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Neeta Karjule

Bio: Neeta Karjule is an academic researcher from Ben-Gurion University of the Negev. The author has contributed to research in topics: Carbon nitride & Photoelectrochemical cell. The author has an hindex of 8, co-authored 25 publications receiving 270 citations. Previous affiliations of Neeta Karjule include Academy of Scientific and Innovative Research & National Chemical Laboratory.

Papers
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TL;DR: In this article, an efficient template-free synthetic route for the preparation of mesoporous nitrogen-doped graphene (NGE) containing a high weight percentage of pyrrolic nitrogen, good specific surface area and comparable electrochemical oxygen reduction activity as that of the state-of-the-art 40 wt% Pt/C catalyst.
Abstract: We report an efficient template-free synthetic route for the preparation of mesoporous nitrogen-doped graphene (NGE) containing a high weight percentage of pyrrolic nitrogen, good specific surface area and comparable electrochemical oxygen reduction activity as that of the state-of-the-art 40 wt% Pt/C catalyst. The desired coordination of nitrogen in the carbon framework of graphene has been conceived by a mutually assisted redox reaction between graphene oxide (GO) and pyrrole, followed by thermal treatment at elevated temperatures. NGE exhibits a high surface area of 528 m2 g−1 and a pore diameter of ∼3 to 7 nm. The heat treatment temperature plays a pivotal role in establishing the desired pyrrolic coordination of nitrogen in graphene for the electrochemical oxygen reduction reaction. The NGE sample obtained after heat treatment at 1000 °C (NGE-1000) has 53% pyrrolic nitrogen content compared to the similar samples prepared by treating at low temperatures. Most importantly, NGE-1000 has displayed a significantly low overpotential for oxygen reduction with the onset potential very closely matching that of the commercial 40 wt% Pt/C. It is noteworthy that the reaction involves the desired 4 electron transfer as observed in the case of the Pt based electrocatalysts, leading to a significantly high kinetic current density of 6 mA cm−2 at −0.2 V. Moreover, the fuel tolerance and durability under the electrochemical environment of the NGE catalyst is found to be superior to the Pt/C catalyst.

154 citations

Journal ArticleDOI
TL;DR: This work combines complementary synthetic approaches to grow tightly packed CN layers forming a type II heterojunction, which results in a CN photoanode with excellent charge separation, high electronic conductivity, and remarkable hole extraction efficiency.
Abstract: Polymeric carbon nitride (CN) has emerged as a promising semiconductor in photoanodes for photoelectrochemical cells (PECs) owing to its suitable electronic structure, tunable band gap, high stability, and low price. However, the poor electron diffusion within the CN layer and hole extraction to the solution still limit its applicability in PECs. Here, we report the fabrication of a CN photoanode with excellent electron diffusion length and remarkable hole extraction properties by careful design of its electronic interfaces. We combine complementary synthetic approaches to grow tightly packed CN layers forming a type-II heterojunction, which results in a CN photoanode with excellent charge separation, high electronic conductivity, and remarkable hole extraction efficiency. The optimized CN photoanode displays excellent PEC performance, reaching up to 270 μA cm-2 in a 0.1 M KOH solution at 1.23 V vs RHE, extremely low onset potential (∼0.0012 V), and long-term stability up to 18 h.

55 citations

Journal ArticleDOI
TL;DR: A simple growth method for polymeric carbon nitride (CN) layers on a conductive substrate, with excellent photoelectrochemical activity, owing to the formation of a type-II heterojunction was proposed in this article.
Abstract: A simple, straightforward growth method for polymeric carbon nitride (CN) layers on a conductive substrate, with excellent photoelectrochemical activity, owing to the formation of a type-II heteroj...

