Gotowa bibliografia na temat „MoS2-rGO”

A new NO2 nanohybrid of a gas sensor (CTAB-MoS2/rGO) was constructed for sensitive room-temperature detection of NO2 by 3D molybdenum disulfide (MoS2) and reduced graphene oxide (rGO), assisted with hexadecyl trimethyl ammonium bromide (CTAB). In comparison with MoS2 and MoS2/rGO, the BET and SEM characterization results depicted the three-dimensional structure of the CTAB-MoS2/rGO nanohybrid, which possessed a larger specific surface area to provide more active reaction sites to boost its gas-sensing performance. Observations of the gas-sensing properties indicated that the CTAB-MoS2/rGO sensor performed a high response of 45.5% for 17.5 ppm NO2, a remarkable selectivity of NO2, an ultra-low detection limit of 26.55 ppb and long-term stability for a 30-day measurement. In addition, the response obtained for the CTAB-MoS2/rGO sensor was about two to four times that obtained for the MoS2/rGO sensor and the MoS2 sensor toward 8 ppm NO2, which correlated with the heterojunction between MoS2 and rGO, and the improvement in surface area and conductivity correlated with the introduction of CTAB and rGO. The excellent performance of the CTAB-MoS2/rGO sensor further suggested the advantage of CTAB in assisting a reliable detection of trace NO2 and an alternative method for highly efficiently detecting NO2 in the environment.

In this paper, we report a facile strategy to design and prepare reduced graphene oxide (rGO) supported MoS2 nanoplatelet (MoS2/rGO) via a solvothermal co-assembly process. It is found that in the as-obtained MoS2/rGO nanocomposite, MoS2 possesses unique platelet structure and rGO is exfoliated due to the in situ growth of MoS2 nanoplatelet, leading to a large specific surface area, facilitating rapid diffusion of lithium ions. The nanocomposite is used as a promising anode material for lithium-ion batteries and displays a high initial charge capacity (1382[Formula: see text]mA[Formula: see text]h[Formula: see text]g[Formula: see text]), excellent rate capability and cycling stability. The remarkable lithium storage performance of MoS2/rGO nanocomposite is mainly ascribed to the inherent nanostructure of the MoS2, and the synergistic effect between rGO nanosheets and MoS2 nanoplatelets.

This study presents three-dimensional (3D) MoS2/reduced graphene oxide (rGO)/graphene quantum dots (GQDs) hybrids with improved gas sensing performance for NO2 sensors. GQDs were introduced to prevent the agglomeration of nanosheets during mixing of rGO and MoS2. The resultant MoS2/rGO/GQDs hybrids exhibit a well-defined 3D nanostructure, with a firm connection among components. The prepared MoS2/rGO/GQDs-based sensor exhibits a response of 23.2% toward 50 ppm NO2 at room temperature. Furthermore, when exposed to NO2 gas with a concentration as low as 5 ppm, the prepared sensor retains a response of 15.2%. Compared with the MoS2/rGO nanocomposites, the addition of GQDs improves the sensitivity to 21.1% and 23.2% when the sensor is exposed to 30 and 50 ppm NO2 gas, respectively. Additionally, the MoS2/rGO/GQDs-based sensor exhibits outstanding repeatability and gas selectivity. When exposed to certain typical interference gases, the MoS2/rGO/GQDs-based sensor has over 10 times higher sensitivity toward NO2 than the other gases. This study indicates that MoS2/rGO/GQDs hybrids are potential candidates for the development of NO2 sensors with excellent gas sensitivity.

Zirconia and 10%, 20%, and 30% cerium-doped zirconia nanoparticles (ZCO), ZCO-1, ZCO-2, and ZCO-3, respectively, were prepared using auto-combustion method. Binary nanohybrids, ZrO2@rGO and ZCO-2@rGO (rGO = reduced graphene oxide), and ternary nanohybrids, ZrO2@rGO@MoS2 and ZCO-2@rGO@MoS2, have been prepared with an anticipation of a fruitful synergic effect of rGO, MoS2, and cerium-doped zirconia on the tribo-activity. Tribo-activity of these additives in paraffin oil (PO) has been assessed by a four-ball lubricant tester at the optimized concentration, 0.125% w/v. The tribo-performance follows the order: ZCO-2@rGO@MoS2 > ZrO2@rGO@MoS2 > ZCO-2@rGO > ZrO2@rGO > MoS2 > ZrO2 > rGO > PO. The nanoparticles acting as spacers control restacking of the nanosheets provided structural augmentation while nanosheets, in turn, prevent agglomeration of the nanoparticles. Doped nanoparticles upgraded the activity by forming defects. Thus, the results acknowledge the synergic effect of cerium-doped zirconia and lamellar nanosheets of rGO and MoS2. There is noncovalent interaction among all the individuals. Analysis of the morphological features of wear-track carried out by scanning electron microscopy (SEM) and atomic force microscopy (AFM) in PO and its formulations with various additives is consistent with the above sequence. The energy dispersive X-ray (EDX) spectrum of ZCO-2@rGO@MoS2 indicates the existence of zirconium, cerium, molybdenum, and sulfur on the wear-track, confirming, thereby, the active role played by these elements during tribofilm formation. The X-ray photoelectron spectroscopy (XPS) studies of worn surface reveal that the tribofilm is made up of rGO, zirconia, ceria, and MoS2 along with Fe2O3, MoO3, and SO42− as the outcome of the tribo-chemical reaction.

