Journal of Photochemistry and Photobiology A-chemistry最新文献

筛选
英文 中文
Nitrogen/sulfur dual-doped porous carbon microtubes prepared from poplar catkins as high-performance counter electrode of dye-sensitized solar cells 杨柳絮制备氮/硫双掺杂多孔碳微管作为染料敏化太阳能电池的高性能对电极
IF 4.1 3区 化学
Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2025-06-08 DOI: 10.1016/j.jphotochem.2025.116561
Jihui Li, Dongsheng Wang, Guiqiang Wang, Fanning Meng
{"title":"Nitrogen/sulfur dual-doped porous carbon microtubes prepared from poplar catkins as high-performance counter electrode of dye-sensitized solar cells","authors":"Jihui Li,&nbsp;Dongsheng Wang,&nbsp;Guiqiang Wang,&nbsp;Fanning Meng","doi":"10.1016/j.jphotochem.2025.116561","DOIUrl":"10.1016/j.jphotochem.2025.116561","url":null,"abstract":"<div><div>The fabrication of low-cost counter electrode using heteroatom-doped porous carbon derived from renewable biomass is a promising strategy to assemble cost-effective dye-sensitized solar cells (DSCs). Here, nitrogen/sulfur dual-doped porous carbon microtubes (NSPCMTs) are prepared by a direct pyrolysis process using poplar catkins as the carbon source and thiourea as the nitrogen (N) and sulfur (S) source. It is found that the as-prepared NSPCMTs inherit the microtube morphology of poplar catkins and the thiourea addition results in the dual-doping of N and S and promotes the pore formation on the wall of carbon microtubes. The obtained NSPCMTs display a specific surface area of 379.55 m<sup>2</sup> g<sup>−1</sup>. The N/S dual-doping and the high surface area enhance the surface accessibility and increase the electrocatalytic active sites of NSPCMTs, which endows NSPCMTs with a superior electrocatalytic performance. Cyclic voltammetry and electrochemical impedance spectroscopy measurements indicates that NSPCMT electrode has the same electrocatalytic activity as conventional Pt electrode. Consequently, the DSC with NSPCMT electrode demonstrates an efficiency of 8.27 %, approaching to the performance of Pt electrode-based cell.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"469 ","pages":"Article 116561"},"PeriodicalIF":4.1,"publicationDate":"2025-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144239976","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Construction and application of Z-scheme heterojunction MOF@COF core-shell materials: Efficient adsorption and synergistic photocatalytic removal of high-concentration organic pollutants z型异质结MOF@COF核壳材料的构建与应用:高效吸附与协同光催化去除高浓度有机污染物
IF 4.1 3区 化学
Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2025-06-07 DOI: 10.1016/j.jphotochem.2025.116554
Yuxin Sun , Binquan Yang , Zhangpei Chen , Linshan Wang , Yuqiu Huo , Jianshe Hu
{"title":"Construction and application of Z-scheme heterojunction MOF@COF core-shell materials: Efficient adsorption and synergistic photocatalytic removal of high-concentration organic pollutants","authors":"Yuxin Sun ,&nbsp;Binquan Yang ,&nbsp;Zhangpei Chen ,&nbsp;Linshan Wang ,&nbsp;Yuqiu Huo ,&nbsp;Jianshe Hu","doi":"10.1016/j.jphotochem.2025.116554","DOIUrl":"10.1016/j.jphotochem.2025.116554","url":null,"abstract":"<div><div>High concentrations of organic pollutants have become a significant environmental issue worldwide. In this study, a hybrid material of metal–organic framework (MOF) and covalent organic framework (COF) was synthesized by covalently modifying NH<sub>2</sub>-MIL-125(Ti) with the COF monomers 1,3,5-tri(4-aminophenyl)benzene (TAPB) and 2,5-di(allyloxy)benzaldehyde (TBAB) via an acetic acid-catalyzed reaction, named NH<sub>2</sub>-MIL-125(Ti)@TAPB-TBAB (NMTT). The resulting NMTT material inherited the advantages of both MOF and COF, including good crystallinity, large surface area, porous structure, and strong visible light absorption capacity. The prepared MOF@COF hybrid demonstrated excellent adsorption performance and photocatalytic activity. Experimental results showed that NMTT was highly effective in removing high concentrations of rhodamine B (RhB) dye, with a removal rate of 100 % for 50 ppm RhB at pH = 5, significantly outperforming both NH<sub>2</sub>-MIL-125(Ti) and TAPB-TBAB. Additionally, NMTT showed broad applicability for the removal of other high-concentration organic pollutants. Through systematic characterization and experimental analysis, a potential Z-scheme heterojunction reaction mechanism was proposed. This study provides new insights for the development of novel MOF@COF composite materials and presents promising potential for environmental remediation of high-concentration organic pollutants.