Graphitic carbon nitride encapsulated sonochemically synthesized β-nickel hydroxide nanocomposites for electrocatalytic hydrogen generation

Hydrogen evolution reaction (HER) carried out from electrocatalysis of water splitting is playing a major role in the production of green and clean hydrogen. In this paper, we report on the synthesis of graphitic carbon nitride on nickel hydroxide (g-C₃N₄/Ni(OH)₂) nanocomposites by a simple ultrasonication method. The characterizations include the XRD, Raman, FESEM and electrochemical studies to analyze the performance of the as developed material over hydrogen evolution reaction. The morphological analysis shows that the aggregated interconnected g-C₃N₄/Ni(OH)₂ (GCN/NH) nanocomposites with an average particle size of ～20 nm. These GCN/NH nanocomposites exhibit the lowest overpotential of 341 mV at 10 mA/cm² which is smaller than that of the pristine Ni(OH)₂ nanosheets at 367 mV. Further, the Tafel slope for GCN/NH nanocomposites reveals a lower value of 131 mV/dec. As a result, g-C₃N₄ decorated sheet-like β-Ni(OH)₂ exhibits the potential hydrogen evolution in alkaline KOH solution. Excitingly, the as developed hybrid β-Ni(OH)₂ nanocomposites show superior electrocatalytic behaviour during the hydrogen evolution reaction and also improve the catalytic stability than pure nanosheets. From these observations, one can say that this g-C₃N₄/Ni(OH)₂ nanocomposite electrocatalyst can play a splendid role in future energy technology.     

Highly-efficient photocatalytic activity of TiO2-AC nanocomposites for hydrogen production from sulphide wastewater

Photocatalytic water splitting is one of the prospective green energy technologies, particularly, for hydrogen production from wastewater under natural sunlight irradiation. Herein, we report experimental data on the synthesis and characteristics of the biomass activated carbon (b-AC)-anchored anatase titanium oxide (a-TiO₂) nanocomposites, which were ultrasonically prepared by using the sol-gel-grown a-TiO₂ spherical nanoparticles and the KOH-activated citron-derived b-AC nanoflakes. The a-TiO₂/b-AC nanocomposites displayed an aggregated morphology with the interconnected spherical nanoparticles, and they showed a high surface area (495 m²/g). When using a-TiO₂/b-AC as a photocatalyst for hydrogen production from sulphide wastewater (0.15 M) under solar irradiation (740 W/m²), the superb hydrogen production efficiency was achieved up to 400 mL/h. The results suggest the a-TiO₂/b-AC nanocomposites to hold an ample potential for photocatalytic hydrogen production from the wastewater.     

Exploration of 1D-2D LaFeO3/RGO S-scheme heterojunction for photocatalytic water splitting

Sustainable energy innovation is spearheading the way to achieve decarbonisation through commercially viable and highly competitive renewable technologies for green hydrogen. Photocatalytic water splitting has received global attention, as it promotes the direct conversion of solar energy to chemical energy and hydrogen production. Lanthanum orthoferrite (LaFeO₃) has been selected due to its narrow bandgap perovskite-oxides (ABO₃) type nature, low cost and high chemical stability but it is limited with fast charge recombination. To circumvent its constraint of fast charge recombination, an efficient graphene-based nanocomposite has been prepared by employing reduced graphene oxide (RGO) nanosheets as charge separators for visible light driven photocatalytic water splitting. Here, we present a thorough physical and spectroscopic characterization of the Lanthanum orthoferrite/Reduced Graphene oxide (LaFeO₃/RGO) nanocomposites, and investigate its photocatalytic and photoelectrochemical performance. The photocurrent density of the nanocomposites demonstrated ∼21 times higher in comparison to pure LaFeO₃. The as-prepared nanocomposites have been successfully used as photocatalysts for H₂ generation through water reduction under visible light. A significant enhancement in H₂ generation has been recorded for nanocomposites (∼82 mmol g⁻¹ h⁻¹) as compared to that of bare LaFeO₃ (∼9 mmol g⁻¹ h⁻¹) which is among the highest values obtained using noble-metal-free graphene-based photocatalytic nanocomposites. This work offers a facile approach for fabricating highly efficient 1D-2D heterostructure for photocatalysis application.     

