Jiaqiang Wang
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Jiaqiang Wang has a total of 300 co-authors. Here are the top co-authors by number of shared publications:
Daomei Chen
24 shared publicationsJiao He
School of Chemical Sciences and Technology, School of Materials and Energy, Yunnan Province Engineering Research Center of Photocatalytic Treatment of Industrial Wastewater, School of Engineering, National Center for International Research on Photoelectric and Energy Materials, Yunnan University, Kunming 650091, P. R. China; Institute of Frontier Technologies in Water Treatment Co., Ltd., Kunming, 650503, P. R. China
22 shared publicationsLiang Jiang
School of Chemical Sciences and Technology, Yunnan Province Engineering Research Center of Photocatalytic Treatment of Industrial Wastewater
20 shared publications- Zhiying Yan
School of Chemical Sciences & Technology, Yunnan University, Kunming 650091, China
17 shared publications - Jiao He
School of Chemical Sciences & Technology, Yunnan University, Kunming 650091, China
15 shared publications Yongjuan Chen
14 shared publications
Latest Publications
- 17 July 2026
- Published by Elsevier in Journal of Environmental Chemical Engineering
- Vol. 14  (5)
Ag@BiPO4/MXene derived from F-containing nitrobenzene wastewater for efficient photocatalytic production of H2O2
- 17 July 2026
- Published by Elsevier in Journal of Environmental Chemical Engineering
- Vol. 14  (5)
Ag@BiPO4/MXene derived from F-containing nitrobenzene wastewater for efficient photocatalytic production of H2O2
- 26 February 2026
- Published by American Chemical Society (ACS) in ACS Sustainable Chemistry & Engineering
- Vol. 14  (9) , 4569-4582
MoS 2 -Decorated Solar Evaporation Aerogel with Sugarcane Vertically Aligned Channels for Water Desalination and Purification
- 26 February 2026
- Published by American Chemical Society (ACS) in ACS Sustainable Chemistry & Engineering
- Vol. 14  (9) , 4569-4582
MoS 2 -Decorated Solar Evaporation Aerogel with Sugarcane Vertically Aligned Channels for Water Desalination and Purification
- 9 October 2025
- Published by American Chemical Society (ACS) in Langmuir
- Vol. 41  (41) , 27868-27879
Urea-Assisted One-Step Pyrolytic Synthesis of Macroporous Carbon Aerogel/MgO Composites for Rapid Phosphate Recovery
Addressing global phosphorus scarcity and eutrophication, MgO-based adsorbents face challenges of slow kinetics and low active-site utilization. In this study, a waste biomass-derived carbon aerogel (CA) was used as a support for a one-step pyrolysis method, simultaneously constructing a porous structure and achieving high-dispersion MgO loading. Results showed a maximum adsorption capacity of 399.8 mg P/g. Kinetic studies indicated 165.4 mg P/g adsorbed within 5 min, with 90% saturation achieved within 40 min. The Pseudo-second-order kinetic constants increased 11-fold compared to commercial MgO. By integrating experiments, machine learning (ML), and density functional theory (DFT), a multiscale investigation revealed the synergistic effect between MgO and the carbon aerogel support. It was demonstrated that the rapid adsorption kinetics originated from the macroporous structure of the support rather than a high specific surface area. Furthermore, urea participation during pyrolysis modulated the pyridinic-N content of the CA, thereby modifying the pH adaptability of the material. Collectively, this study provides a foundation for reusing waste biochar and designing high-performance phosphate adsorbents.
- 9 October 2025
- Published by American Chemical Society (ACS) in Langmuir
- Vol. 41  (41) , 27868-27879
Urea-Assisted One-Step Pyrolytic Synthesis of Macroporous Carbon Aerogel/MgO Composites for Rapid Phosphate Recovery
Addressing global phosphorus scarcity and eutrophication, MgO-based adsorbents face challenges of slow kinetics and low active-site utilization. In this study, a waste biomass-derived carbon aerogel (CA) was used as a support for a one-step pyrolysis method, simultaneously constructing a porous structure and achieving high-dispersion MgO loading. Results showed a maximum adsorption capacity of 399.8 mg P/g. Kinetic studies indicated 165.4 mg P/g adsorbed within 5 min, with 90% saturation achieved within 40 min. The Pseudo-second-order kinetic constants increased 11-fold compared to commercial MgO. By integrating experiments, machine learning (ML), and density functional theory (DFT), a multiscale investigation revealed the synergistic effect between MgO and the carbon aerogel support. It was demonstrated that the rapid adsorption kinetics originated from the macroporous structure of the support rather than a high specific surface area. Furthermore, urea participation during pyrolysis modulated the pyridinic-N content of the CA, thereby modifying the pH adaptability of the material. Collectively, this study provides a foundation for reusing waste biochar and designing high-performance phosphate adsorbents.