In this work, a few layer molybdenum disulfide (MoS2) and reduced graphene oxide (rGO) nanocomposite have been synthesized by liquid exfoliation method. The morphological and structural properties are analyzed using scanning electron microscopy and X-ray diffraction technique. The optical properties are also investigated using absorption and Raman spectroscopy. This report presents quantification of swift heavy ion irradiation induced defects using Raman spectroscopy. We found both Raman mode E12g and A1g corresponding to MoS2 and Raman modes of rGO are strongly affected by increasing ions doses. The defect induced lattice strain in the rGO/MoS2 nanocomposite is also estimated from Raman spectroscopy. MoS2 layers are found to be much more sensitive than rGO in the rGO/MoS2 nanocomposite. These types of study further used in device based application of rGO/MoS2 nanocomposite system.

Fe–Ni-based composites with Ni-coated reduced grapheme oxide (RGO)–MoS2 were fabricated by powder metallurgy technique, and their morphology, phase composition, and tribological properties at different temperatures were investigated systematically. Results showed that Fe–Ni-based composite with Ni-coated RGO–MoS2 possessed much more uniform and denser microstructure, and higher hardness than that with RGO–MoS2. Furthermore, Ni-coated RGO–MoS2 additive greatly allowed increasing the friction-reducing and wear-resistant properties, due to the reinforcing and lubricating effect new phase (Fe3W3C, CrxS1+ x, etc.) and the improvement on interfacial compatibility between Ni-coated RGO–MoS2 and Fe–Ni matrix. In particular, as the content of Ni-coated RGO–MoS2 was 5 wt%, the friction coefficient and wear rate of the corresponding composite was decreased nearly 50% and 75%, respectively. More importantly, Ni-coated RGO–MoS2 reinforced composite kept excellent tribological properties at elevated temperature. Its friction coefficient decreased firstly with the increased temperature from 25℃ to 400℃, then increased slightly when the temperature increased to 600℃. Besides, the wear rate was only 0.73–0.9 × 10−4 mm3/Nm during the whole temperature range. This suggested that Ni-coated RGO–MoS2 was a promising additive of metallic-based composites suitable for high-temperature sliding condition.

MoS2/rGO composites were synthesized by hydrothermal method from the precursors of MoS2 and reduced graphene oxide (rGO) prepared in the former steps. The influence of the synthesis conditions including hydrothermal temperature and mass ratio of MoS2 to rGO on the structure, morphology, and optical absorption capacity of the MoS2/rGO composites was systematically investigated using physicochemical characterizations. The photocatalytic performance of as-prepared samples was investigated on the degradation of Rhodamine B under visible light, in which, the composites obtained at hydrothermal temperature of 180°C and MoS2/rGO mass ratio of 4/1 exhibited the highest photodegradation efficiency of approx. 80% after 4 hours of reaction. This enhancement in photocatalytic behaviour of composites could be assigned to the positive effect of rGO in life time expansion of photoinduced electrons—holes.

A one-step high-temperature solvothermal approach to the synthesis of monolayer or bilayer MoS2 anchored onto reduced graphene oxide (RGO) sheet (denoted as MoS2/RGO) is described. It was found that single-layered or double-layered MoS2 were synthesized directly without an extra exfoliation step and well dispersed on the surface of crumpled RGO sheets with random orientation. The prepared MoS2/RGO composites delivered a high reversible capacity of 900[Formula: see text]mAhg[Formula: see text] after 200 cycles at a current density of 200[Formula: see text]mAg[Formula: see text] as well as good rate capability as anode active material for lithium ion batteries. This one-step high-temperature hydrothermal strategy provides a simple, cost-effective and eco-friendly way to the fabrication of exfoliated MoS2 layers deposited onto RGO sheets.