MoS2-graphene-CuNi2S4 nanocomposite an efficient electrocatalyst for the hydrogen evolution reaction

We present a facile methodology for the synthesis of a novel 2D-MoS₂, graphene and CuNi₂S₄ (MoS₂-g-CuNi₂S₄) nanocomposite that displays highly efficient electrocatalytic activity towards the production of hydrogen. The intrinsic hydrogen evolution reaction (HER) activity of MoS₂ nanosheets was significantly enhanced by increasing the affinity of the active edge sites towards H⁺ adsorption using transition metal (Cu and Ni₂) dopants, whilst also increasing the edge sites exposure by anchoring them to a graphene framework. Detailed XPS analysis reveals a higher percentage of surface exposed S at 17.04%, of which 48.83% is metal bonded S (sulfide). The resultant MoS₂-g-CuNi₂S₄ nanocomposites are immobilized upon screen-printed electrodes (SPEs) and exhibit a HER onset potential and Tafel slope value of – 0.05 V (vs. RHE) and 29.3 mV dec⁻¹, respectively. These values are close to that of the polycrystalline Pt electrode (near zero potential (vs. RHE) and 21.0 mV dec⁻¹, respectively) and enhanced over a bare/unmodified SPE (– 0.43 V (vs. RHE) and 149.1 mV dec⁻¹, respectively). Given the efficient, HER activity displayed by the novel MoS₂-g-CuNi₂S₄/SPE electrochemical platform and the comparatively low associated cost of production for this nanocomposite, it has potential to be a cost-effective alternative to Pt within electrolyser technologies.     

Ferric oxide/date seed activated carbon nanocomposites mediated dark fermentation of date fruit wastes for enriched biohydrogen production

Biohydrogen production from biomass waste, not only addresses the energy demand in a renewable manner but also resolves the safe disposal issues associated with these biowastes. Also, scalable and low-cost techniques to enhance biohydrogen production have gained more attraction and are highly explored. In this research work, date-palm fruit wastes have been studied for their biohydrogen production potential using Enterobacter aerogenes by dark fermentation. Hydrogen yield and productivity were improved through the addition of iron oxide nanoparticles (Fe₃O₄ NPs) and its date seed activated carbon nanocomposites (Fe₃O₄/DSAC) to the fermentation media. Studies on discrete inclusions of these NPs showed that the appropriate dosage of NPs promoted, while higher dosages repressed the hydrogen production performance. Optimal dosage and fermentation time was observed as 150 mg/L and 24 h for both the additives. Fe₃O₄/DSAC nanocomposites showed better hydrogen production enhancement than Fe₃O₄ NPs. Maximum hydrogen yield of 238.7 mL/g was obtained for the 150 mg/L nanocomposites, which was 65.7% higher than that of the standalone Fe₃O₄ NPs and three folds higher than the yield of the control run without any NPs inclusion (78.4 mL/g). Metabolites analysis showed that the hydrogen evolution followed the ethanol-acetate pathway. Formation levels of longer chain propionate and butyrate co-metabolites were significantly low in the presence of Fe₃O₄/DSAC than Fe₃O₄. The carbon support in the nanocomposites acted as an adsorbent-buffer, which favored the medium pH in-addition to the stimulatory effects of Fe₃O₄ NPs. Cell growth and specific hydrogenase activity analysis were also performed to supplement the hydrogen production results. Gompertz and modified Logistic kinetic models were employed for kinetic modeling of experimental hydrogen production values. The Fe₃O₄/DSAC nanocomposites exhibited significant application potential for the production of biohydrogen from date fruit wastes.     

Carbon supported nickel phosphide as efficient electrocatalyst for hydrogen and oxygen evolution reactions

Hydrogen production through water splitting is an efficient and green technology for fulfilling future energy demands. Carbon nanotubes (CNT) supported Ni₂P has been synthesized through a simpler hydrothermal method. Ni₂P/CNT has been employed as efficient electrocatalysts for hydrogen and oxygen evolution reactions in acidic and alkaline media respectively. The electrocatalyst has exhibited low overpotential of 137 and 360 mV for hydrogen and oxygen evolution reactions respectively at 10 mA cm^?2. Lower Tafel slopes, improved electrochemical active surface area, enhanced stability have also been observed. Advantages of carbon support in terms of activity and stability have been described by comparing with unsupported electrocatalyst.     

