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学者姓名：林金国
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Abstract ：
To address the limitations of conventional powdered catalytic materials, including difficulty of recycling, low catalytic activity, and limited applicability to different pollutants, this study developed a wood-based@InCoOS composite catalytic materials with rapid recycling characteristics and suitable for the catalytic reduction of various pollutants. By employing bimetallic oxysulfide in situ decoration, the wood was successfully endowed with catalytic functionality, and the catalytic activities of poplar wood-based (PT@InCoOS) and Chinese fir wood-based (CF@InCoOS) composite catalytic materials were compared across multiple pollutants. The results revealed that both PT@InCoOS and CF@InCoOS showed excellent catalytic reduction performance, but with significant differences. PT@InCoOS achieved complete reduction of new coccine (NC), methylene blue (MB), and rhodamine B (RhB) within 3, 3, and 20 min, respectively, and completely reduced Cr(VI) and p-nitrophenol (4NP) within 22 and 20 min. In contrast, CF@InCoOS required 5, 4, 24, 32, and 30 min for the same pollutants. PT@InCoOS exhibited superior performance due to its higher electron transferring capability and favorable bandgap structure, while the interfacial synergistic effect effectively promoted the photogenerated carrier transport and utilization efficiency. Even after six cycles of use, wood-based@InCoOS composite catalytic materials retained over 88 % of their catalytic efficiency, demonstrating excellent reusability. The materials have low cost, high activity, easy recycling, and environmental friendliness and demonstrate great potential as a microreactor in environmental remediation.
Keyword ：
Bimetallic oxysulfide Bimetallic oxysulfide Catalytic reduction Catalytic reduction Cr (VI) and 4-NP Cr (VI) and 4-NP Organic dyes Organic dyes Recyclable materials Recyclable materials Wastewater treatment Wastewater treatment Wood-based functional materials Wood-based functional materials
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| GB/T 7714 | Bao, Xinde , Yang, Meng , Hong, Yuhao et al. Rapid recyclable wood-based@InCoOS composite catalytic materials: Achieving efficient catalytic reduction and recycling of multiple pollutants [J]. | SEPARATION AND PURIFICATION TECHNOLOGY , 2026 , 380 . |
| MLA | Bao, Xinde et al. "Rapid recyclable wood-based@InCoOS composite catalytic materials: Achieving efficient catalytic reduction and recycling of multiple pollutants" . | SEPARATION AND PURIFICATION TECHNOLOGY 380 (2026) . |
| APA | Bao, Xinde , Yang, Meng , Hong, Yuhao , Guan, Xin , Chen, Xiaoyun , Lin, Jinguo . Rapid recyclable wood-based@InCoOS composite catalytic materials: Achieving efficient catalytic reduction and recycling of multiple pollutants . | SEPARATION AND PURIFICATION TECHNOLOGY , 2026 , 380 . |
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Developing sustainable and economically viable methods is paramount to mitigate the harmful effects of dyes and conserve water resources. This study used the hydrothermal method to effectively synthesize an In2S3/Bi2S3/ BiOBr heterojunction catalyst. The electrochemical properties of the In2S3/Bi2S3/BiOBr were enhanced by the presence of heterovalent In3+ and Bi3+ oxidation states, which facilitated electron transport and pollutant degradation. The heterojunction catalyst synthesized from prefabricated BiOBr, Bi2S3, and In2S3 showed the most pronounced catalytic activity. Its catalytic effectiveness was studied for the degradation of methylene blue (MB), methyl orange (MO), and rhodamine B (RhB), achieving efficiencies of 95.3 %, 99.5 %, and 98.3 % within 120, 100, and 100 min, respectively, in 50 ppm 100 mL of each dye at 10 mg of In2S3/Bi2S3/BiOBr. The In2S3/Bi2S3/ BiOBr featured remarkable stability and efficiency, maintaining a degradation rate of 95.8 % even after five runs. The e- /h + transitions occurring between BiOBr, Bi2S3, and In2S3 led to an enhancement of the electrochemically active surface sites and thereby optimized the catalytic activity. The ability of the In2S3/Bi2S3/BiOBr to absorb visible light led to generating reactive species such as center dot O 2- and h+ free radicals, which were crucial for the degradation of MB, MO, and RhB. These results highlight the exceptional catalytic potential of the In2S3/Bi2S3/ BiOBr heterojunction for the degradation of chemical pollutants, thereby providing a sustainable and effective solution for environmental remediation.
