NO2 gas sensing performance enhancement based on reduced graphene oxide decorated V2O5 thin films.

Here, we demonstrate improved NO2 gas sensing properties based on reduced graphene oxide (rGO) decorated V2O5 thin film. Excluding the DC sputtering grown V2O5 thin film, rGO was spread over V2O5 thin film by the drop cast method. The formation of several p-n heterojunctions was greatly affected by the current-voltage relation of the rGO-decorated V2O5 thin film due to the p-type and n-type nature of rGO and V2O5, respectively. Initially with rGO decoration on V2O5 thin film, current decreased in comparison to the pristine V2O5 thin film, whereas depositing rGO film on a glass substrate drastically increased current. Among all sensors, only the rGO-decorated V2O5 sensor revealed a maximum NO2 gas sensing response for 100 ppm at 150 °C, and it achieved an approximately 61% higher response than the V2O5 sensor. The elaborate mechanism for an extremely high sensing response is attributed to the formation and modulation of p-n heterojunctions at the interface of rGO and V2O5. In addition, the presence of active sites like oxygenous functional groups on the rGO surface enhanced the sensing response. On that account, sensors based on rGO-decorated V2O5 thin film are highly suitable for the purpose of NO2 gas sensing. They enable the timely detection of the gas, further protecting the ecosystem from its harmful effects.

Mechanism for the compressive strain induced oscillations in the conductance of carbon nanotubes.

We report on the monotonic increase and the oscillation of electrical conductance in multiwalled carbon nanotubes with compressive strain. Combined experimental and theoretical analyses confirm that the conductance variation with strain is because of the transition from sp^{2} to sp^{3} configurations that are promoted by the interaction of walls in the nanotubes. The intrawall interaction is the reason for the monotonic increase in the conduction, while the oscillations are attributable to interwall interactions. This explains the observed electromechanical oscillation in multiwalled nanotubes and its absence in single-walled nanotubes, thereby resolving a long-standing debate on the interpretation of these results. Moreover, the current carrying capability of nanotubes can be enhanced significantly by controlling applied strains.

General theories for the electrical transport properties of carbon nanotubes.

We have shown that the general theories of metals and semiconductors can be employed to understand the diameter and voltage dependency of current through metallic and semiconducting carbon nanotubes, respectively. The current through a semiconducting multiwalled carbon nanotube (MWCNT) is associated with the energy gap that is different for different shells. The contribution of the outermost shell is larger as compared to the inner shells. The general theories can also explain the diameter dependency of maximum current through nanotubes. We have also compared the current carrying ability of a MWCNT and an array of the same diameter of single wall carbon nanotubes (SWCNTs) and found that MWCNTs are better suited and deserve further investigation for possible applications as interconnects.

On the paradoxical relation between the melting temperature and forbidden energy gap of nanoparticles.

We comment on the paradox that seems to exist about a correlation between the size-dependent melting temperature and the forbidden energy gap of nanoparticles. By analyzing the reported expressions for the melting temperature and the band gap of nanoparticles, we conclude that there exists a relation between these two physical quantities. However, the variations of these two quantities with size for semiconductors are different from that of metals.

Self-powered, ultrasensitive, room temperature humidity sensors using SnS2 nanofilms.

Humidity monitoring has become extremely vital in various technological fields such as environment control, biomedical engineering, and so on. Therefore, a substantial interest lies in the development of fast and highly sensitive devices with high figures of merit. Self-powered and ultrasensitive humidity sensors based on SnS2 nanofilms of different film thicknesses have been demonstrated in this work. The sensing behavior has been investigated in the relative humidity (RH) range of 2-99%. The observed results reveal a remarkable response and ultrafast detection even with zero applied bias (self-powered mode), with response and recovery times of ~ 10 and ~ 0.7 s, respectively. The self-powered behavior has been attributed to the inhomogeneities and the asymmetry in the contact electrodes. The highest sensitivity of ~ 5.64 × 106% can be achieved at an applied bias of 5 V. This approach of fabricating such highly responsive, self-powered and ultrafast sensors with simple device architectures will be useful for designing futuristic sensing devices.

Synthesis of one-dimensional ZnO nanostructures from Zn powder/granule.

