Next Steps for Hydrogen - physics, technology and the future

Hydrogen has been proposed as a future energy carrier for more than 40 years. In recent decades, impetus has been given by the need to reduce global greenhouse gas emissions from vehicles. In addition, hydrogen has the potential to facilitate the large-scale deployment of variable renewables in the electricity system. Despite such drivers, the long-anticipated hydrogen economy is proving to be slow to emerge. This report stresses the role that physics and physics-based technology could play in accelerating the large-scale deployment of hydrogen in the energy system. Emphasis is given to the potential of cryogenic liquid hydrogen and the opportunities afforded by developments in nanoscience for hydrogen storage and use. The use of low-temperature liquid hydrogen opens up a technological opportunity separate from, but complementary with, energy applications. The new opportunity is the ability to cool novel materials into the superconducting state without the need to use significant quantities of expensive liquid helium. Two of the authors have previously coined the term “hydrogen cryomagnetics” for when liquid hydrogen is utilised in high-field and high-efficiency magnets. The opportunity for liquid hydrogen to displace liquid helium may be a relatively small business opportunity compared to global transport energy demands, but it potentially affords an opportunity to kick-start the wider commercial use of hydrogen. The report considers various important factors shaping the future for hydrogen, such as competing production methods and the importance of safety, but throughout it is clear that science and engineering are of central importance to hydrogen innovation and physics has an important role to play

Gold surface with gold nitride–a surface enhanced Raman scattering active substrate

The nitration of gold surfaces is a nonpolluting method, which can lead to large scale production of substrates with remarkable properties and applications. We present a topographical study of the nanoscale structure of the gold nitride surfaces produced by radio frequency (rf) nitrogen plasma etching of thin gold films. Atomic force microscopy images taken after rf etching reveal the striking appearance of the cluster assembly with large clusters surrounded by small clusters (7.9±1.4 and 2.3±0.9 nm, respectively) appearing to exhibit an attractive interaction. We discuss the possible mechanism for this attraction based on a colloid model by Messina et al. [Phys. Rev. Lett. 85, 872 (2000) ]. This surface exhibits a notable surface enhanced Raman scattering effect demonstrated with L-alanine and rhodamine-6G. The significance of this work is that we found that this SERS active gold nitride surface can be prepared in just one step: by nitrogen plasma etching a thin gold film. Until now most SERS active gold cluster covered surfaces have been prepared in several steps very often requiring complex lithography

Synthesis and characterisation of polyaniline (PAni) membranes for fuel cell

Over the past decade or so, alternative energy plays a pivotal role in addressing challenges posed by nature. Polymer electrolyte membrane fuel cell is one of the promising alternative energy and there has been significant research and technological investments done in this field. The key information and future prospective of the field is energy conversion and storage, both of which are essential in order to meet the challenges of global warming and the limited fossil fuel supply. However, polymer membrane in particular plays a crucial role in advancing this technology further. The utilization of conducting polymers in manufacturing membranes combining their electrochemical properties along with mechanical properties is of primary importance to enhance the efficiency of this system. In the present study blends of high impact polystyrene (HIPS) and polyaniline (PAni) were obtained with the aim of producing membranes for fuel cell. HIPS and PAni were dissolved in tetrachloroethylene, a common solvent for both materials. After dissolution, PAni was dispersed in an HIPS polymeric matrix. The membranes were molded on to glass plates using a laminator to keep thickness constant, and the solvent evaporated slowly for 24 h under room temperature. The amount of polyaniline used was 10 and 20 % weight. The electronic and structural properties were carried out using X-ray photoelectron spectroscopy (XPS), Thermogravimetric Analysis (TGA) Raman spectroscopy, Scanning electronic microscopic (SEM). The analysis indicate that PAni incorporation and its dispersion into the polymeric matrix modifies the membranes properties and show improvement in efficiency

Extracellular electron transfer mechanism in Shewanella loihica PV- 4 biofilms formed at indium tin oxide and graphite electrodes