Keyword ：
In2S3/Bi2S3/BiOBr In2S3/Bi2S3/BiOBr Organic dye pollutant Organic dye pollutant Photocatalytic degradation Photocatalytic degradation Ternary heterojunction Ternary heterojunction Visible light Visible light
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| GB/T 7714 | Mosisa, Mengistu Tadesse , Wu, Binghong , Chen, Longyan et al. Ternary-heterojunction In2S3/Bi2S3/BiOBr catalyst with interfacial effect to enhance the photocatalytic degradation of organic dyes [J]. | JOURNAL OF WATER PROCESS ENGINEERING , 2025 , 70 . |
| MLA | Mosisa, Mengistu Tadesse et al. "Ternary-heterojunction In2S3/Bi2S3/BiOBr catalyst with interfacial effect to enhance the photocatalytic degradation of organic dyes" . | JOURNAL OF WATER PROCESS ENGINEERING 70 (2025) . |
| APA | Mosisa, Mengistu Tadesse , Wu, Binghong , Chen, Longyan , Su, Zhengjie , Zhang, Pengkun , Abdeta, Adugna Boke et al. Ternary-heterojunction In2S3/Bi2S3/BiOBr catalyst with interfacial effect to enhance the photocatalytic degradation of organic dyes . | JOURNAL OF WATER PROCESS ENGINEERING , 2025 , 70 . |
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To reveal the role of bi-vacancy defects and heterovalent states in oxysulfide catalysts for enhancing the photocatalytic hydrogen evolution reaction (PHER), we demonstrate a Br/W co-doped Zn(O,S) catalyst (labeled as Br/W-ZnOS) featuring abundant anionic oxygen vacancies (VO)/cationic zinc vacancies (VZn) bi-defects and heterovalent W5+/W6+ states via a facile hydrolysis method. The co-doping of Br and W induces lattice distortions that enable neighboring atoms to leave the lattice, creating surfaces enriched with anionic VO and cationic VZn defects. The synergistic effect between dual defects forms an efficient electron-hole separation system, enhancing the efficiency of electron-hole pair separation. Density functional theory calculation (DFT) demonstrates that the combination of Br/W co-doping and vacancies significantly reduces the water dissociation barrier and optimizes the surface *H generation rate of the photocatalyst. Thus, Br/W-ZnOS exhibits a PHER rate of 3415.7 mu mol h- 1, which is 12.5 times higher than the undoped Zn(O,S) catalyst, and achieves an apparent quantum yield (AQY) of 15.41 % at 365 nm, while maintaining good stability with a PHER activity of 3288.1 mu mol h- 1 after five repeated cycles. This research provides a promising strategy for designing oxysulfide catalysts with synergistically engineered defects for efficient PHER.
Keyword ：
Heterovalent states Heterovalent states Photocatalytic hydrogen evolution Photocatalytic hydrogen evolution W/Br co-doped W/Br co-doped Zn/O bi-vacancy defects Zn/O bi-vacancy defects
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| GB/T 7714 | Wu, Binghong , Wu, Xinru , Kuo, Dong-Hau et al. W/Br co-doped Zn(O,S) with Zn/O bi-vacancy defects and heterovalent states for enhanced photocatalytic hydrogen evolution [J]. | MATERIALS TODAY ENERGY , 2025 , 49 . |
| MLA | Wu, Binghong et al. "W/Br co-doped Zn(O,S) with Zn/O bi-vacancy defects and heterovalent states for enhanced photocatalytic hydrogen evolution" . | MATERIALS TODAY ENERGY 49 (2025) . |
| APA | Wu, Binghong , Wu, Xinru , Kuo, Dong-Hau , Tang, Xiao , Mao, Xin , Yang, Baoqian et al. W/Br co-doped Zn(O,S) with Zn/O bi-vacancy defects and heterovalent states for enhanced photocatalytic hydrogen evolution . | MATERIALS TODAY ENERGY , 2025 , 49 . |
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A novel AgVOS oxysulfide catalyst for rapid catalytic reduction of toxic organic substances and Cr(VI) under dark is synthesized by a facile method. With the V/O co-doping, the doped Ag2S catalyst has the effectively regulated electron transfer performance, the hydrazine-driven V5+-to-V4+ reduction to disturb charge equilibrium, and the formed sulfur vacancy balanced by oxygen doping to maintain charge equilibrium. The formed sulfur vacancy acts as the active site for electrophilic nucleophilic reaction, while the orbital hybridization of O-2p and S-3p stabilizes the valence state of S2-. A suitable ratio of n(V4+/V5+) is regulated during the hydrazine-driven synthesis to facilitate the electron transfer and enhance the V5+-to-V4+ reduction reaction. V/O co-doped AgVOS-3 prepared by a suitable hydrazine content exhibits super catalytic reduction performance of organic 4-NP (4-nitrophenol), MB (methyl blue), MO (methyl orange), and RhB (Rhodamine B, 20 ppm, 100 mL) dyes, which are completely reduced within 8, 8, 10, and 8 min, respectively. In comparison, Cr6+ (50 ppm, 100 mL) is also completely reduced within 6 min by AgVOS-3, indicating its good catalytic reduction activity for organic and inorganic mixture pollutants. Furthermore, AgVOS-3 has good stability after cyclic tests to maintain a reduction efficiency of 96.5%. Therefore, the AgVOS catalyst shows a promising application for industrial wastewater treatment.
