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学者姓名：温娜
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Abstract ：
Metal-nitrogen co-doped composite (M-N-C) carbon materials exhibit outstanding catalytic performance in oxygen reduction reactions (ORR), making them promising candidates to replace commercial Pt/C catalysts. However, it remains a challenge to achieve a rational design that ensures a uniform dispersion of the metal active centers in the nitrogen-doped carbon materials and an effective construction of the M-N active sites to enhance the ORR performance. This research introduces an innovative in situ pyrolysis technique utilizing the guanine biomolecule in conjunction with ZIF-67. This approach not only circumvents the pitfalls of structural disintegration and cobalt center agglomeration but also creates an abundance of anchoring sites conducive to the atomic dispersion of cobalt. Consequently, this method fosters the synthesis of Co-N and pyridinic-N active sites, which are pivotal for catalytic activity. The G-Co@NC-800 catalyst demonstrates exceptional ORR catalytic prowess, with a half-wave potential of 0.83 V (vs RHE) and a current density of -5.1 mAcm-2, coupled with remarkable stability and methanol tolerance in alkaline media. These attributes surpass those of commercial Pt/C catalysts, underscoring the superiority of this novel catalyst. This pioneering approach promotes the rational design of uniformly dispersed Co nanoparticles and the extensive construction of Co-N sites. Metal-nitrogen co-doped carbon materials are synthesized via a simple and facile in-situ pyrolysis strategy from biomolecules guanine with ZIF-67.The guanine transferred into 2D carbon nanosheets and nanotubes after pyrolysis, which inhibits the structural collapse and Co centers agglomeration of ZIF-67 during pyrolysis.The guanine provides anchoring sites for the Co nanoparticles (Co-Nx).The uniformly dispersed Co nanoparticles, as well as the widely constructed Co-Nx, provide a large number of active centers for catalytic activity of ORR in alkaline conditions.
Keyword ：
electrocatalyst electrocatalyst guanine guanine metal-organic frameworks metal-organic frameworks nitrogen doped carbon materials nitrogen doped carbon materials oxygen reduction reaction oxygen reduction reaction
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| GB/T 7714 | Zhu, Yongchao , Yang, Weibo , Yang, Mingyuan et al. In Situ Fabrication of Nitrogen Co-Doped Carbon Materials from Biomolecule Guanine for Enhanced Oxygen Electrocatalysis [J]. | ECS JOURNAL OF SOLID STATE SCIENCE AND TECHNOLOGY , 2025 , 14 (4) . |
| MLA | Zhu, Yongchao et al. "In Situ Fabrication of Nitrogen Co-Doped Carbon Materials from Biomolecule Guanine for Enhanced Oxygen Electrocatalysis" . | ECS JOURNAL OF SOLID STATE SCIENCE AND TECHNOLOGY 14 . 4 (2025) . |
| APA | Zhu, Yongchao , Yang, Weibo , Yang, Mingyuan , Zhang, Liang , Mao, Aijiao , Lin, Yihui et al. In Situ Fabrication of Nitrogen Co-Doped Carbon Materials from Biomolecule Guanine for Enhanced Oxygen Electrocatalysis . | ECS JOURNAL OF SOLID STATE SCIENCE AND TECHNOLOGY , 2025 , 14 (4) . |
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The persistent threats posed by toxic chemical warfare agents (CWAs) such as mustard gas (bis(2-chloroethyl) sulfide, HD) and bacterial contaminants demand the development of innovative, sustainable mitigation strategies. Photocatalytic processes that generate reactive oxygen species (ROS) offer a promising dual-functional approach for both chemical detoxification and antibacterial defense. In this study, two structurally analogous covalent organic frameworks (COFs), BPY-COF and BD-COF, are synthesized using benzotrithiophene as the donor unit paired with bipyridine and biphenyl, respectively. These COFs exhibit high crystallinity, broad-spectrum light absorption, and efficient charge carrier transport, with BPY-COF demonstrating superior performance due to the incorporation of heteroatoms. BPY-COF achieved ultrafast detoxification of the mustard gas simulant 2-chloroethyl ethyl sulfide (CEES) with a half-life of 35 min and 100% selectivity for 2-chloroethyl sulfoxide (CEESO) under white LED light, outperforming BD-COF. Additionally, electrospun composite fibers containing 40 wt.% BPY-COF maintained comparable CEES degradation rates and exhibited over 99% antibacterial efficiency against Escherichia coli and Bacillus subtilis within 60 min. These findings highlight the potential of BPY-COF as a multifunctional photocatalyst for integrated applications in chemical detoxification and antibacterial defense, addressing critical challenges in public health and safety.
