Junjie Yuan , Zongli Yang , Jiayi Zou , Zhongqiu Wu , Zhaolong Wang , Liang Wang , Wenlong Shen , Quan Zhang , Hui Xu
{"title":"Functionalized sulfonic acid groups enhance solubility and stability of graphene quantum dots for efficient photosynthesis of lettuce","authors":"Junjie Yuan , Zongli Yang , Jiayi Zou , Zhongqiu Wu , Zhaolong Wang , Liang Wang , Wenlong Shen , Quan Zhang , Hui Xu","doi":"10.1016/j.jphotochem.2025.116280","DOIUrl":"10.1016/j.jphotochem.2025.116280","url":null,"abstract":"<div><div>Graphene quantum dots exhibit outstanding fluorescence properties, low cytotoxicity, and exceptional biocompatibility when interacting with plant cells, showcasing significant potential for photosynthesis of plants, such as lettuce. However, the poor dispersion and stability in aqueous solutions have hindered its photosynthetic efficiency. To address this issue, this work demonstrated the sulfonic acid group functionalized graphene quantum dots (SAG-GQDs), in which the sulfonic acid group prominently increased hydrophilicity, thus leading to an enhanced dispersion and stability of SAG-GQDs for efficient lettuce photosynthesis. Results indicated that the functionalized SAG-GQDs with spraying concentration of 3600 mg/L displayed the best photosynthetic efficiency for lettuce growth, including net photosynthetic rate of 8.6 μmol CO<sub>2</sub> m<sup>−2</sup> s<sup>−1</sup>, increased leaf fresh weight of 36%, and nutritional 14 mg/g soluble sugar with biocompatibility availability. Our work suggests the feasibility of functionalized sulfonic acid group in regulating dispersion and stability of graphene quantum dots for promoting photosynthetic efficiency of lettuce plants.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"463 ","pages":"Article 116280"},"PeriodicalIF":4.1,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143142540","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}
Suya Gan , Li-Xin Gao , Zitong Cao , Chun Zhang , Yiqiu Fu , Wen-Long Wang
{"title":"Synthesis, photophysical properties and fluorescent application of novel [1,2,4]triazolo[1,5-a]pyrimidin-7(4H)-one derivatives","authors":"Suya Gan , Li-Xin Gao , Zitong Cao , Chun Zhang , Yiqiu Fu , Wen-Long Wang","doi":"10.1016/j.jphotochem.2025.116294","DOIUrl":"10.1016/j.jphotochem.2025.116294","url":null,"abstract":"<div><div>To extend the application of our theoretical screening method for exploring novel fluorescent fragments, we identified [1,2,4]triazolo[1,5-a]pyrimidin-7(4H)-one as a potential fluorophore, whose optical properties are rarely investigated. In this work, nineteen of novel [1,2,4]triazolo[1,5-a]pyrimidin-7(4H)-one derivatives were designed, synthesized and the relationship between the structure and fluorescence property of [1,2,4]triazolo[1,5-a]pyrimidin-7(4H)-one derivatives was systematically elucidated. The representative compound 5b exhibited notable fluorescence intensity with good fluorescence quantum yield (Φ = 0.285) in PBS. More importantly, compound 5b selectively detected the Fe<sup>3+</sup> ions through fluorescent quenching effect with rapid response, good anti-interference and low detection limit (LOD = 1.82 μM), and could be applied for encryption ink. This work provides an efficient way to explore novel fluorescent molecules.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"464 ","pages":"Article 116294"},"PeriodicalIF":4.1,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143230433","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}
