Publications by authors named "Tofik Ahmed Shifa"

Article Synopsis
  • PEC catalysis is a promising method for producing valuable chemicals from renewable sources, with significant research conducted on various reactions and feedstocks.
  • Challenges remain that hinder the commercialization of PEC processes despite the advancements made.
  • This review summarizes the fundamentals of PEC, highlights photoelectrode fabrication methods, and discusses progress and future prospects for using PEC to create high-value products from sustainable materials.
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In this study, Ce-doped Ni-Al mixed oxides (NACO) were synthesized and comprehensively characterized for their potential application in fluoride adsorption. NACOs were examined using Transmission Electron Microscopy (TEM) and Scanning Electron Microscopy (SEM), revealing a sheet-like morphology with a nodular appearance. X-ray diffraction (XRD) analysis confirmed the formation of mixed oxides of cubic crystal structure, with characteristic planes (111), (200), and (220) at 2 values of 37.

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Excessive fluoride removal from aqueous solutions is of utmost importance as it has an adverse impact on human health. This study investigates the defluoridation efficiency of a novel nano-sized Ce-doped Ni/Al layered double hydroxide (Ni-Al-Ce LDH) for aqueous solutions. The synthesized Ni-Al-Ce LDH exhibited a well-defined nanoscale plate-like morphology and a high surface area with an average size of 11.

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Basic insight into the structural evolution of electrocatalysts under operating conditions is of substantial importance for designing water oxidation catalysts. The first-row transition metal-based catalysts present state-of-the-art oxygen evolution reaction (OER) performance under alkaline conditions. Apparently, confinement has become an exciting strategy to boost the performance of these catalysts.

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An efficient and cost-effective approach for the development of advanced catalysts has been regarded as a sustainable way for green energy utilization. The general guideline to design active and efficient catalysts for oxygen evolution reaction (OER) is to achieve high intrinsic activity and the exposure of more density of the interfacial active sites. The heterointerface is one of the most attractive ways that plays a key role in electrochemical water oxidation.

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The design of highly efficient electrocatalysts containing non-precious metals is crucial for promoting overall water splitting in alkaline media. In particular, Janus catalysts simultaneously facilitating the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) are desirable. Herein, we fabricated a unique hierarchical heterostructure via growing Ni4W6O21(OH)2·4H2O (denoted as Ni-W-O) nanosheets on NiMoO4 rods, which was indispensable for regulating the morphology of the Ni-W-O structure.

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2D magnetic materials have generated an enormous amount of attention due to their unique 2D-limited magnetism and their potential applications in spintronic devices. Recently, most of this research has focused on 2D van der Waals layered magnetic materials exfoliated from the bulk with random size and thicknesses. Controllable growth of these materials is still a great challenge.

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The unique structural and electronic properties of 2D materials, including the metal and metal-free ones, have prompted intense exploration in the search for new catalysts. The construction of different heterostructures based on 2D materials offers great opportunities for boosting the catalytic activity in electo(photo)chemical reactions. Particularly, the merits resulting from the synergism of the constituent components and the fascinating properties at the interface are tremendously interesting.

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2D metal-semiconductor heterostructures based on transition metal dichalcogenides (TMDs) are considered as intriguing building blocks for various fields, such as contact engineering and high-frequency devices. Although, a series of p-n junctions utilizing semiconducting TMDs have been constructed hitherto, the realization of such a scheme using 2D metallic analogs has not been reported. Here, the synthesis of uniform monolayer metallic NbS on sapphire substrate with domain size reaching to a millimeter scale via a facile chemical vapor deposition (CVD) route is demonstrated.

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Two-dimensional layered materials (2DLMs) have attracted a tremendous amount of attention as photodetectors due to their fascinating features, including high potentials in new-generation electronic devices, wide coverage of bandgaps, ability to construct van der Waals heterostructures, extraordinary light-mass interaction, strong mechanical flexibility, and the capability of enabling synthesis of 2D nonlayered materials. Until now, most attention has been focused on the well-known graphene and transition metal dichalcogenides (TMDs). However, a growing number of functional materials (more than 5619) with novel optoelectronic and electronic properties are being re-discovered, thereby widening the horizon of 2D libraries.

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2D layered transition metal phosphorus trichalcogenides (MPX ) possess higher in-plane stiffness and lower cleavage energies than graphite. This allows them to be exfoliated down to the atomic thickness. However, a rational exfoliation route has to be sought to achieve surface-active and uniform individual layers.

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Optoelectronic devices for information storage and processing are at the heart of optical communication technology due to their significant applications in optical recording and computing. The infrared radiations of 850, 1310, and 1550 nm with low energy dissipation in optical fibers are typical optical communication wavebands. However, optoelectronic devices that could convert and store the infrared data into electrical signals, thereby enabling optical data communications, have not yet been realized.

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Considering the sizable band gap and wide spectrum response of tin disulfide (SnS ), ultrathin SnS nanosheets are utilized as solar-driven photocatalyst for water splitting. Designing a heterostructure based on SnS is believed to boost their catalytic performance. Unfortunately, it has been quite challenging to explore a material with suitable band alignment using SnS nanomaterials for photocatalytic hydrogen generation.