Extraordinarily high hydrogen-evolution-reaction activity of corrugated graphene nanosheets derived from biomass rice husks

The metal-free carbonaceous catalysts are one of the promising candidates for efficient electrocatalytic hydrogen production. Aiming at demonstrating the high electrocatalytic activity of the hydrogen evolution reaction (HER), we synthesized the biomass rice husk-derived corrugated graphene (RH-CG) nanosheets via the KOH activation. The 700 °C-activated RH-CG nanosheets exhibited the large specific surface area as well as the high electrical conductivity. When using the RH-CG nanosheets as a HER electrocatalyst in 0.5 M H₂SO₄, the excellent HER activities with a small overpotential (9 mV at 10 mA/cm²) and a small Tafel slope (31 mV/dec) were achieved. The results provide a new strategy for materializing the superb biomass-derived electrocatalyst for highly efficient hydrogen production.     

Heterostructured Co3O4/VO2 nanosheet array catalysts on carbon cloth for hydrogen evolution reaction

Developing highly efficient, low-cost, and robust water splitting hydrogen production catalysts is critical for hydrogen energy applications. This study presents the synthesis of Co₃O₄/VO₂ heterogeneous nanosheet structures on carbon cloth (Co₃O₄/VO₂/CC). The obtained Co₃O₄/VO₂/CC hybrid catalyst has a low overpotential of 108 mV at a current density of 10 mA cm^?2, a Tafel slope of 98 mV dec^?1, and high stability in 1.0 M KOH for 10 h. The experimental results and density functional theory (DFT) calculations results also show that Co₃O₄ coupled with VO₂ in Co₃O₄/VO₂/CC can optimize hydrogen adsorption energy and facilitate electron transport, thereby accelerating the catalytic kinetics for hydrogen evolution reaction (HER). This work also provided an alternative method to design and construct non-noble metal oxide-based catalysts for alkaline hydrogen production.     

Assessment of biotic and abiotic graphite cathodes for hydrogen production in microbial electrolysis cells

Hydrogen represents a promising clean fuel for future applications. The biocathode of a two-chambered microbial electrolysis cell (biotic MEC) was studied and compared with an abiotic cathode (abiotic MEC) in order to assess the influence of naturally selected microorganisms for hydrogen production in a wide range of cathode potentials (from −400 to −1800 mV vs SHE). Hydrogen production in both MECs increased when cathode potential was decreased. Microorganisms present in the biotic MEC were identified as Hoeflea sp. and Aquiflexum sp. Supplied energy was utilized more efficiently in the biotic MEC than in the abiotic, obtaining higher hydrogen production respect to energy consumption. At −1000 mV biotic MEC produced 0.89 ± 0.10 m³ H₂ d⁻¹ m⁻³NCC (Net Cathodic Compartment) at a minimum operational cost of 3.2 USD kg⁻¹ H₂. This cost is lower than the estimated market value for hydrogen (6 USD kg⁻¹ H₂).     

A novel in-situ strategy develops for Mo2C nanoparticles incorporated on N,P co-doped stereotaxically carbon as efficient electrocatalyst for overall water splitting

Developing cost-effective and remarkable electrocatalysts toward oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) performs excelling role in boosting the hydrogen energy application. Herein, a novel in-situ one-pot strategy is developed for the first time to synthesize molybdenum carbide nanoparticles (Mo₂C NPs) incorporated on nitrogen (N) and phosphorous (P) co-doped stereotaxically carbon (SC). The optimized Mo₂C NPs/N, P–SC–800 electrocatalyst exhibits lower overpotentials of 131 and 287 mV for HER and OER to deliver a current density of 10 mA cm^?2 in 1.0 M KOH medium with smaller Tafel slopes of 58.9 and 74.4 mV/dec, respectively. In addition, an electrolyzer using Mo₂C NPs/N, P–SC–800 electrode as cathode and anode delivers a current density of 10 mA cm^?2 at a small voltage of 1.64 V for overall water splitting. The excellent water splitting performance could be ascribed to optimum Mo₂C NPs for more accessible active sites, highly active N, P-SC networks for accelerated electron transfers, and synergetic effect between Mo₂C NPs and N, P-SC networks. The N, P-SC network not only enhances the overall dispersion of Mo₂C NPs but also contributes numerous electroactive edges to enhance the performance of HER, OER, and overall water splitting activity. This research work explores the in-situ one-step strategies of advanced, cost-effective, and non-precious metal electrocatalysts for efficient water splitting and motivates the consideration of a novel class of heteroatom doped stereotaxically carbon nanocomposites for sustainable energy production.     

