Shape-controlled synthesis of Ag@TiO2 cage-bell hybrid structure with enhanced photocatalytic activity and superior lithium storage
Literature Information
Wei Wang, Lixiang Liu, Yunbo He, Cuiping Li, Yapeng Wang
Cage-bell hybrid Ag-modified TiO2 nanoparticle aggregates are fabricated through an environmental template-free route and subsequent facile impregnation method. The intrinsic hollow core–shell microstructure makes multiple reflections of light within the chamber, allowing more efficient use of a light source compared with solid structures. This structure can also shorten the lengths for both electronic and ionic transport, enlarge the surface areas of electrodes, and the improve accommodation of the volume change during Li insertion/extraction cycling. Furthermore, the introduction of Ag is beneficial for the enhancement of the interfacial charge transfer efficiency to adsorbed substrates and for the improvement of its high-rate discharge capacity. Therefore, Ag@TiO2 exhibits remarkable photocatalytic activity under visible light and improved performance as an anode material for lithium ion batteries. This strategy is simple, cheap and amenable to mass-production, which may shed light on a new avenue for large-scale synthesis of cage-bell structural nanofunctional materials for catalysis, energy storage and other applications.
Related Literature
Electrochemical redox signaling of hemoglobin in human whole blood and its relevance to anemia and thalassemia diagnosis
Khairunnisa Amreen, Annamalai Senthil Kumar
DOI: 10.1039/C5AN02646F
A colorimetric probe for the real-time naked eye detection of cyanide and hydroxide ions in tap water: experimental and theoretical studies
Veikko Uahengo, Johannes Naimhwaka, Likius S. Daniel, Ateeq Rahman, Mohamed I. Elzagheid, Ping Cai
DOI: 10.1039/C9AN01481K
A colorimetric and fluorescent dual probe for palladium in aqueous medium and live cell imaging
Jin-wu Yan, Xiao-lin Wang, Qi-feng Tan, Pei-fen Yao, Jia-heng Tan, Lei Zhang
DOI: 10.1039/C6AN00204H
Rapid prototyping of electrochemical lateral flow devices: stencilled electrodes
Miguel Aller Pellitero, Maria Kitsara, Friedrich Eibensteiner, F. Javier del Campo
DOI: 10.1039/C5AN02424B
Improvement of the gas cluster ion beam-(GCIB)-based molecular secondary ion mass spectroscopy (SIMS) depth profile with O2+ cosputtering
Hua-Yang Liao, Kang-Yi Lin, Hsun-Yun Chang, Ding-Yuan Kuo, Yun-Wen You
DOI: 10.1039/C5AN02677F
Characterisation of graphene fibres and graphene coated fibres using capacitively coupled contactless conductivity detector
Emer Duffy, Sinéad Currivan, Andres Ruland, Rouhollah Jalili, Attila J. Mozer, Peter C. Innis, Gordon G. Wallace
DOI: 10.1039/C5AN02534F
FTIR bio-spectroscopy scattering correction using natural biological characteristics of different cell lines
Sara Hariri, Sahar Barzegari B., Kamyar Keshavarz F., Nastaran Nikounezhad, Behnoosh Safaei, Golrokh Farnam
DOI: 10.1039/C9AN00811J
A dual-mode signaling response of a AuNP-fluorescein based probe for specific detection of thiourea
Jian Sun, Xiurong Yang
DOI: 10.1039/C6AN00165C
Development of a ratiometric two-photon fluorescent probe for imaging of hydrogen peroxide in ischemic brain injury
Baoping Zhai, Wei Hu, Ruilin Hao, Wenjing Ni, Zhihong Liu
DOI: 10.1039/C9AN01326A
You might also like
What precautions should be taken when handling 4-(2-Furylmethyl)thiomorpholine 1,1-dioxide (CAS: 79206-94-3)?
When handling 4-(2-Furylmethyl)thiomorpholine 1,1-dioxide (CAS: 79206-94-3), it ...
What precautions should be taken when handling 4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide (CAS: 71320-77-9)?
When handling 4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide (CAS: 71320-77-9), it...
How should waste containing 2-[2-(2-Methoxyethoxy)ethoxy]ethyl 4-methylbenzenesulfonate (CAS: 62921-74-8) be handled?
Waste containing this compound (CAS: 62921-74-8) should be handled according to ...
How should waste containing (S)-Methyl 2-amino-3-cyclohexylpropanoate be handled?
Waste containing (S)-Methyl 2-amino-3-cyclohexylpropanoate should be collected i...
How is 5-({4-[(2S,4R)-4-Hydroxy-2-methyltetrahydro-2H-pyran-4-yl]-2-thienyl}sulfanyl)-1-methyl-1,3-dihydro-2H-indol-2-one (CAS: 166882-70-8) typically synthesized?
This compound can be synthesized using a multi-step process involving the conjug...
Are there alternatives to (2E)-3-(3,4-Dichlorophenyl)acrylic acid (CAS: 7312-27-8) in synthesis?
There are several alternatives to (2E)-3-(3,4-Dichlorophenyl)acrylic acid in syn...
How should Ethyl 6-(2-nitrophenyl)imidazo[2,1-b][1,3]thiazole-3-carboxylate (CAS: 925437-84-9) be stored?
Ethyl 6-(2-nitrophenyl)imidazo[2,1-b][1,3]thiazole-3-carboxylate (CAS: 925437-84...
How should waste containing 2-(1,3-Thiazol-2-yl)ethanamine (CAS: 18453-07-1) be handled?
Waste containing 2-(1,3-Thiazol-2-yl)ethanamine (CAS: 18453-07-1) should be coll...
How is Methyl 5-iodo-2-methylbenzoate (CAS: 103440-54-6) typically synthesized?
Methyl 5-iodo-2-methylbenzoate can be synthesized through the iodination of meth...
How is 5-Chloro[1,2,4]triazolo[1,5-a]pyridine (CAS: 1427399-34-5) typically synthesized?
5-Chloro[1,2,4]triazolo[1,5-a]pyridine is commonly synthesized via the condensat...
Source Journal
Green Chemistry