Noble metal-free cocatalysts have drawn great interest in accelerating the catalytic reactions of metal chalcogenide semiconductor photocatalyst. In particular, great efforts have been made on modifying a semiconductor with dual cocatalysts, which show synergistic effect of a fast transfer of exciton and energy simultaneously. Herein, we report the dual-modified Cu2S with MoS2 and reduced graphene oxides (Cu2S-MoS2/rGO). The in situ growth of Cu2S nanoparticles in the presence of MoS2/rGO resulted in high density of nanoscale interfacial contacts among Cu2S nanoparticles, MoS2, and rGO, which is beneficial for reducing the photogenerated electrons’ and holes’ recombination. The Cu2S-MoS2/rGO system also demonstrated stable photocatalytic activity for H2 evolution reaction for the long term.

Three-dimensional reduced graphene oxide (RGO) matrix decorated with nanoflowers of layered MoS2 (denoted as 3D MoS2/RGO) have been synthesized via a facile one-pot stepwise hydrothermal method. Graphene oxide (GO) is used as precursor of RGO and a 3D GO network is formed in the first-step of hydrothermal treatment. At the second stage of hydrothermal treatment, nanoflowers of layered MoS2 form and anchor on the surface of previously formed 3D RGO network. In this preparation, thiourea not only induces the formation of the 3D architecture at a relatively low temperature, but also works as sulfur precursor of MoS2. The synthesized composites have been investigated with XRD, SEM, TEM, Raman spectra, TGA, N2 sorption technique and electrochemical measurements. In comparison with normal MoS2/RGO composites, the 3D MoS2/RGO composite shows improved electrochemical performance as anode material for lithium-ion batteries. A high reversible capacity of 930[Formula: see text]mAh[Formula: see text][Formula: see text][Formula: see text]g[Formula: see text] after 130 cycles under a current density of 200[Formula: see text]mA[Formula: see text][Formula: see text][Formula: see text]g[Formula: see text] as well as good rate capability and superior cyclic stability have been observed. The superior electrochemical performance of the 3D MoS2/RGO composite as anode active material for lithium-ion battery is ascribed to its robust 3D structures, enhanced surface area and the synergistic effect between graphene matrix and the MoS2 nanoflowers subunit.

Solar energy is by far the most abundant renewable resource available to mankind. However, it is diffused and intermittent, and often geographically separated from that of the production results in underwhelming utilization of this resource. Inspired by photosynthesis, various efforts were made to store solar energy in form of chemical bonds than can be used when the sun is not shining. A promising approach is to produce hydrogen, a carbon-neutral energy carrier is via water splitting which requires electrocatalysts to accelerate the two half-cell reactions, hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). The state-of-art catalysts used for HER is Pt and for OER is IrO2/RuO2 that are prohibitively expensive. We have developed new synthesis methodologies for various earth-abundant electrocatalysts supported heteroatom-doped carbon nanostructures and exploited for water splitting. An in-situ solid state route was developed to integrate ruthenium nanoparticles with N-doped graphene sheets which exhibited an HER activity rivalling state-of-art Pt/C over a wide pH range. In order to find further cost-effective materials, we sought inspiration from NiFe-hydrogenase (the most efficient catalyst for HER) to develop a general solid state method for bimetallic MFe@ N-doped carbon core-shell nanostructures (M = Ni, Cu, Co, Zn, Mn) as efficient total water splitting catalyst. Thereafter, a new, phosphine-free, solid state method to hybridize Co2P with N, P co-doped CNTs was developed which could also be extended to synthesize Fe2P, Ni2P and Cu3P. Moreover, glucose oxidation was attempted as a possible replacement for the kinetically sluggish OER half-cell reaction, wherein Co2P/N, P-CNTs were demonstrated to be an efficient non-enzymatic glucose sensor for the first time. Thereafter, Co-imidazolate frameworks (ZIF-67) were transformed into hierarchal Co-N-Se nanosheets via a simple selenization method. Investigations were carried out to establish a structure-property correlation between the nanostructures evolved over various interval of time along with their OER activity. Finally, an in-situ strategy was developed to hybridize N-doped graphitic carbon seets with Ni and MoxC (Mo2C and MoC) nanoparticles which exhibited resilient HER activity besides effectively accelerating OER, thereby resulting in overall water splitting that can be attributed to favorable electronic modulation between various strongly coupled components.

