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  • Article
    Citation - WoS: 49
    Citation - Scopus: 55
    Synthesis of Α-fe2o3< Heterogeneous Composites by the Sol-Gel Process and Their Photocatalytic Activity
    (Elsevier Science Sa, 2020) Bouziani, Asmae; Park, Jongee; Ozturk, Abdullah
    alpha-Fe2O3/TiO2 heterogeneous composites were synthesized by the sol-gel process to increase the photocatalytic activity of TiO2. The structural, morphological, and optical characteristics of the composites were determined by X-ray diffraction, scanning electron microscope, and UV-vis diffuse reflectance spectroscopy. Results revealed that the incorporation of alpha-Fe2O3 to TiO2 widened the visible light absorption ability of TiO2. It was realized that the calcination temperature plays a crucial role in morphology development hence photocatalytic activity of the alpha-Fe2O3/TiO2 heterogeneous composites. The photocatalytic activity of the composites calcined at various temperatures was evaluated for the degradation of Methylene Blue (MB) and Phenol (Ph) in aqueous medium under UV and sun-like illuminations. The alpha-Fe2O3-TiO2 composites exhibits superior photocatalytic efficiency to degrade both MB and Ph as compared to both pristine TiO2 and pristine alpha-Fe2O3 under sun-like illumination. The alpha-Fe2O3/TiO2 composite degraded approximately 90 % of MB and 50 % of Ph in 180 min sun-like illumination. Improvement in photocatalytic activity is attributed to the separation of photogenerated electron/hole pairs through the interaction of alpha-Fe(2)O(3 )and TiO2.
  • Article
    A Benchmark of Expert-Level Academic Questions to Assess AI Capabilities
    (Nature Portfolio, 2026) Phan, Long; Gatti, Alice; Li, Nathaniel; Khoja, Adam; Kim, Ryan; Ren, Richard; Scaramuzza, Davide; Park, Jongee
    Benchmarks are important tools for tracking the rapid advancements in large language model (LLM) capabilities. However, benchmarks are not keeping pace in difficulty: LLMs now achieve more than 90% accuracy on popular benchmarks such as Measuring Massive Multitask Language Understanding(1), limiting informed measurement of state-of-the-art LLM capabilities. Here, in response, we introduce Humanity's Last Exam (HLE), a multi-modal benchmark at the frontier of human knowledge, designed to be an expert-level closed-ended academic benchmark with broad subject coverage. HLE consists of 2,500 questions across dozens of subjects, including mathematics, humanities and the natural sciences. HLE is developed globally by subject-matter experts and consists of multiple-choice and short-answer questions suitable for automated grading. Each question has a known solution that is unambiguous and easily verifiable but cannot be quickly answered by internet retrieval. State-of-the-art LLMs demonstrate low accuracy and calibration on HLE, highlighting a marked gap between current LLM capabilities and the expert human frontier on closed-ended academic questions. To inform research and policymaking upon a clear understanding of model capabilities, we publicly release HLE at https://lastexam.ai.
  • Article
    Citation - WoS: 44
    Citation - Scopus: 43
    Sol-Gel Synthesis and Photocatalytic Activity of B and Zr Co-Doped Tio2
    (Pergamon-elsevier Science Ltd, 2013) Kapusuz, Derya; Park, Jongee; Ozturk, Abdullah
    Effects of boron (B) and/or zirconium (Zr) doping on photocatalytic activity of sol-gel derived titania (TiO2) powders were investigated. A conventional, non-hydrous sol-gel technique was applied to synthesize the B, Zr doped/co-doped TiO2 powders. Doping was made at molar ratios of Ti/B=1 and Ti/Zr=10. Sol-gel derived xero-gels were calcined at 500 degrees C for 3 h. The crystal chemistry and the morphology of the undoped and B, Zr doped/co-doped TiO2 nanoparticles were investigated using X-ray diffractometer and scanning electron microscope. Nano-scale (9-46 nm) TiO2 crystallites were obtained after calcination. Doping and co-doping decreased the crystallite size. Photocatalytic activity was measured through the degradation of methylene blue (MB) under 1 h UV-irradiation using a UV-vis spectrophotometer. Results revealed that B doping into anatase caused the formation of oxygen vacancies, whereas Zr addition caused Ti substitution. Both B and Zr ions had a profound effect on the particle morphology and photocatalytic activity of TiO2. The photocatalytic activity of B and Zr doped TiO2 particles increased from 27% to 77% and 57%, respectively. The best activity (88.5%) was achieved by co-doping. (C) 2013 Elsevier Ltd. All rights reserved.
