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学者姓名：汪颖
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Abstract ：
The precise regulation of photocatalytic oxygen reduction reaction (ORR) pathways, particularly the more energy-efficient one-step 2e(-) route, is of fundamental importance for optimizing H2O2 production efficiency in rationally designed covalent organic frameworks (COFs). Here, a strengthened donor-acceptor (D-A) structured TPCN-COF [COF synthesized from 2,4,6-hydroxy-1,3,5-benzotricarboxaldehyde and 1,3,5-tris (4-aminophenyl) benzene] photocatalyst was developed through the strategic incorporation of pyridine nitrogen moieties into the COF skeleton. The strengthened D-A structure facilitates effective separation of photogenerated charge carriers while promoting rapid electron transfer kinetics. Concurrently, the introduced pyridine nitrogen units increase the surface polarity, thereby improving hydrophilicity and enabling more efficient proton delivery to active sites. Remarkably, the synergistic combination of enhanced charge separation and optimized proton transport in TPCN-COF effectively shifts the ORR mechanism from two-step 1e(-) pathway to one-step 2e(-) process. As a result, TPCN-COF achieves an exceptional H2O2 production rate of 1320.9 mu molg(-1)h(-1) under visible light irradiation (lambda >= 420 nm) in an air-equilibrated aqueous system, representing a nearly 3-fold enhancement compared to the unmodified TPCC-COF [COF synthesized from 2,4,6-hydroxy-1,3,5-benzotricarboxaldehyde and 5,5 ',5 ''- (benzene-1,3,5-triyl) tris (pyridin-2-ylamino)]. This work establishes an effective design strategy for constructing COFs photocatalysts with strong D-A structures, and elucidates the synergistic regulatory mechanism, by which both electronic structure and surface properties govern ORR pathway selectivity in COF-based systems.
Keyword ：
Covalent organic framework (COF) Covalent organic framework (COF) D-A structure D-A structure H2O2 preparation H2O2 preparation Photocatalysis Photocatalysis Reaction pathway Reaction pathway
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| GB/T 7714 | Wu, Jingyao , Zhao, Qiang , Lv, Yujing et al. Pyridine Nitrogen-modified Covalent Organic Frameworks for Photocatalytic One-step 2e- H2O2 Production [J]. | CHEMICAL RESEARCH IN CHINESE UNIVERSITIES , 2025 , 41 (4) : 822-830 . |
| MLA | Wu, Jingyao et al. "Pyridine Nitrogen-modified Covalent Organic Frameworks for Photocatalytic One-step 2e- H2O2 Production" . | CHEMICAL RESEARCH IN CHINESE UNIVERSITIES 41 . 4 (2025) : 822-830 . |
| APA | Wu, Jingyao , Zhao, Qiang , Lv, Yujing , Wang, Shuo , Wang, Pengzhao , Long, Jinlin et al. Pyridine Nitrogen-modified Covalent Organic Frameworks for Photocatalytic One-step 2e- H2O2 Production . | CHEMICAL RESEARCH IN CHINESE UNIVERSITIES , 2025 , 41 (4) , 822-830 . |
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Photocatalytic conversion of CO2 and H2O to high-value chemicals or fuels provides a crucial pathway for efficiently achieving the conversion and storage of solar-to-chemical energy; however, the overall efficiency is severely restricted by the spatial separation of photogenerated charges. The lifetime of charges in a photoexcited semiconductor particle is mismatched utterly with the rate of interfacial redox reactions, locking kinetically the target reactions. To maximize the availability of photogenerated charges for artificial photosynthesis, constructing various types of heterojunctions including Schottky, p-n, and Z/S-scheme is widely used to manipulate the directional migration of photogenerated charges toward surface active sites, where photoredox catalysis proceeds. Even so, it is unavoidable for the recombination of initially separated charges at the interfacial heterojunctions composed of several atomic layers with less than 1.0 nm thickness, where the Coulomb force remains dominant, leading to the quadratic loss of charges on the surface or interface of catalyst particles. How to eliminate the Coulomb confinement for charges has been a highly interesting topic and yet a formidable challenge in the domain of photocatalysis and solar energy conversion.In this Account, aiming to suppress the recombination of initially separated