Keyword ：
antibacterial antibacterial charge transfer charge transfer covalent organic frameworks covalent organic frameworks photocatalytic degradation photocatalytic degradation
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| GB/T 7714 | Zhu, Yongchao , Qin, Liyang , Yang, Mingyuan et al. Dual-Functional Benzotrithiophene-Based Covalent Organic Frameworks for Photocatalytic Detoxification of Mustard Gas Simulants and Antibacterial Defense [J]. | SMALL , 2025 , 21 (12) . |
| MLA | Zhu, Yongchao et al. "Dual-Functional Benzotrithiophene-Based Covalent Organic Frameworks for Photocatalytic Detoxification of Mustard Gas Simulants and Antibacterial Defense" . | SMALL 21 . 12 (2025) . |
| APA | Zhu, Yongchao , Qin, Liyang , Yang, Mingyuan , Shi, Zhicheng , Chen, Hongxuan , Wen, Na et al. Dual-Functional Benzotrithiophene-Based Covalent Organic Frameworks for Photocatalytic Detoxification of Mustard Gas Simulants and Antibacterial Defense . | SMALL , 2025 , 21 (12) . |
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Rare earth up-conversion nanoparticles (UCNPs) have been used to construct fluorescent nanosensors because of their low toxicity, good chemical stability, and low background fluorescence. Core-shell UCNPs were prepared using the solvothermal method, and water-soluble core-shell UCNPs (Cit-CS-UCNPs) were obtained by surface ligand exchange with sodium citrate. The Cit-CS-UCNPs were used as the energy donor of the fluorescence sensor, and manganese dioxide (MnO2) nanosheets were used as the energy receptor of the fluorescence sensor. Based on the fluorescence resonance energy transfer (FRET) mechanism, a fluorescence nanosensor (Cit-CS-UCNPs-MnO2) was constructed for the detection of hydrogen dioxide (H2O2) and tert-butylhydroquinone (TBHQ ) as food additives. The prepared nanomaterials' morphology, structure, and properties were characterized by scanning electron microscopy (SEM), fluorescence spectrum, and ultraviolet spectrum (UV-vis). The effects of quenching agent concentration, incubation temperature, and incubation time on the detection performance of the fluorescence sensing system were investigated. According to the fluorescence spectra and UV-Vis experimental results, the maximum emission peak of Cit-CS-UCNPs is 654 nm. After the combination of Cit-CS-UCNPs and MnO2, core-shell UCNPs undergo fluorescence quenching. When H2O2 is present, the fluorescence of Cit-CS-UCNPs recovers. The results indicate that H2O2 and MnO2 nanosheets undergo redox reaction at this band, and MnO2 nanosheets are reduced to Mn2+, which gradually dissociates from the surface of Cit-CS-UCNPs. In the presence of TBHQ, the peak of the Cit-CS-UCNPs-MnO2 and TBHQ system was shifted to 253 nm, indicating that the redox reaction occurred between TBHQ and MnO2 nanosheets, and the FRET effect was reduced in the Cit-CS-UCNPs-MnO2 system, and the fluorescence intensity increased. It can be seen from the SEM results that MnO2 nanosheets are uniformly coated around Cit-CS-UCNPs, and maintain good dispersion in water, indicating that MnO2 nanosheets are modified on the surface of Cit-CS-UCNPs. The concentration of the quencher potassium permanganate (KMnO4) was optimized, and the results showed that when the concentration of KMnO4 is 10 mol.L-1, the quenching efficiency can reach 90%. The detection conditions were optimized, and the results showed that when the incubation time of H2O2 was 25 min, the redox reaction between MnO2 and H2O2 was complete. The fluorescence recovery value of Cit-CS-UCNPs-MnO2 was the maximum. The incubation time of TBHQ was 30 min. Under the optimal experimental conditions, the fluorescence intensity of Cit-CS-UCNPs-MnO2 has a good linear relationship with the concentration of H2O2 (0 similar to 1 000 mu mol.L-1) and TBHQ (0 similar to 0.6 mmol.L-1). The optimal experimental conditions were maintained, and representative metal ions (such as K+, Na+, Ca2+ and Mg2+) and common food additives (BA, Glu, PS, Suc, Nat and Ino) in food were selected as research objects. The results showed that compared with H2O2, Cit-CS-UCNPs-MnO2 did not react strongly to other added substances, and the overall fluorescence signal of the sensor did not fluctuate much. Therefore, it can be seen that Cit-CS-UCNPs-MnO2 can detect the specificity of H2O2 and TBHQ.
