{"title":"利用树枝状纳米硅纤维锚定的苯并咪唑连接的微孔共轭聚合物将二氧化碳光还原为甲烷","authors":"Ruijie Xiao, Guirong Cao, Rui Qi","doi":"10.1007/s10562-024-04918-1","DOIUrl":null,"url":null,"abstract":"<div><p>Capturing and transforming diluted CO<sub>2</sub> into energy-rich fuels is a notable and increasingly interesting challenge in renewable energy research. This study successfully developed an enhanced form of silicon oxide with a unique exterior level and a SiO<sub>2</sub>/anatase phase interface. A base complex of Pd (II) and Cu (II) was created using a simple synthetic method, along with 3-chloropropyltriethoxysilane loaded on dendritic fibrous nanosilica (Cu-IL/DFNS and Pd-IL/DFNS). The use of DFNS provided numerous hydroxyl groups for the stable loading of Cu-IL and Pd-IL through chemical bonding interaction. Moreover, Cu-IL and Pd-IL were able to control the appropriate strand dimensions and offer active adsorption locations of metal groups, aiding in the chemical absorption of carbon dioxide. The DFNS composite’s topography and mesoporous structure remained consistent upon Cu-IL and Pd-IL loading, indicating the maintained crystalline form. The use of light-driven biomass valorisation has become a leading field for CO<sub>2</sub> to CH<sub>4</sub> photoreduction due to its sustainable characteristics. Photocatalytic CO<sub>2</sub> reduction is a highly beneficial method to counteract the negative impacts of greenhouse gases and achieve carbon neutrality. The construction of active sites with specific designs that exhibit increased activity and selectivity for photoreduction is a significant challenge. The reduction of carbon dioxide is crucial in today’s era of petroleum refineries. The present paper showcases the initial application of a reusable nanocatalyst with outer magnetism for the efficient and specific light reduction of CO<sub>2</sub> to CH<sub>4</sub> under eco-friendly circumstances that employ earth-friendly reduction, ambient pressure, cool thermal condition, and sustainable dehydration reactants in a shorter duration. This method extends substantial advantages, incorporating substantial financial return and acceptance of functional groups. This investigation emphasizes the possibility of integrating 3D nanoparticle architecture with eco-friendly chemical processes to create highly efficient catalytic reactions for the targeted light reduction of CO<sub>2</sub> to CH<sub>4</sub>.</p><h3>Graphical Abstract</h3>\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":508,"journal":{"name":"Catalysis Letters","volume":"155 2","pages":""},"PeriodicalIF":2.3000,"publicationDate":"2025-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Photoreduction of Carbon Dioxide to Methane Employing Benzimidazole-Linked Microporous Conjugated Polymers Anchored on Dendritic Fibrous Nanosilic\",\"authors\":\"Ruijie Xiao, Guirong Cao, Rui Qi\",\"doi\":\"10.1007/s10562-024-04918-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Capturing and transforming diluted CO<sub>2</sub> into energy-rich fuels is a notable and increasingly interesting challenge in renewable energy research. This study successfully developed an enhanced form of silicon oxide with a unique exterior level and a SiO<sub>2</sub>/anatase phase interface. A base complex of Pd (II) and Cu (II) was created using a simple synthetic method, along with 3-chloropropyltriethoxysilane loaded on dendritic fibrous nanosilica (Cu-IL/DFNS and Pd-IL/DFNS). The use of DFNS provided numerous hydroxyl groups for the stable loading of Cu-IL and Pd-IL through chemical bonding interaction. Moreover, Cu-IL and Pd-IL were able to control the appropriate strand dimensions and offer active adsorption locations of metal groups, aiding in the chemical absorption of carbon dioxide. The DFNS composite’s topography and mesoporous structure remained consistent upon Cu-IL and Pd-IL loading, indicating the maintained crystalline form. The use of light-driven biomass valorisation has become a leading field for CO<sub>2</sub> to CH<sub>4</sub> photoreduction due to its sustainable characteristics. Photocatalytic CO<sub>2</sub> reduction is a highly beneficial method to counteract the negative impacts of greenhouse gases and achieve carbon neutrality. The construction of active sites with specific designs that exhibit increased activity and selectivity for photoreduction is a significant challenge. The reduction of carbon dioxide is crucial in today’s era of petroleum refineries. The present paper showcases the initial application of a reusable nanocatalyst with outer magnetism for the efficient and specific light reduction of CO<sub>2</sub> to CH<sub>4</sub> under eco-friendly circumstances that employ earth-friendly reduction, ambient pressure, cool thermal condition, and sustainable dehydration reactants in a shorter duration. This method extends substantial advantages, incorporating substantial financial return and acceptance of functional groups. 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引用次数: 0