The ever increasing demand for energy due to over consumption of non-renewable fossil fuels has emphasized the need for alternate, sustainable and efficient energy conversion and storage systems. In this direction, electrochemical energy conversion and storage systems involving various fundamental electrochemical redox processes such as hydrogen evolution (HER), oxygen reduction (ORR), oxygen evolution (OER), hydrogen oxidation (HOR) reactions and others become highly important. Electrocatalysts are often used to accelerate the kinetics of these reactions. Platinum (Pt), ruthenium oxide and iridium oxide (RuO2 and IrO2) are known to be the state of the art catalysts for several of these reactions due to favouarable density of states (DOS) near the Fermi level, binding energy with the reactant species, chemical inertness etc. Apart from HER, OER and ORR, chlorine evolution reaction (Cl-ER) is another industrially important reaction associated with water purification, disinfection, bleaching, chemical weapons and pharmaceuticals. Dimensionally stable anodes (RuO2/IrO2 mixed with TiO2 on Ti) are the most commonly used catalysts for this process. Issues related to surface poisoning, corrosion and cost of the catalysts, in addition to selectivity and specificity towards a particular reaction are various aspects to be addressed. For example, Pt is not very specific for ORR in presence of methanol in addition to high cost and corrosion in certain media. On the other hand, DSA can efficiently catalyze both OER and Cl-ER, and hence there is overlap of the two processes in the potential range available. There is an on going search for efficient, cost-effective, stable catalysts that possess high specificity for a particular redox reaction. Towards this goal, the present study explores certain layered (phospho)chalcogenides for catalyzing HER, ORR, OER and Cl-ER. The present thesis is structured in two parts, where the first part explores the multi-functional catalytic aspects of new classes of compounds based on layered transition metal mixed chalcogenides (MoS2(1-x)Se2x) and ternary phosphochalcogenides (FePS3, FePSe3 and MoPS). In addition, lithium insertion and desinsertion has been studied with the aim of using the layered materials for rechargeable batteries. The second part of the thesis explores organic electrode materials with active carbonyl groups such as rufigallol, polydihydroxyanthrachene succinic anhydride (PDASA) as battery electrodes. Additionally, covalently functionalized transition metal phthalocyanines with reduced graphene oxide are studied as counter electrodes in dye sensitized solar cells (DSSCs). MoS2(1-x)Se2x (x = 0 to 1) compositions are solid solutions of MoS2 and MoSe2 in different ratios. They crystallize in hexagonal structure with space group P63/mmc (D6h4) having Mo in trigonal prismatic coordination like the pristine counterparts. X-Ray diffraction studies reveal that Vegard’s law (figure 1a) is followed and hence complete miscibility of MoS2 and MoSe2 is established. MoS2(1-x)Se2x (x = 0 to 1) are layered in nature and the layers are held together by long range, weak van der Waal’s forces. This gives us the flexibility of exfoliation to produce corresponding few-layer materials (figure 1b). Figure 1. (a) Variation of lattice parameter corresponding to (002) reflection of MoS2(1-x)Se2x with different x values. (b) Scanning electron micrograph of few-layer MoS2(1-x)Se2x (x = 0.5). The electrocatalytic activity of the few-layer sulphoselenides have been studied towards HER in aqueous 0.5 M H2SO4 and towards Cl-ER in 3 M aqueous NaCl (pH = 3) solution. The mixed chalcogenides exhibit very good activities for both HER and Cl-ER as compared to the activity of their pristine counter parts (i.e. MoS2 and MoSe2) (figures 2a and 2b). Electrocatalytic activity on different compositions reveal that MoS1.0Se1.0 exhibits the maximum activity. Additionally, it has been observed that MoS1.0Se1.0 shows high specificity for Cl-ER with negligible interference of OER. Figure 2. Voltammetric data for (a) hydrogen evolution reaction (in 0.5 M aqueous H2SO4) and (b) chlorine evolution reaction (in 3 M aqueous NaCl solution, pH = 3) on MoS2(1-x)Se2x (x = 0, 0.5, 1). Figure 3. (a) XRD pattern of MoS2(1-x)Se2x (x = 0.5) electrode after a cycle of Li insersion and deinsersion (red) along with as-synthesized material (black) (b) Cycling behaviour of rGO supported (black) and pristine (red) MoS2(1-x)Se2x (x = 0.5) as electrode in rechargeable lithium-ion battery. The equiatomic MoS1.0Se1.0 has also been studied as an anode material for rechargeable lithium batteries. The cyclic voltammogram and characterization after charge-discharge cycle (figure 3a) indicate intercalation of Li with in the layers followed by conversion type formation of Li-S and Li-Se type compounds. The