Keyword ：
Core shell structures Core shell structures Fluorescent nanosensor Fluorescent nanosensor Up conversion nanoparticles Up conversion nanoparticles
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| GB/T 7714 | Zhang, Xuan , Wang, Ya-sen , Na, Wen et al. Construction of a Rare Earth Up-Conversion Nanoparticle Sensor and Its Application in the Detection of Food Additives [J]. | SPECTROSCOPY AND SPECTRAL ANALYSIS , 2024 , 44 (9) : 2459-2466 . |
| MLA | Zhang, Xuan et al. "Construction of a Rare Earth Up-Conversion Nanoparticle Sensor and Its Application in the Detection of Food Additives" . | SPECTROSCOPY AND SPECTRAL ANALYSIS 44 . 9 (2024) : 2459-2466 . |
| APA | Zhang, Xuan , Wang, Ya-sen , Na, Wen , Lu, Hai-xia , Li, Bao-ming . Construction of a Rare Earth Up-Conversion Nanoparticle Sensor and Its Application in the Detection of Food Additives . | SPECTROSCOPY AND SPECTRAL ANALYSIS , 2024 , 44 (9) , 2459-2466 . |
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The design of a highly active Cu -Co catalyst for catalytic transfer hydrogenolysis of lignin without the use of external hydrogen remains highly challenging. In this work, Cu 2 O was initially encapsulated in ZIF-67, and subsequently Cu 2 O@ZIF-67 was utilized as a precursor and sacrificial template to prepare the unique double core-shell hollow nanocage CuO@Co 3 O 4 . Co and Cu, serving as Lewis acid sites and dehydrogenation sites for the hydrogen -donor solvent isopropanol, respectively, exhibited synergistic enhancement, further increasing the catalytic activity. Under the optimal conditions of 220 degrees C, 1 MPa N 2 , and 4 h, the catalyst achieved 100 % conversion of 2-phenoxy-1-phenylethanol and 100 % yield towards cyclohexanol and ethylbenzene. Furthermore, the catalyst remained stable and reusable after 5 cycles, providing a practicable guidance for the valueadded conversion of lignin.