Electroactive biofilms are capable of extracellular electron transfer to insoluble metal oxides and electrodes; such biofilms are relevant to biogeochemistry, bioremediation, and bioelectricity production. We investigated the extracellular electron transfer mechanisms in Shewanella loihica PV-4 viable biofilms grown at indium tin oxide (ITO) and graphite electrodes in potentiostat-controlled electrochemical cells poised at 0.2 V vs. Ag/AgCl. Chronoamperometry and confocal microscopy showed higher biofilm growth at graphite compared to the ITO electrode. Cyclic voltammetry, differential pulse voltammetry, along with fluorescence spectroscopy showed that direct electron transfer through outer membrane c type cytochromes (Omcs) prevailed at the biofilm/ITO interface, while biofilms formed at graphite electrode reduced the electrode also via secreted redox mediators, such as flavins and quinones. The biofilm age does not affect the prevalent transfer mechanism at ITO electrodes. On the other hand, secreted redox mediators accumulated at biofilm/graphite interface, thus increasing mediated electron transfer as the biofilm grows over five days. Our results showed that the electrode material determined the prevalent electron transfer mechanism and the dynamic of secreted redox mediators in S. loihica PV-4 biofilms. These observations have implications for the optimization of biofilm-based electrochemical systems, such as biosensors and microbial fuel cells

Mediator-free interaction of glucose oxidase, as model enzyme for immobilization, with Al-doped and undoped ZnO thin films laser-deposited on polycarbonate supports

Al doped and undoped ZnO thin films were deposited by pulsed-laser deposition on polycarbonate sheets. The films were characterized by optical transmission, Hall effect measurement, XRD and SEM. Optical transmission and surface reflectometry studies showed good transparency with thicknesses ∼100 nm and surface roughness of 10 nm. Hall effect measurements showed that the sheet carrier concentration was −1.44 × 1015 cm−2 for AZO and −6 × 1014 cm−2 for ZnO. The films were then modified by drop-casting glucose oxidase (GOx) without the use of any mediators. Higher protein concentration was observed on ZnO as compared to AZO with higher specific activity for ZnO (0.042 U mg−1) compared to AZO (0.032 U mg−1), and was in agreement with cyclic voltemmetry (CV). X-ray photoelectron spectroscopy (XPS) suggested that the protein was bound by dipole interactions between AZO lattice oxygen and the amino group of the enzyme. Chronoamperometry showed sensitivity of 5.5 μA mM−1 cm−2 towards glucose for GOx/AZO and 2.2 μA mM−1 cm−2 for GOx/ZnO. The limit of detection (LoD) was 167 μM of glucose for GOx/AZO, as compared to 360 μM for GOx/ZnO. The linearity was 0.28–28 mM for GOx/AZO whereas it was 0.6–28 mM for GOx/ZnO with a response time of 10s. Possibly due to higher enzyme loading, the decrease of impedance in presence of glucose was larger for GOx/ZnO as compared to GOx/AZO in electrochemical impedance spectroscopy (EIS). Analyses with clinical blood serum samples showed that the systems had good reproducibility and accuracy. The characteristics of novel ZnO and AZO thin films with GOx as a model enzyme, should prove useful for the future fabrication of inexpensive, highly sensitive, disposable electrochemical biosensors for high throughput diagnostics

Fast response and low temperature sensing of acetone and ethanol using Al-doped ZnO microrods

We report low temperature acetone and ethanol sensing properties of Al-doped ZnO microrods synthesized using hydrothermal technique. We observe the acetone detection at room temperature as well as ethanol and acetone detection at low temperature of 150 °C using Al-doped ZnO microrods. 3 wt% Al-doped ZnO microrods sensor exhibits the highest response of 231 toward 8100 parts per million (ppm) of ethanol at 150 °C. The response & recovery time are found to be ultrafast of 60 ms & 870 ms for ethanol and 110 ms & 330 ms for acetone of the Al-doped ZnO microrods at an operating temperature of 150 °C, respectively. In addition, sensing mechanism has explained to illuminate the improved sensing performances of Al-doped ZnO microrods. Thus it is revealed that Al-doped ZnO microrods are promising as an ultrafast gas sensor

Engineering work function of graphene oxide from p to n type using a low power atmospheric pressure plasma jet

In this work, we demonstrate doping graphene oxide (GO) films using a low power atmospheric pressure plasma jet (APPJ) with subsequent tuning of the work function. The surface potential of the plasma functionalized GO films could be tuned by 120 ± 10 mV by varying plasma parameters. X-ray spectroscopy used to probe these changes in electronic structure of systematically functionalized GO films by plasma. Detailed investigation using X-ray photoelectron spectroscopy and near edge X-ray absorption fine structure spectroscopy revealed the reactive nitrogen species in the plasma induce finite changes in the surface chemistry of the GO films, introducing additional density of states near the top of the valence band edge. Nitrogen introduced by the atmospheric pressure plasma is predominantly in a graphitic configuration with a varying concentration of pyridinic nitrogen. Additionally, evidence of gradual de-epoxidation of these GO films with increasing plasma exposure was also observed. We attribute this variation in work function values to the configuration of nitrogen in the graphitic structure as revealed by X-ray spectroscopy. With pyridinic nitrogen the electronic states of GO became electron deficient, inducing a p-type doping whereas increase in graphitic nitrogen increased the electron density of GO leading to an n-type doping effect. Nitrogen doping was also found to decrease the resistivity from 138 MΩsq-1 to 4-1MΩsq. These findings are extremely useful in fabricating hetrojunctions like sensor, optoelectronic devices where band structure alignment is key to device performance when GO is used as a charge transport layer. This technique can be extended to other known 2D systems