charges, we introduced a novel strategy of charge tunneling separation to design efficient artificial photosystems for CO2 conversion. An insulator is inserted between the semiconductor and metal to form the metal-insulator-semiconductor (MIS) structure, where the charge donor and acceptor are spatially separated by the insulating layer with a thickness of a few nanometers, different completely from the conventional Schottky junction with a direct contact M/S interface. Photoexcitation of the semiconductor unit generates a large population of hot electrons and holes, and then they immediately tunnel to the metal catalyst for redox reactions across the two M/I and I/S interfaces and the insulating layer. The tunneling separation proceeds within a few attoseconds at a mean free path. These tunneled electrons or holes are trapped, concentrated, and localized on the catalytic units consisting of metallic single atoms, nanoclusters (NCs), or nanoparticles (NPs), and thus the emphasis of this Account will be put on three aspects: (1) understanding the physical fundamentals of quantum tunneling of photogenerated charges for artificial photosynthesis, (2) smartly designing the chemical components and structures of functional units including photoabsorbers, insulators, catalytic active centers and interfaces to maximize the tunneling probability, and (3) constructing a MIS-type all-solar-driven artificial photosynthetic system, where the functional units responsible for CO2 reduction and water oxidation are spatially segregated to enable efficient conversion of solar-to-chemical energy. As a result, a solar-to-chemical conversion efficiency (eta SCC) of 13.6% was achieved for the photosynthetic reaction. This work offers guidance for designing novel, high-performance photocatalysts and photoelectrodes and lays the foundation for producing solar fuels at a large scale. Finally, the challenges and outlook for quantum tunneling-based artificial photosynthesis are discussed. Bidirectional tunneling-enhanced artificial leaf technology is expected to facilitate the development of efficient and durable artificial photosystems capable of converting solar energy to fuels and chemicals.
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| GB/T 7714 | Wang, Ying , Wang, Shuowen , Fu, Xianzhi et al. Quantum Tunneling of Photogenerated Charges for Artificial Photosynthesis [J]. | ACCOUNTS OF CHEMICAL RESEARCH , 2025 , 58 (13) : 2145-2156 . |
| MLA | Wang, Ying et al. "Quantum Tunneling of Photogenerated Charges for Artificial Photosynthesis" . | ACCOUNTS OF CHEMICAL RESEARCH 58 . 13 (2025) : 2145-2156 . |
| APA | Wang, Ying , Wang, Shuowen , Fu, Xianzhi , Long, Jinlin . Quantum Tunneling of Photogenerated Charges for Artificial Photosynthesis . | ACCOUNTS OF CHEMICAL RESEARCH , 2025 , 58 (13) , 2145-2156 . |
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The tightness of pi-pi stacking in supramolecular organic semiconductors plays a crucial role in governing the spatial separation and migration dynamics of photogenerated charge carriers, ultimately determining their photocatalytic performance. To achieve close pi-pi stacking, the suitable design of molecular structure is essential. Therefore, two isomers of pyridine carboxylic acid-modified perylene monoimide (PMI) were designed and synthesized, namely PM5A and PM6A. In aqueous solution, these molecules self-assemble into aggregates, which exhibit distinct stacking properties and optical characteristics. Upon photoexcitation, the loose pi-pi stacking of PM5A favors the generation of charge-transfer excitons (CTEs) over charge-separation excitons (CSEs). In contrast, PM6A, stabilized by intermolecular hydrogen bonds and possessing close pi-pi stacking, undergoes efficient charge separation (CS) to produce CSEs within 4.5 picoseconds. When incorporated into metal-insulator-semiconductor (MIS) photosystems with polyvinylpyrrolidone (PVP)-capped Pt, the Pt/PVP/PM6A system demonstrates a hydrogen evolution rate (HER) of 8100 mu mol g(-1) h(-1), nearly five times higher than that of the Pt/PVP/PM5A system. Additionally, the maximum apparent quantum efficiency (AQE) reaches approximately 2.1% under irradiation with light of a single wavelength of lambda = 425 nm.