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"469 ","pages":"Article 116554"},"PeriodicalIF":4.1,"publicationDate":"2025-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144262216","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Covalent bonded Bi4Ti3O12/covalent organic frameworks inorganic/organic heterojunctions for robust cocatalyst-free photocatalytic hydrogen production 共价键Bi4Ti3O12/共价有机框架无机/有机异质结用于无共催化剂光催化制氢
IF 4.1 3区 化学
Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2025-06-07 DOI: 10.1016/j.jphotochem.2025.116560
Yuqing Gao , Zhen Zhan , Jingxiang Hao , Mingxia Li , Liping Guo , Zhenzi Li , Songhua Cai , Xuepeng Wang , Wei Zhou
{"title":"Covalent bonded Bi4Ti3O12/covalent organic frameworks inorganic/organic heterojunctions for robust cocatalyst-free photocatalytic hydrogen production","authors":"Yuqing Gao ,&nbsp;Zhen Zhan ,&nbsp;Jingxiang Hao ,&nbsp;Mingxia Li ,&nbsp;Liping Guo ,&nbsp;Zhenzi Li ,&nbsp;Songhua Cai ,&nbsp;Xuepeng Wang ,&nbsp;Wei Zhou","doi":"10.1016/j.jphotochem.2025.116560","DOIUrl":"10.1016/j.jphotochem.2025.116560","url":null,"abstract":"<div><div>The high cost of noble metal cocatalysts is impractical for the practical application of photocatalytic hydrogen production. Therefore, the development of photocatalysts to achieve hydrogen production under cocatalyst-free conditions has important economical value. In this work, an excellent visible light responsive covalent organic framework (TpPa-1-COF) and Bi<sub>4</sub>Ti<sub>3</sub>O<sub>12</sub> (BTO) are covalently bonded to construct BTO/TpPa-1-COF inorganic/organic heterojunctions. The obtained BTO/40 %TpPa-1-COF heterojunction achieves high photocatalytic activity without adding cocatalyst. The optimal photocatalytic hydrogen production rate is up to 1055 μmol/g/h, which is 24.3 and 6.2 times higher than that of TpPa-1-COF and physically mixed BTO-40 %TpPa-1-COF. Further studies confirm that the covalent connection between BTO and TpPa-1-COF components can greatly improve the photogenerated charge transfer of TpPa-1-COF, resulting in efficient hydrogen production activity. This provides a new perspective for promoting the practical application of efficient photocatalytic applications.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"469 ","pages":"Article 116560"},"PeriodicalIF":4.1,"publicationDate":"2025-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144239973","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Fabrication and characterization of co-sensitized dye solar cells incorporating cyclodextrin functional layers with energy transfer from spiropyran derivatives to SQ2 dye 含有环糊精功能层并能从螺吡喃衍生物转移到SQ2染料的共敏化染料太阳能电池的制备和表征
IF 4.1 3区 化学
Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2025-06-06 DOI: 10.1016/j.jphotochem.2025.116531
Ryuhei Ejima, Keitaro Ono, Michihiro Hara
{"title":"Fabrication and characterization of co-sensitized dye solar cells incorporating cyclodextrin functional layers with energy transfer from spiropyran derivatives to SQ2 dye","authors":"Ryuhei Ejima,&nbsp;Keitaro Ono,&nbsp;Michihiro Hara","doi":"10.1016/j.jphotochem.2025.116531","DOIUrl":"10.1016/j.jphotochem.2025.116531","url":null,"abstract":"<div><div>We developed dye-sensitized solar cells (DSSCs) using the sensitizing dye 1,5-carboxy-2-[[3-[(2,3-dihydro-1,1-dimethyl-3-ethyl-1H-benzo[e]indol-2-ylidene)methyl]-2-hydroxy-4-oxo-2-cyclobuten-1-ylidene]methyl]-3,3-dimethyl-1-octyl-3H-indolium (SQ2) and the photochromic molecule 1,3,3-trimethyl indolino-6′-nitrobenzopyrylospiran (SPNO<sub>2</sub>). DSSCs incorporating photochromic molecules can regulate photoelectric conversion efficiency (η) through external light irradiation. To enhance η<strong>,</strong> cyclodextrins (CDs) (α-CD, β-CD, γ-CD) were introduced. Among them, γ-CD improved η from 1.2 % to 1.5 % by suppressing SQ2 aggregation. The color of the