Chandran Sudakar

Bio: Chandran Sudakar is an academic researcher from Indian Institute of Technology Madras. The author has contributed to research in topics: Magnetization & Thin film. The author has an hindex of 32, co-authored 140 publications receiving 3204 citations. Previous affiliations of Chandran Sudakar include Wayne State University & Indian Institute of Science.

Tunable Ferromagnetism accompanied by Morphology Control in Li-doped Zn0.97Ni0.03O

Abstract: We report morphological and ferromagnetic property control in ZnO nanorod structures by an optimum doping of Ni and Li. Nanostructures of Zn0.97-xNi0.03LixO (x = 0, 0.03, 0.05, 0.08, and 0.10) are prepared by a solvothermal method. High aspect ratio (5−15) ZnO nanorods transform to particles (with 1−3 aspect ratio) influenced by 3 at. % Ni substitution in ZnO (Zn0.97Ni0.03O). It is remarkable to note that the Zn0.97Ni0.03O particles completely retain the nanorod shape with significantly increased aspect ratio (15−30) when 3 at.% Li ions are codoped in Zn0.97Ni0.03O (Zn0.94Li0.03Ni0.03O). Li substitution also enhances ferromagnetism with largest magnetization (0.8 emu·g−1) observed for Zn0.94Li0.03Ni0.03O. For Li concentration >3 at.%, the aspect ratio as well as the magnetization decreased considerably. These experimental observations are explained by first-principles modeling. At low Li-on-Zn acceptor concentrations, the total magnetization is increased by lower Ni d-state populations, whereas at higher ...

Kinetic Insights into the Mechanism of Oxygen Reduction Reaction on Fe2O3/C Composites.

Abstract: Since the inception of cobalt phthalocyanine for oxygen reduction reaction (ORR), non-platinum group metals have been the central focus in the area of fuel-cell electrocatalysts. Besides Fe-Nx active sites, a large variety of species are formed during the pyrolysis, but studies related to their ORR activity have been given less importance in the literature. Fe2O3 is one among them, and this study describes the role of Fe2O3 in the ORR. The Fe2O3 is carefully synthesized on various carbon supports and characterized using X-ray photoelectron spectroscopy (XPS) spectra, high-resolution transmission electron microscopy (HRTEM) images, and surface area analysis. The characterization techniques reveal that the Fe2O3 nanoparticles are present in the pores of the carbon supports, having a particle size ranging from 4 to 15 nm. The current density of the ORR on Fe2O3/C catalysts is increased compared with bare carbon supports, as discerned from the rotating ring-disk electrode (RRDE) voltammetry experiments, demonstrating the role of size-confined Fe2O3 nanoparticles. The overall number of electrons in the ORR is increased by the introduction of Fe2O3 on the carbon support. Based on the kinetic analysis, the ORR on Fe2O3/C follows a pseudo-4-electron or 2+2-electron ORR, where the first 2-electron ORR to H2O2 and second 2-electron H2O2 reduction reaction (HPRR) to H2O are assigned to the graphitic carbon (carbon defects) and Fe2O3 active sites, respectively. Theoretical studies indicate that the role of Fe2O3 is to decrease the free energy of O2 adsorption and reduce the energy barrier for the reduction of *OOH to OH-. The onset potential estimated from the free energy diagram is 0.42 V, matching with the HPRR activity demonstrated using the potential-dependent rate constants plot. Fe2O3/C shows higher stability by retaining 95% of the initial activity even after 20 000 cycles.

Stability of MAPbI3 perovskite grown on planar and mesoporous electron-selective contact by inverse temperature crystallization

Abstract: Single crystalline perovskite solar cells (PSC) are promising for their inherent stability due to the absence of grain boundaries. While the development of single crystals of perovskite with enhanced optoelectronic properties is known, studies on the growth, device performance and understanding of the intrinsic stability of single crystalline perovskite thin film solar cell devices fabricated on electron selective contacts are scarcely explored. In this work, we examine the impact of mesoporous TiO2 (m-TiO2) and planar TiO2 (p-TiO2) on the growth of single crystalline-methyl ammonium lead iodide (SC-MAPbI3) film, PSC device performance and film stability under harsh weather conditions (T ∼ 85 °C and RH ∼ 85%). Self-grown SC-MAPbI3 films are developed on m-TiO2 and p-TiO2 by inverse temperature crystallization under ambient conditions without the need for sophisticated glove-box processing. The best device with m-TiO2 as an electron transport layer showed a promising power conversion efficiency of 3.2% on an active area of 0.3 cm2 in hole transport material free configuration, whereas, only 0.7% was achieved for the films developed on p-TiO2. Complete conversion of precursor to perovskite phase and better surface coverage of the film leading to enhanced absorption and reduced defects of single crystalline perovskite on m-TiO2 compared to its p-TiO2 leads to this large difference in efficiency. Mesoporous device retained more than 70% of its initial performance when stored at 30 °C under dark for more than 5000 h at 50% RH; while the planar device degraded after 1500 h. Thermal and moisture endurance of SC-MAPbI3 films are investigated by subjecting them to temperatures ranging from 35 °C to 85 °C at a constant relative humidity (RH) of 85%. X-ray diffraction studies show that the SC-MAPbI3 films are stable even at 85 °C and 85% RH, with only slight detection (30–35%) of PbI2 at these conditions. This study highlights the superior stability of SC-MAPbI3 films which paves way for further studies on improving the stability and performance of the ambient processed PSCs.