pristine material shows continuous capacity fading while the composites of sulphoselenides functionalized with conducting carbon supports such as rGO, MWCNT, super P carbon, toray carbon show marked improvement in capacity as well as cycling behavior. The rGO functionalized MoS1.0Se1.0 reveals ~1000 mAh/g of stable specific discharge capacity for 500 cycles (figure 3b). In the next two chapters, new class of transition metal-based layered materials FePS3 and FePSe3, containing both P and chalcogen (S and Se) is indroduced for electrocatalysis. FePS3 crystallizes in monoclinic symmetry with an indirect band gap of ~1.55 eV while FePSe3 possesses rhombohedral crystal structure with comparatively low band gap (~1.3 eV) as shown in figure 4a. The FePS3 and FePSe3 have been exfoliated as has been done for MoS1.0Se1.0 (liquid exfoliation method) using acetone as the solvent. Stable colloids with few-layer nanosheets having lamellar morphology and lateral sizes of ~100 to 200 nm are obtained. Electrical characterization indicates that they are semiconducting and the conductivity of the Se analogue is ~50 times higher than that of the S analogue (figure 4b). Figure 4. (a) Catholuminescence of FePX3 ( X = S and Se) reveals the band gap of the material. Band gap of the S analogue is 1.52 eV and that of the Se analogue is 1.33 eV (b) Resistivity of FePX3 ( X = S and Se) as a function of temperature. The tri-functional electrocatalytic activities on rGO-few layer FePX3 (X = S and Se) have been evaluated for HER over a wide pH range (0.5 M H2SO4, 0.5 M KOH, phosphate Figure 5. Catalytic activity of rGO-few-layer FePX3 (X = S, Se) towards HER in (a) aqueous 0.5 M H2SO4 and (b) 3.5 wt % NaCl solutions. (c) ORR activity of the catalysts in oxygen saturated 0.5 M KOH (d) OER behaviour on the catalysts in 0.5 M KOH at a rotation speed of 1600 rpm. buffer, pH 7 and 3.5 % NaCl), ORR and OER in alkaline media (0.5 M KOH). The studies clearly reveal that both rGO-FePS3 and rGO-FePSe3 exhibit excellent HER activity in acidic media (figure 5a) with high stability. The HER studies in 3.5 wt % aqueous NaCl solution (figure 5b) suggests that the catalysts are effective in evolving hydrogen from sea-water environment. Studies on ORR activity (figure 5c) indicate that the rGO composites of both S and Se analogues follow 4-electron pathways to produce water as the final product. They are also found to be highly methanol tolerant. In the case of OER (figure 5d), XPS characterization of the electrodes after the voltammetric studies reveals the presence of very thin layer of Fe2O3 (not detectable by XRD). All the three reactions (HER, ORR and OER) catalyzed by the Se analogue are better than the S analogue (figure 5). This could be due to the low band gap and high conductivity of FePSe3 as compared to FePS3. The over potential to achieve 10 mAcm-2 current density is ~108 mV for rGO-few-layer FePS3 catalyst where in the case of rGO-few layer FePSe3, it is ~97 mV (table 1). Table 1. Catalytic activities of rGO-few layer FePS3 and rGO-few layer FePSe3 towards HER, ORR and OER. Reaction studied rGO-FePS3 rGO-FePSe3 HER (η @ 10mAcm-2) ~108 mV ~97 mV ORR (peak potential) ~0.81 V ~0.87 V OER (η @ 10mAcm-2) ~470 mV ~430 mV It is likely that there is a strong interaction between FePX3 (metal d-orbital) and rGO, as observed from the downward shift of Fe 2p peak in high resolution XPS studies. This interaction may extend the density of states of metal d-orbitals thereby improving the catalytic activities. The next chapter deals with molybdenum-based phosphosulphide compound (MoPS). Molybdenum-based phosphide catalysts have been explored recently as excellent catalysts for various electrochemical reactions such as HER. It is expected that the catalyst containing both S and P will show positive effects on catalytic activities due to the synergy between S and P. In the present study, P incorporated MoS2 is studied towards HER. The XRD pattern of the as-synthesized crystal suggests the presence of mixed phase of MoS2, MoP2 and MoP while the elemental mapping in microscopy indicates the ratio of Mo, P and S to be 1:1:1. The electrochemical HER in 0.5 M H2SO4 indicates that the activity is improved drastically as compared to bulk and few-layer MoS2. The next section explores the use of different organic electrode materials possessing active carbonyl groups for Li-storage studies. The advantage of the use of carbonyl-based compounds lies in the high reversible activity towards Li ion insersion and de-insersion. Rufigallol (figure 6a) exhibits very stable capacity of ~200 mAh/g (at C/20 rate) upto 500 Figure 6. (a) and (c) Schematic representation of rufigallol and poly-dihydroanthracene succinic anhydride (PDASA) respectively. (b) and (d) Cyclic behaviour of rufigallol (at C/20 rate) and PDASA (at 20 mAg-1 