SQ2/CDs/SPNO<sub>2</sub>-containing photoelectrode changed from blue to purple under UV irradiation and from purple to green under visible light. The η of DSSCs increased after UV irradiation and decreased under visible light. However, direct electron injection from the photochromic molecule appeared to be challenging, suggesting that the efficiency enhancement was primarily due to Förster resonance energy transfer (FRET) from SPNO<sub>2</sub> to SQ2. FRET efficiency calculations showed that β-CD exhibited the highest efficiency among CDs. These findings indicate that the co-sensitization of DSSCs by SPNO<sub>2</sub>-SQ2 and SQ2 alone, facilitated by their respective photoabsorption properties, enables externally tunable photoelectric conversion<strong>.</strong> This study provides insights into high-performance DSSCs with tunable efficiency through CD inclusion effects and photochromic molecular energy transfer<strong>,</strong> contributing to solar energy advancements.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"469 ","pages":"Article 116531"},"PeriodicalIF":4.1,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144253638","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
How do different phase structures of crystalline e-TiO2 nanomaterials affect the UV resistance of unsaturated polyester Resins? 不同相结构的e-TiO2纳米材料如何影响不饱和聚酯树脂的抗紫外线性能?
IF 4.1 3区 化学
Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2025-06-06 DOI: 10.1016/j.jphotochem.2025.116555
Quang-Thuc Dong , Anh-Son Nguyen , Quan-Doan Mai , Anh-Tuan Pham , Anh-Tuan Le
{"title":"How do different phase structures of crystalline e-TiO2 nanomaterials affect the UV resistance of unsaturated polyester Resins?","authors":"Quang-Thuc Dong ,&nbsp;Anh-Son Nguyen ,&nbsp;Quan-Doan Mai ,&nbsp;Anh-Tuan Pham ,&nbsp;Anh-Tuan Le","doi":"10.1016/j.jphotochem.2025.116555","DOIUrl":"10.1016/j.jphotochem.2025.116555","url":null,"abstract":"<div><div>Unsaturated polyester resins (UPRs) are widely used in construction and composite materials due to their good mechanical properties and processability. However, their susceptibility to ultraviolet (UV) resistance limits their long-term outdoor use. To improve UV resistance, electrochemically synthesized TiO<sub>2</sub> nanoparticles (e-TiO<sub>2</sub>) with strong UV absorption were incorporated into the UPR to enhance UV resistance. A critical challenge lies in balancing UV shielding effectiveness with the photocatalytic activity of e-TiO<sub>2</sub>, which can accelerate polymer degradation. This study investigates the influence of three crystalline phases of e-TiO<sub>2</sub> anatase, brookite and rutile on the UV protection performance of UPR/e-TiO<sub>2</sub> nanocomposites. The results showed that UPR reinforced with anatase, brookite and rutile achieved UV protection improvements of 72.2%, 49.2%, and 33.7%, respectively, compared to pure UPR. Anatase phase e-TiO<sub>2</sub> demonstrated the best performance, attributed to its fine particle size and moderate photocatalytic activity, providing a more favorable balance between protection and material stability. These nanocomposites were successfully applied in engineered quartz stone production, showing enhanced UV durability, demonstrating strong potential for large-scale outdoor applications. These findings highlight the importance of the e-TiO<sub>2</sub> crystalline phase and particle properties in optimizing UV protection and open up new possibilities for durable, weather resistant UPR based materials in industrial scale applications.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"469 ","pages":"Article 116555"},"PeriodicalIF":4.1,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144253637","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Boosted photocatalytic NO conversion with inhibited NO2 generation over Nb2O5/g-C3N4 S-scheme heterojunction: nanostructured engineering and mechanism insight Nb2O5/g-C3N4 S-scheme异质结促进光催化NO转化,抑制NO2生成:纳米结构工程和机制洞察
IF 4.1 3区 化学
Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2025-06-05 DOI: 10.1016/j.jphotochem.2025.116545
Lin Cheng , Xueying Guo , Jianmin Luo , Ya Xue , Bin Liu , Haitao Ren , Mohsen Padervand , Xiaoyan Yu , Xinglei Wang
