Strong photoluminescence enhancement of MoS(2) through defect engineering and oxygen bonding.
H. Nan, Zilu Wang, Wenhui Wang
et al.
We report on a strong photoluminescence (PL) enhancement of monolayer MoS2 through defect engineering and oxygen bonding. Micro-PL and Raman images clearly reveal that the PL enhancement occurs at cracks/defects formed during high-temperature annealing. The PL enhancement at crack/defect sites could be as high as thousands of times after considering the laser spot size. The main reasons of such huge PL enhancement include the following: (1) the oxygen chemical adsorption induced heavy p doping and the conversion from trion to exciton; (2) the suppression of nonradiative recombination of excitons at defect sites, which was verified by low-temperature PL measurements. First-principle calculations reveal a strong binding energy of ∼2.395 eV for an oxygen molecule adsorbed on a S vacancy of MoS2. The chemically adsorbed oxygen also provides a much more effective charge transfer (0.997 electrons per O2) compared to physically adsorbed oxygen on an ideal MoS2 surface. We also demonstrate that the defect engineering and oxygen bonding could be easily realized by mild oxygen plasma irradiation. X-ray photoelectron spectroscopy further confirms the formation of Mo-O bonding. Our results provide a new route for modulating the optical properties of two-dimensional semiconductors. The strong and stable PL from defects sites of MoS2 may have promising applications in optoelectronic devices.
1106 sitasi
en
Materials Science, Medicine
Photodegradable Hydrogels for Dynamic Tuning of Physical and Chemical Properties
April M. Kloxin, A. Kasko, Chelsea N. Salinas
et al.
1582 sitasi
en
Materials Science, Medicine
Phase engineering of transition metal dichalcogenides.
D. Voiry, A. Mohite, M. Chhowalla
765 sitasi
en
Medicine, Chemistry
Bioinspired engineering of honeycomb structure – Using nature to inspire human innovation
Qiancheng Zhang, Xiaohu Yang, Peng Li
et al.
711 sitasi
en
Materials Science
An efficient recombination system for chromosome engineering in Escherichia coli.
Daiguan Yu, H. Ellis, E-Chiang Lee
et al.
1787 sitasi
en
Biology, Medicine
Cell surface engineering by a modified Staudinger reaction.
Eliana Saxon, C. Bertozzi
2068 sitasi
en
Chemistry, Medicine
The Science and Engineering of Thermal Spray Coatings
L. Pawłowski
1940 sitasi
en
Materials Science
Chemical vapour deposition of coatings
K. Choy
1466 sitasi
en
Materials Science
Plant cell cultures: Chemical factories of secondary metabolites.
S. Rao, Gokare A. Ravishankar
1469 sitasi
en
Biology, Medicine
The Practical Handbook of Compost Engineering
R. Haug
Chemical and engineering thermodynamics
S. Sandler
Strain engineering in two-dimensional nanomaterials beyond graphene
Shikai Deng, A. Sumant, V. Berry
Abstract Strain engineering is the process of tuning a material's properties by altering its mechanical or structural attributes. Atomically thin two-dimensional nanomaterials (2DNMs), which have been extensively studied in recent years, are particularly well-suited for strain engineering because they can withstand large strain. Thermal vibration, surface adhesion, substrate deformation, pre-stretched substrate, epitaxial grown, thermal expansion mismatch, substrate topography modification, pressurized blisters and tip indentation can lead to strain in 2DNMs. Strain in 2DNMs can modify their atomic structure, lattice vibration, thermal conductivity, electronic and optical, electrical and device performance, and chemical activities. This review focuses on the structural and mechanical properties of various 2DNMs, different experimental strategies to induce strain and modify properties, and applications of strained 2DNMs. Also, the review proposes prospective research areas for future strain engineering studies in 2DNMs.
288 sitasi
en
Materials Science
Investigation of Microstructure and Mechanical Behavior of Nanomodified Cement-Based Materials
Spyridoula G. Farmaki, Dimitrios A. Exarchos, Vasileios Dracopoulos
et al.
