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学者姓名：林华香
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Abstract ：
Photothermal catalytic N-acetylation of aniline has been a promising strategy to synthesize amides, which combined the advantages of thermal catalysis and photocatalysis. Herein, we demonstrate a high-performance strategy to synthesize amides catalyzed by the in-situ formed first-row transition-metal (Fe, Co, Ni, Mn et al.) complexes nanodots (TMC NDs) under solar light excitation without using noble metals or strong acids. The dualfunctional nitriles substrates acted as the ligands to coordinate with transition-metal salts affording photosensitive TMC NDs with high solar-to-thermal energy conversion efficiency. Intramolecular charge transitions reduced the energy barrier of nitriles activation by weakening C---N bond and triggered near-field temperature rise via the electron-phonon scattering non-radiative pathway. The reaction system exhibited good tolerance to different functional groups, affording a series of amide derivatives. Such a dynamic coordination reaction mode and the in-situ formed TMC NDs opens new avenues toward solar-heat conversion via photon-phonon coupling in the field of chemical synthesis.
Keyword ：
Amide synthesis Amide synthesis N-acyl sources N-acyl sources Photon -phonon coupling Photon -phonon coupling Photothermal catalysis Photothermal catalysis Transition-metal complexes nanodots Transition-metal complexes nanodots
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| GB/T 7714 | Ma, Xiong-Feng , Xiao, Rui , Wei, Yingcong et al. Photothermal catalytic conversion of water and inert nitriles to amide activated by in-situ formed transition-metal-complex nanodots [J]. | APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY , 2024 , 344 . |
| MLA | Ma, Xiong-Feng et al. "Photothermal catalytic conversion of water and inert nitriles to amide activated by in-situ formed transition-metal-complex nanodots" . | APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY 344 (2024) . |
| APA | Ma, Xiong-Feng , Xiao, Rui , Wei, Yingcong , Zhang, Shaohui , Hu, Xiaoyi , Zhang, Ling et al. Photothermal catalytic conversion of water and inert nitriles to amide activated by in-situ formed transition-metal-complex nanodots . | APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY , 2024 , 344 . |
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本发明公开了一种具有海胆球形貌的复合光催化剂材料及其制备方法和应用，该复合光催化剂是通过在乙醇热过程中，W18O49材料在2H/3C‑SiC纳米球表面生长从而得到具有海胆球形貌的SiC‑W18O49复合材料。该复合光催化剂制备原料价廉易得，制备方案便捷可行，并且与单一组分的W18O49材料和2H/3C‑SiC材料相比，光催化还原二氧化碳性能显著增强。
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| GB/T 7714 | 张子重 , 柳勇志 , 王绪绪 et al. 一种具有海胆球形貌的复合光催化剂材料及其制备方法和应用 : CN202210788518.0[P]. | 2022-07-06 00:00:00 . |
| MLA | 张子重 et al. "一种具有海胆球形貌的复合光催化剂材料及其制备方法和应用" : CN202210788518.0. | 2022-07-06 00:00:00 . |
| APA | 张子重 , 柳勇志 , 王绪绪 , 龙金林 , 林华香 , 沈锦妮 et al. 一种具有海胆球形貌的复合光催化剂材料及其制备方法和应用 : CN202210788518.0. | 2022-07-06 00:00:00 . |
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本发明公开了一种含稀土元素的硫化物光催化剂及其制备方法和应用，采用简单的水热法或溶剂热法制备含稀土元素的硫化物催化剂，并将其应用于光催化CO2还原体系中。本发明的制备方法简单易行、温和低能耗。制得的催化剂具有显著提高光催化CO2还原性能，且产物选择性高的优点，在光催化领域具有较广泛的应用前景，同时也为新型光催化剂的制备提供了新的思路。
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| GB/T 7714 | 丁正新 , 王文静 , 何春娴 et al. 一种含稀土元素的硫化物光催化剂及其制备方法和应用 : CN202210039689.3[P]. | 2022-01-14 00:00:00 . |
| MLA | 丁正新 et al. "一种含稀土元素的硫化物光催化剂及其制备方法和应用" : CN202210039689.3. | 2022-01-14 00:00:00 . |
| APA | 丁正新 , 王文静 , 何春娴 , 魏芬 , 韩世同 , 龙金林 et al. 一种含稀土元素的硫化物光催化剂及其制备方法和应用 : CN202210039689.3. | 2022-01-14 00:00:00 . |
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A AgBr-Ag2MoO4 heterojunction with high inactivation of E. coli under visible-light illumination was constructed. The crystal structure, morphology, elemental composition, and optical properties were characterized by TEM, SEM, XRD, XPS and DRS. The photocatalytic inactivation of E. coli by AgBr, Ag2MoO4, and AgBr-Ag2MoO4 was investigated. The results indicate that AgBr-Ag2MoO4 shows the best disinfection activity compared to AgBr and Ag2MoO4, with the E. coli being almost completely inactivated after illumination for 80 min. In addition, the cell structure of the bacteria is destroyed after visible-light irradiation in the presence of the catalyst. The UV absorption detection confirms that the bacterial protein leak and the concentration of nucleic acid in the solution also increase with the increase of the reaction time, indicating that the integrity of the bacterial cell membrane is damaged. The detection of ROS scavengers indicates that the reactive species (h(+), OH, e(-) and O-2(-)) play an important role in the inactivation of bacteria. The EPR tests confirm that the amount of OH is higher than that of O-2(-) during the illumination process, which is consistent with the results of the free-radical capture tests. The heterojunction of AgBr-Ag2MoO4 is beneficial for the separation of photogenerated electrons and holes during the illumination process, resulting in an improvement of the antibacterial properties.