{"title":"Fluorometric detection of Hg2+ via metal displacement of BODIPY-Fe(III) complex in aqueous media","authors":"Pornthip Piyanuch , Jirapat Santatiwongchai , Sarawoot Impeng , Anyanee Kamkaew , Suttipong Wannapaiboon , Kantapat Chansaenpak","doi":"10.1016/j.jphotochem.2025.116291","DOIUrl":"10.1016/j.jphotochem.2025.116291","url":null,"abstract":"<div><div>A selective and sensitive fluorogenic chemosensor based on Fe<sup>3+</sup>-BODIPY complex (<strong>BPH-Fe</strong>) was developed for the specific binding toward Hg<sup>2+</sup> in aqueous system. This sensor reveals rapid recognition and simple detection of Hg<sup>2+</sup> via metal displacement approach. The <strong>BPH-Fe</strong> complex showed excellently selective chelation to Hg<sup>2+</sup> and was not affected by other interfering metal ions. This developed sensor exhibited the quenching of green fluorescence emission along with yellow to orange color change upon exposure to Hg<sup>2+</sup> ion. The stoichiometric ratio of <strong>BPH-Fe</strong> complex to Hg<sup>2+</sup> was established to be 1:1 by Job’s method. The detection limit of the sensor in the determination of Hg<sup>2+</sup> was calculated as 1.8 ppb, which is lower than WHO and U.S. EPA allowable level (2 ppb). The X-ray absorption spectroscopy (XAS) probed at Hg L3-edge and Fe K-edge revealed the metal displacement of Fe<sup>3+</sup> in <strong>BPH-Fe</strong> complex to form <strong>BPH-Hg<sup>2+</sup></strong> complex upon sensing process. Furthermore, <strong>BPH-Fe</strong> had been successfully employed to determine Hg<sup>2+</sup> in living cancer cells.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"463 ","pages":"Article 116291"},"PeriodicalIF":4.1,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143142927","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}
Tonghan Zhao , Dengke Song , Jing Wang , Huadong Chen, Wenqian Chen, Xiaohui Zhu
{"title":"Nanoshell-mediated color tuning of erbium-sensitized upconversion nanoparticles for advanced phototherapy above 1500 nm","authors":"Tonghan Zhao , Dengke Song , Jing Wang , Huadong Chen, Wenqian Chen, Xiaohui Zhu","doi":"10.1016/j.jphotochem.2025.116285","DOIUrl":"10.1016/j.jphotochem.2025.116285","url":null,"abstract":"<div><div>Conventional phototherapy, including photodynamic therapy (PDT) and photothermal therapy (PTT), is often limited by the risk of serious photodamage and shallow tissue caused by the excitation light. Lanthanide-doped upconversion nanoparticles (UCNPs) enable to convert long-wavelength light to short-wavelength emission, which, in principle, can address these issues in phototherapy. However, traditional UCNPs are mainly excitable in the near-infrared I region (700–900 nm), which still faces challenges such as strong light absorption/scattering and overheating side effects. Herein, we have developed an Er<sup>3+</sup>-sensitized upconversion nanoparticle (NaErF<sub>4</sub>@NaYbF<sub>4</sub>@NaYF<sub>4</sub>) in response to 1550 nm excitation light in the far NIR-II region. Through a core–shell–shell engineering strategy, the emissive signal of Er<sup>3+</sup> ion can be finely tailored from red-dominant to green-dominant, offering great flexibility in optical tuning of Er<sup>3+</sup> sensitized UCNPs under 1550 nm light excitation. Upon surface modification by a mesoporous silica shell and loading of dual photosensitive agents (MC540 (merocyanine 540) and FePc (iron phthalocyanine)), a synergistic PDT/PTT phototherapeutic nanoagent was constructed. Results showed that as-developed nanotherapeutic platform could solve the overheating problem and further enhance tissue penetration upon illumination by 1550 nm light, thus demonstrating great efficiency of combinational PDT/PTT for tumor treatment.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"463 ","pages":"Article 116285"},"PeriodicalIF":4.1,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143142935","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}
Subhendu Sekhar Bag , Hiranya Gogoi , Sujata Roy , Manoj Kumar Pradhan , Sangita Talukdar