Keyword ：
bimetal oxysulfide bimetal oxysulfide heterovalent states heterovalent states pollutant reduction pollutant reduction sulfur vacancy sulfur vacancy V/O co-doped Ag2S V/O co-doped Ag2S
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| GB/T 7714 | Wu, Xinru , Zhang, Pengkun , Insua, Benjamin Kunkadma et al. V-/O-Doping to Endow Ag2S-based Bimetal Oxysulfide with Sulfur Vacancies and Heterovalent States for Rapid Reduction of Organic and Cr(VI) Pollutants in the Dark [J]. | ADVANCED SUSTAINABLE SYSTEMS , 2025 , 9 (3) . |
| MLA | Wu, Xinru et al. "V-/O-Doping to Endow Ag2S-based Bimetal Oxysulfide with Sulfur Vacancies and Heterovalent States for Rapid Reduction of Organic and Cr(VI) Pollutants in the Dark" . | ADVANCED SUSTAINABLE SYSTEMS 9 . 3 (2025) . |
| APA | Wu, Xinru , Zhang, Pengkun , Insua, Benjamin Kunkadma , Yang, Baoqian , Kuo, Dong-Hau , Lu, Dongfang et al. V-/O-Doping to Endow Ag2S-based Bimetal Oxysulfide with Sulfur Vacancies and Heterovalent States for Rapid Reduction of Organic and Cr(VI) Pollutants in the Dark . | ADVANCED SUSTAINABLE SYSTEMS , 2025 , 9 (3) . |
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Traditional Ag3SbS3 exhibits low efficiency in the catalytic reduction of pollutants due to its surface hydrophobicity, which limits its practical application. Herein, we demonstrate a hydrophilic oxygen-doped Ag3SbS3 bimetal oxysulfide (AgSbOS or Ag3SbS3) catalyst with heterovalent valence states for the efficient reduction of toxic phenolic compounds (4-NP), organic dyes (MO, MB, RhB), and heavy metal ions (Cr6 +)The O-doping transforms the hydrophobic Ag3SbS3 into hydrophilic AgSbOS, increasing the adsorption sites and electrochemical active sites on the surface of AgSbOS. Hydrogen peroxide-driven oxidizing the Sb3+ into Sb5+, regulation of the AgSbOS with optimal heterovalent n(Sb5+)/n(Sb3+ + Sb5+) states facilitates the rapid hopping of electrons between Sb3+ <-> Sb5+ to transfer for the catalytic reduction of pollutants, accelerating the catalytic reduction activity. Oxygen doping also regulates the energy band structure to facilitate electron transfer and enhances the specific surface area, further improving the catalytic reduction activity. AgSbOS with an appropriate amount of oxygen doping significantly enhances the catalytic reduction efficiency, with 10 mg of AgSbOS3 reducing 100 mL of 20 ppm 4-NP and Cr6+ in 12 and 8 min, respectively. Furthermore, this catalyst achieves a complete reduction of 100 mL of 50 ppm MO, MB, and RhB in 4, 6, and 8 min, respectively. AgSbOS-3 is also effective in treating mixed pollutants, demonstrating high activity over a wide pH range and good reuse stability. AgSbOS exhibits significant potential for wastewater treatment applications.
