ZnO nanorods-PANI heterojunction dielectric,electrochemical properties,and photodegradation study of organic pollutant under solar light

In the last years, the development of photocatalysts has gained a growing interest in the photoelectrochemical conversion. Here, we report a hetero-junction organic/inorganic (Polyaniline (PANI)) on n type Silicon substrate prepared by electrophoretic deposition (EPD). ZnO nanorods (NRs) are grown by chemical bath deposition (CBD) on seed layer of ZnO prepared by dip coating onto the PANI layer. The relief and morphological properties are investigated by both atomic force microscope (AFM) and scanning electron microscopy (SEM). The forbidden bands (E_g) of 1.12 and 3.26 eV are obtained for PANI and ZnO_NRS respectively. The optical and dielectric constants are determined by the diffuse reflectance where the extinction coefficient (k), the refractive index (n), optical conductivity, dissipation factor and relaxation time are extracted. The semi conductivity is highlighted by the capacitance measurement; a flat band potential (E_fb = 0.541 V) for ZnO_NRs-PANI is deduced from the Mott-Schottky plot. The contributions of the bulk and grain boundaries of the electrode are evidenced from the electrochemical impedance spectroscopy (EIS). The as-fabricated samples show improved photoactivity compared to PANI and ZnO_NRs. Indeed, the hetero-junction exhibits a high stability and recyclability for the photodegradation of Orange II (OII) after six cycling runs. The current research offers a new understanding of designing a high performance of the photocatalyst under solar light based on PANI for the wastewater treatment.     

Well-defined core/shell pDA@Ni-MOF heterostructures with photostable polydopamine as electron-transfer-template for efficient photoelectrochemical H2 evolution

Here, novel core/shell polydopamine@Ni-MOF (pDA@Ni-MOF) heterogeneous nanostructures are synthesized via a simple one-pot nucleation-growth technique. This rational core/shell design method provide a uniform Ni-MOF shell thickness (shell: ～ 10 nm) as well as homogeneous wrapping of pDA templates with quite narrow size distributions. The obtained band properties of bare pDA (E_CB = ?0.35 eV and E_VB = 2.95 eV vs normal hydrogen electrode (NHE)) and bare Ni-MOF (E_CB = ?0.49 eV and E_VB = 2.85 eV vs NHE) clearly revealed charge separation is occurred on pDA by absorbing light due to π-π1 transition, and photogenerated electrons on conduction band (CB) of pDA was migrated to CB of Ni-MOF. Specifically, the photoelectrochemical (PEC) water performance of pDA@Ni-MOF photoanodes with highest current density is recorded as 8.61 mA/cm² at 0.77 V vs. RHE under visible LED irradiation, which is significantly higher than bare pDA (0.008 V vs. RHE) and bare Ni-MOF (0.011 V vs. RHE) at the same conditions. Note that, the higher photon absorption properties of pDA in core together with high interaction valence bond between two semiconductors could generate electron rich state giving rise to faster electron transfer kinetics as next generation of MOF based hybrid materials with regular morphologies.     

Influence of microstructure on hydrogen trapping and diffusion in a pre-deformed TRIP steel

Austenitic steels are known to exhibit a low hydrogen diffusion coefficient and hence a good resistance to hydrogen embrittlement. Therefore, it is an experimental challenge to investigate their hydrogen diffusion properties. In this study, the electrochemical permeation technique is used to determine the hydrogen diffusion coefficients in different pre-deformed states (φ = 0, 0.32, 0.39, 0.49) of the high-alloy austenitic TRIP steel X3CrMnNiMoN17-8-4 in a temperature range of 323 K–353 K. In combination with microstructural analysis, a correlation between phase transformation from γ-austenite to α′-martensite and dislocation density is shown. As a result of the lattice transformation from fcc to bcc, the diffusion rate of hydrogen is significantly increased (D_{app, φ = 0} = 3.6 × 10^?12 cm² s^?1, D_{app, φ = 0.32} = 1.6 × 10^?11 cm² s^?1at 323 K). With higher degrees of deformation, the dislocation density also increased in the martensite islands, resulting in a degressive growth of the diffusion coefficient (D_{app, φ = 0.39} = 5.3 × 10^?11 cm² s^?1, D_{app, φ = 0.49} = 1.1 × 10^?10 cm² s^?1at 323 K). Moreover, detailed calculations are performed to describe the way of hydrogen trapping and to give a possible mechanism of diffusion.     