Recent advances in nanotechnology have highlighted the transformative potential of carbon-based nanomaterials, such as carbon nanofibers, carbon nanotubes, and graphene, in cementitious systems. These materials have shown a remarkable ability to enhance the mechanical strength, fracture toughness, and overall functional performance of cementitious composites. Their nanoscale dimensions and exceptional intrinsic properties allow for effective stress bridging, crack arrest, and matrix densification. Despite these promising features, the current understanding remains limited, particularly regarding their application to concrete. Furthermore, literature lacks systematic, parallel evaluations of their respective effectiveness in improving both mechanical performance and long-term durability, as well as their potential to impart true multifunctionality to concrete structures. It is worth noting that significant and statistically significant improvements in fracture behavior were observed at specific nanofiller concentrations, suggesting strong potential for the material system in next-generation innovative infrastructure applications. Experimental results demonstrated that both CNTs and GNPs significantly enhanced the mechanical performance of concrete, with flexural strength increases of approximately 49% and 38%, and compressive strength improvements of 22% and 47%, respectively, at optimum contents of 0.6 wt.% CNTs and 0.8 wt.% GNPs. SEM analyses confirmed improved matrix densification and interfacial bonding at these concentrations, while higher dosages led to agglomeration and reduced performance. This gap highlights the need for targeted experimental studies to elucidate the structure-property relationships governing these advanced materials.
Engineering (General). Civil engineering (General)
Work function engineering of graphene electrode via chemical doping.
Yumeng Shi, Ki Kang Kim, A. Reina
et al.
520 sitasi
en
Materials Science, Medicine
An overview of process systems engineering approaches for process intensification: State of the art
Yuhe Tian, S. Demirel, M. Hasan
et al.
Abstract Process intensification offers the potential to drastically reduce the energy consumption and cost of producing chemicals from both bulk and distributed feedstocks. This review article aims to offer an extensive survey on state-of-the-art process systems engineering (PSE) approaches for process intensification. From both academic and industrial perspectives, this paper provides an overview of the development of various process intensification technologies, specifically those under the categories of separation, reaction, hybrid reaction/separation, and alternative energy sources. A current status analysis in the areas of modeling and simulation is then provided. An indicative list of PSE publications specialized on process intensification is presented to illustrate the progresses made so far towards the deployment of novel process intensification technologies. We also highlight some recent advances for the modeling, design, and synthesis of intensified systems, as well as for the assessment of their controllability/operability/safety performance. Key open questions in these areas include: (i) how to systematically derive intensified designs, and (ii) how to ensure the operability and optimality of the derived intensified structures while delivering their expected functionality.
242 sitasi
en
Computer Science
Crystal Engineering: An Outlook for the Future.
A. Nangia, G. Desiraju
Crystal Engineering has traditionally dealt with molecular crystals. It is the understanding of intermolecular interactions in the context of crystal packing and in the utilization of such understanding in the design of new solids with desired physical and chemical properties. We outline here five areas which come under the umbrella of Crystal Engineering and where we feel that a proper planning of research efforts could lead to higher dividends for science together with greater returns for humankind. We touch on themes and domains where science funding and translation efforts could be directed in the current climate of a society that increasingly expects applications and utility products from science and technology. The five topics are: 1) pharmaceutical solids; 2) industrial solid state reactions; 3) mechanical properties with practical applications; 4) MOFs and COFs framework solids; 5) new materials for solar energy harvesting and advanced polymers.
206 sitasi
en
Medicine, Engineering
Development of 2,1,3-Benzothiadiazole-Based Room-Temperature Fluorescent Nematic Liquid Crystals
Muhammad Suhail bin Uzair, Yoshimichi Shimomura, Takuya Tanaka
et al.