- 2 September 2025
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 61  (79) , 15457-15460
Accelerated sonochemical fabrication of a polydopamine@COF hierarchical structure for boosting H2O2 photosynthesis
A core–shell structured polydopamine@covalent organic framework (PDA@COF) was rapidly constructed via a facile sonochemical strategy. The resulting organic heterostructure exhibited excellent photocatalytic activity for H2O2 production.
- 2 September 2025
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 61  (79) , 15457-15460
Accelerated sonochemical fabrication of a polydopamine@COF hierarchical structure for boosting H2O2 photosynthesis
A core–shell structured polydopamine@covalent organic framework (PDA@COF) was rapidly constructed via a facile sonochemical strategy. The resulting organic heterostructure exhibited excellent photocatalytic activity for H2O2 production.
- 23 August 2025
- Published by Elsevier in Environmental Research
- Vol. 285  (Pt 5) , 122677
Synthesis and highly selective adsorption of hydroxyapatite in situ self-Co-doped by magnesium-fluorine in phosphate tailings
- 23 August 2025
- Published by Elsevier in Environmental Research
- Vol. 285  (Pt 5) , 122677
Synthesis and highly selective adsorption of hydroxyapatite in situ self-Co-doped by magnesium-fluorine in phosphate tailings
- 16 June 2025
- Published by Elsevier in Journal of Hazardous Materials
- Vol. 495, 138874
Chlorophyll-regulated BiOBr (110) facets for enhanced photocatalytic coupling of secondary amines and methamphetamine detoxification
- 16 June 2025
- Published by Elsevier in Journal of Hazardous Materials
- Vol. 495, 138874
Chlorophyll-regulated BiOBr (110) facets for enhanced photocatalytic coupling of secondary amines and methamphetamine detoxification
- Open Access
- 27 March 2025
- Published by MDPI AG in Nanomaterials
- Vol. 15  (7) , 504
TiO2 Decorated onto Three-Dimensional Carbonized Osmanthus Fragrans Leaves for Solar-Driven Clean Water Generation
Solar steam generation (SSG) has garnered significant attention for its potential in water purification applications. While composites with physically combined structures based on semiconductors or biomass have been developed for SSG, there remains a critical need for low-cost, high-efficiency devices. In this study, TiO2 composites exhibiting excellent stability, high solar absorption, porous microstructure, and hydrophilic surfaces were identified as effective materials for SSG and water purification for the first time. A novel SSG device was designed by decorating TiO2 onto three-dimensional carbonized Osmanthus fragrans leaves (TiO2/carbonized OFL). Compared to directly carbonized OFL (without TiO2) and Osmanthus fragrans leaves with templated TiO2 (OFL-templated TiO2), the TiO2/carbonized OFL carbon composites demonstrated enhanced solar absorption, achieving over 99% in the visible region and more than 80% in the near-infrared region. Under solar illumination of 1 kW·m−2, the TiO2/carbonized OFL device achieved a high water evaporation rate of 2.31 kg·m−2·h−1, which is 1.6 times higher than that of carbonized OFL and 3.45 times higher than OFL-templated TiO2. Additionally, the TiO2/carbonized OFL system exhibited remarkable efficiency in treating pharmaceutical wastewater, with a chemical oxygen demand (COD) removal efficiency of 98.9% and an ammonia nitrogen removal efficiency of 90.8% under solar radiation.
