Optimization of biohydrogen production using acid pretreated corn stover hydrolysate followed by nickel nanoparticle addition

The dilute acid hydrolysis using corn stover (CS) to produce reducible sugars was optimized by the response surface methodology. The electron-equivalent balances of the main metabolites during the dark fermentation (DF) using acid hydrolysate were investigated to identify the evolutions of the electron sinks over the course of DF. The additions of nickel ion and Ni⁰ nanoparticles (NPs) were found to effectively enhance the hydrogen production at experimental conditions. The optimal condition (HCl 2.5 wt%, hydrolyzing duration 105 minutes, pH=5, S/B=3.5, Ni⁰ NPs=10 mg/L^-1) was achieved with Y_H2/S reaching 1.18 (mol.mol^-1-glucose). The Y_H2/S increased from 0.7 (mol.mol^-1-glucose) to 1.18 (mol.mol^-1-glucose) reaching 40% hydrogen yield increase when Ni⁰ NPs was added to the fermentation broth. Among the investigated significant soluble metabolites, the butyric acid was found to serve as the largest e-sink in the electron-equivalent balance. The additions of Ni⁰ NPs at low level (below 10 mg/L) were found to appreciably increase the hydrogen production. The increased pH and substrate to biomass ratio were found to skew the metabolic balance from hydrogen production to the biosynthesis (an increase of biomass). The proposed anaerobic digestion model with consideration of the inhibitory factors model presents a good agreement with the experimental data. The chemical addition such as nickel ions, Ni⁰ NPs was found to be a practical approach in enhancing biohydrogen production using CS acid hydrolysate as cultivation broth.     

Magnetite nanoparticles enhanced glucose anaerobic fermentation for bio-hydrogen production using an expanded granular sludge bed (EGSB) reactor

The feasibility and efficiency of magnetite nanoparticles (Fe₃O₄NPs) enhanced bio-hydrogen production from glucose anaerobic fermentation were evaluated in this study. The results demonstrated that the maximum hydrogen yield (HY) of 12.97 mL H₂/g-VSS was obtained with 50 mg/L and 40–60 nm of Fe₃O₄NPs in batch experiments. Moreover, the optimum dosage of Fe₃O₄NPs produced hydrogen production (HP) of 4.95 L H₂/d in an expanded granular sludge bed (EGSB) reactor. Fe₃O₄NPs involved could promote ethanol and acetic acid accumulation. Fe²⁺ as by-product of iron corrosion could effectively promote the activity of key coenzymes and soluble microbial products (SMPs). Importantly, Fe₃O₄NPs addition resulted in the formation of electronic conductor chains to enhance the electron transport efficiency in the granular sludge. Microbial community analysis revealed that the relative abundance of butyrate-hydrogen-producing bacteria (Clostridium) decreased from 40.55% to 11.45%, while the relative abundance of ethanol-hydrogen-producing bacteria (Acetanaerobacterium and Ethanoligenens) increased from 19.62% to 35.35% with Fe₃O₄NPs involved, confirming that the fermentation type was transformed from butyrate-type to ethanol-type, which finally facilitated more hydrogen production.     

In situ synthesis of dendrimer-encapsulated palladium(0) nanoparticles as catalysts for hydrogen production from the methanolysis of ammonia borane

Addressed herein is the in situ synthesis of a PAMAM dendrimer-encapsulated palladium(0) NPs (Pd(0)/Dnd) during the methanolysis of ammonia borane (AB) and the catalytic performance of the yielded Pd(0)/Dnd nanocatalysts in hydrogen production from the methanolysis of AB under ambient conditions. A two-step procedure that includes the impregnation of Pd(II) ions via their coordination to –NH₂ groups of the dendrimer and then reduction of Pd(II) ions into the dendrimer-encapsulated Pd(0) NPs by AB during the methanolysis reaction was followed for the synthesis of Pd(0)/Dnd nanocatalysts. However, apart from the existing reports on the synthesis of dendrimer-encapsulated metal NPs, the present study includes for the first time the examination of effect of generation size (G4-G6), core type (ethylene diamine (E) or Jeffamine (P)) and terminal groups (-NH₂, –COOH and –OH) of a PAMAM dendrimer on the stability, particle size, morphology and catalytic activity of metal NPs. After finding the optimum Pd(0)/Dnd catalysts considering all these effects, a detailed kinetic study comprising the effect of catalyst and AB concentrations as well as temperature was conducted by monitoring the hydrogen production from the methanolysis of AB. The best catalytic activity in the methanolysis of AB was obtained by using a PAMAM dendrimer with generation G6, amine terminal groups and Jeffamine core (P6.NH₂) encapsulated Pd(0) NPs, providing the highest initial turnover frequency (TOF) of 55.8 mol H₂.mol Pd⁻¹.min⁻¹ and apparent activation energy (Ea^app) of 48 ± 3 kJ.mol⁻¹ at room temperature.     