Semiconductor-based Photocatalytic Hydrogen Generation

Abstract: 2.3. Evaluation of Photocatalytic Water Splitting 6507 2.3.1. Photocatalytic Activity 6507 2.3.2. Photocatalytic Stability 6507 3. UV-Active Photocatalysts for Water Splitting 6507 3.1. d0 Metal Oxide Photocatalyts 6507 3.1.1. Ti-, Zr-Based Oxides 6507 3.1.2. Nb-, Ta-Based Oxides 6514 3.1.3. W-, Mo-Based Oxides 6517 3.1.4. Other d0 Metal Oxides 6518 3.2. d10 Metal Oxide Photocatalyts 6518 3.3. f0 Metal Oxide Photocatalysts 6518 3.4. Nonoxide Photocatalysts 6518 4. Approaches to Modifying the Electronic Band Structure for Visible-Light Harvesting 6519

Understanding TiO2 photocatalysis: mechanisms and materials.

Abstract: Jenny Schneider,*,† Masaya Matsuoka,‡ Masato Takeuchi,‡ Jinlong Zhang, Yu Horiuchi,‡ Masakazu Anpo,‡ and Detlef W. Bahnemann*,† †Institut fur Technische Chemie, Leibniz Universitaẗ Hannover, Callinstrasse 3, D-30167 Hannover, Germany ‡Faculty of Engineering, Osaka Prefecture University, 1 Gakuen-cho, Sakai Osaka 599-8531, Japan Key Lab for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, Shanghai 200237, China

Ferromagnetic materials

Abstract: In this chapter, we will restrict our attention to the ferrites and a few other closely related materials. The great interest in ferrites stems from their unique combination of a spontaneous magnetization and a high electrical resistivity. The observed magnetization results from the difference in the magnetizations of two non-equivalent sub-lattices of the magnetic ions in the crystal structure. Materials of this type should strictly be designated as “ferrimagnetic” and in some respects are more closely related to anti-ferromagnetic substances than they are to ferromagnetics in which the magnetization results from the parallel alignment of all the magnetic moments present. We shall not adhere to this special nomenclature except to emphasize effects, which are due to the existence of the sub-lattices.

Advanced Nanoarchitectures for Solar Photocatalytic Applications

Abstract: UV-Visible ار راد ن .د TiO2 ( تیفرظ راون مان هب نورتکلا یاراد یژرنا زارت لماش VB و ) رگید زارت ی یژرنا اب ( ییاناسر راون مان هب نورتکلا زا یلاخ و رتلااب VB یم ) .دشاب ت ود نیا نیب یژرنا توافت یژرنا فاکش زار ، پگ دناب هدیمان یم .دوش هک ینامز زا نورتکلا لاقتنا VB هب VB یم ماجنا دریگ ، TiO2 اب ودح یژرنا بذج د ev 2 / 3 ، نورتکلا تفج کی دیلوت یم هرفح .دیامن و نورتکلا هرفح ی نا اب هدش دیلوت یم کرتشم حطس هب لاقت ثعاب دناوت شنکاو ماجنا اه یی ددرگ . TiO2 دربراک ،دراد یدایز یاه هلمج زا یم ناوت اوه یگدولآ هیفصت یارب (CO2) و بآ و ... نآ زا هدافتسا درک .

Titanium dioxide-based nanomaterials for photocatalytic fuel generations.

Abstract: Generations Yi Ma,† Xiuli Wang,† Yushuai Jia,† Xiaobo Chen,‡ Hongxian Han,*,† and Can Li*,† †State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences and Dalian National Laboratory for Clean Energy, 457 Zhongshan Road, Dalian 116023, China ‡Department of Chemistry, College of Arts and Sciences, University of Missouri-Kansas City, 5100 Rockhill Road, Kansas City, Missouri 64110, United States