Keyword ：
Bimetal oxysulfide Bimetal oxysulfide Heterovalent states Heterovalent states Hydrophobic-to-hydrophilic Hydrophobic-to-hydrophilic Oxygen-doped Ag3SbS3 Oxygen-doped Ag3SbS3 Pollutant reduction Pollutant reduction
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| GB/T 7714 | Xiang, Kening , Wang, Haoyu , Liu, Tao et al. Oxygen-doped Ag3SbS3 with the hydrophobic-to-hydrophilic transformation for efficient reduction of organic and hexavalent chromium pollutants [J]. | JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING , 2025 , 13 (5) . |
| MLA | Xiang, Kening et al. "Oxygen-doped Ag3SbS3 with the hydrophobic-to-hydrophilic transformation for efficient reduction of organic and hexavalent chromium pollutants" . | JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING 13 . 5 (2025) . |
| APA | Xiang, Kening , Wang, Haoyu , Liu, Tao , Li, Cuizhu , Su, Zhengjie , Zhang, Pengkun et al. Oxygen-doped Ag3SbS3 with the hydrophobic-to-hydrophilic transformation for efficient reduction of organic and hexavalent chromium pollutants . | JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING , 2025 , 13 (5) . |
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Although the efficiency of perovskite solar cells (PSCs) keeps breaking new records, their stability and cost are still limited by using the conventional hole transport material of 2,2 ',7,7 '-tetrakis(N,N-di-p-methoxyphenylamine)-9,9 '-spirobifluorene (Spiro-OMeTAD). Herein, we use 3,4-ethylenedioxythiophene (EDOT) as a solubilizer to enhance the dissolution of lithium bis(trifluoromethane)sulfonylimide (Li-TFSI) and reduce the 4-tert-bultypyridine (TBP) dosage. Then, EDOT undergoes in situ oxidative polymerization to generate PEDOT by an oxidizing agent of iodine (I2). Moreover, I2 can also accelerate the oxidation of Spiro-OMeTAD. Therefore, the generated PEDOT can synergistically enhance hole transport capability with the oxidized Spiro-OMeTAD, and the generated I- ions can compensate for the I vacancies and inhibit the migration of I- in the perovskite film, resulting in an enhanced stability and efficiency of PSCs. A PSC based on the composite hole transport system achieves a power conversion efficiency (PCE) of 24.79%. Moreover, the PSC retains 92% of its initial PCE for over 2000 h under ambient conditions of 25 degrees C and 35% relative humidity. Furthermore, the quantities of Spiro-OMeTAD and TBP have, respectively, decreased by 24.9 and 37.5% in the composite hole transport system, thereby lowering the production cost of the PSC and facilitating its industrialization development.
Keyword ：
3,4-ethylenedioxythiophene 3,4-ethylenedioxythiophene holetransporting material holetransporting material perovskitesolar cell perovskitesolar cell solubilizer solubilizer synergistic effect synergistic effect
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| GB/T 7714 | Jiang, Jianmei , Xiao, Yaoming , Yang, Wenjing et al. In Situ Oxidative Polymerization of PEDOT, Reducing the TBP Dosage, and Synergizing with Spiro-OMeTAD to Enhance the Efficiency and Stability of Perovskite Solar Cells [J]. | ACS APPLIED MATERIALS & INTERFACES , 2025 , 17 (37) : 52779-52788 . |
| MLA | Jiang, Jianmei et al. "In Situ Oxidative Polymerization of PEDOT, Reducing the TBP Dosage, and Synergizing with Spiro-OMeTAD to Enhance the Efficiency and Stability of Perovskite Solar Cells" . | ACS APPLIED MATERIALS & INTERFACES 17 . 37 (2025) : 52779-52788 . |
| APA | Jiang, Jianmei , Xiao, Yaoming , Yang, Wenjing , Wen, Chao , Liu, Biye , Wang, Lidan et al. In Situ Oxidative Polymerization of PEDOT, Reducing the TBP Dosage, and Synergizing with Spiro-OMeTAD to Enhance the Efficiency and Stability of Perovskite Solar Cells . | ACS APPLIED MATERIALS & INTERFACES , 2025 , 17 (37) , 52779-52788 . |
