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Functional metal-organic frameworks derived electrode materials for electrochemical energy storage: a review. 功能性金属有机框架衍生的电化学储能电极材料:综述。
IF 4.3 2区 化学
Chemical Communications Pub Date : 2024-11-12 DOI: 10.1039/d4cc04086d
Basree, Arif Ali, Khusboo Kumari, Musheer Ahmad, Ganesh Chandra Nayak
{"title":"Functional metal-organic frameworks derived electrode materials for electrochemical energy storage: a review.","authors":"Basree, Arif Ali, Khusboo Kumari, Musheer Ahmad, Ganesh Chandra Nayak","doi":"10.1039/d4cc04086d","DOIUrl":"10.1039/d4cc04086d","url":null,"abstract":"<p><p>Pristine metal-organic frameworks (MOFs) are built through self-assembly of electron rich organic linkers and electron deficient metal nodes <i>via</i> coordinate bond. Due to the unique properties of MOFs like highly tunable frameworks, huge specific surface areas, flexible chemical composition, flexible structures and a large volume of pores, they are being used to design the electrode materials for electrochemical energy storage devices. As per the literature, MOFs (including manganese, nickel, copper, and cobalt-based zeolitic imidazolate frameworks (ZIFs), University of Oslo (UiO) MOFs, Hong Kong University of Science and Technology (HKUST) MOFs and isoreticular MOFs (IRMOFs)) have attracted much attention in the field of supercapacitors (SCs)/batteries. According to their dimensionality such as 1D, 2D and 3D, pristine MOFs are mainly used as SC materials. Highly porous materials and their composites are capable for intercalation of metal ions (Na<sup>+</sup>/Li<sup>+</sup>). Moreover, the supramolecular features (π⋯π, C-H⋯π, hydrogen bond interactions) of redox stable MOFs provide better insight for electrochemical stability. So, this review provides an in-depth analysis of pure MOFs and MOF derived composites (MOF composites and MOF derived porous carbon) as electrode materials and also discusses their metal ion charge storage mechanism. Finally, we provide our perspectives on the current issues and future opportunities for supercapacitor materials.</p>","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":null,"pages":null},"PeriodicalIF":4.3,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142491235","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Fluorination of antimonene hexagons. 锑六边形的氟化。
IF 4.3 2区 化学
Chemical Communications Pub Date : 2024-11-12 DOI: 10.1039/d4cc03423f
Michael Fickert, Rebeca Martinez-Haya, Diego López-Alcalá, Frank Hauke, José J Baldoví, Andreas Hirsch, Gonzalo Abellán
{"title":"Fluorination of antimonene hexagons.","authors":"Michael Fickert, Rebeca Martinez-Haya, Diego López-Alcalá, Frank Hauke, José J Baldoví, Andreas Hirsch, Gonzalo Abellán","doi":"10.1039/d4cc03423f","DOIUrl":"10.1039/d4cc03423f","url":null,"abstract":"<p><p>Fluorination of two-dimensional (2D) antimonene hexagons synthesized through a colloidal bottom-up approach has been explored using microwave-induced plasma and reactive ion etching fluorination strategies through the generation of CF<sub>4</sub>. The stability of the fluorine bond has been corroborated through DFT calculations. This work paves the way for further halogen-derivative modifications of heavy 2D pnictogens.</p>","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":null,"pages":null},"PeriodicalIF":4.3,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11446181/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142360776","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Enhancing the performance of ionic conductivity for solid-state electrolytes: an effective strategy of injecting lithium ions within anionic metal-organic frameworks. 提高固态电解质的离子导电性能:在阴离子金属有机框架内注入锂离子的有效策略。
IF 4.3 2区 化学
Chemical Communications Pub Date : 2024-11-12 DOI: 10.1039/d4cc04515g
Lu Shi, Xin Wang, Zhiliang Liu
{"title":"Enhancing the performance of ionic conductivity for solid-state electrolytes: an effective strategy of injecting lithium ions within anionic metal-organic frameworks.","authors":"Lu Shi, Xin Wang, Zhiliang Liu","doi":"10.1039/d4cc04515g","DOIUrl":"10.1039/d4cc04515g","url":null,"abstract":"<p><p>Metal-organic frameworks (MOFs) are considered as potential solid-state electrolyte (SSE) materials due to their structural diversity and porosity. Adding lithium ions into the anionic frameworks of MOFs and then realizing single-ion transport is an efficient way to enhance the performance of ionic conductivity of SSE materials. Herein, an ionotropic MOF (Li<sup>+</sup>[Cu-BTC]<sup>-</sup>) with lithium ions in the pores of the lattice was synthesized through an ion exchange strategy, which exhibits outstanding lithium ionic conducting properties over a wide temperature range (ionic conductivity: 0.11-2.96 × 10<sup>-3</sup> S cm<sup>-1</sup> in the temperature range of -40 to 100 °C). The strategy of injecting Li<sup>+</sup> within anionic metal-organic frameworks provides a new opportunity for exploring advanced SSEs.</p>","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":null,"pages":null},"PeriodicalIF":4.3,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142520362","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Solid-state synthesis of ligand-assisted lead halide nanoclusters. 配体辅助的卤化铅纳米团簇的固态合成。