Biohydrogen production via integrated sequential fermentation using magnetite nanoparticles treated crude enzyme to hydrolyze sugarcane bagasse

This study presents a potential approach to enhance integrated sequential biohydrogen production from waste biomass using magnetite nanoparticle (Fe₃O₄ NPs) which is synthesized through waste seeds of Syzygium cumini. Consequences of 0.5% Fe₃O₄ NPs have been investigated on the thermal and pH stability of fungal crude cellulase. It is noticed that Fe₃O₄ NPs treated enzyme and control exhibits 100% activity in the temperature range of 45–60 °C and 45–55 °C, respectively. Moreover, Fe₃O₄ NPs treated enzyme showed extended thermal stability in the temperature range of 50–60 °C up to 12 h. Beside this, Fe₃O₄ NPs treated enzyme possesses 100% stability in the pH range of 5.0–7.0 whereas control exhibited only at pH 6.0. Enzymatic hydrolysis via Fe₃O₄ NPs treated enzyme has been employed which produces ～68.0 g/L reducing sugars from sugarcane bagasse. Subsequently, sugar hydrolyzate has been utilized as substrate in the sequential integrated fermentation that produces ～3427.0 mL/L cumulative hydrogen after 408 h. This approach may have potential for the pilot scale production of biohydrogen from waste biomass at low-cost in an eco-friendly manner.     

Methanolysis of ammonia borane catalyzed by magnetically isolable RHODIUM(0) nanoparticles

This article reports the preparation and employment of rhodium (0) nanoparticles (Rh⁰NPs) on the surface of magnetite nanospheres, denoted as Rh⁰@Fe₃O₄, as magnetically isolable nanocatalyst in the methanolysis of ammonia borane (MAB). The monodispersed Fe₃O₄ nanospheres are fabricated by a simple technique and used as nanosupport for Rh⁰NPs which are well stabilized and homogeneously distributed on the surface of nanospheres with a mean particle size of 2.8 ± 0.5 nm. The as-synthesized Rh⁰@Fe₃O₄ has a remarkable TOF value of 184 min⁻¹ in the MAB to produce H₂ gas in RT. Most of all, Rh⁰@Fe₃O₄ nanocatalyst can be reused, evolving 3.0 mol of H₂ gas for a mole of AB, keeping 100% of its initial activity even in the fourth reuse of MAB at 25 °C. Recovery of the Rh⁰@Fe₃O₄ nanocatalyst can be accomplished by simply approaching an external magnet, which eliminates many laborious catalyst removal steps in catalytic reactions. Reported are the outcomes of kinetic investigation, done by altering the concentration of substrate and catalyst together with temperature. Kinetic studies reveal that the catalytic MAB shows dependence on the concentration of reactants and temperature.     

The effect of Ni,Fe and Mg concentration on photo-hydrogen production by Rhodopseudomonas faecalis RLD-53

In the present study, the effect of Ni²⁺ (0–10 μmol/l), Fe²⁺ (0–200 μmol/l) and Mg²⁺ (0–15 mmol/l) concentration on photo-hydrogen production from acetate was investigated by batch culture. Results showed that under a proper concentration range, Ni²⁺ was able to enhance the hydrogen production rate and the hydrogen yield; Fe²⁺ was able to increase the hydrogen yield, and hydrogen production rate was enhanced only when the culturing time was 24–72 h. Ni²⁺ and Fe²⁺ at a higher concentration inhibited cell growth. When Ni²⁺ and Fe²⁺ concentrations were 4 μmol/l and 80 μmol/l, respectively, maximal hydrogen yield of 2.87 and 2.78 mol H₂/mol acetate was obtained when batch culturing at 35 °C with initial pH 7.0. Mg²⁺ did not significantly affect hydrogen production and hydrogen yield which maintained at about 2.45 mol H₂/mol acetate, but it was favorable to cell growth.     

