FTIR). Thermal properties were measured using differential scanning calorimetry and thermogravimetric analysis. Tensile properties were also measured with a tensile tester. Results showed that when the molar ratio of NCO/OH was 1 : 1, T g can be increased from the original 54 to 60°C. The weight loss temperature of 4,4'-methylene diphenyl diisocyanate chaining PDLLA was also enhanced from 10 to 190°C. Tensile strength increased from 19.00 to 39.00 MPa. Hydrolytic stability was approximately 1.5 times that of pure PDLLA. In this manner, PDLLA materials with excellent mechanical properties, thermal stability, and degradation resistance of poly(lactic acid) material were easily obtained.
- 1 December 2025
- Published by Pleiades Publishing Ltd in Polymer Science, Series B
- Vol. 67 (6) , 31
Chain Extension of PDLLA with 4,4'-Methylene diphenyl diisocyanate and Its Degradation Performance
In this paper, PDLLA was end-capped with 1,4-butanediol to control hydroxyl groups, ensuring a 1 : 1 NCO/OH ratio for MDI chain extension.The chemical degradation, hydrolytic stability, and thermal and mechanical properties of poly(D,L-lactic acid) (PDLLA), as well as its extended polymer obtained by reacting with 4,4'-methylene diphenyl diisocyanate (MDI), were improved. The resulting samples were characteriяed by Fourier transform infrared spectroscopy (FTIR). Thermal properties were measured using differential scanning calorimetry and thermogravimetric analysis. Tensile properties were also measured with a tensile tester. Results showed that when the molar ratio of NCO/OH was 1 : 1, T g can be increased from the original 54 to 60°C. The weight loss temperature of 4,4'-methylene diphenyl diisocyanate chaining PDLLA was also enhanced from 10 to 190°C. Tensile strength increased from 19.00 to 39.00 MPa. Hydrolytic stability was approximately 1.5 times that of pure PDLLA. In this manner, PDLLA materials with excellent mechanical properties, thermal stability, and degradation resistance of poly(lactic acid) material were easily obtained.
- 22 November 2025
- Published by American Chemical Society (ACS) in ACS Applied Materials & Interfaces
- Vol. 18 (2) , 3723-3730
Micro/Nano-Crystal 3D Growth on Graphene Oxide Plates for a Bioinspired Air–Water Harvester
Water-augmentation materials have drawn more attention recently. Here, a micro/nano-NaCl-crystal 3D growth on graphene oxide plates (GONC) is designed and synthesized by using anticaking agents. After thermal reduction, it was found that rGONC particles formed an alternating hydrophilic/hydrophobic micro/nanostructure, where NaCl functions as a hydrophilic region, while rGO acts as a hydrophobic region. This structure is similar to the surface microstructure of desert beetles for efficient water vapor harvesting. It was shown to deliquesce at lower environmental 58-62% RH than RHd, ∼75% RH of NaCl, and form larger water droplets, ∼4-7 times its original measured area. These are attributed to the synergistic water-molecule-gathering effects from the surface energy gradient (F, ∼9.86 × 10-8 N) of the bioinspired nanostructure and vapor pressure gradient (F', ∼1.59 × 10-9 N) of NaCl deliquescence. The benefits of rGONC particles for water vapor harvesters are verified through in situ observation under environmental scanning electron microscopy (E-SEM) at the microscale and by 3D environment chamber experiments at the macroscale. The excellent and consistent performances positively corroborate its promising application to solve the present major environmental concern from smog/fog as an effective water-augmentation technology.
- 22 November 2025
- Published by American Chemical Society (ACS) in ACS Applied Materials & Interfaces
- Vol. 18 (2) , 3723-3730
Micro/Nano-Crystal 3D Growth on Graphene Oxide Plates for a Bioinspired Air–Water Harvester
Water-augmentation materials have drawn more attention recently. Here, a micro/nano-NaCl-crystal 3D growth on graphene oxide plates (GONC) is designed and synthesized by using anticaking agents. After thermal reduction, it was found that rGONC particles formed an alternating hydrophilic/hydrophobic micro/nanostructure, where NaCl functions as a hydrophilic region, while rGO acts as a hydrophobic region. This structure is similar to the surface microstructure of desert beetles for efficient water vapor harvesting. It was shown to deliquesce at lower environmental 58-62% RH than RHd, ∼75% RH of NaCl, and form larger water droplets, ∼4-7 times its original measured area. These are attributed to the synergistic water-molecule-gathering effects from the surface energy gradient (F, ∼9.86 × 10-8 N) of the bioinspired nanostructure and vapor pressure gradient (F', ∼1.59 × 10-9 N) of NaCl deliquescence. The benefits of rGONC particles for water vapor harvesters are verified through in situ observation under environmental scanning electron microscopy (E-SEM) at the microscale and by 3D environment chamber experiments at the macroscale. The excellent and consistent performances positively corroborate its promising application to solve the present major environmental concern from smog/fog as an effective water-augmentation technology.
- 9 August 2025
- Published by Springer Nature in Journal of Materials Science
- Vol. 60 (34) , 15127-15139
3D porous MXene/RGO aerogels induced by template method for high-capacity supercapacitors
- 9 August 2025
- Published by Springer Nature in Journal of Materials Science
- Vol. 60 (34) , 15127-15139
3D porous MXene/RGO aerogels induced by template method for high-capacity supercapacitors