Browsing by Author "Nizamoglu, Sedat"

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Antibacterial type-II InP/ZnO quantum dots via multimodal reactive oxygen species
(ELSEVIER SCIENCE SA, 2024) Khan, Saad Ullah; Eren, Guncem Ozgun; Atac, Nazli; Onal, Asim; Qureshi, Mohammad Haroon; Cooper, Francis Korshe; Almammadov, Toghru; Kolemen, Safacan; Sahin, Mehmet; Can, Fusun; Nizamoglu, Sedat; 0000-0002-9419-1711; AGÜ, Mühendislik Fakültesi, Malzeme Bilimi ve Nanoteknoloji Mühendisliği Bölümü; Sahin, Mehmet
The emergence of multidrug-resistant bacteria as a global health threat has necessitated the exploration of alternative treatments to combat bacterial infections. Among these, photocatalytic nanomaterials such as quantum dots (QDs) have shown great promise and type-I QDs have been investigated thus far. In this study, we introduce type-II InP/ZnO core/shell QDs that are ligand-exchanged with a short-chain inorganic sulfide ion (S2-) for antibacterial activity. Interestingly, InP/ZnO QDs simultaneously generate reactive oxygen species (ROS) including hydroxyl (center dot OH) and superoxide (O-2(center dot-) ) radicals, while only O-2(center dot-) radicals can be released by the type-I sulfide-capped InP/ZnS QDs. The optimized nanostructure achieved effective inhibition of Pseudomonas aeruginosa and Escherichia coli bacteria growth to the level of 99.99% and 70.31% under low-intensity green light illumination of 5 mW.cm(-2). Our findings highlight the importance of type-II QDs as a new avenue for developing effective antibacterial agents against drug-resistant pathogens.
Cadmium-Free and Efficient Type-II InP/ZnO/ZnS Quantum Dots and Their Application for LEDs
(AMER CHEMICAL SOC1155 16TH ST, NW, WASHINGTON, DC 20036, 2021) Eren, Guncem Ozgun; Sadeghi, Sadra; Jalali, Houman Bahmani; Ritter, Maximilian; Han, Mertcan; Baylam, Isinsu; Melikov, Rustamzhon; Onal, Asim; Oz, Fatma; Sahin, Mehmet; Ow-Yang, Cleva W.; Sennaroglu, Alphan; Lechner, Rainer T.; Nizamoglu, Sedat; AGÜ, Mühendislik Fakültesi, Malzeme Bilimi ve Nanoteknoloji Mühendisliği Bölümü; Sahin, Mehmet
It is a generally accepted perspective that type-II nanocrystal quantum dots (QDs) have low quantum yield due to the separation of the electron and hole wavefunctions. Recently, high quantum yield levels were reported for cadmium-based typeII QDs. Hence, the quest for finding non-toxic and efficient type-II QDs is continuing. Herein, we demonstrate environmentally benign type-II InP/ZnO/ZnS core/shell/shell QDs that reach a high quantum yield of similar to 91%. For this, ZnO layer was grown on core InP QDs by thermal decomposition, which was followed by a ZnS layer via successive ionic layer adsorption. The small-angle Xray scattering shows that spherical InP core and InP/ZnO core/ shell QDs turn into elliptical particles with the growth of the ZnS shell. To conserve the quantum efficiency of QDs in device architectures, InP/ZnO/ZnS QDs were integrated in the liquid state on blue light-emitting diodes (LEDs) as down-converters that led to an external quantum efficiency of 9.4% and a power conversion efficiency of 6.8%, respectively, which is the most efficient QD-LED using type-II QDs. This study pointed out that cadmium-free type-II QDs can reach high efficiency levels, which can stimulate novel forms of devices and nanomaterials for bioimaging, display, and lighting.
Cation exchange mediated synthesis of bright Au@ZnTe core-shell nanocrystals
(IOP PUBLISHING LTD, TEMPLE CIRCUS, TEMPLE WAY, BRISTOL BS1 6BE, ENGLAND, 08.01.2021) Sadeghi, Sadra; Melikov, Rustamzhon; Sahin, Mehmet; Nizamoglu, Sedat; 0000-0002-8569-1626; 0000-0003-2214-7604; AGÜ, Mühendislik Fakültesi, Malzeme Bilimi ve Nanoteknoloji Mühendisliği Bölümü
The synthesis of heterostructured core-shell nanocrystals has attracted significant attention due to their wide range of applications in energy, medicine and environment. To further extend the possible nanostructures, non-epitaxial growth is introduced to form heterostructures with large lattice mismatches, which cannot be achieved by classical epitaxial growth techniques. Here, we report the synthetic procedure of Au@ZnTe core-shell nanostructures by cation exchange reaction for the first time. For that, bimetallic Au@Ag heterostructures were synthesized by using PDDA as stabilizer and shape-controller. Then, by addition of Te and Zn precursors in a step-wise reaction, the zinc and silver cation exchange was performed and Au@ZnTe nanocrystals were obtained. Structural and optical characterization confirmed the formation of the Au@ZnTe nanocrystals. The optimization of the synthesis led to the bright nanocrystals with a photoluminescence quantum yield up to 27%. The non-toxic, versatile synthetic route, and bright emission of the synthesized Au@ZnTe nanocrystals offer significant potential for future bio-imaging and optoelectronic applications.