Photocatalytic hydrogen production over CuO and TiO2 nanoparticles mixture

Cheap and efficient photocatalysts were fabricated by simply mixing TiO₂ nanoparticles (NPs) and CuO NPs. The two NPs combined with each other to form TiO₂/CuO mixture in an aqueous solution due to the opposite surface charge. The TiO₂/CuO mixture exhibited photocatalytic hydrogen production rate of up to 8.23 mmol h⁻¹ g⁻¹ under Xe lamp irradiation when the weight ratio of P25 to CuO was optimized to 10. Although the conduction band edge position of CuO NPs is more positive than normal hydrogen electrode, the TiO₂/CuO mixture exhibited good photocatalytic hydrogen production performance because of the inter-particle charge transfer between the two NPs. The detailed mechanism of the photocatalytic hydrogen production is discussed. This mixing method does not require a complicated chemical process and allows mass production of the photocatalysts.     

Synergistic enhancement of biohydrogen production by supplementing with green synthesized magnetic iron nanoparticles using thermophilic mixed bacteria culture

The production of biohydrogen can be improved by focusing on the nutrients needed by fermentative bacteria like iron. Iron reacts with the [Fe-Fe]-hydrogenase enzyme within the mixed bacteria culture for optimum hydrogen release. Iron nanoparticles (NPs) are attractive due to its unique properties and high reactivity. It can be produced through green synthesis, a more eco-friendly and relatively lower cost process, by using iron salt as precursor and green coconut shell extracted by deep eutectic solvent (DES) as reducing agent. The coconut shell extract consists of phytochemicals that help in producing polydisperse magnetic iron oxide nanoparticles at ～75 nm in size. The addition of optimum concentration of 200 mg Fe/L magnetic iron NPs resulted in the maximum cumulative hydrogen production, glucose utilization and hydrogen yield of 101.33 mL, 9.12 g/L and 0.79 mol H₂/mol glucose respectively. Furthermore, the kinetic analysis on Gompertz model using the optimum magnetic iron NPs concentration showed that the hydrogen production potential (P) and hydrogen production rate (R_m) increased to 50.69 mL and 3.30 mL/h respectively and the lag phase time reduced about 7.12 h as compared with the control experiment (0 mg Fe/L). These results indicated the positive effects of magnetic iron NPs supplementation on fermentative biohydrogen production of mixed bacteria culture and proved the feasibility of adding the magnetic iron NPs as the micronutrient for enhancement of such hydrogen production system.     

Green synthesis of magnetite nanoparticle and its regulatory effect on fermentative hydrogen production from lignocellulosic hydrolysate by Klebsiella sp.

This study describes the synthesis and characterization of magnetite nanoparticles (NPs) from water hyacinth (WH) extract and its regulatory effect on fermentative hydrogen production from lignocellulosic hydrolysate by Klebsiella sp. Characterization of WH-magnetite-NP revealed that it was a pure magnetite NP in a spherical shape with an average particle size of 13.5 ± 3.7 nm. The maximum cumulative hydrogen production with an increment of 23.49% and an optimum Y(H₂/S) of 83.20 ± 2.19 mL/g_substrate was obtained with WH-magnetite-NP at 20 mg/L. Monitoring of key node metabolites further established the potential of WH-magnetite-NP to increase the flux distribution of the hydrogen synthesis pathway. The hydrogenase activity was enhanced via WH-magnetite-NP addition, with peak value 2.1 times of the control. The expression of functional genes in key pathways assessed via RT-PCR highlighted the effect of WH-magnetite-NP on the evident promotion of hydrogenase and formate-hydrogen lyase. This is the first attempt to detect the expression of multiple functional genes in key metabolic pathways to explain the regulatory mechanism upon NP addition.     