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Due to the novel physical properties, high flexibility, and strong compatibility with Si-based electronic techniques, 2D nonlayered structures have become one of the hottest topics. However, the realization of 2D structures from nonlayered crystals is still a critical challenge, which requires breaking the bulk crystal symmetry and guaranteeing the highly anisotropic crystal growth. CdTe owns a typical wurtzite crystal structure, which hinders the 2D anisotropic growth of hexagonal-symmetry CdTe.

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Two-dimensional transition-metal dichalcogenides (TMDs) have attracted much research interest in the hydrogen evolution reaction (HER) due to their superior electrocatalytic properties. Beyond binary TMDs, ternary TMD alloys, as electrocatalysts, were also gradually acknowledged for their remarkable efficiency in HER. Herein, we successfully synthesized monolayer dendritic ternary WSSe flakes possessing abundant active edge sites on a single crystalline SrTiO (STO(100)).

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Developing earth-abundant and efficient bifunctional electrocatalysts for realizing the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) under alkaline conditions is an intriguing challenge. Here, ternary necklace-like CoPSe nanowire arrays are synthesized via simultaneously phosphorizing and selenizing Co(OH) nanowires. Owing to the substitution of the P atom in the ternary system, the optimal electronic structure of CoPSe can be obtained and the stability can also be enhanced for hydrogen evolution.

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The rational design of Earth abundant electrocatalysts for efficiently catalyzing hydrogen evolution reaction (HER) is believed to lead to the generation of carbon neutral energy carrier. Owing to their fascinating chemical and physical properties, transition metal dichalcogenides (TMDs) are widely studied for this purpose. Of particular note is that doping by foreign atom can bring the advent of electronic perturbation, which affects the intrinsic catalytic property.

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Group III-VI compounds MX (M = Ga, In; X = S, Se, Te) are one class of important 2D layered materials and are currently attracting increasing interest due to their unique electronic and optoelectronic properties and their great potential applications in various other fields. Similar to 2D layered transition metal dichalcogenides (TMDs), MX also have the significant merits of ultrathin thickness, ultrahigh surface-to-volume ratio, and high compatibility with flexible devices. More impressively, in contrast with TMDCs, MX demonstrate many superior properties, such as direct band gap electronic structure, high carrier mobility, rare p-type electronic behaviors, high charge density, and so on.

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Molybdenum disulfide (MoS) has attracted a great deal of attention in optoelectronic applications due to its high mobility, low off-state current and high on/off ratio. However, its intrinsic large bandgap limits its application in infrared detection. Here, we have developed a high-performance infrared photodetector by integrating nonlayered PbS and layered MoS nanostructures via van der Waals epitaxy.

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2D nonlayered semiconductors attract intense interest due to their unique planar structure and various fascinating optoelectronic properties. Here, a method is developed to design orientation-controlled and well-defined single-crystalline PbS nanoplates arrays on mica. Furthermore, the single PbS nanoplate device displays great photoresponsivity, detectivity, and photogain values as high as 1621 A W , 1.

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Transition metal dichalcogenides (TMDs), as one of potential electrocatalysts for hydrogen evolution reaction (HER), have been extensively studied. Such TMD-based ternary materials are believed to engender optimization of hydrogen adsorption free energy to thermoneutral value. Theoretically, cobalt is predicted to actively promote the catalytic activity of WS2 .

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To address the urgent need for clean and sustainable energy, the rapid development of hydrogen-based technologies has started to revolutionize the use of earth-abundant noble-metal-free catalysts for the hydrogen evolution reaction (HER). Like the active sites of hydrogenases, the cation sites of pyrite-type transition-metal dichalcogenides have been suggested to be active in the HER. Herein, we synthesized electrodes based on a Se-enriched NiSe2 nanosheet array and explored the relationship between the anion sites and the improved hydrogen evolution activity through theoretical and experimental studies.

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Binary transition metal dichalcogenides (TMDs) have emerged as efficient catalysts for the hydrogen evolution reaction (HER). Co-based TMDs, such as CoS2 and CoSe2, demonstrate promising HER performance due to their intrinsic metallic nature. Recently, the ternary electrocatalysts were widely acknowledged for their prominent efficiency as compared to their binary counterparts due to increased active sites caused by the incorporation of different atoms.

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The desire for sustainable and clean energy future continues to be the concern of the scientific community. Researchers are incessantly targeting the development of scalable and abundant electro- or photo-catalysts for water splitting. Owing to their suitable band-gap and excellent stability, an enormous amount of transition-metal dichalcogenides (TMDs) with hierarchical nanostructures have been extensively explored.

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Layered chalcogenide materials (LCMs) are emerging materials in recent years for their great potential in applications of electronics and optoelectronics. As a member of LCMs, SnSe2, an n-type semiconductor with a band gap of ∼1.0 eV, is of great value to explore.

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