We report the growth of one-dimensional ZnO nanostructures with different morphologies such as nanoneedles, nanorods, nanobelts from Zn powder/granule. The growth process is different from the conventional vapor-solid mechanism. The advantage of this method is that neither a catalyst nor any gas flow is required for the synthesis of nanostructures. Depending upon the Zn powder or Zn granules as the starting material different nanostructures have been synthesized which demonstrates the versatility of the technique.

Self-Powered, Broad Band, and Ultrafast InGaN-Based Photodetector.

A self-powered, broad band and ultrafast photodetector based on n+-InGaN/AlN/n-Si(111) heterostructure is demonstrated. Si-doped (n+ type) InGaN epilayer was grown by plasma-assisted molecular beam epitaxy on a 100 nm thick AlN template on an n-type Si(111) substrate. The n+-InGaN/AlN/n-Si(111) devices exhibit excellent self-powered photoresponse under UV-visible (300-800 nm) light illumination. The maximum response of this self-powered photodetector is observed at 580 nm for low-intensity irradiance (0.1 mW/cm2), owing to the deep donor states present near the InGaN/AlN interface. It shows a responsivity of 9.64 A/W with rise and fall times of 19.9 and 21.4 µs, respectively. A relation between the open circuit voltage and the responsivity has been realized.

Possible application of carbon nanotube bundles for low temperature sensing.

We report on the R-T measurement of carbon nanotube bundles from room temperature down to 1 K. The resistance at a particular temperature depends on the diameter of the bundle. The larger the bundle diameter is, the lower the value of the resistance. The resistance increases with the decrease in temperature as in the case of carbon, carbon glass resistance thermometer, and carbon nanotubes reported in the literature. The rate of the variation of resistance depends on the resistance of the bundle at room temperature which can be explored for the low temperature thermometry. Overall, the resistance and the sensitivity of the bundle depend on the bundle diameter which can be monitored easily.

Note: Simultaneous water quality monitoring and degradation of hazardous organic pollutants.

Here, we report a simple technique that uses mesoporous SnO2 to monitor the water quality and degrade the hazardous organic pollutants simultaneously. The technique generates hydroxyl radicals and a voltage that is hindered by the presence of hazardous organic pollutants. Pollutant as low as 1 ppb concentration level can easily be detected. The developed system not only monitors the water quality but also is capable of degrading hazardous dyes (organic pollutants) through its self-power, not relying on any external stimuli such as light, heat, radiation, and current. A simple digital laboratory multimeter is shown to be useful for the overall study. Overall, the study indicates that spectrophotometer generally used to monitor the dye concentration can be avoided.

In-Plane Anisotropic Photoconduction in Nonpolar Epitaxial a-Plane GaN.

Nonpolar a-plane GaN epitaxial films were grown on an r-plane sapphire using the plasma-assisted molecular beam epitaxy system, with various nitrogen plasma power conditions. The crystallinity of the films was characterized by high-resolution X-ray diffraction and reciprocal space mapping. Using the X-ray "rocking curve-phi scan", [0002], [1-100], and [1-102] azimuth angles were identified, and interdigitated electrodes along these directions were fabricated to evaluate the direction-dependent UV photoresponses. UV responsivity ( R) and internal gain ( G) were found to be dependent on the azimuth angle and in the order of [0002] > [1-102] > [1-100], which has been attributed to the enhanced crystallinity and lowest defect density along [0002] azimuth. The temporal response was very stable irrespective of growth conditions and azimuth angles. Importantly, response time, responsivity, and internal gain were 210 ms, 1.88 A W-1, and 648.9%, respectively, even at a bias as low as 1 V. The results were validated using the Silvaco Atlas device simulator, and experimental observations were consistent with simulated results. Overall, the photoresponse is dependent on azimuth angles and requires further optimization, especially for materials with in-plane crystal anisotropy.

Rational geometrical engineering of palladium sulfide multi-arm nanostructures as a superior bi-functional electrocatalyst.