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| GB/T 7714 | Rao, Qin , Xian, Xiao , Lin, Huaxiang et al. Construction of a AgBr-Ag2MoO4 heterojunction and its photocatalytic sterilization activity [J]. | NEW JOURNAL OF CHEMISTRY , 2023 , 47 (32) : 15151-15161 . |
| MLA | Rao, Qin et al. "Construction of a AgBr-Ag2MoO4 heterojunction and its photocatalytic sterilization activity" . | NEW JOURNAL OF CHEMISTRY 47 . 32 (2023) : 15151-15161 . |
| APA | Rao, Qin , Xian, Xiao , Lin, Huaxiang , Yuan, Rusheng , Zhang, Zizhong , Long, Jinlin et al. Construction of a AgBr-Ag2MoO4 heterojunction and its photocatalytic sterilization activity . | NEW JOURNAL OF CHEMISTRY , 2023 , 47 (32) , 15151-15161 . |
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In a novel approach that capitalized on the differential solubility product (K-sp) of ZnSe and Ag2Se, a unique ZnSe/Ag2Se binary heterostructure was efficiently synthesized in situ. ZnSe/Ag2Se exhibited excellent antimicrobial efficiency under visible light. Incorporating Ag2Se into ZnSe significantly enhanced the photoelectric performance of the catalyst, greatly accelerating the separation of the photogenerated electrons in the system. Active species removal experiments determined that O-2(-) and H2O2 played crucial roles in photocatalytic antibacterial efficiency. Further investigation into the levels of cellular membrane peroxidation, bacterial morphology, and intracellular contents concentration revealed that during the photocatalytic antimicrobial process, reactive oxygen species initially oxidize phospholipids in the cell membrane, leading to damage to the external structure of the cell and leakage of the intracellular contents, ultimately resulting in bacteria inactivation. The photocatalytic antimicrobial process of ZnSe/Ag2Se fundamentally deviates from conventional methods, offering new insights into efficient disinfection and photocatalytic antimicrobial mechanisms.
Keyword ：
antibacterial mechanism antibacterial mechanism binary heterojunction binary heterojunction photocatalysis photocatalysis photocatalytic disinfection photocatalytic disinfection ZnSe ZnSe
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| GB/T 7714 | Wang, Qian , Wang, Qin , Yuan, Rusheng et al. Facile Preparation of the ZnSe/Ag2Se Binary Heterojunction for Photocatalytic Antibacterial Efficiency [J]. | ACS APPLIED MATERIALS & INTERFACES , 2023 , 15 (43) : 50155-50165 . |
| MLA | Wang, Qian et al. "Facile Preparation of the ZnSe/Ag2Se Binary Heterojunction for Photocatalytic Antibacterial Efficiency" . | ACS APPLIED MATERIALS & INTERFACES 15 . 43 (2023) : 50155-50165 . |
| APA | Wang, Qian , Wang, Qin , Yuan, Rusheng , Zhang, Zizhong , Long, Jinlin , Lin, Huaxiang . Facile Preparation of the ZnSe/Ag2Se Binary Heterojunction for Photocatalytic Antibacterial Efficiency . | ACS APPLIED MATERIALS & INTERFACES , 2023 , 15 (43) , 50155-50165 . |
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Iodine(i) doped ZnO nanoarray films (ZnO/I-X) were prepared on a silicon wafer by the in situ growth method. The structure and morphology of the samples were tested by XRD, SEM, DRS. The hydrophobic properties were characterized by the water contact angle on the surface. The results show that the doped iodine extended the light absorption range of the ZnO nanofilm and the nanoarray film (ZnO/I-X) are super hydrophobic. The antimicrobial activity of iodine(i)-doped ZnO nanofilms towards E. coli under visible light illumination is much higher than that of the ZnO film. In addition, ZnO/I-3 exhibits the best antimicrobial activity.