- 27 March 2025
- Published by MDPI AG in Nanomaterials
- Vol. 15  (7) , 504
Open AccessTiO2 Decorated onto Three-Dimensional Carbonized Osmanthus Fragrans Leaves for Solar-Driven Clean Water Generation
Solar steam generation (SSG) has garnered significant attention for its potential in water purification applications. While composites with physically combined structures based on semiconductors or biomass have been developed for SSG, there remains a critical need for low-cost, high-efficiency devices. In this study, TiO2 composites exhibiting excellent stability, high solar absorption, porous microstructure, and hydrophilic surfaces were identified as effective materials for SSG and water purification for the first time. A novel SSG device was designed by decorating TiO2 onto three-dimensional carbonized Osmanthus fragrans leaves (TiO2/carbonized OFL). Compared to directly carbonized OFL (without TiO2) and Osmanthus fragrans leaves with templated TiO2 (OFL-templated TiO2), the TiO2/carbonized OFL carbon composites demonstrated enhanced solar absorption, achieving over 99% in the visible region and more than 80% in the near-infrared region. Under solar illumination of 1 kW·m−2, the TiO2/carbonized OFL device achieved a high water evaporation rate of 2.31 kg·m−2·h−1, which is 1.6 times higher than that of carbonized OFL and 3.45 times higher than OFL-templated TiO2. Additionally, the TiO2/carbonized OFL system exhibited remarkable efficiency in treating pharmaceutical wastewater, with a chemical oxygen demand (COD) removal efficiency of 98.9% and an ammonia nitrogen removal efficiency of 90.8% under solar radiation.
- Open Access
- 7 January 2025
- Published by MDPI AG in Nanomaterials
- Vol. 15  (2) , 80
One-Pot Synthesis and Enhanced Vis-NIR Photocatalytic Activity of NiTiO3/TiO2 Templated by Waste Tobacco Stem-Silks
Synthesis of the photocatalysts with near-infrared light response usually involves upconversion materials or plasmon-assisted noble metals. Herein, NiTiO3/TiO2 was synthesized by using waste tobacco stem-silks as biotemplates and tetra-tert-butyl orthotitanate and nickel nitrate as precursors in a one-pot procedure. NiTiO3(1.0)/TiO2(TSS) with a mass percent of Ni 1.0% exhibited very high visible-light photocatalytic efficiency in photodegradation of tetracycline hydrochloride (TC), which is 8.0 and 2.3 times higher than TiO2 prepared without templates and TiO2(TSS) prepared without Ni, respectively. Interestingly, NiTiO3(1.5)/TiO2(TSS) even exhibited good activity under NIR light (λ = 840~850 nm) without upconversion materials or plasmon-assisted noble metals, which is 2.8 and 2.2 times than TiO2 prepared without templates and TiO2(TSS), respectively. The boosting photocatalytic activity has been shown to be attributed to efficient charge separation and transfer across a direct Z-scheme heterojunction between NiTiO3 and TiO2 and enhanced light-harvesting ability of special flaky structure reduplicated from tobacco stem-silks. This reported strategy provides a new idea for the multifunctional utilization of waste tobacco stem-silks and the synthesis of novel photocatalysts for the potential application in wastewater treatment.
- 7 January 2025
- Published by MDPI AG in Nanomaterials
- Vol. 15  (2) , 80
Open AccessOne-Pot Synthesis and Enhanced Vis-NIR Photocatalytic Activity of NiTiO3/TiO2 Templated by Waste Tobacco Stem-Silks
Synthesis of the photocatalysts with near-infrared light response usually involves upconversion materials or plasmon-assisted noble metals. Herein, NiTiO3/TiO2 was synthesized by using waste tobacco stem-silks as biotemplates and tetra-tert-butyl orthotitanate and nickel nitrate as precursors in a one-pot procedure. NiTiO3(1.0)/TiO2(TSS) with a mass percent of Ni 1.0% exhibited very high visible-light photocatalytic efficiency in photodegradation of tetracycline hydrochloride (TC), which is 8.0 and 2.3 times higher than TiO2 prepared without templates and TiO2(TSS) prepared without Ni, respectively. Interestingly, NiTiO3(1.5)/TiO2(TSS) even exhibited good activity under NIR light (λ = 840~850 nm) without upconversion materials or plasmon-assisted noble metals, which is 2.8 and 2.2 times than TiO2 prepared without templates and TiO2(TSS), respectively. The boosting photocatalytic activity has been shown to be attributed to efficient charge separation and transfer across a direct Z-scheme heterojunction between NiTiO3 and TiO2 and enhanced light-harvesting ability of special flaky structure reduplicated from tobacco stem-silks. This reported strategy provides a new idea for the multifunctional utilization of waste tobacco stem-silks and the synthesis of novel photocatalysts for the potential application in wastewater treatment.