Fabrication of large area nanorod like structured CdS photoanode for solar H2 generation using spray pyrolysis technique

Large area nanorod like structured CdS films (9 × 9 cm²) were deposited on the FTO glass substrate using simple and economic spray pyrolysis deposition technique for photoelectrochemical (PEC) hydrogen production. With an intention of electrode scaling-up, the deposition area of photoanode was varied to evaluate its effect on the PEC hydrogen generation capability. High photocurrent of 5 mA has been achieved from the PEC active area of 37.5 cm². Its unit area (1 cm²) counterpart yielded Solar-to-Hydrogen (STH) conversion efficiency of 0.20% at a bias of 0.2 V vs Ag/AgCl using sacrificial reagents under solar simulator (AM1.5) with 80 mW/cm² irradiance. The 500 nm thick film exhibiting uniformly distributed nano-rod features yielded 3-times more photocurrent, as well as hydrogen evolution than other films. It exhibited an enhanced photo-activity as indicated by the higher IPCE values (5–9%) in the wavelength range of 450–550 nm. It exhibited superior optical properties (E_g ∼2.4 eV), and formation of high crystallinity hexagonal CdS phase with space group P63MC. The superior performance of the photoanode is attributed to the nanostructured morphology acquired under optimized spray pyrolysis conditions. Large area photoanodes showed unaltered photo-activity indicating the homogeneity in the film properties even in scaled-up version.     

Enhanced photocatalytic performance of NiFe2O4 nanoparticle spinel for hydrogen production

The spinel NiFe₂O₄, prepared from nitrates precursors, was characterized by thermal analyses, X-Ray Diffraction, UV-Vis diffuse reflectance, Scanning electron microscopy, X-Ray Fluorescence spectrometry, X-ray photoelectron spectroscopy and photo-electrochemistry measurements. The X-ray diffrcation analysis of the powder indicates a cubic phase with a lattice constant of 8.327(8) Å and crystallite size of 19 nm. The X-Ray Fluorescence spectrometry indicates a stoichiometry, very close to NiFe₂O₄ catalyst calcined at 900 °C The X-ray photoelectron spectroscopy analysis confirmed the valences and crystallographic sites of the transition elements. The direct optical gap of NiFe₂O₄ (1.78 eV), due to the crystal field splitting of the 3d orbital in the octahedral site, is well suited for the solar spectrum and attractive for photo-electrochemical H₂ production. The flat band potential (E_fb = 0.47 V_SCE) was obtained from the capacitance-potential (C^?2 - E) characteristic in NaOH (0.1 M) electrolyte. A conduction band of ?1.11 V_SCE, more cathodic than the H₂ level (?0.8 V_SCE), enabled the use of NiFe₂O₄ for the water reduction into hydrogen. The H₂ evolution rate of 46.5 μmol g^?1 min^?1 was obtained under optimal conditions (1 mg of catalyst/mL, NaOH and 50 °C) in the presence of SO₃^2? (10^?3 M) as hole scavenger under visible light flux of 23 mW cm^?2. A deactivation effect of only 1% was obtained.     

Battery-type and binder-free MgCo2O4-NWs@NF electrode materials for the assembly of advanced hybrid supercapacitors

In this study, the hetero-structure of MgCo₂O₄ nanowires (MCO-NWs) and microcubes (MCO-MCs) on the skeleton of nickel foam (NF) was realized through a simple hydrothermal method and subsequent annealing treatment, and then served as a binder-free cathode for assembly of high-performance hybrid supercapacitor (HSC). Such synthetic methodology avoided the traditional usage of conductive and binder reagents for the electrode fabrication. The electrochemical tests indicated its battery-type characteristics, and the MCO-NWs@NF exhibited a huge specific capacity (C_s) of 389.0 C g^?1 as well as 86.2% capacity retention when the current density boosted from 1 to 10 A g^?1. The assembled HSC with activated carbon (AC) as anode further demonstrated the advantages of this electrode material. After 5000 cycles at 6 A g^?1, the MCO-NWs@NF//AC HSC showed good long-term cycling stability without any decay in capacitance, and could deliver an energy density (E_d) of 37.9 W h kg^?1 at the power density (P_d) of 958.1 W kg^?1, higher than the 30.4 W h kg^?1 of MCs-based HSC. These impressive results regarding electrochemical performance suggest that MCO-NWs@NF may be a promising candidate to serve as a battery-type material in electrochemical energy storage applications such as HSCs, batteries, and so on.     