current rate) in Li-storage devices. (e) and (f) represent the coulombic efficiency of rufigallol (at C/20 rate) and PDASA (at 20 mAg-1 current rate) as a function of number of cycles. cycles along (figure 6b) and with very good rate capability. A triptycene-based mesoporous polymer, PDASA (figure 6c) is introduced and explored as efficient electrode material for Li-storage. PDASA exhibits very high capacity of ~1000 mAh/g at a current rate of 50 mA/g upto 1000 cycles (figure 6d). Even at very high current rates (3A/g) excellent cyclability is observed. The mechanistic details of lithium uptake and release are studied using various spectroscopic techniques. In both the cases the coulombic efficiency observed is ~80 to 90 % (figures 6e and f). Figure 7. (a) Digital photograph of the dye sensitized solar cell with rGO-Co-TAPc counter electrode. (b) Photoconversion efficiency of DSSCs with different counter electrodes as mentioned in the figure. (c) Photo conversion efficiency of Pt and rGO-Co-TAPc based DSSCs as function of storage time. (d) Schematic illustration of DSSC wherein the energy level of the counter electrodes and electrolyte are shown for different M-TAPcs. In a slightly different direction, metal phthalocyanine - rGO composites (rGO-M-TAPc; M = Co, Zn, Fe) have been explored as counter electrodes in DSSC. Figure 7a depicts the digital image of a DSSC constructed using rGO-Co-TAPc as the counter electrode. It has been observed that rGO-cobalt tetraamino phthalocyanine (rGO-Co-TAPc) counter electrode exhibits ~6.6 % of solar conversion efficiency (figure 7b) and is close to that of standard DSSC (Pt counter electrode) under identical experimental conditions and are highly stable (figure 7c). Other metal phthalocyanines show less efficiency and is analysed based on the relative positions of HOMO energy levels of the materials and the energy level of the redox system (I-/I3- system) as given in figure 7d. The thesis contains eight chapters on aspects discussed above along with summary and future perspectives given at the end. It is devided into various chapters in two sections, one comprising inorganic chalcogenide-based electrocatalysts and another comprising organic electrode materials. Appendix I discusses the Na-storage behaviour of MoS1.0Se1.0 and appendix II describes the Li-storage behaviour of rGO functionalized benzoquinone and diamino anthraquinone electrode materials.

The ever increasing demand for energy due to over consumption of non-renewable fossil fuels has emphasized the need for alternate, sustainable and efficient energy conversion and storage systems. In this direction, electrochemical energy conversion and storage systems involving various fundamental electrochemical redox processes such as hydrogen evolution (HER), oxygen reduction (ORR), oxygen evolution (OER), hydrogen oxidation (HOR) reactions and others become highly important. Electrocatalysts are often used to accelerate the kinetics of these reactions. Platinum (Pt), ruthenium oxide and iridium oxide (RuO2 and IrO2) are known to be the state of the art catalysts for several of these reactions due to favouarable density of states (DOS) near the Fermi level, binding energy with the reactant species, chemical inertness etc. Apart from HER, OER and ORR, chlorine evolution reaction (Cl-ER) is another industrially important reaction associated with water purification, disinfection, bleaching, chemical weapons and pharmaceuticals. Dimensionally stable anodes (RuO2/IrO2 mixed with TiO2 on Ti) are the most commonly used catalysts for this process. Issues related to surface poisoning, corrosion and cost of the catalysts, in addition to selectivity and specificity towards a particular reaction are various aspects to be addressed. For example, Pt is not very specific for ORR in presence of methanol in addition to high cost and corrosion in certain media. On the other hand, DSA can efficiently catalyze both OER and Cl-ER, and hence there is overlap of the two processes in the potential range available. There is an on going search for efficient, cost-effective, stable catalysts that possess high specificity for a particular redox reaction. Towards this goal, the present study explores certain layered (phospho)chalcogenides for catalyzing HER, ORR, OER and Cl-ER. The present thesis is structured in two parts, where the first part explores the multi-functional catalytic aspects of new classes of compounds based on layered transition metal mixed chalcogenides (MoS2(1-x)Se2x) and ternary phosphochalcogenides (FePS3, FePSe3 and MoPS). In addition, lithium insertion and desinsertion has been studied with the aim of using the layered materials for rechargeable batteries. The second part of the thesis explores organic electrode materials with active carbonyl groups such as rufigallol, polydihydroxyanthrachene