  • Article
    Citation - WoS: 12
    Citation - Scopus: 11
    Enhanced Bioactivity and Low Temperature Degradation Resistance of Yttria Stabilized Zirconia/Clay Composites for Dental Applications
    (Elsevier Sci Ltd, 2022) Tufan, Yigithan; Park, Jongee; Ozturk, Abdullah; Ercan, Batur
    Yttria stabilized zirconia (YSZ)/clay composites were produced to improve osseointegration and undesired tetragonal-to-monoclinic phase transformation (low temperature degradation, LTD) of YSZ ceramics so that long-term clinical success of YSZ implants is achieved. Various amounts (0.5,1,2, and 4 wt%) of clay was incorporated to YSZ. Predetermined amounts of clay and YSZ were mixed and pressed uniaxially at 15 MPa into compacts that were subsequently pressureless sintered at 1450 degrees C. Density, compressive strength, hardness and indentation crack resistance of 4 wt% clay incorporated YSZ/clay composite were 5.77 +/- 0.01 g/cm3, 1188 +/- 121 MPa, 1223 +/- 9 HV, and 4.4 +/- 0.1 MPa root m, respectively. Additionally, biological properties of YSZ/clay composites were assessed in vitro using bone cells. Incorporation of 4 wt% clay significantly enhanced bone cell prolifer-ation, spreading, and functions. Moreover, a significant increase in the LTD resistance of YSZ was achieved upon 4 wt% clay incorporation. The findings collectively suggest that YSZ/clay composites have a potential to be used as an alternative material for dental applications.
  • Article
    Citation - WoS: 25
    Citation - Scopus: 26
    Identifying the Potentials for Charge Transport Layers Free N-P Homojunction-Based Perovskite Solar Cells
    (Pergamon-elsevier Science Ltd, 2022) Khan, Danish; Sajid, Sajid; Khan, Suliman; Park, Jongee; Ullah, Ihsan
    Perovskite solar cells (PSCs) with no charge transport layers (CTLs) could be one of the major device architectures for the production of simple and low-cost devices. However, CTLs-free PSCs based on n-p homojunction have yet to show high power conversion efficiency (PCE), which is most likely due to inadequate light-and charge-management in the p-type perovskite. The device operation is examined using Solar Cell Capacitance Simulator (SCAPS)-software, and a novel n-p homojunction design is proposed to attempt efficient CTLs-free PSCs. Several aspects of p-type layer that can affect device performance, such as acceptor density, photon harvesting capability, defects density, and resistances to the transport of charge-carriers are scrutinized and adjusted. Furthermore, the effects of different work-functions of metal electrodes are examined. A suitable acceptor concentration is required for oriented charge transport. It is determined that a p-type perovskite with a thickness of 0.3 mu m is advantageous for high performance. A metal electrode with a high work-function is essential for efficient device. Consequently, a PCE of 15.60% is obtained with an optimal defect density of E15 cm(-3), indicating that n-p homojunction-based CTLs-free PSCs are promising since they simplify the device design and fabrication process while retaining an acceptable PCE.