Fluorescent liquid crystals (LCs) have attracted considerable interest owing to their unique combination of fluidity, anisotropy, and intrinsic emission. However, most reported fluorescent LCs exhibit high phase transition temperatures and/or smectic phases, limiting their practical applications. To address this, we designed and synthesized a series of 2,1,3-benzothiadiazole (BTD)-based fluorescent nematic liquid crystals incorporating donor (D) or acceptor (A) groups to form D–A–D or D–A–A structures. Most of the synthesized derivatives exhibited supercooled nematic phases at room temperature. They composed various functional groups, such as secondary alkylamine, branched alkyl chain, and trifluoroacetyl groups, which are rarely used in calamitic nematic LCs. Notably, dimethylamine- and carbonyl-substituted derivatives exhibited relatively high fluorescence quantum yields (Φ<sub>fl</sub>) in both solid and mesophase states, demonstrating their potential as efficient fluorescent materials. Our findings underscore the versatility of BTD-based mesogenic skeletons for designing room-temperature fluorescent nematic LCs with various functional groups. These materials offer promising opportunities for next-generation display technologies, optical sensors, and photonic applications.
Bioconversion of Date Waste into Bacterial Nanocellulose by a New Isolate <i>Komagataeibacter</i> sp. IS22 and Its Use as Carrier Support for Probiotics Delivery
Islam Sayah, Ibtissem Chakroun, Claudio Gervasi
et al.
Bacterial nanocellulose (BNC) has gained considerable interest over the last decade due to its unique properties and versatile applications. However, the low yield and the high production cost significantly limit its industrial scalability. The proposed study explores the isolation of new BNC producers from date palm sap and the use of date waste extract as a sustainable carbon source to improve BNC productivity. Results revealed three potential BNC producers identified as <i>Komagataeibacter</i> sp. IS20, <i>Komagataeibacter</i> sp. IS21, and <i>Komagataeibacter</i> sp. IS22 with production yield of 1.7 g/L, 0.8 g/L and 1.8 g/L, respectively, in Hestrin-Schramm (HS) medium. The biopolymer characterization indicated the presence of type I cellulose, a high thermal stability, and a highly dense network made of cellulose nanofibrils for all BNC samples. The isolate IS22, showing the highest productivity, was selected for an optimization procedure using a full factorial design with date waste extract as a carbon source. The BNC yield increased to 6.59 g/L using 4% date waste extract and 2% ethanol after 10 days of incubation compared to the standard media (1.8 g/L). Two probiotic strains, including <i>Bacillus subtilis</i> (BS), and <i>Lactobacillus plantarum</i> (LP) were successfully encapsulated into BNC matrix through a co-culture approach. The BNC-LP and BNC-BS composites showed antibacterial activity against <i>Pseudomonas aeruginosa</i>. BNC–probiotic composites have emerged as a promising strategy for the effective delivery of viable probiotics in a wide range of applications. Overall, this study supports the use of date waste extract as a sustainable carbon source to enhance BNC productivity and reduce the environmental footprint using a high-yielding producer (IS22). Furthermore, the produced BNC demonstrated promising potential as an efficient carrier matrix for probiotic delivery.
Pt/IrO x enables selective electrochemical C-H chlorination at high current
Bo Wu, Ruihu Lu, Chao Wu
et al.
Abstract Employing electrochemistry for the selective functionalization of liquid alkanes allows for sustainable and efficient production of high-value chemicals. However, the large potentials required for C(sp 3)-H bond functionalization and low water solubility of such alkanes make it challenging. Here we discover that a Pt/IrO x electrocatalyst with optimized Cl binding energy enables selective generation of Cl free radicals for C-H chlorination of alkanes. For instance, we achieve monochlorination of cyclohexane with a current up to 5 A, Faradaic efficiency (FE) up to 95% and stable performance over 100 h in aqueous KCl electrolyte. We further demonstrate that our system can directly utilize concentrated seawater derived from a solar evaporation reverse osmosis process, achieving a FE of 93.8% towards chlorocyclohexane at a current of 1 A. By coupling to a photovoltaic module, we showcase solar-driven production of chlorocyclohexane using concentrated seawater in a membrane electrode assembly cell without any external bias. Our findings constitute a sustainable pathway towards renewable energy driven chemicals manufacture using abundant feedstock at industrially relevant rates.
Polymeric scaffolds in tissue engineering: a literature review.
Maissa Jafari, Zahrasadat Paknejad, M. Rad
et al.
263 sitasi
en
Materials Science, Medicine