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| GB/T 7714 | Xiao, Yingxin , Han, Shitong , Xi, Hailing et al. Super-hydrophobic and photocatalytic antimicrobial activity of iodine-doped ZnO nanoarray films [J]. | NEW JOURNAL OF CHEMISTRY , 2022 , 46 (7) : 3140-3145 . |
| MLA | Xiao, Yingxin et al. "Super-hydrophobic and photocatalytic antimicrobial activity of iodine-doped ZnO nanoarray films" . | NEW JOURNAL OF CHEMISTRY 46 . 7 (2022) : 3140-3145 . |
| APA | Xiao, Yingxin , Han, Shitong , Xi, Hailing , Jin, Yubo , Lin, Huaxiang , Yuan, Rusheng et al. Super-hydrophobic and photocatalytic antimicrobial activity of iodine-doped ZnO nanoarray films . | NEW JOURNAL OF CHEMISTRY , 2022 , 46 (7) , 3140-3145 . |
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采用溶剂热法和煅烧处理制备了I掺杂ZnO微米棒,系统表征了ZnO微米棒的结构、形貌及光吸收性能.以大肠杆菌为研究对象,用菌落计数法测试了样品的可见光光催化抗菌活性.结果表明,溶剂热法合成的pre-I-ZnO含较多体相缺陷,而经过在空气中以400℃高温煅烧2 h处理可得到富含表面氧空位的I-ZnO.单一的ZnO在可见光照射下的抗菌能力很低,而I掺杂ZnO的可见光光催化抗菌活性得到明显提高.煅烧处理的I-ZnO对细菌的杀灭率明显高于pre-I-ZnO和ZnO.在可见光光照4 h后,I-ZnO的反应体系中菌液的浓度由106～7 cfu/mL降到26 cfu/mL,杀菌率达99.999％以上.在光催化抗菌过程产生的活性物种中,光生电子、·O2-和H2O2起了主要作用.
Keyword ：
光催化 光催化 可见光 可见光 抗菌 抗菌 碘-氧化锌 碘-氧化锌
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| GB/T 7714 | 周塘华 , 林华香 , 龙金林 et al. I掺杂ZnO的制备及其光催化抗菌性能探究 [J]. | 防化研究 , 2022 , 1 (1) : 59-66 . |
| MLA | 周塘华 et al. "I掺杂ZnO的制备及其光催化抗菌性能探究" . | 防化研究 1 . 1 (2022) : 59-66 . |
| APA | 周塘华 , 林华香 , 龙金林 , 员汝胜 , 付贤智 . I掺杂ZnO的制备及其光催化抗菌性能探究 . | 防化研究 , 2022 , 1 (1) , 59-66 . |
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Mustard gas is a kind of erosive poison with great harm and used as a chemical weapon since World War. It has suggested that the photocatalytic technology is an effective method to eliminate it. Because the small difference in molecular structure between 2-CEES and Mustard gas, and the less toxic of 2-CEES, 2-CEES is often used as a simulator to evaluate the photocatalytic activity of catalysts. In this work, symbiotic mixture of Bi2WO6 and Bi6O6 (OH)(3)(NO3)(3)center dot 1.5H(2)O nanosheets doped with Mo (Mo-B-B) have been synthesized by a facile hydrothermal treatment. The samples were characterized by XRD, DRS, XPS, SEM, TEM, Raman, and PL. The photocatalytic activity of the samples was evaluated by measuring the degradation of 2-CEES under visible light irradiation. The results showed that the doped Mo reduce the Eg of bare symbiotic mixture and improve the separation efficiency of photo-generated carriers that is beneficial to photocatalytic activity. The optimum amount of doped Mo is 5% that exhibits the best activity for degradation for 2-CEES.