Green Chemistry provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on, but not limited to, the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998). Green chemistry is the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry is at the frontiers of this continuously-evolving interdisciplinary science and publishes research that attempts to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. Submissions on all aspects of research relating to the endeavour are welcome. The journal publishes original and significant cutting-edge research that is likely to be of wide general appeal. To be published, work must present a significant advance in green chemistry. Papers must contain a comparison with existing methods and demonstrate advantages over those methods before publication can be considered. For more information please see this Editorial. Coverage includes the following, but is not limited to: Design (e.g. biomimicry, design for degradation/recycling/reduced toxicity…) Reagents & Feedstocks (e.g. renewables, CO2, solvents, auxiliary agents, waste utilization…) Synthesis (e.g. organic, inorganic, synthetic biology…) Catalysis (e.g. homogeneous, heterogeneous, enzyme, whole cell…) Process (e.g. process design, intensification, separations, recycling, efficiency…) Energy (e.g. renewable energy, fuels, photovoltaics, fuel cells, energy storage, energy carriers…) Applications (e.g. electronics, dyes, consumer products, coatings, pharmaceuticals, preservatives, building materials, chemicals for industry/agriculture/mining…) Impact (e.g. safety, metrics, LCA, sustainability, (eco)toxicology…) Green chemistry is, by definition, a continuously-evolving frontier. Therefore, the inclusion of a particular material or technology does not, of itself, guarantee that a paper is suitable for the journal. To be suitable, the novel advance should have the potential for reduced environmental impact relative to the state of the art. Green Chemistry does not normally deal with research associated with 'end-of-pipe' or remediation issues.










![tert-Butyl N-[(2-chloropyridin-4-yl)methyl]carbamate structure tert-Butyl N-[(2-chloropyridin-4-yl)methyl]carbamate structure](https://static.chemtradehub.com/structs/916/916210-27-0-9f95.webp)
![4-Chloro-3-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine structure 4-Chloro-3-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine structure](https://static.chemtradehub.com/structs/869/869335-75-1-a9d0.webp)

![1-[3-(4-Morpholinylsulfonyl)phenyl]methanamine structure 1-[3-(4-Morpholinylsulfonyl)phenyl]methanamine structure](https://static.chemtradehub.com/structs/933/933989-32-3-51af.webp)