Effects of dark/light bacteria ratio on bio-hydrogen production by combined fed-batch fermentation of ground wheat starch

Bio-hydrogen production by combined dark and light fermentation of ground wheat starch was investigated using fed-batch operation. Serum bottles containing heat-treated anaerobic sludge and a mixture of Rhodobacter sp. was fed with a medium containing 20 g dm^?3 wheat powder (WP) at a constant flow rate. The system was operated at different initial dark/light biomass ratios (D/L). The optimum D/L ratio was 1/2 yielding the highest cumulative hydrogen (1548 cm³), yield (65.2 cm³ g^?1 starch), and specific hydrogen production rate (5.18 cm³ g^?1 h^?1). Light fermentation alone yielded higher hydrogen production than dark fermentation due to fermentation of volatile fatty acids (VFAs) to H₂ and CO₂. The lowest hydrogen formation was obtained with D/L ratio of 1/1 due to accumulation of VFAs in the medium.     

Synthesis,physical, optical and electrochemical properties of the ilmenite CrFeO3: Application to photo-reduction of Ni2+

During the last decade, there is a growing interest in developing efficient photocatalysts with a visible light sensitivity. Herein, visible-light-driven photoactivity of CrFeO₃ prepared by nitrate route was studied. The photocatalysis was evaluated through the Ni²⁺ reduction. The X-ray diffraction (XRD) is characteristic of a single phase crystallizing in the ilmenite structure with a good crystallinity. It was characterized by the SEM, TEM/HRTEM, FTIR spectroscopy and thermal analysis (TG). The optical and dielectric constants are determined from the diffuse reflectance data. The refractive index (n), extinction coefficient (k), relaxation time (τ), dissipation factor (tan δ) and optical conductivity are extracted. The forbidden band E_g (= 1.65 eV), was computed and confirmed by different methods. The electrical conductivity (σ) augments exponentially with 1000/T and activation energy of 0.22 eV was calculated. The p-type conduction is evidenced from the capacitance measurements with a flat band potential (E_fb = ?0.38 V_Ag/AgCl) and a hole concentration (N_A = 5.87 × 10¹⁸ cm^?3). The novel hetero-system CrFeO₃/TiO₂ showed improved efficiency by 47% compared to CrFeO₃. An optimal mass ratio CrFeO₃/TiO₂ (25%/75%) gives to a Ni²⁺ reduction of 88% at pH ～ 7.2 within 4 h irradiation for an initial Ni²⁺ concentration of 15 mg/L. A first order kinetic was found from the Ni²⁺ photoreduction with a half photocatalytic life of 61 min^?1 and a higher photodegradation under sunlight is obtained. More interestingly, the photocatalyst showed a good stability and recyclability after four runs.     

Growth of ultrathin nanosheets of nickel iron layered double hydroxide for the oxygen evolution reaction