Geometrical tunability offers sharp edges and an open-armed structure accompanied with a high electrochemical active surface area to ensure the efficient and effective utilization of materials by exposing the electrochemical active sites for facile accessibility of reactant species. Herein, we report a one-step, single-pot, surfactant-free, electroless, and economic route to synthesize palladium sulfide nanostructures with different geometries at mild temperatures and their catalytic properties towards the oxygen reduction reaction (ORR) and methanol electro-oxidation (MOR). For ORR, the positive on-set, half wave potentials, smaller Tafel slope, high electrochemical active surface area, large roughness factor, and better cyclic stability of the proposed nanostructures as compared to those of the commercial state-of-the-art Pt-C/PdS catalysts suggest their superiority in an alkaline medium. In addition, high mass activity (Jf ∼ 715 mA mg-1), in comparison with that of the commercial state-of-the-art Pt-C/PdS catalysts (Jf ∼ 138/41 mA mg-1, respectively), and high Jf/Jb (1.52) along with the superior operational stability of the multi-arm palladium sulfide nanostructures towards MOR advocates the bi-functional behavior of the catalyst and its potential as a promising Pt-free anode/cathode electrocatalyst in fuel cells.

Sequential Elemental Dealloying Approach for the Fabrication of Porous Metal Oxides and Chemiresistive Sensors Thereof for Electronic Listening.

Highly porous materials, with large surface area and accessible space, variable chemical compositions, and porosity at different length scales, have captivated the attention of researchers in recent years as an important family of functional materials. Here, we report a novel approach to grow porous metal oxides (PMOs) by sequential elemental dealloying in which a highly mobile element gets dealloyed first under the thermal treatment (annealing) and facilitates the formation of PMOs. Subsequently, a chemiresistive sensor based on porous SnO2 was fabricated for humidity sensing at room temperature which shows a high sensitivity of 348 in a fully humid [>99% relative humidity (RH)] atmosphere with an accuracy of 1% RH change. In addition, the sensor is highly durable and reproducible. Eventually, the chemiresistive sensor has been exploited for electronic listening toward speaking, whistling, and breath monitoring. Overall, the results advocate the fabrication of PMOs and the development of resistive humidity sensors for electronic listening as well as for biomedical applications.

Phenomenological predictions of cohesive energy and structural transition of nanoparticles.

In this paper, it is shown that a liquid-drop model (LDM) can predict the size-dependent cohesive energy (SDCE) of large nanoparticles and clusters (particles with few atoms) quantitatively. The cohesive energy decreases linearly with the inverse of the particle size both for large nanoparticles and clusters though the slopes are different. This indicates that there are three different regions (I-III) of SDCE in the complete size range. Regions I and II represent the SDCE of large nanoparticles and clusters, respectively, while region II represents the intermediate region where the cohesive energy is almost size-independent. Different regions of SDCE correspond to different structures of nanoparticles, and structural transition associated with the particle size can easily be predicted from the SDCE. Analyzing the cohesive energy data on the basis of LDM, it is shown that the surface tension decreases with decreasing size for very small nanoparticles. The Tolman equation can account for the variation of surface tension by predicting the size dependency of the Tolman length.

Temperature-Dependent Photoluminescence of g-C3N4: Implication for Temperature Sensing.

We report the temperature-dependent photoluminescence (PL) properties of polymeric graphite-like carbon nitride (g-C3N4) and a methodology for the determination of quantum efficiency along with the activation energy. The PL is shown to originate from three different pathways of transitions: σ*-LP, π*-LP, and π*-π, respectively. The overall activation energy is found to be ∼73.58 meV which is much lower than the exciton binding energy reported theoretically but ideal for highly sensitive wide-range temperature sensing. The quantum yield derived from the PL data is 23.3%, whereas the absolute quantum yield is 5.3%. We propose that the temperature-dependent PL can be exploited for the evaluation of the temperature dependency of quantum yield as well as for temperature sensing. Our analysis further indicates that g-C3N4 is well-suited for wide-range temperature sensing.

Reduced Graphene Oxide-Ag3PO4 Heterostructure: A Direct Z-Scheme Photocatalyst for Augmented Photoreactivity and Stability.