Functionalized 2D materials F–MoS2 and F-g-C3N4 with TiO2 as Composite Electrocatalysts for Electrochemical Hydrogen Evolution

Electrochemical hydrogen evolution is an important research field to produce renewable energy. Nanostructured two dimensional (2D) materials such as g-C₃N₄ and MoS₂ are potential electrocatalysts for hydrogen evolution reaction (HER). The incorporation of semiconducting material into 2D material enhances the hydrogen evolution. Here in, we have developed composite of acid functionalized MoS₂ and g-C₃N₄ with TiO₂ (F–MoS₂/TiO₂, F-g-C₃N₄/TiO₂). The F–MoS₂/TiO₂ composite exhibited excellent electrochemical HER activity with an overpotential of 103 mV Vs RHE at 20 mA/cm² compared to pristine F–MoS₂ of 232 mV, TiO₂ of 455 mV Vs RHE. In addition F-g-C₃N₄/TiO₂ showed high overpotential of 322 mV at 5 mA/cm² than pristine F-g-C₃N₄ and TiO₂ of 433 mV and 448 mV Vs RHE at 2.7 mA/cm² respectively.     

Enhancing biohydrogen production from sugar industry wastewater using metal oxide/graphene nanocomposite catalysts in microbial electrolysis cell

Biohydrogen production through Microbial Electrolysis Cell (MEC) has drifted towards the development of suitable cost-effective cathode catalysts. In this study, two graphene hybrid metal oxide nanocomposites were used as catalysts to investigate hydrogen production in the MEC operated with sugar industry wastewater as substrate against phosphate buffer catholyte. Electrochemical characterizations exposed the better performance of NiO.rGO coated cathode which showed lesser overpotential at 600 mV and overall lowest resistance in the Nyquist plots than Ni-foam and Co₃O₄.rGO cathodes. The experimental results showed that at an applied voltage 1.0 V, NiO.rGO nanocomposite had exhibited maximum hydrogen production rate of 4.38 ± 0.11 mmol/L/D, Coloumbic efficiency of 65.6% and Cathodic hydrogen recovery of 20.8% respectively. The MEC performance in terms of biohydrogen production was 1.19 and 2.68 times higher than Co₃O₄.rGO and uncoated Ni-Foam. Hence, economical hybrid nanocomposite catalysts were demonstrated in MEC using industrial effluent for energy and environment sustainability.     

Modified cobalt oxalate heterostructure catalyst P–FeOOH@CoC2O4/NF for a highly efficient oxygen evolution reaction

Oxygen evolution reaction (OER) has been recognized as the key role to determine the overall efficiency of hydrogen production by electrolysis of water. The development of green, low-cost and high stability electrocatalysts which can effectively reduce the reaction energy barrier is a key to promote the large-scale application of hydrogen energy. Herein, a modified transition metal oxalate loaded on nickel foam (NF), P–FeOOH@CoC₂O₄/NF heterostructure catalyst was synthesized by simple hydrothermal and electrodeposition methods. By constructing heterostructures and phosphorous doping, the morphology and electronic structure of CoC₂O₄ were optimized, thus, P–FeOOH@CoC₂O₄/NF shows excellent electrocatalytic performance, the overpotentials of 211/264/295 mV were needed to reach the current densities of 10/100/200 mA cm^?2, with a low Tafel slope of 41.33 mV dec^?1 and almost constant long-term stability. The results revealed that the construction of the heterostructure led to the superficial electrochemical reconstruction of the cobalt oxalate microrod, which effectually accelerated the transformation of the active species and primely realized the efficient alkaline water oxidation.     