Keyword ：
C-O bonds cleavage C-O bonds cleavage CuCo-based catalyst CuCo-based catalyst Double core-shell hollow nanocage structure Double core-shell hollow nanocage structure Lignin Lignin
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| GB/T 7714 | Chen, Feng , Lin, Xuebin , Chen, Wei et al. Double core-shell hollow nanocage CuO@Co 3 O 4 for the selective hydrogenolysis of C-O bonds of lignin without external hydrogen [J]. | CHEMICAL ENGINEERING JOURNAL , 2024 , 491 . |
| MLA | Chen, Feng et al. "Double core-shell hollow nanocage CuO@Co 3 O 4 for the selective hydrogenolysis of C-O bonds of lignin without external hydrogen" . | CHEMICAL ENGINEERING JOURNAL 491 (2024) . |
| APA | Chen, Feng , Lin, Xuebin , Chen, Wei , Wen, Na , Jin, Yanqiao . Double core-shell hollow nanocage CuO@Co 3 O 4 for the selective hydrogenolysis of C-O bonds of lignin without external hydrogen . | CHEMICAL ENGINEERING JOURNAL , 2024 , 491 . |
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Bacterial infections are a major public health challenge around the world. The development of novel surface coatings that effectively inhibit bacterial adhesion, proliferation and growth is a critical step in addressing this global challenge. Photocatalytic antibacterial therapy has proven to be an effective approach and has received increasing attention. However, it is still a challenge to obtain coatings with both antibacterial adhesion and durable photocatalytic antibacterial functions. Herein, an acridine-based coating with antibacterial adhesion and photocatalytic antibacterial properties was prepared by simple methods (i.e., spin-coating, spray-coating, and drop-coating) and can be applied to various substrates. The bacterial anti-adhesion test results showed that the coating could effectively prevents the adhesion of Escherichia coli (E. coli), Staphylococcus aureus (S. aureus), and Pseudomonas aeruginosa (P. aeruginosa), indicating the strong anti-fouling capability. The acridine-based coating demonstrated durable photocatalytic antimicrobial activity, remaining 99.3 % antibacterial effective against all three bacterial strains even after 30 days exposed to visible light. The coating can significantly reduce or eliminate the risk of contamination and cross-contamination, making it ideal for use in public healthcare environments.
Keyword ：
Antibacterial Antibacterial Anti-fouling Anti-fouling Coating Coating Photocatalytic Photocatalytic
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| GB/T 7714 | Kang, Linfeng , Peng, Houqian , Yang, Mingyuan et al. Dual-functional acridine-based coatings with anti-bacterial adhesion and durable photocatalytic antibacterial [J]. | PROGRESS IN ORGANIC COATINGS , 2024 , 194 . |
| MLA | Kang, Linfeng et al. "Dual-functional acridine-based coatings with anti-bacterial adhesion and durable photocatalytic antibacterial" . | PROGRESS IN ORGANIC COATINGS 194 (2024) . |
| APA | Kang, Linfeng , Peng, Houqian , Yang, Mingyuan , Hu, Ke , Lin, Yihui , Zhu, Yongchao et al. Dual-functional acridine-based coatings with anti-bacterial adhesion and durable photocatalytic antibacterial . | PROGRESS IN ORGANIC COATINGS , 2024 , 194 . |
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The electrocatalytic conversion of inert CO2 to value-added chemical fuels powered by renewable energy is one of the benchmark approaches to address excessive carbon emissions and achieve carbon-neutral energy restructuring. However, the adsorption/activation of supersymmetric CO2 is facing insurmountable challenges that constrain its industrial-scale applications. Here, this theory-guided study confronts these challenges by leveraging the synergies of bimetallic sites and defect engineering, where pyrochlore-type semiconductor A(2)B(2)O(7) is employed as research platform and the conversion of CO2-to-HCOOH as the model reaction. Specifically, defect engineering intensified greatly the chemisorption-induced CO2 polarization via the bimetallic coordination, thermodynamically beneficial to the HCOOH production via the *HCO2 intermediate. The optimal V-BSO-430 electrocatalyst with abundant surface oxygen vacancies achieved a superior HCOOH yield of 116.7 mmol h(-1) cm(-2) at -1.2 V-RHE, rivalling the incumbent similar reaction systems. Furthermore, the unique catalytic unit featured with a Bi-1-Sn-Bi-2 triangular structure, which is reconstructed by defect engineering, and altered the pathway of CO2 adsorption and activation to allow the preferential affinity of the suspended O atom in *HCO2 to H. As a result, V-BSO-430 gave an impressive FEHCOOH of 93% at -1.0 V-RHE. This study held promises for inspiring the exploration of bimetallic materials from the massive semiconductor database.