succinic anhydride (PDASA) as battery electrodes. Additionally, covalently functionalized transition metal phthalocyanines with reduced graphene oxide are studied as counter electrodes in dye sensitized solar cells (DSSCs). MoS2(1-x)Se2x (x = 0 to 1) compositions are solid solutions of MoS2 and MoSe2 in different ratios. They crystallize in hexagonal structure with space group P63/mmc (D6h4) having Mo in trigonal prismatic coordination like the pristine counterparts. X-Ray diffraction studies reveal that Vegard’s law (figure 1a) is followed and hence complete miscibility of MoS2 and MoSe2 is established. MoS2(1-x)Se2x (x = 0 to 1) are layered in nature and the layers are held together by long range, weak van der Waal’s forces. This gives us the flexibility of exfoliation to produce corresponding few-layer materials (figure 1b). Figure 1. (a) Variation of lattice parameter corresponding to (002) reflection of MoS2(1-x)Se2x with different x values. (b) Scanning electron micrograph of few-layer MoS2(1-x)Se2x (x = 0.5). The electrocatalytic activity of the few-layer sulphoselenides have been studied towards HER in aqueous 0.5 M H2SO4 and towards Cl-ER in 3 M aqueous NaCl (pH = 3) solution. The mixed chalcogenides exhibit very good activities for both HER and Cl-ER as compared to the activity of their pristine counter parts (i.e. MoS2 and MoSe2) (figures 2a and 2b). Electrocatalytic activity on different compositions reveal that MoS1.0Se1.0 exhibits the maximum activity. Additionally, it has been observed that MoS1.0Se1.0 shows high specificity for Cl-ER with negligible interference of OER. Figure 2. Voltammetric data for (a) hydrogen evolution reaction (in 0.5 M aqueous H2SO4) and (b) chlorine evolution reaction (in 3 M aqueous NaCl solution, pH = 3) on MoS2(1-x)Se2x (x = 0, 0.5, 1). Figure 3. (a) XRD pattern of MoS2(1-x)Se2x (x = 0.5) electrode after a cycle of Li insersion and deinsersion (red) along with as-synthesized material (black) (b) Cycling behaviour of rGO supported (black) and pristine (red) MoS2(1-x)Se2x (x = 0.5) as electrode in rechargeable lithium-ion battery. The equiatomic MoS1.0Se1.0 has also been studied as an anode material for rechargeable lithium batteries. The cyclic voltammogram and characterization after charge-discharge cycle (figure 3a) indicate intercalation of Li with in the layers followed by conversion type formation of Li-S and Li-Se type compounds. The pristine material shows continuous capacity fading while the composites of sulphoselenides functionalized with conducting carbon supports such as rGO, MWCNT, super P carbon, toray carbon show marked improvement in capacity as well as cycling behavior. The rGO functionalized MoS1.0Se1.0 reveals ~1000 mAh/g of stable specific discharge capacity for 500 cycles (figure 3b). In the next two chapters, new class of transition metal-based layered materials FePS3 and FePSe3, containing both P and chalcogen (S and Se) is indroduced for electrocatalysis. FePS3 crystallizes in monoclinic symmetry with an indirect band gap of ~1.55 eV while FePSe3 possesses rhombohedral crystal structure with comparatively low band gap (~1.3 eV) as shown in figure 4a. The FePS3 and FePSe3 have been exfoliated as has been done for MoS1.0Se1.0 (liquid exfoliation method) using acetone as the solvent. Stable colloids with few-layer nanosheets having lamellar morphology and lateral sizes of ~100 to 200 nm are obtained. Electrical characterization indicates that they are semiconducting and the conductivity of the Se analogue is ~50 times higher than that of the S analogue (figure 4b). Figure 4. (a) Catholuminescence of FePX3 ( X = S and Se) reveals the band gap of the material. Band gap of the S analogue is 1.52 eV and that of the Se analogue is 1.33 eV (b) Resistivity of FePX3 ( X = S and Se) as a function of temperature. The tri-functional electrocatalytic activities on rGO-few layer FePX3 (X = S and Se) have been evaluated for HER over a wide pH range (0.5 M H2SO4, 0.5 M KOH, phosphate Figure 5. Catalytic activity of rGO-few-layer FePX3 (X = S, Se) towards HER in (a) aqueous 0.5 M H2SO4 and (b) 3.5 wt % NaCl solutions. (c) ORR activity of the catalysts in oxygen saturated 0.5 M KOH (d) OER behaviour on the catalysts in 0.5 M KOH at a rotation speed of 1600 rpm. buffer, pH 7 and 3.5 % NaCl), ORR and OER in alkaline media (0.5 M KOH). The studies clearly reveal that both rGO-FePS3 and rGO-FePSe3 exhibit excellent HER activity in acidic media (figure 5a) with high stability. The HER studies in 3.5 wt % aqueous NaCl solution (figure 5b) suggests that the catalysts are effective in evolving hydrogen from sea-water environment. Studies on ORR activity (figure 5c) indicate that the rGO composites of both S and Se analogues follow 4-electron pathways to produce water as the final product. They are also found to be