Hydrogen adsorption and interactions in self-reducing shell hosted palladium nanoparticles on magnetite support

The nanoparticles (NP), consisting of hydrazine grafted organo-silica with PdNPs embedded shell on the Fe₃O₄ core, were prepared to study the adsorption and interactions of hydrogen in PdNPs and their support matrix. This material is expected to find the applications in the hydrogen technology including catalysis. The PdNPs were formed spontaneously in the organo-silica shell on magnetite nanoparticles by the reduction of Pd²⁺ ions with grafted hydrazine in the organo-silica shell. Thus formed NPs, termed as Fe₃O₄-GTEOS@PdNPs, were also thermally treated at 1033 K in Ar atmosphere to convert organic components to carbon. The chemical composition, physical structure, and magnetic properties were studied by high resolution transmission electron microscopy, X-rays diffraction, Mössbauer spectroscopy and X-ray photoelectron spectroscopy for the characterizations of physical, chemical and magnetic changes occurred in the Fe₃O₄-GTEOS@PdNPs after hydrogen adsorption-desorption at varying temperatures with respect to that in unused one. The hydrogen adsorption pressure-composition (PC) isotherms in Fe₃O₄-GTEOS@PdNPs followed the expected trend from 173 to 303 K as expected from PdNPs. However, thermally treated Fe₃O₄-GTEOS@PdNPs were found to adsorb lower amount of hydrogen due to oxidation of Pd⁰ to PdO and morphological changes during heating in Ar atmosphere. The comparison of n_H/n_Pd value (0.49) obtained for the PdNPs in Fe₃O₄-GTEOS@PdNPs with the values those reported in the literature for different Pd materials showed the decrease in n_H/n_Pd value with decrease in the size of Pd particles. This was attributed to stronger Pd–H bond in a nanoscale palladium, which prevented hydrogen transfer to interior matrix as compared to bigger Pd particles. The hydrogen adsorption PC isotherm at 373 K in Fe₃O₄-GTEOS@PdNPs could not be obtained as the unknown chemical reaction happened in the sample during the experiment. The considerably higher H₂ consumption in the Fe₃O₄-GTEOS@PdNPs occurred at 373 K than that expected from the hydrogen adsorption in the PdNPs alone.     

Well-designed NiS/CdS nanoparticles heterojunction for efficient visible-light photocatalytic H2 evolution

Heterojunction photocatalysts based on semiconducting nanoparticles show excellent performance in many photocatalytic reactions. In this study, 0D/0D heterojunction photocatalysts containing CdS and NiS nanoparticles (NPs) were successfully synthesized by a chemical precipitation method. The NiS NPs were grown in situ on CdS NPs, ensuring intimate contact between the semiconductors and improving the separation efficiency of hole-electron pairs. The obtained NiS/CdS composite delivered a photocatalytic H₂ evolution rate (7.49 mmol h^?1 g^?1), which was 39.42 times as high as that of pure CdS (0.19 mmol h^?1 g^?1). This study demonstrates the advantages of 0D/0D heterojunction photocatalysts for visible light-driven photocatalytic hydrogen production.     

Ni–Fe + SDC composite as anode material for intermediate temperature solid oxide fuel cell

Composite materials of Sm_0.2Ce_0.8O_1.9 (SDC) with various Ni–Fe alloys were synthesized and evaluated as the anode for intermediate temperature solid oxide fuel cell. The performance of single cells consisting of the Ni–Fe + SDC anode, SDC buffer layer, La_0.8Sr_0.2Ga_0.83Mg_0.17O_2.815 (LSGM) electrolyte, and SrCo_0.8Fe_0.2O_3 − δ (SCF) cathode were measured in the temperature range of 600–800 °C with wet H₂ as fuel. It was found that the anodic overpotentials of the different Fe–Ni compositions at 800 °C were in the following order: Ni_0.8Fe_0.2 < Ni_0.75Fe_0.25 < Ni < Ni_0.7Fe_0.3 < Ni_0.9Fe_0.1 < Ni_0.95Fe_0.05 < Ni_0.33Fe_0.67. The single cell with the Ni_0.8Fe_0.2 + SDC anode exhibited a maximum power density of 1.43 W cm⁻² at 800 °C and 0.62 W cm⁻² at 700 °C. The polarization resistance of the Ni_0.8Fe_0.2 + SDC anode was as low as 0.105 Ω cm² at 800 °C under open circuit condition. A stable performance with essentially negligible increase in anode overpotential was observed during about 160 h operation of the cell with the Ni_0.8Fe_0.2 + SDC anode at 800 °C with a fixed current density of 1875 mA cm⁻². The possible mechanism responsible for the improved electrochemical properties of the composite anodes with the Ni_0.8Fe_0.2 and Ni₀₇₅Fe_0.25 alloys was discussed.     