{"title":"Fluorescent tetrazolylpyrene unnatural nucleoside in sensing BSA protein","authors":"Subhendu Sekhar Bag , Hiranya Gogoi , Sujata Roy , Manoj Kumar Pradhan , Sangita Talukdar","doi":"10.1016/j.jphotochem.2025.116290","DOIUrl":"10.1016/j.jphotochem.2025.116290","url":null,"abstract":"<div><div>A spectroscopic investigation of the interaction of a fluorescent unnatural tetrazolylpyrene nucleoside (<strong><sup>TPy</sup>B<sub>Do</sub></strong>) with model protein BSA is presented herein. The probe nucleoside shows a good interaction with BSA, which is reflected by the enhanced fluorescence intensity with an increase in the concentration of BSA. The enhancement is found to be linear with respect to the BSA concentration. Thus, the probe might find applications in chemical biology. The results infer that exploiting weak non-covalent interactions, such as H-bonding/hydrophobic, is an efficient strategy for sensing biomolecules. Further, the result would also help in designing other novel fluorescent probes capable of interacting with biomolecules via such forces with the generation of enhanced signals.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"463 ","pages":"Article 116290"},"PeriodicalIF":4.1,"publicationDate":"2025-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143142926","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}
{"title":"Synthesis of novel Ce3+ doped NaLi2PO4 UV-A emitting phosphor","authors":"Sanjeev Kumar , Manveer Singh , Siddhartha , Kuldeep Kumar , Bhawani Shankar , Nimmi Singh","doi":"10.1016/j.jphotochem.2025.116289","DOIUrl":"10.1016/j.jphotochem.2025.116289","url":null,"abstract":"<div><div>Ce<sup>3+</sup> doped NaLi<sub>2</sub>PO<sub>4</sub> orthophosphate material was successfully synthesized via the solid-state diffusion method. The phase purity of synthesized phosphor was confirmed by Powder X-ray Diffraction (PXRD). Elemental analysis and surface morphology of phosphor material were analyzed by Field Emission Scanning Electron Microscope (FE-SEM) and Energy Dispersive X-Ray Spectroscopy (EDX) respectively. In addition, chemical states and their elemental bonding of material were investigated by X-ray Photoelectron Spectroscopy (XPS). Whereas Diffuse Reflectance Spectra (DRS) is utilized to examine the optical energy band gap of NaLi<sub>2</sub>PO<sub>4</sub> and NaLi<sub>2</sub>PO<sub>4</sub>:Ce<sup>3+</sup> phosphors. First principle study was employed to explain the energy band gap deviation between the theoretical and experimental results of phosphors. Fluorescence properties of NaLi<sub>2</sub>PO<sub>4</sub>:Ce<sup>3+</sup> phosphor (0.0 to 0.3 mol %) were studied at excitation wavelength of 277 nm. NaLi<sub>2</sub>PO<sub>4</sub>:Ce<sup>3+</sup>phosphor exhibited intense emission peaks centred at 335 and 360 nm due to spin orbit splitting of <sup>2</sup>F<sub>5/2</sub> and <sup>2</sup>F<sub>7/2</sub>. Beyond the optimal limit of dopant ions, non-radiative energy transfer phenomena occurred due to dipole–dipole interaction between the acceptor and the donor. Minimum stokes shift between the excitation and emission bands of phosphor leads it to persistent UV emission. These properties of NaLi<sub>2</sub>PO<sub>4</sub>:Ce<sup>3+</sup> phosphor predicts its possible use in the development of UV-A phosphor LEDs.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"463 ","pages":"Article 116289"},"PeriodicalIF":4.1,"publicationDate":"2025-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143142534","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}
Wen-Xin Chu , Xiao-Min Tang , Fei-Yang Lu , Bao-Li An , Ji-Ming Zhang , Xiao-Hong Wang , Yue-Ling Bai , Jiaqiang Xu