Colloidal Aluminum Antimonide Quantum Dots
(AMER CHEMICAL SOC, 1155 16TH ST, NW, WASHINGTON, DC 20036 USA, 2019) Jalali, Houman Bahmani; Sadeghi, Sadra; Sahin, Mehmet; Ozturk, Hande; Ow-Yang, Cleva W.; Nizamoglu, Sedat; AGÜ, Mühendislik Fakültesi, Malzeme Bilimi ve Nanoteknoloji Mühendisliği Bölümü;
AlSb is a less studied member of the III-V semiconductor family, and herein, we report the colloidal synthesis of AlSb quantum dots (QDs) for the first time. Different sizes of colloidal AlSb QDs (5 to 9 nm) were produced by the controlled reaction of AlCl3 and Sb[N(Si(Me)(3))(2)](3) in the presence of superhydride. These colloidal AlSb quantum dots showed excitonic transitions in the UV-A region and a tunable band edge emission (quantum yield of up to 18%) in the blue spectral range. Among all III-V quantum dots, these quantum dots show the brightest core emission in the blue spectral region.
Effective Neural Photostimulation Using Indium-Based Type-II Quantum Dots
(AMER CHEMICAL SOC, 1155 16TH ST, NW, WASHINGTON, DC 20036 USA, 2018) Jalali, Houman Bahmani; Aria, Mohammad Mohammadi; Dikbas, Ugur Meric; Sadeghi, Sadra; Kumar, Baskaran Ganesh; Sahin, Mehmet; Kavakli, Ibrahim Halil; Ow-Yang, Cleva W.; Nizamoglu, Sedat; AGÜ, Mühendislik Fakültesi, Malzeme Bilimi ve Nanoteknoloji Mühendisliği Bölümü;
Light-induced stimulation of neurons via photoactive surfaces offers rich opportunities for the development of therapeutic methods and high-resolution retinal prosthetic devices. Quantum dots serve as an attractive building block for such surfaces, as they can be easily functionalized to match the biocompatibility and charge transport requirements of cell stimulation. Although indium based colloidal quantum dots with type-I band alignment have attracted significant attention as a nontoxic alternative to cadmium-based ones, little attention has been paid to their photovoltaic potential as type-II heterostructures. Herein, we demonstrate type-II indium phosphide/zinc oxide core/shell quantum dots that are incorporated into a photoelectrode structure for neural photostimulation. This induces a hyperpolarizing bioelectrical current that triggers the firing of a single neural cell at 4 mu W mm(-2), 26-fold lower than the ocular safety limit for continuous exposure to visible light. These findings show that nanomaterials can induce a biocompatible and effective biological junction and can introduce a route in the use of quantum dots in photoelectrode architectures for artificial retinal prostheses.
Quantum dot and electron acceptor nano-heterojunction for photo-induced capacitive charge-transfer
(NATURE RESEARCHHEIDELBERGER PLATZ 3, BERLIN 14197, GERMANY, 2021) Karatum, Onuralp; Eren, Guncem Ozgun; Melikov, Rustamzhon; Onal, Asim; Ow-Yang, Cleva W.; Sahin, Mehmet; AGÜ, Mühendislik Fakültesi, Malzeme Bilimi ve Nanoteknoloji Mühendisliği Bölümü; Nizamoglu, Sedat
Capacitive charge transfer at the electrode/electrolyte interface is a biocompatible mechanism for the stimulation of neurons. Although quantum dots showed their potential for photostimulation device architectures, dominant photoelectrochemical charge transfer combined with heavy-metal content in such architectures hinders their safe use. In this study, we demonstrate heavy-metal-free quantum dot-based nano-heterojunction devices that generate capacitive photoresponse. For that, we formed a novel form of nano-heterojunctions using type-II InP/ZnO/ZnS core/shell/shell quantum dot as the donor and a fullerene derivative of PCBM as the electron acceptor. The reduced electron-hole wavefunction overlap of 0.52 due to type-II band alignment of the quantum dot and the passivation of the trap states indicated by the high photoluminescence quantum yield of 70% led to the domination of photoinduced capacitive charge transfer at an optimum donor-acceptor ratio. This study paves the way toward safe and efficient nanoengineered quantum dot-based next-generation photostimulation devices.