Tungsten(VI) oxide supported rhodium(0) nanoparticles; highly efficient catalyst for H2 production from dimethylamine borane

It reports the preparation and characterization of tungsten(VI) oxide supported rhodium(0) nanoparticles (Rh⁰/WO₃ NPs) being used as catalysts in releasing H₂ from dimethylamine borane (DMAB). The reducible nature of WO₃ plays a significant role in the catalytic efficiency of rhodium(0) nanoparticles in the dehydrogenation of DMAB. The Rh⁰/WO₃ NPs were in-situ generated from the reduction of Rh²⁺ ions on the surface of WO₃ during the catalytic dehydrogenation of dimethylamine borane in toluene and isolated from the reaction solution after the dehydrogenation to be characterized by using SEM, TEM, XPS, ATR-IR and XRD. The results reveal the formation of Rh⁰ NPs with a mean particle size of 1.92 ± 0.34 nm dispersed on the surface of tungsten(VI) oxide. Rh⁰/WO₃ NPs are found to be very active catalyst releasing 1.0 equiv. H₂ per mole of dimethylamine borane under ambient conditions. Among the various WO₃ supported Rh⁰ NPs with different metal loadings, the sample with 0.1% wt. Rh provide the record catalytic activity (TOF = 2816 h^?1) which is one of the highest value ever reported for rhodium-based catalysts in H₂ generation from DMAB at 60.0 ± 0.5 °C. Rh⁰/WO₃ NPs were also reusable catalyst in dehydrogenation of DMAB retaining 55% of their initial catalytic activity in the 3rd run of the dehydrogenation reaction. Control experiments were performed at various catalyst concentrations and temperatures to investigate the kinetics of dehydrogenation and to calculate the activation parameters for the reaction.     

Rapid preparation of Ru(0) nanoparticles stabilized with water-soluble biopolymer for hydrogen production from ammonia borane: Development of battery-like hydrolysis media

The biohybrid Na-Alg@Ru catalyst was prepared as a result of stabilizing Ru(0) nanoparticles with biopolymer chains of sodium alginate. The in-situ prepared Ru(0) nanoparticles had an average particle size of 1.023 ± 0.097 nm. The monodisperse Ru(0) nanoparticles prepared with a very practical, inexpensive and rapid method were used as a catalyst in hydrogen production by the hydrolysis reaction of ammonia borane (AB). The Na-Alg@Ru catalyst containing 3 mg Ru(0) metal catalyzed the hydrolysis of 50 mM AB with 100% yield, and the activation energy (E_a) of the reaction was estimated as 61.05 kJ mol⁻¹. In addition, the Na-Alg@Ru nanoparticles were prepared with acrylamide as p(AAm)/Na-Alg@Ru hydrogel films suitable for use in hydrogen production in fuel cells, which represents a battery-like environment, and used for hydrogen production from AB. Thus, it was shown that the catalysts prepared in a few nm size could easily be used in battery-like environments.     

PdCoNi nanoparticles supported on nitrogen-doped porous carbon nanosheets for room temperature dehydrogenation of formic acid

The development of cost-effective heterogeneous catalysts for the dehydrogenation of formic acid (FA) is the key challenge for the commercialization of FA as a hydrogen-storage medium. Herein, PdCoNi nanoparticles (NPs) with different element ratios supported on N-doped carbon nanosheets (N-CN) were designed, which exhibit excellent catalytic dehydrogenation performance for FA. Compared with PdCoNi NPs loaded on the carbon nanosheets (CN), the introduction of pyrrolic N to CN induces the formation of ultrafine, monodispersed and amorphous Pd_0.6Co_0.2Ni_0.2 NPs with a size of 1.60 nm, which significantly increases the number of active sites and the instant contact between FA and catalysts. The as-prepared Pd_0.6Co_0.2Ni_0.2/N-CN catalyst shows more than 99% conversion and 100% H₂ selectivity at room temperature, with a record-high initial turnover frequency (TOF_initial) of 1249.0 h⁻¹ among non-noble containing Pd-based catalysts, which demonstrates the high potential of Pd_0.6Co_0.2Ni_0.2/N-CN as a practical catalyst for the hydrogen generation from FA.     