Co/Mo2C composites for efficient hydrogen and oxygen evolution reaction

Non-precious transition metal electrocatalysts with high catalytic performance and low cost enable the scalable and sustainable production of hydrogen energy through water splitting. In this work, based on the polymerization of CoMoO₄ nanorods and pyrrole monomer, a heterointerface of carbon-wrapped and Co/Mo₂C composites are obtained by thermal pyrolysis method. Co/Mo₂C composites show considerable performance for both hydrogen and oxygen evolution in alkaline media. In alkaline media, Co/Mo₂C composites show a small overpotential, low Tafel slope, and excellent stability for water splitting. Co/Mo₂C exhibits a small overpotential of 157 mV for hydrogen evolution reaction and 366 mV for oxygen evolution reaction at current density of 10 mA cm⁻², as well as a low Tafel slope of 109.2 mV dec⁻¹ and 59.1 mV dec⁻¹ for hydrogen evolution reaction and oxygen evolution reaction, respectively. Co/Mo₂C composites also exhibit an excellent stability, retaining 94% and 93% of initial current value for hydrogen evolution reaction and oxygen evolution reaction after 45,000 s, respectively. Overall water splitting via two-electrode water indicates Co/Mo₂C can hold 91% of its initial current after 40,000 s in 1 M KOH.     

Biological hydrogen production by Anabaena sp. - Yield, energy and CO2 analysis including fermentative biomass recovery

This paper presents laboratory results of biological production of hydrogen by photoautrotophic cyanobacterium Anabaena sp. Additional hydrogen production from residual Cyanobacteria fermentation was achieved by Enterobacter aerogenes bacteria. The authors evaluated the yield of H₂ production, the energy consumption and CO₂ emissions and the technological bottlenecks and possible improvements of the whole energy and CO₂ emission chain.The authors did not attempt to extrapolate the results to an industrial scale, but to highlight the processes that need further optimization.The experiments showed that the production of hydrogen from cyanobacteria Anabaena sp. is technically viable. The hydrogen yield for this case was 0.0114 kgH₂/kg_biomass which had a rough energy consumption of 1538 MJ/MJH₂ and produced 114640 gCO₂/MJH₂. The use of phototrophic residual cyanobacteria as a substrate in a dark-fermentation process increased the hydrogen yield by 8.1% but consumed 12.0% more of energy and produced 12.1% more of CO₂ showing that although the process increased the overall efficiency of hydrogen production it was not a viable energy and CO₂ emission solution. To make cyanobacteria-based biofuel production energy and environmentally relevant, efforts should be made to improve the hydrogen yield to values which are more competitive with glucose yields (0.1 kgH₂/kg_biomass). This could be achieved through the use of electricity with at least 80% of renewables and eliminating the unessential processes (e.g. pre-concentration centrifugation).     

Electro-catalyst [ZrO2/ZnO/PdO]-NPs green functionalization: Fabrication,characterization and water splitting potential assessment

Present investigation reports the biomimetic synthesis of mixed metallic oxides nanoparticles (NPs) comprising of zirconia, zinc oxide and palladium oxide ([ZrO₂/ZnO/PdO]-NPs) functionalized via nature's bio-factories for the first time. [ZrO₂/ZnO/PdO]-NPs express reduction revealed via Fourier transform infra-red spectroscopy and gas chromatography and mass spectrometry. X-ray diffraction express poly-crystallinity. The fabrication of green NPs is confirmed via energy-dispersive X-ray spectroscopy with irregular morphologies visible by scanning electron micrographs. A direct bandgap of 2.11 eV is obtained for [ZrO₂/ZnO/PdO]-NPs. Promising surficial features are disclosed via X-ray photoelectron spectroscopy. The electro-catalytic potential is studied using linear sweep voltammetry and electrochemical impedance spectroscopy for investigation of oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) activities with low over-potential of 0.37 V and Tafel slope of 74 mV/dec, indicating the suitability for OER. [ZrO₂/ZnO/PdO]-NP electro-catalyst is also tested for HER, demonstrating remarkable results with the overpotential and Tafel slope value of 157 mV and 151 mV/dec.     

Zinc oxide functionalized molybdenum disulfide heterostructures as efficient electrocatalysts for hydrogen evolution reaction

Technology urges to replace the state-of-the-art catalysts such as platinum with low cost, earth abundant and durable electrocatalysts for efficient hydrogen evolution (HER) reaction which is going to become the major sustainable production of energy in future. Herein, we present the heterostructure based MoS₂.ZnO (MZO) heterostructures for successful electrochemical water splitting process. For HER, the prepared MoS₂.ZnO nanocomposites show the over potential as low as 239 mV at cathodic current density 10 mAcm⁻² with an exchange current density of 3.2 μAcm⁻². A Tafel slope of about 62 mV per decade suggested to have the Volmer-Heyrovsky mechanism for the HER process with MoS₂.ZnO nanocomposite as the catalyst. The small Tafel slope indicates a promising electrocatalyst for HER in practical application. The strong interface formation at the MoS₂.ZnO heterostructure facilitates higher catalytic activity and excellent cycling stability. The heterostructure formation based on semiconductor two dimensional (2D) transition metal dichalcogenides (TMDC) open up new avenues for effective manipulation of HER catalysts.     