Keyword ：
2-CEES 2-CEES Mo-doping Mo-doping Photocatalytic degradation Photocatalytic degradation
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| GB/T 7714 | Yang, Haoguo , Guo, Yijun , Han, Shitong et al. Synthesis of Mo-doped symbiotic mixture of Bi2WO6 and Bi6O6(OH)(3)(NO3)(3)center dot 1.5H(2)O nanosheets with enhanced photocatalytic degradation for mustard gas simulator 2-CEES [J]. | RESEARCH ON CHEMICAL INTERMEDIATES , 2022 . |
| MLA | Yang, Haoguo et al. "Synthesis of Mo-doped symbiotic mixture of Bi2WO6 and Bi6O6(OH)(3)(NO3)(3)center dot 1.5H(2)O nanosheets with enhanced photocatalytic degradation for mustard gas simulator 2-CEES" . | RESEARCH ON CHEMICAL INTERMEDIATES (2022) . |
| APA | Yang, Haoguo , Guo, Yijun , Han, Shitong , Xi, Hailing , Lin, Huaxiang , Yuan, Rusheng et al. Synthesis of Mo-doped symbiotic mixture of Bi2WO6 and Bi6O6(OH)(3)(NO3)(3)center dot 1.5H(2)O nanosheets with enhanced photocatalytic degradation for mustard gas simulator 2-CEES . | RESEARCH ON CHEMICAL INTERMEDIATES , 2022 . |
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Tailoring the surficial chemical environment of two-dimensional materials by organic modification is an effective way to optimize their catalytic behaviors. Herein, we present a dynamic coordination approach to improve the photocatalytic performance of ultrathin Co2CO3(OH)(2) nanosheets (u-CoCH) in NIR light (lambda > 780 nm) driven carbonylation reaction by using the reacting substrates (diamines) as the ligands. The coordination of diamines with surface Co2+ ions form a binuclear complex at the crystallographic planes of u-CoCH. The as-formed complexes can reduce the energy barrier of carbonylation reaction by weaking the N-H bond of the substrate on u-CoCH, and afford enhanced light response as well as the prolonged photogenerated electron lifetime. Together with the successful synthesis of a series of important structural motifs in pharmaceuticals and bioactive agents, the promoted photosynthesis reaction mode via in-situ formed surface complexes offers a model toward full-spectrum-solar-energy conversion in the field of chemical synthesis.
Keyword ：
Binuclear complex Binuclear complex Carbonylation Carbonylation NIR light excitation NIR light excitation Photocatalysis Photocatalysis Ultrathin Co2CO3(OH)(2) nanosheets Ultrathin Co2CO3(OH)(2) nanosheets
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| GB/T 7714 | Wei, Yingcong , Zha, Wenying , Wang, Lele et al. In-situ Formed Surface Complexes Promoting NIR-Light-Driven Carbonylation of Diamine with CO on Ultrathin Co2CO3(OH)(2) Nanosheets [J]. | APPLIED CATALYSIS B-ENVIRONMENTAL , 2022 , 306 . |
| MLA | Wei, Yingcong et al. "In-situ Formed Surface Complexes Promoting NIR-Light-Driven Carbonylation of Diamine with CO on Ultrathin Co2CO3(OH)(2) Nanosheets" . | APPLIED CATALYSIS B-ENVIRONMENTAL 306 (2022) . |
| APA | Wei, Yingcong , Zha, Wenying , Wang, Lele , Ma, Xiongfeng , Zhang, Shaohui , Sa, Rongjian et al. In-situ Formed Surface Complexes Promoting NIR-Light-Driven Carbonylation of Diamine with CO on Ultrathin Co2CO3(OH)(2) Nanosheets . | APPLIED CATALYSIS B-ENVIRONMENTAL , 2022 , 306 . |
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本发明公开了一种用于光解水产氢的直接Z型光催化剂的制备方法，其采用共沉淀法制备钛基钙钛矿材料NiTiO3前驱体，通过进一步高温煅烧制备NiTiO3载体，再利用共沉淀法以及进一步水热法原位制备NiTiO3/CdxZn(1‑x)S直接Z型光催化剂。该催化剂独特的直接Z型异质结可以改善硫化物固溶体的稳定性并提高电荷的分离和迁移速度，显著降低光生电子和空穴的复合速率，进而提高光解水产氢反应的效率。同时，该催化剂制备方法简单易行，无助催化剂负载，在光催化领域具有广阔的应用前景。
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| GB/T 7714 | 丁正新 , 李碧芳 , 熊壮 et al. 一种直接Z型光催化剂及其制备方法和应用 : CN202110014140.4[P]. | 2021-01-06 . |
| MLA | 丁正新 et al. "一种直接Z型光催化剂及其制备方法和应用" : CN202110014140.4. | 2021-01-06 . |
| APA | 丁正新 , 李碧芳 , 熊壮 , 韩世同 , 龙金林 , 林华香 . 一种直接Z型光催化剂及其制备方法和应用 : CN202110014140.4. | 2021-01-06 . |
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