Electrocatalytic hydrogen evolution on metallic and bimetallic Pd–Co alloy nanoparticles

Increasing world energy demands and crises led to alternative energy production methods, such as fuel cells using hydrogen gas which is the half electrochemical reaction of water splitting process. Herein, we synthesize polyvinylpyrrolidone coated Pd, Co and Pd_xCo_1-x (x: 0.5, 0.12, 0.23, 0.49, 0.55, 0.62) metallic and bimetallic nanoparticles (NPs) via polyol process alternative to Pt-based catalysts for hydrogen evolution reaction (HER). Detailed structural analyses of Pd, Co and Pd_xCo_1-x NPs revealed that fcc-Pd, fcc/hcp-Co and fcc-PdCo NPs crystal structures, and the lattice parameters were calculated as 3.5358 Å for Co NPs and 3.9777 Å for Pd NPs. The average size confirmed below 9 nm via TEM imaging and XPS data confirmed the formation of a bimetallic PdCo structure. Although Pd catalyst is mostly responsible for HER process, Pd₆₂Co₃₈ catalysts reduced the onset potential to about 197 mV and provided greater current density. Although E_a values were slightly higher against the Pt/C (20 wt %) benchmark which is reported as 16 kJ mol⁻¹, PdCo NPs provided considerably reduced activation energy (E_a) values compared to Pd/C catalyst of 31 kJ mol⁻¹. The best onset potential was recorded for Pd₆₂Co₃₈ catalysts for HER activity which is 16 mV higher compared to commercially available Pt/C catalyst.     

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.     

Nitrogen-phosphorus co-functionalized reduced graphene oxide supported NiCoPd-CeOx nanoparticles as a highly efficient and stable catalyst for formic acid dehydrogenation

Formic acid (HCOOH, FA), a common liquid hydrogen storage material, has attracted tremendous research interest. However, the development of efficient, low-cost and high-stable heterogeneous catalyst for selective dehydrogenation of FA remains a major challenge. In this paper, a simple co-reduction method is proposed to synthesize nitrogen-phosphorus co-functionalized rGO (NPG) supported ultrafine NiCoPd-CeO_x nanoparticles (NPs) with a mean size of 1.2 nm. Remarkably, the as-prepared Ni_0.2Co_0.2Pd_0.6-CeO_x/NPG shows outstanding catalytic activity for FA dehydrogenation, affording a high TOF value of 6506.8 mol H₂ mol Pd^?1 h^?1 at 303 K and a low activation energy of 17.7 kJ mol^?1, which is better than most of the reported heterogeneous catalysts, and can be ascribed to the combined effect of well-dispersed ultrafine NiCoPd-CeO_x NPs, modified Pd electronic structure, and abundant active sites. The reaction mechanism of dehydrogenation of FA is also discussed. Furthermore, the optimized Ni_0.2Co_0.2Pd_0.6-CeO_x/NPG shows excellent stability over 10^th run with 100% conversion and 100% H₂ selectivity, which may provide more possibilities for practical application of FA system on fuel cells.     

Synthesis and characterization of Nanocrystalline Ba0·6Sr0·4Co0·8Fe0·2O3 for application as an efficient anode in solid oxide electrolyser cell

Nanocrystalline Ba_0·6Sr_0·4Co_0·8Fe_0·2O₃ (BSCF-6482) powder is synthesized by combustion synthesis technique. Powder calcined at 1000 °C reveals phase pure cubic perovskite. Transmission electron microscopic (TEM) analysis exhibits soft agglomerates of average size ∼50 nm wherein interplanar spacing for (110) and (221) resembles to the cubic lattice. While DC electrical conductivity of 23 S cm⁻¹@800 °C is observed, interfacial polarization measured by electrochemical impedance spectroscopy is found to be the least @850 °C (0.18 Ω cm²). Cell performance has been compared among BSCF-6482, BSCF-5582 and LSCF-6482 mixed ionic and electronic conducting (MIEC) and conventional electrode (LSM). Higher performance (1.37 A/cm²@1.3 V,800 °C) with high hydrogen generation rate (0.57 Nl/cm²/h) is found during steam electrolysis with cell fabricated using BSCF-6482 having minimal area specific resistance 0.33 Ω cm². Under similar operating condition, BSCF-5582, LSCF-6482 and LSM exhibit hydrogen generation rate of 0.35, 0.28 and 0.23 Nl/cm²/h respectively. Cell microstructure is clinically correlated with the higher reactivity of BSCF-6482 air electrode in steam electrolysis.