Keyword ：
A(2)B(2)O(7) A(2)B(2)O(7) bimetallic sites bimetallic sites CO2 reduction CO2 reduction electrocatalysis electrocatalysis pyrochlore pyrochlore
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| GB/T 7714 | Zhao, Jiwu , Wang, Jiashun , Xue, Lan et al. Surface Oxygen Defect Engineering of A2B2O7 Pyrochlore Semiconductors Boosts the Electrocatalytic Reduction of CO2-to-HCOOH [J]. | SMALL , 2024 , 20 (38) . |
| MLA | Zhao, Jiwu et al. "Surface Oxygen Defect Engineering of A2B2O7 Pyrochlore Semiconductors Boosts the Electrocatalytic Reduction of CO2-to-HCOOH" . | SMALL 20 . 38 (2024) . |
| APA | Zhao, Jiwu , Wang, Jiashun , Xue, Lan , Wang, Ying , Wen, Na , Huang, Haowei et al. Surface Oxygen Defect Engineering of A2B2O7 Pyrochlore Semiconductors Boosts the Electrocatalytic Reduction of CO2-to-HCOOH . | SMALL , 2024 , 20 (38) . |
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Polypropylene (PP) nonwovens have been widely used in disposable protective masks and protective clothing, which are essential to protect healthcare workers from highly infectious diseases such as COVID-19. However, realizing the disinfection reusable function of PP nonwovens to reduce carbon emission or white waste pollution after extensive use has been still a great challenge. Herein, Durable Antimicrobial and Anti-fungal Post-disinfection polypropylene nonwovens were developed by co-grafting of Triclosan and Chitosan. The antibacterial performance test results showed that the as-prepared co-grafted polypropylene nonwoven has a > 99.9% of antimicrobial efficiency against E. coli, S. aureus as well as multi-drug-resistant P. aeruginosa, and the excellent anti-fungal performance against fungus (C. albicans) and mold (A. niger). Moreover, it retained excellent Antimicrobial and Anti-fungal Properties after disinfection 3 times with boiling water, 40 x diluted 84 disinfectant and 75% alcohol for 5 min. This work provided ideas for developing more effective pathogen protection and longer-lasting personal protective equipment to reduce the environmental impact of medical masks and personal protective equipment in terms of energy consumption, carbon emissions and waste generation.
Keyword ：
Antibacterial Antibacterial Anti-fungal Anti-fungal Polypropylene nonwovens Polypropylene nonwovens UV irradiation modification UV irradiation modification
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| GB/T 7714 | Hu, Ke , Chen, Hongxuan , Lin, Yihui et al. Synthesis and Durable Antimicrobial and Anti-fungal Properties of Triclosan and Chitosan Co-grafted Polypropylene Nonwovens [J]. | FIBERS AND POLYMERS , 2024 , 25 (11) : 4245-4256 . |
| MLA | Hu, Ke et al. "Synthesis and Durable Antimicrobial and Anti-fungal Properties of Triclosan and Chitosan Co-grafted Polypropylene Nonwovens" . | FIBERS AND POLYMERS 25 . 11 (2024) : 4245-4256 . |
| APA | Hu, Ke , Chen, Hongxuan , Lin, Yihui , Han, Shitong , Wang, Qi , Peng, Houqian et al. Synthesis and Durable Antimicrobial and Anti-fungal Properties of Triclosan and Chitosan Co-grafted Polypropylene Nonwovens . | FIBERS AND POLYMERS , 2024 , 25 (11) , 4245-4256 . |
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Converting clean solar energy into chemical energy through artificial photosynthesis is an effective solution to solve the energy and environmental issues. Here, we report a Cs3Bi2Br9/Bi2WO6 (CBB/BWO) Z-scheme heterojunction constructed via electrostatic self-assembly, which facilitates efficient separation of photogenerated carriers and ensures the corresponding redox capacity of both components. By sharing Bi atoms, a Br-Bi-O bond is established between CBB and BWO, serving as an "electron bridge". The electrons generated by BWO are efficiently channeled to CBB through the heterojunction-formed "electron bridge", thereby achieving effective photocatalytic CO2 reduction. Under simulated sunlight conditions, it exhibits the highest CO yield of 72.52 mu mol g(-1) (without the addition of any precious metal, photosensitizers or sacrifices), which is approximately 7-fold and 18-fold greater than that of pure CBB and BWO, respectively. This work provides a more profound comprehension of the regulation of electron transfer through interfacial chemical bonds, thereby proposing a promising strategy for the development of efficient heterojunction photocatalysts for CO2 photoreduction.