27 citations


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TL;DR: The unique advances on ultrathin 2D nanomaterials are introduced, followed by the description of their composition and crystal structures, and the assortments of their synthetic methods are summarized.
Abstract: Since the discovery of mechanically exfoliated graphene in 2004, research on ultrathin two-dimensional (2D) nanomaterials has grown exponentially in the fields of condensed matter physics, material science, chemistry, and nanotechnology. Highlighting their compelling physical, chemical, electronic, and optical properties, as well as their various potential applications, in this Review, we summarize the state-of-art progress on the ultrathin 2D nanomaterials with a particular emphasis on their recent advances. First, we introduce the unique advances on ultrathin 2D nanomaterials, followed by the description of their composition and crystal structures. The assortments of their synthetic methods are then summarized, including insights on their advantages and limitations, alongside some recommendations on suitable characterization techniques. We also discuss in detail the utilization of these ultrathin 2D nanomaterials for wide ranges of potential applications among the electronics/optoelectronics, electrocat...

3,628 citations

Journal ArticleDOI
TL;DR: This paper presents a probabilistic procedure for estimating the polymethine content of carbon dioxide using a straightforward two-step procedure, and shows good results in both the stationary and the liquid phase.
Abstract: Liming Dai,*,†,‡ Yuhua Xue,†,‡ Liangti Qu,* Hyun-Jung Choi, and Jong-Beom Baek* †Center of Advanced Science and Engineering for Carbon (Case4Carbon), Department of Macromolecular Science and Engineering, Case Western Reserve University, 10900 Euclid Avenue, Cleveland, Ohio 44106, United States Key Laboratory of Cluster Science, Ministry of Education of China, Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, Department of Chemistry, School of Science, Beijing Institute of Technology, Beijing 100081, People’s Republic of China School of Energy and Chemical Engineering/Center for Dimension-Controllable Covalent Organic Frameworks, Ulsan National Institute of Science and Technology (UNIST), 100 Banyeon, Ulsan, 689-798, South Korea

1,967 citations

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TL;DR: In this paper, a review focuses on recent progress in the experimental and computational studies of the roles of heteroatoms in heterogeneous nanocarbons for electrocatalytic oxygen reduction reaction (ORR).
Abstract: Heterogeneous nanocarbon materials are being increasingly investigated and deployed in numerous new technologies and devices for sustainable energy conversion and storage. Nanocarbons often consist of fullerene, graphene and carbon nanotubes. Their derivatives include quantum dots, nanofibres, nanoribbons, nanospheres/capsules and other nanostructured morphologies. The heterogeneous forms of these nanocarbons stem from the implantation of alien atoms into the aromatic carbon lattice or the covalent grafting of functional groups onto the carbon basal plane or edge sites. Heterogeneous nanocarbons have shown remarkable advantages in solar cells, water splitting, supercapacitors, lithium ion batteries and catalysis. This review focuses on recent progress in the experimental and computational studies of the roles of heteroatoms in heterogeneous nanocarbons for electrocatalytic oxygen reduction reaction (ORR). Critical perspectives are devoted to the ambiguous phenomena in this emerging research area. The long standing debate about the active sites is discussed with an emphasis on more rational development of advanced nanocarbon-based electrocatalysts for ORR.

869 citations

Journal ArticleDOI
TL;DR: In this paper, a comprehensive overview and description of graphene-based nanomaterials explored in recent years for catalyst supports and metal-free catalysts for polymer electrolyte membrane (PEM) fuel cell oxygen reduction reactions (ORR) is presented.
Abstract: A comprehensive overview and description of graphene-based nanomaterials explored in recent years for catalyst supports and metal-free catalysts for polymer electrolyte membrane (PEM) fuel cell oxygen reduction reactions (ORR) is presented. The catalyst material structures/morphologies, material selection, and design for synthesis, catalytic performance, catalytic mechanisms, and theoretical approaches for catalyst down-selection and catalyzed ORR mechanisms are emphasized with respect to the performance of ORR catalysts in terms of both activity and stability. When graphene-based materials, including graphene and doped graphene, are used as the supporting materials for both Pt/Pt alloy catalysts and non-precious metal catalyst, the resulting ORR catalysts can give superior catalyst activity and stability compared to those of conventional carbon-supported catalysts; when they are used as metal-free ORR catalysts, significant catalytic activity and stability are observed. The nitrogen-doped graphene materials even show superior performance compared to supported metal catalysts. Challenges including the lack of material mass production, unoptimized catalyst structure/morphology, insufficient fundamental understanding, and testing tools/protocols for performance optimization and validation are identified, and approaches to address these challenges are suggested.

420 citations