IF 4.3 2区 化学
Chemical Communications Pub Date : 2024-11-12 DOI: 10.1039/d4cc04623d
David C Zeitz, Kai-Chun Chou, Jin Z Zhang
{"title":"Solid-state synthesis of ligand-assisted lead halide nanoclusters.","authors":"David C Zeitz, Kai-Chun Chou, Jin Z Zhang","doi":"10.1039/d4cc04623d","DOIUrl":"10.1039/d4cc04623d","url":null,"abstract":"<p><p>A solid-state synthesis of blue-emitting lead halide nanoclusters has been demonstrated for the first time. The solid-state grinding synthesis provides a facile method to produce highly confined lead bromide clusters under ambient conditions. Both CH<sub>3</sub>NH<sub>3</sub>PbBr<sub>3</sub> perovskite magic-sized clusters and lead halide molecular clusters have been produced, as confirmed by comparison to those synthesized using a ligand-assisted reprecipitation method in terms of electronic absorption, photoluminescence, and solid state characterization.</p>","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":null,"pages":null},"PeriodicalIF":4.3,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142491236","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Bioinspired hydrogels: polymeric designs towards artificial photosynthesis. 生物启发水凝胶:实现人工光合作用的聚合物设计。
IF 4.3 2区 化学
Chemical Communications Pub Date : 2024-11-12 DOI: 10.1039/d4cc04033c
Reina Hagiwara, Ryo Yoshida, Kosuke Okeyoshi
{"title":"Bioinspired hydrogels: polymeric designs towards artificial photosynthesis.","authors":"Reina Hagiwara, Ryo Yoshida, Kosuke Okeyoshi","doi":"10.1039/d4cc04033c","DOIUrl":"10.1039/d4cc04033c","url":null,"abstract":"<p><p>Aquatic environments host various living organisms with active molecular systems, such as the enzymes in the thylakoid membrane that realise photosynthesis. Various challenges in achieving artificial photosynthesis, such as water splitting, have been studied using both inorganic and organic molecules. However, several problems persist, including diffusion-limited reactions and multiple redox reactions in the liquid phase. In this Feature Article, we discuss the significant challenges in using polymer networks as active mediators for photoinduced water splitting. In the creation of artificial chloroplasts, polymer networks offer various advantages, such as stable dispersions of multiple types of functional molecules and close molecular arrangements. To incorporate these features, stepwise synthesis and integration can be utilized during the hierarchical construction of polymer networks. The constituent molecules such as ruthenium complex and platinum nanoparticles in the photoinduced electron transfer circuits are closely arranged to smoothly operate forward reactions by polymer networks. The quantum efficiency of photoinduced H<sub>2</sub> generation in gel systems is considerably higher than that of conventional solution systems. Additionally, a thermoresponsive poly(<i>N</i>-isopropylacrylamide) (PNIPAAm) network of microgels can be used to integrate catalytic nanoparticles into the inside by using the electrostatic interaction and the mesh size changes. By focusing on the redox changes of copolymerised molecules that induce swelling/shrinking at a constant temperature, active electron transfer can be precisely achieved using the coil-globule transition of the PNIPAAm having viologen. This article highlights the potential of polymer networks to develop strategies for active electron transfer and energy conversion systems similar to those found in living organisms.</p>","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":null,"pages":null},"PeriodicalIF":4.3,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142556584","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Separation of Rare Earth Elements and Nickel Harnessing Electrochemistry and Reactive CO2 Capture and Mineralization 利用电化学和反应性二氧化碳捕获与矿化分离稀土元素和镍
IF 4.9 2区 化学
Chemical Communications Pub Date : 2024-11-09 DOI: 10.1039/d4cc04632c
Akanksha Srivastava, Prarabdh Jain, Greeshma Gadikota, Prince Ochonma, Christopher Noe, Tianhe Yin
{"title":"Separation of Rare Earth Elements and Nickel Harnessing Electrochemistry and Reactive CO2 Capture and Mineralization","authors":"Akanksha Srivastava, Prarabdh Jain, Greeshma Gadikota, Prince Ochonma, Christopher Noe, Tianhe Yin","doi":"10.1039/d4cc04632c","DOIUrl":"https://doi.org/10.1039/d4cc04632c","url":null,"abstract":"The aim is to probe the chemical mechanisms underlying the use of multifunctional solvents to simultaneously capture and convert CO2 into insoluble Rare Earth Element (REE)-carbonates, while forming soluble complexes with nickel for separation. Subsequent nickel electrodeposition regenerates the CO2-loaded solvent for reuse.","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":null,"pages":null},"PeriodicalIF":4.9,"publicationDate":"2024-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142596875","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Varied CO2 photoreduction activity over UiO-66-NH2 with different aggregation morphology 具有不同聚集形态的 UiO-66-NH2 的二氧化碳光还原活性各异