{"title":"Synthesis of red carbon quantum dots with solvatochromic properties as a selective luminescence probe of MnO4−","authors":"Wen-Xin Chu , Xiao-Min Tang , Fei-Yang Lu , Bao-Li An , Ji-Ming Zhang , Xiao-Hong Wang , Yue-Ling Bai , Jiaqiang Xu","doi":"10.1016/j.jphotochem.2025.116288","DOIUrl":"10.1016/j.jphotochem.2025.116288","url":null,"abstract":"<div><div>Red efficient luminescent carbon quantum dots are still difficult to be synthesized. In this work, red carbon quantum dots (RCQDs) isopropanol solution with quantum yield of 43.9 % have been synthesized using isopropanol as carbon source and solvent, N1-phenylbenzene-1,2,4-triamine as carbon and nitrogen source. The solvothermal synthesis was catalyzed surprisingly by SnO<sub>2</sub> nanoparticles, the optimal synthesis temperature was lowered to 130 °C, and the optimal synthesis time was reduced to 1 h. Moreover, the RCQDs nanoparticles showed excellent solvatochromic properties. The maximum emission wavelength for RCQDs in <em>N</em>, <em>N</em>-dimethylformamide dilute solution blue shifted to 504 nm, and the maximum emission wavelengths for RCQDs in acetone, isopropanol, dimethyl sulfoxide and water solutions were in the range of 592 nm ∼ 624 nm. The reason was investigated by the in-situ infrared absorption spectra. MnO<sub>4</sub><sup>−</sup> ions could be selectively detected using RCQDs in PBS buffer solution (pH = 5.0), the linear range of MnO<sub>4</sub><sup>−</sup> concentration was 0.1 μM ∼ 2.0 μM. This work provides a new synthesis method of efficient red carbon quantum dots, and it supplies a friendly candidate for detection of MnO<sub>4</sub><sup>−</sup> ions in water.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"463 ","pages":"Article 116288"},"PeriodicalIF":4.1,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143142936","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}
Bo Li , Yongfeng Wan , Caifeng Xiu , Yuliang Liu , Qi Li , Lixia Zhu , Hang Yin , Ying Shi
{"title":"Enhanced fluorescence resonance energy transfer in CsPbBr3 quantum dot-rhodamine 640 molecule hybrid system: Toward high-efficiency and high-rate capability","authors":"Bo Li , Yongfeng Wan , Caifeng Xiu , Yuliang Liu , Qi Li , Lixia Zhu , Hang Yin , Ying Shi","doi":"10.1016/j.jphotochem.2025.116283","DOIUrl":"10.1016/j.jphotochem.2025.116283","url":null,"abstract":"<div><div>The fluorescence resonance energy transfer (FRET) process plays a crucial role in improving the efficiency of optoelectronic and photosynthetic devices. CsPbBr<sub>3</sub> perovskite quantum dot (QD) serves as efficient photon absorbers and exciton generators, thus offering the potential to enhance FRET performance. However, a high-efficiency FRET process with high-rate capability has not been achieved in the CsPbBr<sub>3</sub> perovskite QD-based system. Herein, we reported that the FRET process is improved in CsPbBr<sub>3</sub> perovskite QD-rhodamine 640 molecule hybrid system in n-hexane solution. This phenomenon stems from an increased number of adsorbed acceptor and a decreased distance between donor and acceptor. When the adsorbed number reached 4.2, a near-unity FRET efficiency of 99.3 % was achieved. Meanwhile, femtosecond transient absorption spectroscopy reveals that the FRET process exhibits a high-rate capability of 0.57 ps<sup>−1</sup>. Consequently, this research will stimulate the development of high-performance light-emitting device of perovskite-based system.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"463 ","pages":"Article 116283"},"PeriodicalIF":4.1,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143142928","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}
Mohamed I. Chouiter , Yunsheng Xue , Ali Belfaitah , Gilles Ulrich , Houssem Boulebd