  • Article
    First-Principles Investigation of Kaolinite/YSZ Heterostructure for Solar-Driven Photocatalytic Hydrogen Production
    (Pergamon-Elsevier Science Ltd, 2025) Park, Jongee; Yu, Eunmi; Fatima, Syeda Afrinish
    This work employs density functional theory (DFT) to elucidate the structural, electronic, and photocatalytic properties of a kaolinite/yttria-stabilized zirconia (Kaol/YSZ) heterostructure tailored for solar-driven hydrogen generation. The lattice mismatch between Kaol(001) and YSZ(111) was determined to be 4.4 % along the a-axis and 2.2 % along the b-axis. Two interface terminations were modeled: an O-terminated Si-O surface and an OH-terminated Al-OH surface. The OH-terminated interface demonstrated a stronger interfacial binding energy (-9.32 eV per cell) and enhanced thermodynamic stability, indicating its suitability for photocatalytic water splitting. Electronic structure analysis reveals that the Kaol/YSZ heterostructure exhibits a narrowed band gap of 1.46 eV relative to the isolated components, which promotes enhanced visible-light absorption. A type-II band alignment is observed, facilitating photoinduced electron transfer from the conduction band of YSZ to the conduction band of Kaol and promoting efficient charge separation. Hirshfeld charge analysis confirms the existence of a built-in electric field at the interface that further drives charge migration. Calculated optical absorption spectra shows a red shift in the heterostructure's absorption edge, extending its photoresponse into the visible region. Under simulated solar irradiation, photogenerated electrons preferentially migrate to Kaol for proton reduction, while holes remain on the YSZ surface to oxidize water, enabling simultaneous H2 evolution and O2 evolution pathways. These findings highlight the promise of the Kaol/YSZ heterostructure as a robust visible-light photocatalyst for sustainable hydrogen production and environmental remediation.
  • Article
    Citation - WoS: 20
    Citation - Scopus: 24
    Lead-Free Perovskite Homojunction-Based Htm-Free Perovskite Solar Cells: Theoretical and Experimental Viewpoints
    (Mdpi, 2023) Sajid, Sajid; Alzahmi, Salem; Salem, Imen Ben; Park, Jongee; Obaidat, Ihab M.
    Simplifying the design of lead-free perovskite solar cells (PSCs) has drawn a lot of interest due to their low manufacturing cost and relative non-toxic nature. Focus has been placed mostly on reducing the toxic lead element and eliminating the requirement for expensive hole transport materials (HTMs). However, in terms of power conversion efficiency (PCE), the PSCs using all charge transport materials surpass the environmentally beneficial HTM-free PSCs. The low PCEs of the lead-free HTM-free PSCs could be linked to poorer hole transport and extraction as well as lower light harvesting. In this context, a lead-free perovskite homojunction-based HTM-free PSC was investigated, and the performance was then assessed using a Solar Cell Capacitance Simulator (SCAPS). A two-step method was employed to fabricate lead-free perovskite homojunction-based HTM-free PSCs in order to validate the simulation results. The simulation results show that high hole mobility and a narrow band gap of cesium tin iodide (CsSnI3) boosted the hole collection and absorption spectrum, respectively. Additionally, the homojunction's built-in electric field, which was identified using SCAPS simulations, promoted the directed transport of the photo-induced charges, lowering carrier recombination losses. Homojunction-based HTM-free PSCs having a CsSnI3 layer with a thickness of 100 nm, defect density of 10(15) cm(-3), and interface defect density of 10(18) cm(-3) were found to be capable of delivering high PCEs under a working temperature of 300 K. When compared to formamidinium tin iodide (FASnI(3))-based devices, the open-circuit voltage (V-oc), short-circuit density (J(sc)), fill factor (FF), and PCE of FASnI(3)/CsSnI3 homojunction-based HTM-free PSCs were all improved from 0.66 to 0.78 V, 26.07 to 27.65 mA cm(-2), 76.37 to 79.74%, and 14.62 to 19.03%, respectively. In comparison to a FASnI(3)-based device (PCE = 8.94%), an experimentally fabricated device using homojunction of FASnI(3)/CsSnI3 performs better with V-oc of 0.84 V, J(sc) of 22.06 mA cm(-2), FF of 63.50%, and PCE of 11.77%. Moreover, FASnI(3)/CsSnI3-based PSC is more stable over time than its FASnI(3)-based counterpart, preserving 89% of its initial PCE. These findings provide promising guidelines for developing highly efficient and environmentally friendly HTM-free PSCs based on perovskite homojunction.
  • Article
    Citation - WoS: 21
    Citation - Scopus: 25
    Inorganic Hole Transport Materials in Perovskite Solar Cells Are Catching Up
    (Elsevier Sci Ltd, 2023) Sajid, Sajid; Alzahmi, Salem; Ben Salem, Imen; Park, Jongee; Obaidat, Ihab M.