Electrochemical micro analytical device interfaced with portable potentiostat for rapid detection of chlorpyrifos using acetylcholinesterase conjugated metal organic framework using Internet of things

An Electrochemical micro Analytical Device (EµAD) was fabricated for sensitive detection of organophosphate pesticide chlorpyrifos in the food chain. Gold microelectrode (µE) modified with Zinc based Metal Organic Framework (MOF-Basolite Z1200) and Acetylcholinesterase (AChE) enzyme served as an excellent electro-analytical transducer for the detection of chlorpyrifos. Electrochemical techniques such as Cyclic Voltammetry (CV), Electrochemical Impedance Spectroscopy (EIS) and Differential Pulse Voltammetry (DPV) were performed for electrochemical analysis of the developed EµAD. The sensor needs only 2 µL of the analyte and it was tested within the linear range of 10 to 100 ng/L. The developed EµAD’s limit of detection (LoD) and sensitivity is 6 ng/L and 0.598 µ A/ng L−1/mm2 respectively. The applicability of the device for the detection of chlorpyrifos from the real vegetable sample was also tested within the range specified. The fabricated sensor showed good stability with a shelf-life of 20 days. The EµAD’s response time is of 50 s, including an incubation time of 20 s. The developed EµAD was also integrated with commercially available low-cost, handheld potentiostat (k-Stat) using Bluetooth and the results were comparable with a standard electrochemical workstation

Microwave- and Formaldehyde-Assisted Synthesis of Ag–Ag₃PO₄ with Enhanced Photocatalytic Activity for the Degradation of Rhodamine B Dye and Crude Oil Fractions

The release of crude oil and water-soluble dyes into our marine environment is a major global problem. An efficient semiconductor Ag–Ag3PO4 photocatalyst was synthesized using formaldehyde as a reducing agent to form surface active Ag on Ag3PO4 under microwave radiation for heating, and its potential in destroying environmental pollutants has been examined. The diffuse reflectance spectroscopy of Ag–Ag3PO4 revealed an enhanced absorption in the visible light region. The rate of photocatalytic degradation of rhodamine B by Ag–Ag3PO4 was over 4-fold compared to Ag3PO4. The potential application of Ag–Ag3PO4 in oil spill remediation was also examined through photocatalytic degradation of benzene, n-hexane, and 1:1 v/v benzene/methanol crude oil-soluble fractions. UV–vis and gas chromatography–mass spectrometry analysis of the crude oil components after visible light irradiation showed excellent degradation. The photocatalytic efficiency enhancement of Ag–Ag3PO4 is attributed to the excellent electron trapping of silver nanoparticles deposited on the surface of Ag3PO4. This work will motivate future studies to develop recyclable visible light photocatalysts for many applications

Electro-deposited nano-webbed structures based on polyaniline/multi walled carbon nanotubes for enzymatic detection of organophosphates

We report the development of an ultrasensitive electrochemical sensor using polyaniline (PANi) and carboxyl functionalized multi-walled carbon nanotubes (fMWCNT) for the detection of organophosphates (OPs) in real samples. The sensor was tested in the linear concentration range of 10 ng/L to 120 ng/L. The limit of detection (LoD) was found to be 8.8 ng/L with sensitivity 0.41 mA/ng/L/cm2 for chlorpyrifos (CPF); and 10.2 ng/L with sensitivity 0.58 mA/ng/L/cm2 for methyl parathion (MP). The vegetable samples (cucumber) were also tested. The average % recovery for CPF and MP were found to be 98.05% and 96.63% respectively. The developed sensor showed stability for a period of 30 days. The interference of the sensor was studied with heavy metals (cadmium (Cd), chromium (Cr), lead (Pb), arsenic (As)) which was found to be < 10%. The developed sensor will play a major role in real-time monitoring of food products, leading to food safety