IF 4.9 2区 化学
Chemical Communications Pub Date : 2024-11-09 DOI: 10.1039/d4cc04919e
Shuran Zhang, Yan-Hong Zou, Hai-Ning Wang, Guangjuan Xu, Wei Xie, Na Xu, Yanhong Xu, Yaqian Lan
{"title":"Varied CO2 photoreduction activity over UiO-66-NH2 with different aggregation morphology","authors":"Shuran Zhang, Yan-Hong Zou, Hai-Ning Wang, Guangjuan Xu, Wei Xie, Na Xu, Yanhong Xu, Yaqian Lan","doi":"10.1039/d4cc04919e","DOIUrl":"https://doi.org/10.1039/d4cc04919e","url":null,"abstract":"UiO-66-NH2 with different aggregation morphology are prepared to verify the morphology of photocatalysts could influence the charge transfer. Among them, UiO-66-NH2 with the poor aggregation exhibits superior performances over CO2 photoreduction, owing to the high separation efficiency of photo-generated electron-holes because of small particle sizes induced by the poor aggregation.","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":null,"pages":null},"PeriodicalIF":4.9,"publicationDate":"2024-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142596876","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Direct π-extension of a Conjugated Carbon Nanohoop Using a Zipper Method 利用拉链法直接π延伸共轭碳纳米环
IF 4.9 2区 化学
Chemical Communications Pub Date : 2024-11-08 DOI: 10.1039/d4cc04976d
kang Wei, Zaitian Cheng, Xingyu Zhang, Qiang Huang, Pingwu Du
{"title":"Direct π-extension of a Conjugated Carbon Nanohoop Using a Zipper Method","authors":"kang Wei, Zaitian Cheng, Xingyu Zhang, Qiang Huang, Pingwu Du","doi":"10.1039/d4cc04976d","DOIUrl":"https://doi.org/10.1039/d4cc04976d","url":null,"abstract":"The π-extension of carbon nanorings towards ultrashort carbon nanotubes (CNTs) is a great challenge for synthetic chemists. Herein, we report the synthesis, characterization, and properties of a nanographene-embedded carbon nanoring (NECR) by a direct zipper method. In this approach, a long linear phenyl chain is fused onto the CPP backbone by a simple Scholl reaction, similar to zipping two pieces of fabric together. Its photophysical properties were studied by UV‒Vis and photoluminescence spectroscopy. The potential application of NECR in electron-transport devices were further investigated.","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":null,"pages":null},"PeriodicalIF":4.9,"publicationDate":"2024-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142596882","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
ARCaDia: Single-round screening of a DNA-type targeted covalent binder possessing a latent warhead ARCaDia:拥有潜伏弹头的 DNA 型靶向共价粘合剂的单轮筛选
IF 4.9 2区 化学
Chemical Communications Pub Date : 2024-11-08 DOI: 10.1039/d4cc04594g
Masumi Taki, Masayasu Kuwahara, Chaohui Li, Naoko Tomoda, Naoyuki Miyashita, Tetsuo Kan, Jay Yang
{"title":"ARCaDia: Single-round screening of a DNA-type targeted covalent binder possessing a latent warhead","authors":"Masumi Taki, Masayasu Kuwahara, Chaohui Li, Naoko Tomoda, Naoyuki Miyashita, Tetsuo Kan, Jay Yang","doi":"10.1039/d4cc04594g","DOIUrl":"https://doi.org/10.1039/d4cc04594g","url":null,"abstract":"A covalent binder for a target protein was obtained by a direct single-round screening of a latent-warhead-modified DNA library via affinity/reactivity-based co-selection of aptameric deoxyribonucleic acid (ARCaDia), followed by a top k-mer analysis. The optimal position of the conjugated warhead on the selected aptamer was simultaneously identified.","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":null,"pages":null},"PeriodicalIF":4.9,"publicationDate":"2024-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142596877","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Rapid identification of P-C bonds in phosphorus-carbon anode materials 快速识别磷碳阳极材料中的 P-C 键
IF 4.9 2区 化学
Chemical Communications Pub Date : 2024-11-08 DOI: 10.1039/d4cc03317e
Yadong Ye, Qiang Xiao, Huanyu Xie, Hongchang Jin, Hengxing Ji
{"title":"Rapid identification of P-C bonds in phosphorus-carbon anode materials","authors":"Yadong Ye, Qiang Xiao, Huanyu Xie, Hongchang Jin, Hengxing Ji","doi":"10.1039/d4cc03317e","DOIUrl":"https://doi.org/10.1039/d4cc03317e","url":null,"abstract":"Phosphorus-carbon composites in alkali metal-ion batteries benefit from P-C bonds, enhancing stability and performance. Rapid P-C bond detection is crucial. X-ray photoelectron spectroscopy (XPS), balancing convenience and accuracy, was chosen in this study for its efficiency in analyzing P-C bond energies, aiding in the quick identification of these bonds in phosphorus-carbon anodes.","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":null,"pages":null},"PeriodicalIF":4.9,"publicationDate":"2024-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142596879","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
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