{"title":"Boosted photocatalytic NO conversion with inhibited NO2 generation over Nb2O5/g-C3N4 S-scheme heterojunction: nanostructured engineering and mechanism insight","authors":"Lin Cheng ,&nbsp;Xueying Guo ,&nbsp;Jianmin Luo ,&nbsp;Ya Xue ,&nbsp;Bin Liu ,&nbsp;Haitao Ren ,&nbsp;Mohsen Padervand ,&nbsp;Xiaoyan Yu ,&nbsp;Xinglei Wang","doi":"10.1016/j.jphotochem.2025.116545","DOIUrl":"10.1016/j.jphotochem.2025.116545","url":null,"abstract":"<div><div>The critical challenge in the photocatalytic treatment of low-concentration nitrogen oxides (NO<sub>x</sub>) is to achieve deep oxidation of NO while suppressing the formation of toxic intermediate NO<sub>2</sub>. Herein, a Nb<sub>2</sub>O<sub>5</sub>/g-C<sub>3</sub>N<sub>4</sub> S-scheme heterojunction is designed to address this challenge through tailored charge dynamics. Experimental results and theoretical calculations synergistically validate the S-scheme heterojunction featuring an interfacial electric field (IEF)-driven directional charge separation mechanism. This configuration synergistically enhances charge separation efficiency while maintaining robust redox potentials, thereby effectively activating hydroxyl radicals (<sup><img></sup>OH). As the dominant reactive species, <sup><img></sup>OH facilitates deep oxidation of NO while effectively inhibiting toxic NO<sub>2</sub> by-product formation. At an initial NO concentration of 800 ppb, the Nb<sub>2</sub>O<sub>5</sub>/g-C<sub>3</sub>N<sub>4</sub> S-scheme heterojunction achieved an excellent removal rate of 68.3 % with suppressed NO<sub>2</sub> byproduct generation (24.6 ppb) under visible light irradiation (λ ≥ 420 nm) within 20 min. Furthermore, the reaction intermediates were monitored by in-situ diffused reflection Fourier transform infrared spectroscopy (DRIFTS), identifying nitrate as the terminal oxidation product. This work advances the rational design of S-scheme photocatalysts and offers a viable strategy for environmental remediation of NO<sub>x</sub> contaminants under visible-light-driven conditions.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"469 ","pages":"Article 116545"},"PeriodicalIF":4.1,"publicationDate":"2025-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144239974","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dual antioxidant-oxidant activity, optical properties and thermal stability of 1,5-diaminonaphthalene 1,5-二氨基萘的双抗氧化活性、光学性质和热稳定性
IF 4.1 3区 化学
Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2025-06-04 DOI: 10.1016/j.jphotochem.2025.116541
Federico Fiori , Federico Olia , Marta Cadeddu , Stefano Livraghi , Alessia Zollo , Laura Caggiu , Sebastiano Garroni , Roberto Anedda , Davide Carboni , Luca Malfatti , Plinio Innocenzi
{"title":"Dual antioxidant-oxidant activity, optical properties and thermal stability of 1,5-diaminonaphthalene","authors":"Federico Fiori ,&nbsp;Federico Olia ,&nbsp;Marta Cadeddu ,&nbsp;Stefano Livraghi ,&nbsp;Alessia Zollo ,&nbsp;Laura Caggiu ,&nbsp;Sebastiano Garroni ,&nbsp;Roberto Anedda ,&nbsp;Davide Carboni ,&nbsp;Luca Malfatti ,&nbsp;Plinio Innocenzi","doi":"10.1016/j.jphotochem.2025.116541","DOIUrl":"10.1016/j.jphotochem.2025.116541","url":null,"abstract":"<div><div>1,5-Diaminonaphthalene (DAN) is a small polyaromatic molecule known for its remarkable antioxidant properties. While its effective radical-scavenging activity under ambient conditions has been previously documented, this study unveils an equally compelling yet contrasting duality in the nature of this molecule. Indeed, DAN can also act as a photosensitizer under UV light irradiation, generating reactive singlet oxygen species, <sup>1</sup>O<sub>2</sub>. We have studied the mechanisms underlying this dual behavior using a combination of characterization techniques, including FTIR, XRD, thermogravimetric analysis, UV–Vis spectroscopy, and electronic paramagnetic resonance. Without light, DAN efficiently neutralizes the 2,2-Diphenyl-1-picrylhydrazyl (DPPH<sup>·</sup>) radicals used as probe molecules through hydrogen atom transfer and exhibits antioxidant properties. However, under UV-light irradiation, DAN nature shifts dramatically. The photo-stimulation enables the production of reactive singlet oxygen with significant oxidative response, as demonstrated by the test with the standard probe indocyanine green. This light-triggered transformation highlights the versatility of DAN, bridging its use as a radical scavenger and pro-oxidant. The findings pave the way for exploiting the dynamic redox properties of DAN in designing multifunctional nanomaterials where controlled oxidative and antioxidative responses are critical.