Keyword ：
Hydrogen evolution Hydrogen evolution Perylene monoimide Perylene monoimide Photocatalysis Photocatalysis pi-pi stacking pi-pi stacking Supramolecular semiconductor Supramolecular semiconductor
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| GB/T 7714 | Wu, Shuhong , Han, Wanying , Wang, Ying et al. Close π-π stacking facilitated intermolecular charge separation in self-assembled perylene monoimide for photocatalytic hydrogen production [J]. | CHINESE JOURNAL OF STRUCTURAL CHEMISTRY , 2025 , 44 (6) . |
| MLA | Wu, Shuhong et al. "Close π-π stacking facilitated intermolecular charge separation in self-assembled perylene monoimide for photocatalytic hydrogen production" . | CHINESE JOURNAL OF STRUCTURAL CHEMISTRY 44 . 6 (2025) . |
| APA | Wu, Shuhong , Han, Wanying , Wang, Ying , Zhuang, Yan , Niu, Hui , Li, Lurong et al. Close π-π stacking facilitated intermolecular charge separation in self-assembled perylene monoimide for photocatalytic hydrogen production . | CHINESE JOURNAL OF STRUCTURAL CHEMISTRY , 2025 , 44 (6) . |
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H2 and O2 evolutions occur simultaneously for conventional particulate photocatalytic overall water splitting (PPOWS), leading to a significant backward reaction and the formation of an explosive H2/O2 gas mixture. This is an issue that must be addressed prior to industrialization of PPOWS. Here, a convenient, cost-effective, and scalable concept is introduced to uncouple hydrogen and oxygen production for PPOWS. Based on this idea, a three-component photocatalyst, Co(5 %)-HPCN/(rGO/Pt), is constructed, consisting of a photoresponsive chip (HPCN), a H2 evolution cocatalyst (rGO/Pt), and a cobalt complex capable of reversibly binding O2 (Co), to achieve the decoupling of PPOWS under alternating UV and visible light irradiations. The asynchronous O2 and H2 evolution strategy have considerable flexibility regarding the photocatalyst structure and light sources suitable for PPOWS.
Keyword ：
carbon nitride chips carbon nitride chips overall water splitting overall water splitting photocatalytic photocatalytic PPOWS decoupling PPOWS decoupling reaction mechanism reaction mechanism
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| GB/T 7714 | Liu, Dan , Xu, Huihui , Shen, Jinni et al. Decoupling H2 and O2 Release in Particulate Photocatalytic Overall Water Splitting Using a Reversible O2 Binder [J]. | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION , 2025 , 64 (9) . |
| MLA | Liu, Dan et al. "Decoupling H2 and O2 Release in Particulate Photocatalytic Overall Water Splitting Using a Reversible O2 Binder" . | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 64 . 9 (2025) . |
| APA | Liu, Dan , Xu, Huihui , Shen, Jinni , Wang, Xun , Qiu, Chengwei , Lin, Huaxiang et al. Decoupling H2 and O2 Release in Particulate Photocatalytic Overall Water Splitting Using a Reversible O2 Binder . | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION , 2025 , 64 (9) . |
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The persistent threats posed by toxic chemical warfare agents (CWAs) such as mustard gas (bis(2-chloroethyl) sulfide, HD) and bacterial contaminants demand the development of innovative, sustainable mitigation strategies. Photocatalytic processes that generate reactive oxygen species (ROS) offer a promising dual-functional approach for both chemical detoxification and antibacterial defense. In this study, two structurally analogous covalent organic frameworks (COFs), BPY-COF and BD-COF, are synthesized using benzotrithiophene as the donor unit paired with bipyridine and biphenyl, respectively. These COFs exhibit high crystallinity, broad-spectrum light absorption, and efficient charge carrier transport, with BPY-COF demonstrating superior performance due to the incorporation of heteroatoms. BPY-COF achieved ultrafast detoxification of the mustard gas simulant 2-chloroethyl ethyl sulfide (CEES) with a half-life of 35 min and 100% selectivity for 2-chloroethyl sulfoxide (CEESO) under white LED light, outperforming BD-COF. Additionally, electrospun composite fibers containing 40 wt.% BPY-COF maintained comparable CEES degradation rates and exhibited over 99% antibacterial efficiency against Escherichia coli and Bacillus subtilis within 60 min. These findings highlight the potential of BPY-COF as a multifunctional photocatalyst for integrated applications in chemical detoxification and antibacterial defense, addressing critical challenges in public health and safety.