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Lignin, a negatively charged, three-dimensional natural biopolymer, serves as an ideal support for metal catalysts due to its abundant functional groups and tunable chemical properties, which enable strong metal coordination and effective immobilization. Herein, we demonstrate a lignin-mediated Co/O co-doped Ag2S, symbolized as LAgCoOS, bimetal oxysulfide catalyst via a facile hydrolysis method for the efficient reduction of toxic phenolic compounds (4-nitrophenol, 4-NP), organic dyes (methyl orange (MO), methylene blue (MB), rhodamine B (RhB), and heavy metal ions Cr(VI)) under dark conditions. Lignin, used to immobilize catalysts, also contributes to increasing the number of active catalytic sites and enhancing catalytic activity. The co-doping of transition metal cations and anions was employed to effectively regulate the electron transfer property of the catalyst, with oxygen doping modifying the energy band structure and cobalt providing heterovalent Co3+/Co2+ states that facilitate rapid electron hopping between Co2+ and Co3+ (Co2+ <-> Co3+) to transfer for catalytic reduction of pollutants. Furthermore, the hybridization of O 2p and S 3p orbitals improved the structural stability of the catalyst. L-AgCoOS with an appropriate level of cobalt doping exhibited significantly enhanced catalytic reduction efficiency. Specifically, 5 mg of L-AgCoOS-2 could completely reduce 100 ml of 20 ppm 4-NP within 8 min, with the reaction rate constant of 0.26 min-1. Additionally, it achieved a complete reduction of 100 ml of 50 ppm MB, MO, RhB, and Cr(VI) in 4, 3, 4, and 4 min, respectively, with the reaction rate constant of 0.49, 0.51, 0.57, and 0.54 min-1. L-AgCoOS-2 also demonstrated excellent performance in treating mixed pollutants, maintaining high activity across a wide pH range, and good reusability. These results highlight the significant potential of L-AgCoOS-2 for practical applications in wastewater treatment.
Keyword ：
Bimetal oxysulfide catalyst Bimetal oxysulfide catalyst Lignin Lignin Pollutants reduction Pollutants reduction Under dark Under dark
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| GB/T 7714 | Liu, Tao , Wu, Zhenjie , Liu, Yang et al. Lignin-mediated AgCoOS bimetal oxysulfide catalysts for highly efficient catalytic reduction of organic and Cr(VI) pollutants in the dark [J]. | INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES , 2025 , 328 . |
| MLA | Liu, Tao et al. "Lignin-mediated AgCoOS bimetal oxysulfide catalysts for highly efficient catalytic reduction of organic and Cr(VI) pollutants in the dark" . | INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES 328 (2025) . |
| APA | Liu, Tao , Wu, Zhenjie , Liu, Yang , Xiang, Kening , Wang, Haoyu , Li, Cuizhu et al. Lignin-mediated AgCoOS bimetal oxysulfide catalysts for highly efficient catalytic reduction of organic and Cr(VI) pollutants in the dark . | INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES , 2025 , 328 . |
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The efficient removal of lignin is crucial for process optimization, as it enhances the exposure of polar groups in wood and provides interfacial binding sites for subsequent material modifications. In this study, an environmentally friendly peracetic acid/ hydrogen peroxide system was employed to delignify fast-growing wood. The results indicated mass loss rates of 30.7% for poplar and 31.3% for Chinese fir, with corresponding decreases in relative lignin content by 95.3% and 87.2%, respectively. Additionally, the specific surface area increased by 6.4% in poplar and 30.9% in Chinese fir. The relative crystallinity was enhanced by 31.2% in poplar and 15.7% in Chinese fir, and the O/C ratio increased by 29.6% and 19.7%, respectively. Microsocopic morphological analysis revealed noticeably thinner and slightly collapsed cell walls in the treated samples. The disappearance of lignin-specific peaks at 1507 cm-1, 1460 cm-1, and 1264 cm-1 confirmed the effective removal of lignin. Additionally, delignification resulted in a lower pyrolysis temperature, increased surface brightness, and reduced color variation. Due to the differences in internal structures and chemical compositions between poplar and Chinese fir, the effects of lignin removal varied, leading to significant changes in their physicochemical properties. These findings provide a theoretical foundational for lignin removal from wood and support future efforts in wood functionalization.