{"title":"New pyrazoline-imidazole derivatives as highly fluorescent small organic compounds: Synthesis, photoluminescence properties, and DFT/TD-DFT calculations","authors":"Mohamed I. Chouiter , Yunsheng Xue , Ali Belfaitah , Gilles Ulrich , Houssem Boulebd","doi":"10.1016/j.jphotochem.2025.116272","DOIUrl":"10.1016/j.jphotochem.2025.116272","url":null,"abstract":"<div><div>In this paper we present the synthesis, photoluminescence properties and quantum chemical calculations of a series of novel 1,3,5-trisubstituted 2-pyrazoline derivatives incorporating an imidazole nucleus. These compounds were synthesized in good to excellent yields through the reaction of α,β-unsaturated ketones (chalcones) with phenylhydrazine derivatives. Structural elucidation of all synthesized compounds was performed using spectroscopic techniques including IR, <sup>1</sup>H NMR, <sup>13</sup>C NMR, and HR-MS. The photoluminescence properties of the pyrazolines were evaluated using UV–visible absorption and fluorescence spectroscopy. These compounds exhibited strong fluorescence in liquid solution, with fluorescence lifetimes ranging from 3.2 ns to 4.3 ns and quantum yields between 50 % and 74 %. The absorption spectra of the compounds revealed peaks in the near-ultraviolet region (325 to 364 nm), while the emission spectra displayed wavelengths in the blue region (434 to 476 nm). Additionally, density functional theory (DFT) and time-dependent density functional theory (TD-DFT) calculations, performed at the PBE0/TZVP level of theory, provided insight into the mechanisms underlying the fluorescence properties of the synthesized molecules.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"463 ","pages":"Article 116272"},"PeriodicalIF":4.1,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143142934","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}
{"title":"Maltose-functionalized MAPbBr3 fluorescent perovskite quantum dots with strong water resistance for detection of γ-aminobutyric acid as a neurological biomarker","authors":"Suresh Kumar Kailasa , Mayurkumar Revabhai Patel , Madhura Pradeep Deshpande , Eunji Shin , Yoojin Choi , Tae Jung Park","doi":"10.1016/j.jphotochem.2025.116282","DOIUrl":"10.1016/j.jphotochem.2025.116282","url":null,"abstract":"<div><div>Zero-dimensional perovskite nanostructures have always been shown outstanding applications in recognizing gases and molecular species. Herein, maltose (Malt) was introduced as an encapsulating agent for the synthesis of MAPbBr<sub>3</sub> fluorescent perovskite quantum dots (Malt@MAPbBr<sub>3</sub> PQDs), showing strong water resistance and good quantum yield (QY). The as-synthesized Malt@MAPbBr<sub>3</sub> PQDs have an average size of 7.25 ± 2.63 nm. The structure and elemental composition of Malt@MAPbBr<sub>3</sub> PQDs are confirmed by various analytical techniques. The as-synthesized Malt@MAPbBr<sub>3</sub> PQDs display remarkable fluorescence characteristics (λ<sub>Ex/Em</sub> = 430/535 nm) with QY of 23.74 %. The selectivity of various biomarkers (epinephrine, normetanephrine, creatinine, dehydroepiandrosterone, uric acid, bilirubin, methyl nicotinate, γ-aminobutyric acid (GABA), Se-methylselenocystiene, and cortisone) on the fluorescence quenching of Malt@MAPbBr<sub>3</sub> PQDs was studied through fluorescence emission spectroscopy. Interestingly, Malt@MAPbBr<sub>3</sub> PQDs exhibit a noticeable fluorescence quenching (>90 %) with the limit of detection (8.37 nM) in the presence of GABA. The developed Malt@MAPbBr<sub>3</sub> PQDs-based fluorescent sensor is successfully applied to detect GABA in biofluids.</div></div>","PeriodicalId":16782,"journal":{"name":"Journal of Photochemistry and Photobiology A-chemistry","volume":"463 ","pages":"Article 116282"},"PeriodicalIF":4.1,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143142535","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}