Keyword ：
antibacterial antibacterial charge transfer charge transfer covalent organic frameworks covalent organic frameworks photocatalytic degradation photocatalytic degradation
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| GB/T 7714 | Zhu, Yongchao , Qin, Liyang , Yang, Mingyuan et al. Dual-Functional Benzotrithiophene-Based Covalent Organic Frameworks for Photocatalytic Detoxification of Mustard Gas Simulants and Antibacterial Defense [J]. | SMALL , 2025 , 21 (12) . |
| MLA | Zhu, Yongchao et al. "Dual-Functional Benzotrithiophene-Based Covalent Organic Frameworks for Photocatalytic Detoxification of Mustard Gas Simulants and Antibacterial Defense" . | SMALL 21 . 12 (2025) . |
| APA | Zhu, Yongchao , Qin, Liyang , Yang, Mingyuan , Shi, Zhicheng , Chen, Hongxuan , Wen, Na et al. Dual-Functional Benzotrithiophene-Based Covalent Organic Frameworks for Photocatalytic Detoxification of Mustard Gas Simulants and Antibacterial Defense . | SMALL , 2025 , 21 (12) . |
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This work proposes a sigma-pi hyperconjugation strategy to establish interlayer charge transport channels (CTC) in supramolecular organic nanostructures. A series of ullazine-based molecular semiconductors were designed and synthesized successfully by engineering end groups to demonstrate the sigma-pi hyperconjugation that unlocks the quantum confinement of photogenerated charges in pi-conjugated planes. Ullazine grafted with tert-butyl (U-t-Bu) showed a J-cross-stacking model in which the cross-stacked U-t-Bu molecular pair smoothly glides along the elongated dimension, forming a Z-schemed interlayer CTC by sigma-pi hyperconjugations between C-H sigma-bonds of tert-butyl end group and pi-bonds of ullazines in adjacent layers along the stacking dimension. Consequently, upon photoexcitation of ullazine-based supramolecular nanoaggregates in aqueous solution, the formed Frenkel excitons are dissociated to charge-separated excitons by the interlayer charge separation channels, undergoing an ultrafast charge transfer within 0.58 ps and an ultrafast charge separation within 0.67 ps. The Z-schemed charge separation between adjacent layers leads to a significantly enhanced hydrogen yield over U-t-Bu/PVP/Pt, with a hydrogen evolution rate of 369.9 mu molg-1h-1 and an apparent quantum yield of 1.46% at 420 nm. It is 3.8-fold larger than that of ullazine modified with methoxy (U-OMe), without the sigma-pi hyperconjugation.
Keyword ：
exciton dynamics exciton dynamics HER HER hyperconjugation effect hyperconjugation effect photocatalysis photocatalysis supramolecule supramolecule
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| GB/T 7714 | Yang, Qin , Li, Wanqing , Wang, Ying et al. σ-π Hyperconjugation Unlocks Interlayer Charge Separation of Ullazine-Based Supramolecular Nanostructures for Photocatalytic Hydrogen Evolution [J]. | ACS CATALYSIS , 2025 , 15 (4) : 3267-3275 . |
| MLA | Yang, Qin et al. "σ-π Hyperconjugation Unlocks Interlayer Charge Separation of Ullazine-Based Supramolecular Nanostructures for Photocatalytic Hydrogen Evolution" . | ACS CATALYSIS 15 . 4 (2025) : 3267-3275 . |
| APA | Yang, Qin , Li, Wanqing , Wang, Ying , Zhuang, Yan , Wu, Shuhong , Wang, Shuo et al. σ-π Hyperconjugation Unlocks Interlayer Charge Separation of Ullazine-Based Supramolecular Nanostructures for Photocatalytic Hydrogen Evolution . | ACS CATALYSIS , 2025 , 15 (4) , 3267-3275 . |
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Achieving fast exciton dissociation is a critical factor for optimizing the performance of organic photocatalysts in solar energy conversion. This work demonstrates the end-group-dependent ultrafast exciton dissociation in supramolecular perylene monoimide (PMI) nanostructures. A series of PMI molecules are designed by connecting the amide site with methylene carboxyl (& horbar;CH2 & horbar;COOH), methylene phosphonic acid (& horbar;CH2 & horbar;PO3H2), and methylene sulfonic acid (& horbar;CH2 & horbar;SO3H) to increase the dipole moment and built-in electric field, thereby effectively diminishing exciton binding energy. Upon photoexcitation, self-assembled PMI-CH2-SO3H nanoribbons (NRs), which exhibit the lowest exciton binding energy of 29.4 meV, achieve ultrafast exciton dissociation within 0.25 ps, leading to the formation of charge-separated excitons from charge-transfer states. This dissociation rate is approximate to 40 and 16 times faster than that observed in PMI-CH2-COOH (NRs) and PMI-CH2-PO3H2 (NRs), respectively. Following the deposition of Pt nanoparticles on PMI NRs, Pt/PMI-CH2-SO3H (NRs) demonstrates an H-2 evolution of 21.2 mmol g(-1) h(-1) under visible light irradiation (lambda > 420 nm), outperforming Pt/PMI-CH2-COOH (NRs) and Pt/PMI-CH2-PO3H2 (NRs) by factors of 53 and 5.4, respectively.