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"469 ","pages":"Article 116541"},"PeriodicalIF":4.1,"publicationDate":"2025-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144253609","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dual-Functional 2D-3D Zn2In2S5 for photocatalytic degradation of azo dye and hydrogen production 双功能2D-3D Zn2In2S5光催化降解偶氮染料和制氢
IF 4.1 3区 化学
Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2025-06-04 DOI: 10.1016/j.jphotochem.2025.116542
Zongwen Zhang , Yuge Zhang , Yi Zhang , Yueyue Kong , Xiang Li , Muhammad Tayyab , Shifu Chen , Sugang Meng
{"title":"Dual-Functional 2D-3D Zn2In2S5 for photocatalytic degradation of azo dye and hydrogen production","authors":"Zongwen Zhang ,&nbsp;Yuge Zhang ,&nbsp;Yi Zhang ,&nbsp;Yueyue Kong ,&nbsp;Xiang Li ,&nbsp;Muhammad Tayyab ,&nbsp;Shifu Chen ,&nbsp;Sugang Meng","doi":"10.1016/j.jphotochem.2025.116542","DOIUrl":"10.1016/j.jphotochem.2025.116542","url":null,"abstract":"<div><div>In this study, we synthesized a two-dimensional-three-dimensional (2D-3D) flower-like Zn<sub>2</sub>In<sub>2</sub>S<sub>5</sub> (ZIS225) photocatalyst via the hydrothermal method. The photocatalytic performance of ZIS225 was systematically evaluated for the degradation of methyl orange (MO) and hydrogen production under visible light irradiation. ZIS225 achieved a 100 % degradation rate of MO within 60 min, with a reaction rate constant of 6.11 h<sup>−1</sup>, significantly outperforming commercial anatase TiO<sub>2</sub> (degradation rate of 42.7 % and reaction rate constant of 0.54 h<sup>−1</sup>). Moreover, ZIS225 demonstrated the ability to simultaneously degrade MO and produce hydrogen, with a hydrogen production rate of 4.9 μmol g<sup>−1</sup>h<sup>−1</sup> and a MO degradation rate of 99.7 %. The hydrogen production rate increased to 35.3 μmol g<sup>−1</sup>h<sup>−1</sup> upon in-situ photodeposition of 1 % Pt, maintaining stable performance over three cycles. Photoelectrochemical and electron paramagnetic resonance (EPR) analyses identified superoxide radicals (•O<sub>2</sub><sup>−</sup>) and photogenerated holes (h<sup>+</sup>) as the primary active species. This research provides valuable insights for the development of efficient photocatalytic materials and offers technical references for dye pollution treatment and clean energy conversion.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"469 ","pages":"Article 116542"},"PeriodicalIF":4.1,"publicationDate":"2025-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144231079","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Green validation of synchronous fluorometry study applied on binary mixture (risperidone and biperiden hydrochloride as a co-administered drugs) used for treatment of schizophrenia 同步荧光法研究应用于治疗精神分裂症的二元混合物(利培酮和盐酸双培脲共同给药)的绿色验证
IF 4.1 3区 化学
Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2025-06-03 DOI: 10.1016/j.jphotochem.2025.116536
Hesham Salem , Ramy M. Elsabaa , Nadeen Emad , Mahmoud A. Abdelmajed , Mohamed Karem , Mohamed Rafat , Abdullah Hamed , Manar Wael , Mariam Mohamed , Asmaa A. Hamed
{"title":"Green validation of synchronous fluorometry study applied on binary mixture (risperidone and biperiden hydrochloride as a co-administered drugs) used for treatment of schizophrenia","authors":"Hesham Salem ,&nbsp;Ramy M. Elsabaa ,&nbsp;Nadeen Emad ,&nbsp;Mahmoud A. Abdelmajed ,&nbsp;Mohamed Karem ,&nbsp;Mohamed Rafat ,&nbsp;Abdullah Hamed ,&nbsp;Manar Wael ,&nbsp;Mariam Mohamed ,&nbsp;Asmaa A. Hamed","doi":"10.1016/j.jphotochem.2025.116536","DOIUrl":"10.1016/j.jphotochem.2025.116536","url":null,"abstract":"<div><div>Risperidone and biperiden hydrochloride concentration levels<!--> <!-->have been successfully quantified in laboratory prepared mixture, tablets for each studied drug and spiked human plasma<!