A visible light driven, direct Z-scheme reduced graphene oxide-Ag3PO4 (RGO-Ag3 PO4 ) heterostructure was synthesized by means of a simple one-pot photoreduction route by varying the amount of RGO under visible light illumination. The reduction of graphene oxide (GO) and growth of Ag3PO4 took place simultaneously. The effect of the amount of RGO on the textural properties and photocatalytic activity of the heterostructure was investigated under visible light illumination. Furthermore, total organic carbon (TOC) analysis confirmed 97.1 % mineralization of organic dyes over RGO-Ag3PO4 in just five minutes under visible-light illumination. The use of different quenchers in the photomineralization suggested the presence of hydroxyl radicals ((.)OH), superoxide radicals ((.)O2 (-)), and holes (h(+)), which play a significant role in the mineralization of organic dyes. In addition to that, clean hydrogen fuel generation was also observed with excellent reusability. The 4 RGO-Ag3PO4 heterostructure has a high H2 evolution rate of 3690 µmol h(-1) g(-1), which is 6.15 times higher than that of RGO.

Changes in Ascorbic Acid Content during Growth and Development of Panicum miliaceum.

The present paper deals with changes in the ascorbic acid content of the shoot apex during its transformation from the vegetative to the reproductive state and its further development in Panicum miliaceum var. Samai Co. 1. Seedlings were exposed to 24-hour illumination, natural day, and 8 hours of illumination per day. Ascorbic acid was determined for the growing apex, stem, and leaf of the main shoot and for the individual branches produced on it at successive developmental stages.A several-fold increase in ascorbic acid content of the growing apex of the main shoot of plants grown under 8-hour illumination synchronizes with its transformation from the vegetative to the reproductive state. In plants grown under natural day and continuous illumination, which continue to grow vegetatively, the ascorbic acid content remains at a low level. Moving these plants to 8-hour illumination results in floral initiation and an increase in the ascorbic acid content. The high level of ascorbic acid is maintained through the gametogenic and embryogenic phases, but decreases during seed formation. A rise in ascorbic acid content of branch apices always occurs later than that in the main shoot but the increase again coincides with floral initiation in the branch apex. The ascorbic acid contents of stem and leaf are not significantly affected by the photoperiod. Hence, a massive upsurge in ascorbic acid content synchronizes with the transformation of the vegetative branch and shoot apices to the reproductive state.

Photoperiodic studies on growth and development of Impatiens balsamina L. : II. Floral bud initiation, flower opening and extension growth.

In the short-day plant Impatiens balsamina it was found that, while floral buds are initiated with 3 short-day (SD) cycles, at least 8 such cycles are required for flowering. The numbers of floral buds and open flowers bear a linear relationship with the number of SD cycles. The induced floral buds revert to vegetative growth unless the plants receive the minimum number of SD cycles needed for flowering, this reversion occurring in a basipetal direction. The rate of extension growth of the stem increases with increasing numbers of SD cycles. The high rate is maintained longer in plants receiving 32 or more SD cycles, but the subsequent fall is also steeper in these plants than in plants receiving less inductive cycles. Senescence also occurs in these plants and appears to be related to the magnitude of reproductive development and the high rate of extension growth.

Photoperiodic studies on growth and development of Impatiens balsamina L. : I. Lateral bud development and its relationship with senescence.

Seedlings of Impatiens balsamina raised under ND and LD conditions were divided into two sub-groups each when they had reached 5-leaf stage. While one sub-group was left under the same condition (NDND or LDLD), the other was transferred to the other photoperiod (NDLD or LDND). NDND plants were subdivided into 2 lots. One of these was transferred to SD in May. The dates of emergence of individual branches and floral buds were recorded and the vegetative period was calculated in each case.It was found that in NDND plants floral buds were produced from all the nodes except the lowermost which produced a single vegetative branch. In LDND plants the vegetative branches were produced from the lower 9 nodes but floral buds from those above these. Small leafy structures which ultimately dried up were produced from a few top nodes in both these cases. In contrast to this in LDLD plants only vegetative branches were produced from all the nodes. In NDLD plants floral buds were produced from the lower 3-5 nodes prior to transfer to LD condition, but vegetative branches were produced from the upper nodes after this transfer. Even some of the lower floral buds reverted to vegetative state under this condition.The production of floral buds or the vegetative branches as the case may be, occurred in acropetal succession under all the photoperiodic conditions and never in basipetal manner.LDLD and NDLD plants, which did not flower at all, continued to produce lateral branches without showing any sign of senescence, while LDND and NDND ones showed yellowing of the apical growing point which spread downwards and lead ultimately to the death of the plant. The senescence was hastened when these plants were transferred to SD condition towards the end of May. The senescence therefore, appears to be related with reproductive development. The results are discussed in the light of current literature.