摘要
在可再生能源研究中,捕获并将稀释后的二氧化碳转化为富含能量的燃料是一项引人注目且日益有趣的挑战。该研究成功地开发了一种具有独特外部水平和SiO2/锐钛矿相界面的增强型氧化硅。用简单的方法合成了Pd (II)和Cu (II)的碱配合物,并将3-氯丙基三乙氧基硅烷负载在树枝状纤维纳米二氧化硅上(Cu- il /DFNS和Pd- il /DFNS)。DFNS的使用为Cu-IL和Pd-IL通过化学键相互作用的稳定负载提供了大量的羟基。此外,Cu-IL和Pd-IL能够控制适当的链尺寸,并提供金属基团的活性吸附位置,有助于二氧化碳的化学吸收。负载Cu-IL和Pd-IL后,DFNS复合材料的形貌和介孔结构保持一致,表明其晶体形态保持不变。由于其可持续的特性,使用光驱动生物质增值已成为CO2光还原为CH4的领先领域。光催化CO2还原是一种非常有益的方法,可以抵消温室气体的负面影响,实现碳中和。构建具有特定设计的活性位点,以增加光还原的活性和选择性是一个重大挑战。在今天的炼油厂时代,二氧化碳的减少是至关重要的。本论文展示了一种可重复使用的外磁纳米催化剂的初步应用,在环境友好的环境下,利用环境压力、低温条件和可持续的脱水反应物,在较短的时间内,将二氧化碳高效、特异地光还原为CH4。这种方法扩展了大量的优势,包括大量的财务回报和功能组的接受。这项研究强调了将3D纳米颗粒结构与环保化学工艺相结合的可能性,以创造高效的催化反应,将二氧化碳定向光还原为CH4。图形抽象
Photoreduction of Carbon Dioxide to Methane Employing Benzimidazole-Linked Microporous Conjugated Polymers Anchored on Dendritic Fibrous Nanosilic
Capturing and transforming diluted CO2 into energy-rich fuels is a notable and increasingly interesting challenge in renewable energy research. This study successfully developed an enhanced form of silicon oxide with a unique exterior level and a SiO2/anatase phase interface. A base complex of Pd (II) and Cu (II) was created using a simple synthetic method, along with 3-chloropropyltriethoxysilane loaded on dendritic fibrous nanosilica (Cu-IL/DFNS and Pd-IL/DFNS). The use of DFNS provided numerous hydroxyl groups for the stable loading of Cu-IL and Pd-IL through chemical bonding interaction. Moreover, Cu-IL and Pd-IL were able to control the appropriate strand dimensions and offer active adsorption locations of metal groups, aiding in the chemical absorption of carbon dioxide. The DFNS composite’s topography and mesoporous structure remained consistent upon Cu-IL and Pd-IL loading, indicating the maintained crystalline form. The use of light-driven biomass valorisation has become a leading field for CO2 to CH4 photoreduction due to its sustainable characteristics. Photocatalytic CO2 reduction is a highly beneficial method to counteract the negative impacts of greenhouse gases and achieve carbon neutrality. The construction of active sites with specific designs that exhibit increased activity and selectivity for photoreduction is a significant challenge. The reduction of carbon dioxide is crucial in today’s era of petroleum refineries. The present paper showcases the initial application of a reusable nanocatalyst with outer magnetism for the efficient and specific light reduction of CO2 to CH4 under eco-friendly circumstances that employ earth-friendly reduction, ambient pressure, cool thermal condition, and sustainable dehydration reactants in a shorter duration. This method extends substantial advantages, incorporating substantial financial return and acceptance of functional groups. This investigation emphasizes the possibility of integrating 3D nanoparticle architecture with eco-friendly chemical processes to create highly efficient catalytic reactions for the targeted light reduction of CO2 to CH4.
期刊介绍:
Catalysis Letters aim is the rapid publication of outstanding and high-impact original research articles in catalysis. The scope of the journal covers a broad range of topics in all fields of both applied and theoretical catalysis, including heterogeneous, homogeneous and biocatalysis.
The high-quality original research articles published in Catalysis Letters are subject to rigorous peer review. Accepted papers are published online first and subsequently in print issues. All contributions must include a graphical abstract. Manuscripts should be written in English and the responsibility lies with the authors to ensure that they are grammatically and linguistically correct. Authors for whom English is not the working language are encouraged to consider using a professional language-editing service before submitting their manuscripts.