    More research is required to further optimize device efficiency, stability, and reduce the materials cost as perovskite solar cells (PSCs) approach to industrialization. Modulating the optoelectronic features and chemical coupling of the hole transport materials (HTMs) remains a prominent field of study in PSCs due to the significant impact these materials have on the device performance and stability. In order to speed up the commercialization of these cells, it is also important to use cost-effective HTMs in PSCs. InorganicHTMs are superior to other types of HTMs in terms of their advantages in boosting device performance and producing PSCs at a reasonable cost, in addition to their superior charge transport capabilities, desired energy levels, and intrinsic thermal and chemical stability. A detailed overview of inorganicHTMs, including metal oxides, cyanates, phthalocyanines, chalcogenides, nitrides, and carbides, is presented in this review. After briefly discussing the primary physical and optoelectronic characteristics of inorganic-HTMs, the critical functions of the above-mentioned materials as HTMs in PSCs are addressed. This review concludes by offering suggestions for future research that could considerably boost the performance of the PSCs with cost-effective inorganic-HTMs.
  • Article
    Citation - WoS: 18
    Citation - Scopus: 19
    Synthesis and Enhanced Photocatalytic Activity of Nitrogen-Doped Triphasic Tio2 Nanoparticles
    (Elsevier Science Sa, 2019) Erdogan, Nursev; Bouziani, Asmae; Park, Jongee; Micusik, Matej; Kim, Soo Young; Majkova, Eva; Ozturk, Abdullah
    TiO2 nanoparticles of the single anatase phase, binary anatase-brookite phases, and ternary anatase-brookite-rutile phases were synthesized using an HNO3-catalyzed hydrothermal process. The types and amounts of phases varied depending on the hydrothermal synthesis conditions. The results revealed that N dissolves in different amounts and chemical states, depending on the phases present and their proportions in the nano particles. Brookite and rutile nanoparticles oriented through one direction were found to be crystallized by the surface transformation from anatase. Photocatalytic activity tests, evaluated by degradation of methylene blue (MB) under ultraviolet (UV) and visible light illumination, revealed that the N-doped TiO2 nanoparticles containing a ternary-phase mixture had the best photocatalytic activity. The MB degradation of the visible light-active nanoparticles was three times better than that of a commercially available well-known TiO2 powder, P25 under UV illumination. The enhanced photoactivity was attributed to the following: i) a high surface area, ii) suppression of the recombination of electron-hole pairs with ternary-phase mixture crystallized in heterojunctions, iii) larger anatase phase content, and iv) narrower band gap and facilitation of charge separation by dissolved N atoms.
  • Article
    Citation - WoS: 6
    Citation - Scopus: 6
    Diethanolamine Modified Perovskite-Substrate Interface for Realizing Efficient Esl-Free Pscs
    (Mdpi, 2023) Sajid, Sajid; Alzahmi, Salem; Wei, Dong; Ben Salem, Imen; Park, Jongee; Obaidat, Ihab M.
    Simplifying device layout, particularly avoiding the complex fabrication steps and multiple high-temperature treatment requirements for electron-selective layers (ESLs) have made ESL-free perovskite solar cells (PSCs) attractive. However, the poor perovskite/substrate interface and inadequate quality of solution-processed perovskite thin films induce inefficient interfacial-charge extraction, limiting the power conversion efficiency (PCEs) of ESL-free PSCs. A highly compact and homogenous perovskite thin film with large grains was formed here by inserting an interfacial monolayer of diethanolamine (DEA) molecules between the perovskite and ITO substrate. In addition, the DEA created a favorable dipole layer at the interface of perovskite and ITO substrate by molecular adsorption, which suppressed charge recombination. Comparatively, PSCs based on DEA-treated ITO substrates delivered PCEs of up to 20.77%, one of the highest among ESL-free PSCs. Additionally, this technique successfully elongates the lifespan of ESL-free PSCs as 80% of the initial PCE was maintained after 550 h under AM 1.5 G irradiation at ambient temperature.