Keyword ：
Chinese fir wood Chinese fir wood Delignification treatment Delignification treatment Fast growing wood Fast growing wood Lignin Lignin Poplar wood Poplar wood
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| GB/T 7714 | Bao, Xinde , Yang, Meng , Zhu, Junjie et al. Efficient delignification of poplar and Chinese fir wood using a peroxyacetic acid/hydrogen peroxide system [J]. | JOURNAL OF WOOD SCIENCE , 2025 , 71 (1) . |
| MLA | Bao, Xinde et al. "Efficient delignification of poplar and Chinese fir wood using a peroxyacetic acid/hydrogen peroxide system" . | JOURNAL OF WOOD SCIENCE 71 . 1 (2025) . |
| APA | Bao, Xinde , Yang, Meng , Zhu, Junjie , Xu, Hui , Dang, Huiying , Guo, Kai et al. Efficient delignification of poplar and Chinese fir wood using a peroxyacetic acid/hydrogen peroxide system . | JOURNAL OF WOOD SCIENCE , 2025 , 71 (1) . |
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Abstract ：
NH
Keyword ：
Zn Zn
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| GB/T 7714 | 张鹏坤 , 吴秦汉 , 王昊昱 et al. Z型异质结Zn [J]. | Chinese Journal of Catalysis , 2025 , 74 (07) : 279-293 . |
| MLA | 张鹏坤 et al. "Z型异质结Zn" . | Chinese Journal of Catalysis 74 . 07 (2025) : 279-293 . |
| APA | 张鹏坤 , 吴秦汉 , 王昊昱 , 郭东昊 , 赖雨洁 , 陆东芳 et al. Z型异质结Zn . | Chinese Journal of Catalysis , 2025 , 74 (07) , 279-293 . |
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Herein, we established a Zn3(OH)2(V2O7)(H2O)2/V-Zn(O,S) Z-scheme heterojunction (labeled ZnVO/V-Zn(O,S) with a heterovalent V4+/V5+ states and oxygen vacancies in both phases via a one-step in-situ hydrolysis method. The NaBH4 regulated the ZnVO/V-Zn(O,S)-3 with rich Vo and suitable n(V4+)/n(V5+) ratio achieved an excellent photocatalytic nitrogen fixation activity of 301.7 mu mol/(g center dot h) and apparent quantum efficiency of 1.148% at 420 nm without any sacrificial agent, which is 11 times than that of V-Zn(O,S). The Vo acts as the active site to trap and activate N2 molecules and to trap and activate H2O to produce the H for N2 molecules photocatalytic reduction. The rich Vo defects can also reduce the competitive adsorption of H2O and N2 molecules on the surface active site of the catalyst. The heterovalent vanadium states act as the photogenerated electrons, quickly hopping between V4+ and V5+ to transfer for the photocatalytic N2 reduction reaction. Additionally, the Z-scheme heterojunction effectively minimizes photogenerated carrier recombination. These synergistic effects collectively boost the photocatalytic nitrogen fixation activity. This study provides a practical method for designing Z-scheme heterojunctions for efficient photocatalytic N2 fixation under mild conditions. (c) 2025, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
Keyword ：
Heterovalent valence states Heterovalent valence states Oxygen vacancy Oxygen vacancy Photocatalytic N2 fixation Photocatalytic N2 fixation Z-scheme heterojunction Z-scheme heterojunction
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| GB/T 7714 | Zhang, Pengkun , Wu, Qinhan , Wang, Haoyu et al. Z-scheme heterojunction Zn3(OH)2(V2O7)(H2O)2/V-Zn(O,S) for enhanced visible-light photocatalytic N2 fixation via synergistic heterovalent vanadium states and oxygen vacancy defects [J]. | CHINESE JOURNAL OF CATALYSIS , 2025 , 74 : 279-293 . |
| MLA | Zhang, Pengkun et al. "Z-scheme heterojunction Zn3(OH)2(V2O7)(H2O)2/V-Zn(O,S) for enhanced visible-light photocatalytic N2 fixation via synergistic heterovalent vanadium states and oxygen vacancy defects" . | CHINESE JOURNAL OF CATALYSIS 74 (2025) : 279-293 . |
| APA | Zhang, Pengkun , Wu, Qinhan , Wang, Haoyu , Kuo, Dong-Hau , Lai, Yujie , Lu, Dongfang et al. Z-scheme heterojunction Zn3(OH)2(V2O7)(H2O)2/V-Zn(O,S) for enhanced visible-light photocatalytic N2 fixation via synergistic heterovalent vanadium states and oxygen vacancy defects . | CHINESE JOURNAL OF CATALYSIS , 2025 , 74 , 279-293 . |
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