--> <!-->through an innovative spectrofluorimetric approach. In order to successfully estimate risperidone at 302 nm and biperiden hydrochloride at 405 nm in the presence of each other at Δλ of 60 nm, the spectrofluorometric technique’s selectivity is increased by combining both derivative and synchronous spectrofluorometric approaches. The technique was extensively validated by following the validation requirements of the International Conference on Harmonization, and linearity was achieved for the two medicines across the range of 20–200 ng mL<sup>−1</sup>. The technique was successfully used to commercial tablets, combination made in the lab and spiked<!--> <!-->human plasma. The results showed good agreement with the approaches that have been published. The measurement of risperidone and biperiden hydrochloride in spiked human plasma samples was relevant. The quantitation limits were 11.626 and 11.522 ngmL<sup>−1</sup> and the detection limits were 3.873 and 5.023 ng ml<sup>−1</sup> for risperidone and biperiden hydrochloride, respectively. A statistical comparison of the results with other published analytical techniques revealed no significant difference. The validation of the procedure was successfully completed in compliance with ICH guidelines. The suggested approach included an environmentally beneficial element by using water as the ideal diluting solvent.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"469 ","pages":"Article 116536"},"PeriodicalIF":4.1,"publicationDate":"2025-06-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144279613","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
An experimental evidence for the isotropic absorption by cis isomers of azo compounds in the n−π∗ band 偶氮化合物顺式异构体在n−π *波段各向同性吸收的实验证据
IF 4.1 3区 化学
Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2025-06-03 DOI: 10.1016/j.jphotochem.2025.116509
S. Grebenkin, V.M. Syutkin
{"title":"An experimental evidence for the isotropic absorption by cis isomers of azo compounds in the n−π∗ band","authors":"S. Grebenkin,&nbsp;V.M. Syutkin","doi":"10.1016/j.jphotochem.2025.116509","DOIUrl":"10.1016/j.jphotochem.2025.116509","url":null,"abstract":"<div><div>Polymeric materials and molecular glasses containing azo moieties have been the subject of many investigations due to the light driven behavior of such materials. The primary photochemical process in these systems is the light-induced <em>trans-cis</em> isomerization of azo moieties. It is commonly accepted that the <em>trans</em> molecules of azo chromophores absorb light by dipole mechanism, i.e., proportionally to the square cosine of the angle between the transition dipole moment and the light polarization. However, there is no consensus regarding the anisotropy of the absorption cross section of <em>cis</em> molecules. In this study, <em>p</em>-azotoluene (AT) and 1-naphthyl-<em>p</em>-azo-methoxybenzene (NAMB) dissolved in <em>ortho</em>-terphenyl (OTP) are irradiated with linearly polarized light in the region of the <span><math><mrow><mi>n</mi><mo>−</mo><msup><mrow><mi>π</mi></mrow><mrow><mo>∗</mo></mrow></msup></mrow></math></span> absorption band in a wide temperature range including the glass transition temperature of OTP, <span><math><msub><mrow><mi>T</mi></mrow><mrow><mi>g</mi></mrow></msub></math></span>. Upon irradiation, the <em>trans-cis</em> isomerization and the reorientation of azo chromophores occur. Near <span><math><msub><mrow><mi>T</mi></mrow><mrow><mi>g</mi></mrow></msub></math></span>, a kink in temperature dependence of the photostationary absorbance is observed. This fact together with modeling the time profiles of absorbance and anisotropy lead us to conclude that <em>cis</em> molecules of both azo chromophores absorb light isotropically upon irradiation in the <span><math><mrow><mi>n</mi><mo>−</mo><msup><mrow><mi>π</mi></mrow><mrow><mo>∗</mo></mrow></msup></mrow></math></span> absorption band.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"469 ","pages":"Article 116509"},"PeriodicalIF":4.1,"publicationDate":"2025-06-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144222684","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信