NH2-MIL-125(Ti) doped CdS/Graphene composite as electro and photo catalyst in basic medium under light irradiation.

The development of active electrocatalysts and photocatalysts for hydrogen evolution reaction (HER) and for environmental remediation is a huge challenge. Research is still underway on the development of low-cost catalytic materials with appreciable efficiency for HER. In the present study, a composite of metal organic framework (MOF) with CdS and graphene (NH2-MIL-125(Ti)/CdS-graphene) composites were developed with different loadings of graphene material via solvothermal technique. Further the electrocatalytic activity of the synthesized catalysts were investigated for HER and photocatalytic degradation of dye. Results show that the synthesized catalyst with a less amount of graphene was more active. HER results showed a less Tafel slope of 70.8 and 61.9 mVdec-1 with 15.6 mA/cm2 and 15.46 mA/cm2 current densities under light on and off conditions. Further the dye degradation activity of the synthesized catalysts was tested with Rhodamine B dye and results showed that the catalyst showed excellent activity for low weight loading of graphene with a degradation efficiency of 95 % and followed pseudo first order kinetic model. Overall results showed that the synthesized composites are promising for HER and photocatalytic applications.

Effect of Thermally Induced Oxygen Vacancy of α-MnO2 Nanorods toward Oxygen Reduction Reaction.

MnO2 has been explored for various applications in environmental and energy aspects. However, the thermal sensitivity of the MnO2 crystal structure never been studied. As a potential cathode material for fuel cell, α-MnO2 has a higher specific activity than Pt/C based on per metals cost. In this work, the physical and electrochemical properties of α-MnO2 nanorods were explored for the first time under thermal treatment with different temperatures (300, 400, and 500 °C). Under thermal treatment, oxygen vacancies were induced. The high-angle annular dark-field (HAADF) images and electron energy loss spectroscopy (EELS) have been taken to explore oxygen vacancies of α-MnO2 materials. From EELS and X-ray photoelectron spectroscopy (XPS) analysis, the oxygen vacancies on the α-MnO2 nanorods were strengthened with the temperature increasing. The sample with 400 °C treatment exhibited the best performance toward ORR, excellent methanol tolerance and higher stability compared to commercial Pt/C in alkaline media due to its combination of preferable growth on (211) plane and moderate oxygen vacancies as well as coexistence of Mn (IV)/ Mn (III) species. It was also observed the α-MnO2 nanorods tended to become longer and thinner with increasing temperature. This work suggests that the α-MnO2 nanorods are thermal sensitive materials and their performance for ORR can be boosted under certain temperatures.

Cross-linked glucose oxidase clusters for biofuel cell anode catalysts.

The efficient localization of increased levels of active enzymes onto conducting scaffolds is important for the development of enzyme-based biofuel cells. Cross-linked enzyme clusters (CEC) of glucose oxidase (GOx) constrained to functionalized carbon nanotubes (CEC-CNTs) were generated in order to evaluate the potential of using CECs for developing GOx-based bioanodes functioning via direct electron transfer from the GOx active site to the CNT scaffold. CEC-CNTs generated from several weight-to-weight ratios of GOx:CNT were examined for comparable catalytic activity to free GOx into the solution, with CEC-CNTs generated from a 100% GOx solution displaying the greatest enzymatic activity. Scanning transmission electron microscopic analysis of CEC-CNTs generated from 100% GOx to CNT (wt/wt) ratios revealed that CEC clusters of ∼78 µm2 localized to the CNT surface. Electrochemical analysis indicates that the enzyme is engaged in direct electron transfer, and biofuel cells generated using GOx CEC-CNT bioanodes were observed to have a peak power density of ∼180 µW cm(-2). These data indicate that the generation of nano-to-micro-sized active enzyme clusters is an attractive option for the design of enzyme-specific biofuel cell powered implantable devices.

Influence of cell fabrication procedure on the performance of the dye sensitized solar cell.

The recent technological advancements of the Dye Sensitized Solar Cells (DSSCs) fabrication technology is gaining momentum as a low cost and simple fabrication technology to convert solar energy into electric energy. A systematic study of the DSSC fabrication procedure and its influence on the cell efficiency are presented in this paper. Preparation of the titanium dioxide (TiO2) layer on the working electrode was the most significant process improvement made to enhance cell efficiency. The Coatema tool was used to develop an automated TiO2 coating process, which yielded layer thicknesses with minimum micro cracks and repeatable TiO2 weight loading in the range of 8-13 microm. Secondary process improvements implemented were: vacuum drying step for the TiO2 layer, dilution ratio of the sensitized dye and sealant thickness. These optimized cell fabrication steps enhanced cell efficiencies over 200% and reduced total process time. The work in progress demonstrated higher cell efficiency slightly greater than 9% by reducing the cell size using the optimized fabrication process described in this paper. We are confident that higher efficiency cells can be fabricated with this optimized fabrication process illustrated in this paper.

Bio-batteries and bio-fuel cells: leveraging on electronic charge transfer proteins.

Bio-fuel cells are alternative energy devises based on bio-electrocatalysis of natural substrates by enzymes or microorganisms. Here we review bio-fuel cells and bio-batteries based on the recent literature. In general, the bio-fuel cells are classified based on the type of electron transfer; mediated electron transfer and direct electron transfer or electronic charge transfer (ECT). The ECT of the bio-fuel cells is critically reviewed and a variety of possible applications are considered. The technical challenges of the bio-fuel cells, like bioelectrocatalysis, immobilization of bioelectrocatalysts, protein denaturation etc. are highlighted and future research directions are discussed leveraging on the use of electron charge transfer proteins. In addition, the packaging aspects of the bio-fuel cells are also analyzed and the found that relatively little work has been done in the engineering development of bio-fuel cells.