Because of low cost and abundance, nickel-iron double layered hydroxide (NiFe LDH) is seen as a viable substitute for noble-metal-based electrodes for the oxygen evolution reaction (OER). Herein, we report the growth of NiFe LDH in the form of fine nanosheets in a single step using benzyl alcohol-mediated chemistry. The electrochemical studies clearly suggest that benzyl alcohol is capable of inducing effective chemical interaction between Ni and Fe in the NiFe LDH. The overpotential to produce benchmark 10 mA cm^?2 (η₁₀) for the NiFe LDH electrode is only ～270 mV_RHE, which is much smaller than those of benchmark IrO₂ (η₁₀ = 318 mV_RHE), nickel hydroxide (η₁₀ = 370 mV_RHE) and iron hydroxide (η₁₀ = 410 mV_RHE) for the OER. The difference of the overpotential requirement increases further with increasing current density, indicating faster kinetics of the OER at the catalytic interface of the NiFe LDH. Estimation of Tafel values verifies this notion – the Tafel slopes of NiFe LDH, Ni(OH)₂, and FeOOH are calculated to be 48.6, 55.8, and 59.3 mV dec^?1, respectively. At η = 270 mV, the turnover frequency (TOF) of the NiFe LDH is 0.48 s^?1, which is ～8 and ～11 folds higher than those of Ni(OH)₂ (0.059 s^?1) and FeOOH (0.042 s^?1). In addition to Tafel and TOF, the NiFe LDH electrode has favorable electrochemically active surface area and electrochemical impedance. The electrochemical stability of the NiFe LDH electrode is assessed by conducting potentiostatic measurements at η = 270 mV_RHE (～10 mA cm^?2) and at η = 355 mV_RHE (～30 mA cm^?2) for 24 h of continuous oxygen production.     

Usage of natural leaf as a bio-template to inorganic leaf: Leaf structure black TiO2/CdS heterostructure for efficient photocatalytic hydrogen evolution

Herein, first time we report that highly efficient sheet like leaf structure black TiO₂ (LBT)/CdS hetero-structure (LBT/CdS). Photocatalytic hydrogen generation was tested for different material in the presence of visible light (λ ≥ 420 nm) irradiation. 10 wt% of LBT loaded CdS (10LBT/CdS) exhibit maximum photocatalytic H₂ generation rate about ~10 mmol h^?1 g^?1, which is higher than the H₂ production results of pristine CdS (6 mmol h^?1 g^?1) and leaf black-TiO₂ 5.1 mmol h^?1 g^?1) respectively. Detailed characterization revealed that higher photocatalytic activity was mainly attributed to enormous spatial transfer efficiency of photo-excited charge carriers at the hetero-junction between LBT and CdS in LBT/CdS. Additionally, introduction of 2D black leaf-TiO₂ to CdS act as a mat and enhances the mobility of charge carriers. In addition, presence of anatase-rutile surface-phase junction in leaf TiO₂ (synthesized at 750 °C) and more edges, steps and corners on the CdS synergistically increased the photocatalytic H₂ generation and photocurrent response of LBT/CdS.     

Synthesis,physical and electrochemical properties of the spinel CoFe2O4: Application to the photocatalytic hydrogen production

This research is achieved for the preparation of CoFe₂O₄ with a high purity and crystanillity by nitrate route followed by a calcination at 850 °C. The material exhibits a single phase with a cubic symmetry. The electrochemistry performed in Na₂SO₄ solution shows a stable semiconductor with a small exchange current density (112 μA cm^?2). The capacitance-potential measurement indicates p-type behavior, typically related to the metal insertion in octahedral sites. The narrow band gap semiconductor with a direct optical transition of 1.27 eV is due to the lifting of degeneracy of Fe³⁺: 3d orbital in 6-fold coordination, making it attractive for the photo-electrochemical (PEC) conversion. Moreover, its cathodic comportment evidenced from the negative conduction band compared to the potential of the water reduction makes it an ideal candidate for the hydrogen production. The experimental data shows a great activity for the evolution of hydrogen with an average rate of 74 μmol min^?1 g_cat^?1 and a quantum efficiency of 0.34% under visible illumination (23 mW cm^?2). The use of C₂O₄^2? as reducing agent increased substantially the performances by a factor of 57%.     