Keyword ：
built-in electric fields built-in electric fields hydrogen evolution hydrogen evolution perylene monoimide perylene monoimide photocatalysis photocatalysis supramolecular organic semiconductors supramolecular organic semiconductors
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| GB/T 7714 | Wu, Shuhong , Cheng, Xiuyan , Huang, Haowei et al. End Group-Induced Ultrafast Exciton Dissociation of Supramolecular Perylene Monoimide Nanoribbons for Efficient Photocatalytic Hydrogen Evolution [J]. | SMALL , 2025 , 21 (14) . |
| MLA | Wu, Shuhong et al. "End Group-Induced Ultrafast Exciton Dissociation of Supramolecular Perylene Monoimide Nanoribbons for Efficient Photocatalytic Hydrogen Evolution" . | SMALL 21 . 14 (2025) . |
| APA | Wu, Shuhong , Cheng, Xiuyan , Huang, Haowei , Yang, Qin , Wang, Ying , Zhuang, Yan et al. End Group-Induced Ultrafast Exciton Dissociation of Supramolecular Perylene Monoimide Nanoribbons for Efficient Photocatalytic Hydrogen Evolution . | SMALL , 2025 , 21 (14) . |
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Heterogeneous photocatalysis offers potential solutions for energy conversion, yet its effectiveness is compromised by the intermittent nature of solar energy. This research explores the "dark" photocatalysis, with a specific emphasis on the electron storing process in cyanamide-functionalized carbon nitride. In this study, cyanamide-functionalized carbon nitride with distinct ionic binding characteristics is synthesized. By tuning the ionic composition, an unprecedented electron storage capacity of 1.46 mmol g-1 is attained postvisible light illumination, which is about 1.5 times greater than the previously reported carbon nitride materials. The electrons retained in carbon nitride demonstrate lifetimes of up to 10 days, and the efficiency of electron utilization during subsequent dark reactions ranges from 69% to >99%. Spectroscopic analysis reveals that ions significantly alter the electronic structure of the heptazine unit, affecting electron storage. Furthermore, it is demonstrated that stored electrons efficiently reduce aryl halides in the dark, demonstrating a robust photocharging-discharging process. The dehalogenation efficiency in the absence of illumination positively correlates with trapped charge accumulation in the carbon nitride framework, suggesting that charge storage enhances electron utilization. This research not only advances the understanding of electron storage in carbon nitride but also provides significant implications for the development of more efficient photocatalytic systems.
Keyword ：
carbon nitride carbon nitride "dark" photocatalysis "dark" photocatalysis hydro-dehalogenation reaction hydro-dehalogenation reaction photocharging-discharging photocharging-discharging
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| GB/T 7714 | Wang, Yingqi , Yang, Mingcheng , Wang, Ying et al. Cyanamide-Functionalized Carbon Nitride with Ion Modification for Enhanced "Dark" Photocatalysis [J]. | ADVANCED FUNCTIONAL MATERIALS , 2025 . |
| MLA | Wang, Yingqi et al. "Cyanamide-Functionalized Carbon Nitride with Ion Modification for Enhanced "Dark" Photocatalysis" . | ADVANCED FUNCTIONAL MATERIALS (2025) . |
| APA | Wang, Yingqi , Yang, Mingcheng , Wang, Ying , Cheng, Jiajia . Cyanamide-Functionalized Carbon Nitride with Ion Modification for Enhanced "Dark" Photocatalysis . | ADVANCED FUNCTIONAL MATERIALS , 2025 . |
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Photocatalytic CO2 reduction reaction (CO2RR) is a desired solution to overcome current energy and environmental problems. As a main competitive reaction, hydrogen evolution reaction (HER) urgently needs to be restrained to improve the conversion rate and selectivity of CO2RR. Here, we report a Cu2O/MXene-g-C3N4 (Cu2O/MX-CN) p-n heterojunction that achieves highly selective CO2 reduction of 93% (competing with HER) under visible light. CO is the only product of CO2RR, which yielded 28.4 mu mol g(-1) h(-1). The introduction of Ti3C2 MXene in g-C3N4 promotes the energy of photoelectrons and the transport efficiency of photogenerated carriers at the p-n heterojunction interface via hot electron injection induced by the localized surface plasmonic resonance (LSPR) and band structure regulation. Meanwhile, apart from the component of p-n heterojunction, Cu2O also acts as the adsorption site of CO2, inhibiting HER by blocking the adsorption of protons. This study provides a novel strategy to fabricate multifunctional composite for efficient and highly selective CO2 reduction.