Thermal oxidation–electroreduction modified 3D NiCu for efficient alkaline hydrogen evolution reaction

The preparation of high-efficiency and low-cost electrocatalysts is vital to the development of green hydrogen energy. In this study, 3D NiCu electrodes with hierarchical micro-nano structure was constructed by a simple direct-write 3D printing technology and followed by the treatment of thermal oxidation - electroreduction steps. The composite structure of Cu NWs/Cu₂O and Ni/NiO in the prepared 3D NiCu promotes the dissociation of water and the conversion of hydrogen, and the special micro-nano structure displays a large active surface area. Therefore, the 3D NiCu exhibits a low overpotential of 70 mV to deliver a current density of 10 mA cm^?2. It demonstrates outstanding stability in the hydrogen evolution reaction experiment for 100 h in 1 M KOH. Overall, this research provides a pioneer of modified 3D printing to hydrogen production by water electrolysis.     

Biohydrogen and biogas production from mashed and powdered vegetable residues by an enriched microflora in dark fermentation

This study conducted the utilization of vegetable residues by an enriched microflora inoculum to produce biohydrogen via anaerobic batch reactor. Dark fermentation processes were carried out with 3 kinds of vegetable residue substrates including broccoli (Brassica oleracea var. italica.), onion (Alium cepa Linn.), and sweet potato (Ipomoea batatas (L.) Lam). Vegetable wastes were pretreated into 2 forms, i.e. mashed and powdered vegetable, prior to the fermentation. The substrate used for the biohydrogen production were vegetable residues and inoculum at the vegetable residues/inoculum ratio of 1:1 (based on TS). The digestion processes were performed under 120 rpm speed of shaking bottle in the incubator with control temperature of 35^?C. In this work, the maximum hydrogen production was achieved by anaerobic digestion at mashed onion with bioreactor inoculum that produced total hydrogen of 424.1 mL H₂ with hydrogen yield and hydrogen concentration of 151.67 mL H₂/g VS_added and 43.54%, respectively. In addition, the hydrogen production continues took only 7 days for the vegetables blended with the bioreactor inoculum. Finally, it was found that the high potential of degradation of vegetable wastes an enriched microflora in dark fermentation also showed alternative solution to eliminate agricultural wastes to produce green energy.     

Improvement of photobiological hydrogen production in Chlorococcum minutum using various oxygen scavengers

The depletion of non-renewable energy resources such as fossil fuels urge the human society to concentrate more on renewable energy including production of biological hydrogen (H₂) from algae. Biological hydrogen or biohydrogen is one of the cleanest and efficient alternate energy sources for human needs. It is a well-known fact that hydrogenase (H₂ase) will work in anoxic condition which is the key enzyme in H₂ generation from photosynthetic algae or advanced plants. Keeping in view the significance of anoxic condition, the present study deals with screening of three oxygen scavengers/removers such as sodium sulfite (Na₂SO₃), sodium metabisulfite (Na₂S₂O₅) and sodium dithionite (Na₂S₂O₄) individually along with universal tris-acetate-phosphate (TAP) medium for improvement of biohydrogen production in green alga Chlorococcum minutum (C. minutum) under in vitro conditions. To the best of our knowledge, for the first time improvement in hydrogen production was achieved using sodium sulfite and sodium metabisulfite individually with algal cultures. Efficient photobiological H₂ production was observed at 24 h in C. minutum in the presence of all the three oxygen scavengers when compared to untreated samples via limiting the oxygen levels but output was more with sodium sulfite treatment. Particularly 0.8 mM Na₂SO₃ is best for enhancement of H₂ production at 24 h when compared to other two scavengers and this may be due to high oxidation state and more electron negativity of this compound. Apart from augmentation in H₂ production in this species, present screening may also be helpful for researchers working in the area of biological H₂ generation.