Transitional metal alloyed nanoparticles entrapped into the highly porous N-doped 3D honeycombed carbon: A high-efficiency bifunctional oxygen electrocatalyst for boosting rechargeable Zn-air batteries

Rational development of low-cost, durable and high-performance bifunctional oxygen catalysts is highly crucial for metal-air batteries. Herein, transition metal alloyed FeCo nanoparticles (NPs) embedded into N-doped honeycombed carbon (FeCo@N-HC) was efficiently prepared by a one-step carbonization method in the existence of NH₄Cl and citric acid. Benefiting from the honeycomb-like architectures and the synergistic effects of the FeCo alloy with the doped-carbon matrix, the as-synthesized FeCo@N-HC exhibited outstanding oxygen reduction reaction (ORR) with the more positive onset potential (E_onset = 0.98 V vs. RHE) and half-wave potential (E_1/2 = 0.85 V vs. RHE), coupled with outstanding oxygen evolution reaction (OER) with the lower overpotential (318 mV) at 10 mA cm^?2. Besides, the home-made Zn-air battery has the larger power density of 144 mW cm^?2 than Pt/C + RuO₂ (80 mW cm^?2). This research offers some valuable guidelines for constructing robust oxygen catalysts in clean energy storage and conversion technologies.     

Physicochemical properties and electrochemical hydrogen storage performance of Li2M(WO4)2 (M = Co,Ni and Cu)

In this work, new materials of the Li₂M(WO₄)₂ type with (M = Co, Ni and Cu) have been studied for the first time as electrodes for electrochemical hydrogen storage. The three double tungstates compounds, have been synthesized by a one-step solid-state reaction and carefully characterized, using X-ray diffraction, scanning electron microscopy, UV–visible and FTIR spectroscopy. The presence of a pure and single phase is confirmed by XRD with the Rietveld refinement for all the studied materials, while SEM observation reveals the granular microstructure of these compounds (1-10 μm). Very close energy gaps of 1.60 eV, 1.62 eV and 1.64 eV are respectively attributed to Li₂Cu(WO₄)₂, Li₂Co(WO₄)₂ and Li₂Ni(WO₄)₂. Cyclic voltametry shows the characteristic redox peaks of these samples and clearly elucidates the redox behavior of the battery type. EIS results show good contact between the surface of the studied materials and the H₂SO₄ electrolyte, with a surface resistance of (~2 Ω/cm²). The charge-discharge galvanostatic cycling gives a specific storage capacity of 120.1 mA h.g⁻¹ Li₂Ni(WO₄)₂, 98.88 mA h.g⁻¹ Li₂Co(WO₄)₂ and 84.44 mA h.g⁻¹ Li₂Cu(WO₄)₂ at 1 A g⁻¹. They also exhibit a good life cycle stability that exceeds 84%–90% of the retention capacity of Li₂Ni(WO₄)₂ after 50 cycles at 1 A g⁻¹.     

Effect of synthesis method on the oxygen reduction performance of Co–N–C catalyst

In recent years, Co, N co-doped carbon (Co–N–C) materials as oxygen reduction reaction (ORR) catalysts have attracted great attention because of their good ORR stability as well as decent activity. Co-doped zeolitic imidazolate framework-8 (Co@ZIF-8) as the precursor for synthesizing Co–N–C has attracted great interest recently. Co@ZIF-8 synthesis method may affect the properties of the as-synthesized Co@ZIF-8 precursors, which will surely affect the properties and ORR performance of Co@ZIF-8-derived Co–N–C catalysts. Herein, three methods, viz. room-temperature stirring method, reflux method, and hydrothermal method, were used to synthesize Co@ZIF-8 precursors. Physical characterization shows that the synthesis method has a great influence on the textural properties, composition, and graphitization degree of the as-synthesized Co–N–C catalysts. Electrochemical characterization shows that Co–N–C-R synthesized with reflux method exhibits an onset potential (E_onset) of 0.905 V, a half-wave potential (E_1/2) of 0.792 V and a limiting current density (J_L) of 5.85 mA cm^?2 in acidic media, which are higher than those of Co–N–C–S (E_onset = 0.870 V, E_1/2 = 0.770 V, J_L = 4.71 mA cm^?2) and Co–N–C–H (E_onset = 0.892 V, E_1/2 = 0.785 V, J_L = 4.68 mA cm^?2) synthesized with room-temperature stirring method and hydrothermal method, respectively. The better ORR activity observed on Co–N–C-R can be attributed to its larger graphitization degree and larger mesopore volume. Catalytic stability test shows that Co–N–C-R has negligible activity loss after 5000 potential cycles. This work demonstrates that reflux method is a more suitable method for synthesizing Co–N–C catalysts for ORR.     