Keyword ：
CO2 Reduction CO2 Reduction Cu2O Cu2O G-C3N4 G-C3N4 Photocatalysis Photocatalysis Ti3C2 MXene Ti3C2 MXene
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| GB/T 7714 | Gao, Yuan , Wang, Ying , Sun, Ruihong et al. Interfacial hot electron injection in Cu2O/MXene-g-C3N4 p-n heterojunction for efficient photocatalytic CO2 reduction [J]. | COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS , 2024 , 684 . |
| MLA | Gao, Yuan et al. "Interfacial hot electron injection in Cu2O/MXene-g-C3N4 p-n heterojunction for efficient photocatalytic CO2 reduction" . | COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS 684 (2024) . |
| APA | Gao, Yuan , Wang, Ying , Sun, Ruihong , Luo, Yining , Xin, Liantao , Wang, Debao . Interfacial hot electron injection in Cu2O/MXene-g-C3N4 p-n heterojunction for efficient photocatalytic CO2 reduction . | COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS , 2024 , 684 . |
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Wound dressings play a critical role in the wound healing process; however, conventional dressings often address singular functions, lacking versatility in meeting diverse wound healing requirements. Herein, dual-network, multifunctional hydrogels (PSA/CS-GA) have been designed and synthesized through a one-pot approach. The in vitro and in vivo experiments demonstrate that the optimized hydrogels have exceptional antifouling properties, potent antibacterial effects and rapid hemostatic capabilities. Notably, in a full-thickness rat wound model, the hydrogel group displays a remarkable wound healing rate exceeding 95% on day 10, surpassing both the control group and the commercial 3M group. Furthermore, the hydrogels exert an anti-inflammatory effect by reducing inflammatory factors interleukin 6 (IL-6) and tumor necrosis factor-alpha (TNF-alpha), enhance the release of the vascular endothelial growth factor (VEGF) to promote blood vessel proliferation, and augment collagen deposition in the wound, thus effectively accelerating wound healing in vivo. These innovative hydrogels present a novel and highly effective approach to wound healing. Dual network multifunctional hydrogels are developed using a one-pot synthesis approach. The in vitro and in vivo experiments demonstrate that these hydrogels have exceptional antifouling properties, potent antibacterial effects and rapid hemostatic capabilities.
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| GB/T 7714 | Jiang, Hongzhi , Huang, Xueping , Yang, Jiachao et al. Dual network composite hydrogels with robust antibacterial and antifouling capabilities for efficient wound healing [J]. | JOURNAL OF MATERIALS CHEMISTRY B , 2024 , 12 (20) : 4909-4921 . |
| MLA | Jiang, Hongzhi et al. "Dual network composite hydrogels with robust antibacterial and antifouling capabilities for efficient wound healing" . | JOURNAL OF MATERIALS CHEMISTRY B 12 . 20 (2024) : 4909-4921 . |
| APA | Jiang, Hongzhi , Huang, Xueping , Yang, Jiachao , Yu, Xunbin , Yang, Weibo , Song, Yunhao et al. Dual network composite hydrogels with robust antibacterial and antifouling capabilities for efficient wound healing . | JOURNAL OF MATERIALS CHEMISTRY B , 2024 , 12 (20) , 4909-4921 . |
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