Keyword ：
Bi2WO6 Bi2WO6 CO2 reduction CO2 reduction Perovskite Perovskite Photocatalysis Photocatalysis Z-scheme Z-scheme
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| GB/T 7714 | Liu, Haolan , Sun, Jingjing , Lin, Qianying et al. An Electron Bridge of Shared Atoms Mediated Cs3Bi2Br9/Bi2WO6 Z-Scheme Heterojunction for Photocatalytic CO2 Reduction [J]. | CHEMCATCHEM , 2024 , 16 (22) . |
| MLA | Liu, Haolan et al. "An Electron Bridge of Shared Atoms Mediated Cs3Bi2Br9/Bi2WO6 Z-Scheme Heterojunction for Photocatalytic CO2 Reduction" . | CHEMCATCHEM 16 . 22 (2024) . |
| APA | Liu, Haolan , Sun, Jingjing , Lin, Qianying , Wang, Ying , Wang, Shuo , Wang, Shuowen et al. An Electron Bridge of Shared Atoms Mediated Cs3Bi2Br9/Bi2WO6 Z-Scheme Heterojunction for Photocatalytic CO2 Reduction . | CHEMCATCHEM , 2024 , 16 (22) . |
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稀土上转换纳米粒子(UCNPs)因其具有毒性小、化学稳定性好和背景荧光低等优点被用于构建荧光纳米传感器.通过溶剂热法制备核壳UCNPs,采用柠檬酸钠对其进行表面配体交换得到水溶性核壳UCNPs(Cit-CS-UCNPs),以Cit-CS-UCNPs作为荧光传感器的能量供体,二氧化锰(MnO2)纳米片作为荧光传感器的能量受体,采用荧光共振能量转移(FRET)机理,构建了一种用于食品添加剂二氧化氢(H2O2)和叔丁基对苯二酚(TBHQ)检测的荧光纳米传感器(Cit-CS-UCNPs-MnO2).通过扫描电镜(SEM)、荧光光谱和紫外可见吸收光谱(UV-Vis)等分析测试手段对制备的纳米材料的形貌结构和性能进行表征.考察了猝灭剂浓度、孵育温度及孵育时间等实验条件对荧光传感体系检测性能的影响.荧光光谱和UV-Vis实验结果表明,Cit-CS-UCNPs最大发射峰位于654 nm,Cit-CS-UCNPs与MnO2结合后,核壳UCNPs发生荧光猝灭,当存在H2O2时,Cit-CS-UCNPs的荧光恢复,说明在此波段H2O2与MnO2纳米片发生氧化还原反应,MnO2纳米片被还原成Mn2+,逐渐从Cit-CS-UCNPs的表面解离下来;存在TBHQ时,Cit-CS-UCNPs-MnO2与TBHQ体系峰位与TBHQ偏移到253 nm,为TBHQ与MnO2纳米片发生氧化还原反应,使得Cit-CS-UCNPs-MnO2体系中FRET效应减弱,荧光强度回升.SEM结果表明,MnO2纳米片均匀包覆在Cit-CS-UCNPs的周围,在水中仍可保持良好的分散性,表明MnO2纳米片修饰到Cit-CS-UCNPs表面.对猝灭剂高锰酸钾(KMnO4)的浓度进行了优化.结果表明,当KMnO4浓度为10 mol·L-1时,猝灭效率可达90％.对检测条件进行优化,结果表明H2O2的检测孵育时间为25 min时,MnO2和H2O2之间氧化还原反应基本完全,Cit-CS-UCNPs-MnO2荧光恢复值最大;TBHQ的检测孵育时间为30 min.在最佳实验条件下,Cit-CS-UCNPs-MnO2 的荧光强度变化比率与 H2O2 浓度(0～1 000 μmol·L-1)及 TBHQ 浓度(0～0.6 mmol·L-1)分别具有良好的线性关系.保持最佳实验条件,选取食品中存在的代表性金属离子(如K+、Na+、Ca2+和Mg2+)和常见的食品添加剂苯甲酸(BA)、D-葡萄糖(Glu)、山梨酸钾(PS)、蔗糖(Suc)、纳他霉素(Nat)和肌醇(Ino)作为研究对象进行选择性测试,发现与H2O2相比,Cit-CS-UCNPs-MnO2对其他添加物质没有强烈的反应,传感器整体荧光信号波动不大,因此Cit-CS-UCNPs-MnO2对H2O2和TBHQ可进行特异性检测.