Photocatalytic hydrogen production on the hetero-junction CuO/ZnO

The co-precipitation is successfully used for the synthesis of the hetero-junction CuO/ZnO. Thermal analysis, ATR spectroscopy and diffuse reflectance were used to assess the photoactivity of the hetero-system for the hydrogen formation upon visible light. As expected, the X-ray diffraction shows mixed phases of CuO (tenorite) and ZnO (Wurtzite). The specific surface area is around ~7 m² g⁻¹ with a crystallite size lying between 20 and 49 nm. The diffuse reflectance indicates an indirect transition at 3.13 eV for ZnO and a direct transition at 1.60 eV for the sensitizer CuO. The capacitance-potential (C⁻² - E) characteristic of CuO plotted in Na₂SO₄ electrolyte exhibits p-type comportment with a flat band potential of −0.315 V_RHE and a holes concentration of 8.7 × 10¹⁸cm⁻³. The Electrochemical Impedance Spectroscopy exhibits a semicircle characteristic of the bulk material with an impedance of 1725 Ω cm² which decreases down to 453 Ω cm² under irradiation, supporting the semiconducting character of CuO. ZnO mediates the electrons transport thanks to its conduction band, formed from Zn²⁺: 4s orbital (−0.92 V_RHE); it is positioned cathodically with respect to the H₂O/H₂ level (~-0.74 V_RHE), producing a H₂ evolution under visible light illumination. The performance peaks at pH ~7 on 5% CuO/ZnO for a catalyst dose of 0.25 mg of catalyst/mL of solution in the presence of SO₃²⁻ as holes scavenger. A liberation rate of 340 μmol h⁻¹ (g of catalyst)⁻¹ is obtained with a quantum efficiency of 0.38% under a photons flux of 2.09 × 10¹⁹ s⁻¹.     

Hydrogen production on the new hetero-system Pr2NiO4/SnO2 under visible light irradiation

The Pr₂NiO₄/SnO₂ heterojunction with a mass ratio equal to unity was tested with success for the hydrogen production under visible light irradiation. Pr₂NiO₄, prepared by nitrate route, crystallizes in a tetragonal symmetry with K₂NiF₄ type structure. The physical, electrical and photo-electrochemical characterizations are correlated to show the feasibility of Pr₂NiO₄ for the hydrogen formation under visible light. The enhanced hydrogen production activity is due to electron injection of activated conduction band Pr₂NiO₄-CB (−1.53 V_SCE) into SnO₂-CB (−0.87 V_SCE) which acts as an electron pump, resulting in better water reduction. The band gap of the semiconductor Pr₂NiO₄ is 1.81 eV with a direct optical transition. Pr₂NiO₄ acquired p type conductivity, due to oxygen insertion in the layered lattice with an activation energy of 0.09 eV. The flat band potential (E_fb, 0.18 V_SCE), very close to the photocurrent onset potential (0.13 V_SCE) and the density of the holes (N_A, 1.85 10²⁰ cm⁻³) were obtained from the Mott-Schottky characteristic. H₂ production rate of 24.3 μmol g⁻¹ min⁻¹ is obtained with a quantum yield of 1.45% within 30 min under optimal conditions (1 mg of catalyst/mL, pH ~12 and 50 °C) in presence of S₂O₂⁻³ as hole scavenger under visible light flux of 29 mW cm⁻².     

Impact of surface oxide on hydrogen permeability of chromium membranes

Hydrogen permeation through pure and oxidised bulk chromium membranes was measured by the classical gas technique to get insight into oxide as a hydrogen permeation barrier (HPB). An additional palladium-coated reference chromium membrane was tested to avoid the influence of native Cr oxide. Key parameters for Cr permeability: P₀ = 3.23 × 10^?7 mol H₂/s/m/Pa^0.5 and E_a = 0.68 eV and Cr diffusivity D₀ = 9.0 × 10^?5 m²/s and E_a = 0.59 eV. In the sample preparation stage, a thin ～2 nm thick oxide was formed. Additional oxidation in pure oxygen at 400 °C increased the thickness from 20 to 50 nm. At this temperature, its efficiency as HPB was evaluated by comparing permeation rates to the reference chromium membrane. The highest permeation reduction factor of ～3900 corresponded to only a ～28 nm thick Cr oxide layer. Surface morphology and oxide thickness were investigated by SEM, while the thickness and type of chromium oxide by XPS.     