highly methanol tolerant. In the case of OER (figure 5d), XPS characterization of the electrodes after the voltammetric studies reveals the presence of very thin layer of Fe2O3 (not detectable by XRD). All the three reactions (HER, ORR and OER) catalyzed by the Se analogue are better than the S analogue (figure 5). This could be due to the low band gap and high conductivity of FePSe3 as compared to FePS3. The over potential to achieve 10 mAcm-2 current density is ~108 mV for rGO-few-layer FePS3 catalyst where in the case of rGO-few layer FePSe3, it is ~97 mV (table 1). Table 1. Catalytic activities of rGO-few layer FePS3 and rGO-few layer FePSe3 towards HER, ORR and OER. Reaction studied rGO-FePS3 rGO-FePSe3 HER (η @ 10mAcm-2) ~108 mV ~97 mV ORR (peak potential) ~0.81 V ~0.87 V OER (η @ 10mAcm-2) ~470 mV ~430 mV It is likely that there is a strong interaction between FePX3 (metal d-orbital) and rGO, as observed from the downward shift of Fe 2p peak in high resolution XPS studies. This interaction may extend the density of states of metal d-orbitals thereby improving the catalytic activities. The next chapter deals with molybdenum-based phosphosulphide compound (MoPS). Molybdenum-based phosphide catalysts have been explored recently as excellent catalysts for various electrochemical reactions such as HER. It is expected that the catalyst containing both S and P will show positive effects on catalytic activities due to the synergy between S and P. In the present study, P incorporated MoS2 is studied towards HER. The XRD pattern of the as-synthesized crystal suggests the presence of mixed phase of MoS2, MoP2 and MoP while the elemental mapping in microscopy indicates the ratio of Mo, P and S to be 1:1:1. The electrochemical HER in 0.5 M H2SO4 indicates that the activity is improved drastically as compared to bulk and few-layer MoS2. The next section explores the use of different organic electrode materials possessing active carbonyl groups for Li-storage studies. The advantage of the use of carbonyl-based compounds lies in the high reversible activity towards Li ion insersion and de-insersion. Rufigallol (figure 6a) exhibits very stable capacity of ~200 mAh/g (at C/20 rate) upto 500 Figure 6. (a) and (c) Schematic representation of rufigallol and poly-dihydroanthracene succinic anhydride (PDASA) respectively. (b) and (d) Cyclic behaviour of rufigallol (at C/20 rate) and PDASA (at 20 mAg-1 current rate) in Li-storage devices. (e) and (f) represent the coulombic efficiency of rufigallol (at C/20 rate) and PDASA (at 20 mAg-1 current rate) as a function of number of cycles. cycles along (figure 6b) and with very good rate capability. A triptycene-based mesoporous polymer, PDASA (figure 6c) is introduced and explored as efficient electrode material for Li-storage. PDASA exhibits very high capacity of ~1000 mAh/g at a current rate of 50 mA/g upto 1000 cycles (figure 6d). Even at very high current rates (3A/g) excellent cyclability is observed. The mechanistic details of lithium uptake and release are studied using various spectroscopic techniques. In both the cases the coulombic efficiency observed is ~80 to 90 % (figures 6e and f). Figure 7. (a) Digital photograph of the dye sensitized solar cell with rGO-Co-TAPc counter electrode. (b) Photoconversion efficiency of DSSCs with different counter electrodes as mentioned in the figure. (c) Photo conversion efficiency of Pt and rGO-Co-TAPc based DSSCs as function of storage time. (d) Schematic illustration of DSSC wherein the energy level of the counter electrodes and electrolyte are shown for different M-TAPcs. In a slightly different direction, metal phthalocyanine - rGO composites (rGO-M-TAPc; M = Co, Zn, Fe) have been explored as counter electrodes in DSSC. Figure 7a depicts the digital image of a DSSC constructed using rGO-Co-TAPc as the counter electrode. It has been observed that rGO-cobalt tetraamino phthalocyanine (rGO-Co-TAPc) counter electrode exhibits ~6.6 % of solar conversion efficiency (figure 7b) and is close to that of standard DSSC (Pt counter electrode) under identical experimental conditions and are highly stable (figure 7c). Other metal phthalocyanines show less efficiency and is analysed based on the relative positions of HOMO energy levels of the materials and the energy level of the redox system (I-/I3- system) as given in figure 7d. The thesis contains eight chapters on aspects discussed above along with summary and future perspectives given at the end. It is devided into various chapters in two sections, one comprising inorganic chalcogenide-based electrocatalysts and another comprising organic electrode materials. Appendix I discusses the Na-storage behaviour of MoS1.0Se1.0 and appendix II describes the Li-storage behaviour of rGO functionalized benzoquinone and diamino anthraquinone electrode materials.