Keyword ：
上转换纳米粒子 上转换纳米粒子 核壳结构 核壳结构 荧光纳米传感器 荧光纳米传感器
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| GB/T 7714 | 张璇 , 王雅森 , 温娜 et al. 基于稀土上转换纳米粒子传感器的构建及其在食品添加剂检测中的应用 [J]. | 光谱学与光谱分析 , 2024 , 44 (9) : 2459-2466 . |
| MLA | 张璇 et al. "基于稀土上转换纳米粒子传感器的构建及其在食品添加剂检测中的应用" . | 光谱学与光谱分析 44 . 9 (2024) : 2459-2466 . |
| APA | 张璇 , 王雅森 , 温娜 , 吕海霞 , 李宝铭 . 基于稀土上转换纳米粒子传感器的构建及其在食品添加剂检测中的应用 . | 光谱学与光谱分析 , 2024 , 44 (9) , 2459-2466 . |
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Efficient photocatalytic reduction of CO2 to high-calorific-value CH4, an ideal target product, is a blueprint for C-1 industry relevance and carbon neutrality, but it also faces great challenges. Herein, we demonstrate unprecedented hybrid SiC photocatalysts modified by Fe-based cocatalyst, which are prepared via a facile impregnation-reduction method, featuring an optimized local electronic structure. It exhibits a superior photocatalytic carbon-based products yield of 30.0 mu mol g(-1) h(-1) and achieves a record CH4 selectivity of up to 94.3%, which highlights the effectiveness of electron-rich Fe cocatalyst for boosting photocatalytic performance and selectivity. Specifically, the synergistic effects of directional migration of photogenerated electrons and strong pi-back bonding on low-valence Fe effectively strengthen the adsorption and activation of reactants and intermediates in the CO2 -> CH4 pathway. This study inspires an effective strategy for enhancing the multielectron reduction capacity of semiconductor photocatalysts with low-cost Fe instead of noble metals as cocatalysts.
Keyword ：
artificial synthesis of CH4 artificial synthesis of CH4 electronic structure optimization electronic structure optimization Fe species cocatalyst Fe species cocatalyst photocatalytic CO2 reduction photocatalytic CO2 reduction SiC SiC
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| GB/T 7714 | Lin, Qianying , Zhao, Jiwu , Zhang, Pu et al. Highly selective photocatalytic reduction of CO2 to CH4 on electron-rich Fe species cocatalyst under visible light irradiation [J]. | CARBON ENERGY , 2024 , 6 (1) . |
| MLA | Lin, Qianying et al. "Highly selective photocatalytic reduction of CO2 to CH4 on electron-rich Fe species cocatalyst under visible light irradiation" . | CARBON ENERGY 6 . 1 (2024) . |
| APA | Lin, Qianying , Zhao, Jiwu , Zhang, Pu , Wang, Shuo , Wang, Ying , Zhang, Zizhong et al. Highly selective photocatalytic reduction of CO2 to CH4 on electron-rich Fe species cocatalyst under visible light irradiation . | CARBON ENERGY , 2024 , 6 (1) . |
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