Enhanced performance for photocatalytic hydrogen evolution using MoS2/graphene hybrids

A MoS₂/graphene hybrid (MSG) is synthesized by microwave hydrothermal method. Both of the charge transfer resistance and the photocurrent are tuned in graphene modified MoS₂ by enhancing photocatalytic nature, where the charge transfer resistance significantly decreases from 36,000 Ω–8.49 Ω and the photocurrent promotes from 0.29 mA cm^?2 to 16.47 mA cm^?2. In this article, the result reveals that the appropriate modification of graphene can reach the maximum yield of hydrogen gas. In addition, the appropriate conditions, such as the concentration of 0.32 M formic acid and the MoS₂ photocatalyst with 0.8 wt% graphene (MSG_0.8) dose of 0.013 g L^?1, can complete the outstanding photocatalytic hydrogen evolution, where the hydrogen evolution using MSG_0.8 composite photocatalyst has the maximum yield of 667.2 μmol h^?1 g^?1.     

Sodium alginate assisted preparation of oxygen-doped microporous carbons with enhanced electrochemical energy storage and hydrogen uptake

Microporous carbons with large oxygen content have been successful synthesized from biomass by the sodium alginate assisted strategy. During the activation process, the Na₂O formed by the decomposition of sodium alginate combines with the activator KOH to undergo a redox reaction in situ with precursor, thereby forming a rich porosity in the samples. The obtained samples possess not only high SSA (2310~3001 m² g^?1) and large pore volume (0.89~1.19 cm³ g^?1) arising almost completely (>90%) from micropores, but also retains a high content of oxygen (21.86~32.47 wt %). As supercapacitor electrodes, the oxygen-doped microporous carbons display a high specific capacitance of 385 F g^?1 at 0.5 A g^?1 with capacity stability of 91.5% after 20 000 cycles at 5 A g^?1. As hydrogen storage materials, the oxygen-doped microporous carbons exhibit enhanced hydrogen storage capacity of 2.84 wt% (77 K, 1 bar) and 0.91 wt% (303 K, 50 bar). Experimental data indicate that this work provides a simple-efficient and universal strategy for preparing oxygen-doped microporous carbon for high-performance energy and hydrogen storage.     

Study of the influence of Nafion/C composition on electrochemical performance of PEM single cells with ultra-low platinum load

The electrochemical performance of membrane electrode assemblies (MEAs) with ultra-low platinum load (0.02 mg_Pt cm^?2) and different compositions of Nafion/C in the catalytic layer have been investigated. The electrodes were fabricated depositing the catalytic ink, prepared with commercial catalyst (HiSPEC 2000), onto the gas diffusion layers by wet powder spraying. The MEAs were electrochemically tested using current-voltage curves and electrochemical impedance spectroscopy measurements. The experiments were carried out at 70 °C in H₂/O₂ and H₂/air as reactant gases at 1 and 2 bar pressure and 100% of relative humidity. For all MEAs tested, power density increases when the gasses pressure is increased from 1 to 2 bar. On the other hand, power density also increased when oxygen is used instead of air as oxidant gas in cathode. The lower power density (34 mW cm^?2) and power per Pt loading (0.86 kW g_Pt^?1) corresponds to the MEA prepared without Nafion in anode and cathode catalytic layers working with hydrogen and air at 1 bar pressure as reactants gas. The MEA with 30% wt Nafion/C reached the highest power density (422 mW cm^?2) and power per Pt loading (10.60 kW g_Pt^?1) using hydrogen and oxygen at 2 bar pressure. Finally, electrode surface microstructure and cross sections of MEAs were analyzed by Scanning Electron Microscopy (SEM). Examination of the electrodes, revealed that the most uniform ionomer network surface corresponds to the electrode with 40 wt% Nafion/C, and MEA ionomer-free catalytic layer shows delamination, it leads to low electrochemical performance.