Abstract:Photoelectrochemical (PEC) water splitting for hydrogen generation has been considered as a promising route to convert and store solar energy into chemical fuels. In terms of its large-scale application, seeking semiconductor photoelectrodes with high efficiency and good stability should be essential. Although an enormous number of materials have been explored for solar water splitting in the last several decades, challenges still remain for the practical application. P-type copper-based chalcogenides, such as… Show more
“…Electrocatalytic and photocatalytic hydrogen generation from water are promising schemes for sustainable hydrogen generation. [1][2][3][4][5][6] The key issue of these techniques is to develop highly efficient and low-cost hydrogen evolution reaction (HER) catalysts. Noble metals (e.g., Pt) are commonly examined HER catalysts at present.…”
The development of efficient noble-metal-free hydrogen evolution catalysts is quite appealing with the aim of providing cost-competitive hydrogen.Herein, nickel sulfides (NiS x ) with tunable NiS/Ni 3 S 4 molar ratios were synthesized via a simple hydrothermal method. Detailed electrochemical studies under neutral conditions indicated that the electrocatalytic property of NiS x catalysts was determined by the composition. Notably, the NiS x sample with the NiS/Ni 3 S 4 molar ratio of 1.0 exhibited the lowest overpotential and charge-transfer resistance. As analyzed from the Tafel plots, the rate determining step of NiS x catalysts for hydrogen generation was the Volmer step, in which the proton adsorption played a key role.Theoretical calculation revealed that NiS and Ni 3 S 4 exhibited the metallic behaviors with different work functions. Consequently, the NiS x sample with the NiS/Ni 3 S 4 molar ratio of 1.0 owned the most adsorbed protons, which led to the highest electrocatalytic property. Meanwhile, NiS x was demonstrated to be efficient cocatalysts to promote photocatalytic hydrogen generation. NiS x /CdS with the S 4 molar ratio of 1.0 showed the best photocatalytic activity with the apparent quantum efficiency of 56.5% at 420 nm. This result was in good agreement with the electrocatalytic activities of NiS x samples, indicating the intrinsic property for efficient hydrogen generation.
“…Electrocatalytic and photocatalytic hydrogen generation from water are promising schemes for sustainable hydrogen generation. [1][2][3][4][5][6] The key issue of these techniques is to develop highly efficient and low-cost hydrogen evolution reaction (HER) catalysts. Noble metals (e.g., Pt) are commonly examined HER catalysts at present.…”
The development of efficient noble-metal-free hydrogen evolution catalysts is quite appealing with the aim of providing cost-competitive hydrogen.Herein, nickel sulfides (NiS x ) with tunable NiS/Ni 3 S 4 molar ratios were synthesized via a simple hydrothermal method. Detailed electrochemical studies under neutral conditions indicated that the electrocatalytic property of NiS x catalysts was determined by the composition. Notably, the NiS x sample with the NiS/Ni 3 S 4 molar ratio of 1.0 exhibited the lowest overpotential and charge-transfer resistance. As analyzed from the Tafel plots, the rate determining step of NiS x catalysts for hydrogen generation was the Volmer step, in which the proton adsorption played a key role.Theoretical calculation revealed that NiS and Ni 3 S 4 exhibited the metallic behaviors with different work functions. Consequently, the NiS x sample with the NiS/Ni 3 S 4 molar ratio of 1.0 owned the most adsorbed protons, which led to the highest electrocatalytic property. Meanwhile, NiS x was demonstrated to be efficient cocatalysts to promote photocatalytic hydrogen generation. NiS x /CdS with the S 4 molar ratio of 1.0 showed the best photocatalytic activity with the apparent quantum efficiency of 56.5% at 420 nm. This result was in good agreement with the electrocatalytic activities of NiS x samples, indicating the intrinsic property for efficient hydrogen generation.
“…Photocatalytic water splitting has continuously been a hot academic topic since Fujishima and Honda′s work in hydrogen production from water using a TiO 2 electrode [1]. Over the past decades, metal sulfides [2] and chalcogenides [3] have attracted broad interest from scientists engaged in photocatalysis. Of those compounds, cadmium sulfide (CdS) is an attractive semiconductor photocatalyst under continuous research due to its optimal band gap and suitable position of the conduction band and valence band edge [4,5,6].…”
Abstract:Ultrasonic spray pyrolysis is a superior method for preparing and synthesizing spherical particles of metal oxide or sulfide semiconductors. Cadmium sulfide (CdS) photocatalysts with different sizes and doped-CdS with different dopants and doping levels have been synthesized to study their properties of photocatalytic hydrogen production from water. The CdS photocatalysts were characterized with scanning electron microscopy (SEM), X-ray fluorescence-spectrometry (XRF), UV-Vis absorption spectra and X-ray diffraction (XRD) to study their morphological and optical properties. The sizes of the prepared CdS particles were found to be proportional to the concentration of the metal nitrates in the solution. The CdS photocatalyst with smaller size showed a better photocatalytic activity. In addition, Cu doped CdS were also deposited and their photocatalytic activities were also investigated. Decreased bandgaps of CdS synthesized with this method were found and could be due to high density surface defects originated from Cd vacancies. Incorporating the Cu elements increased the bandgap by taking the position of Cd vacancies and reducing the surface defect states. The optimal Cu-doped level was found to be 0.5 mol % toward hydrogen evolution from aqueous media in the presence of sacrificial electron donors (Na 2 S and Na 2 SO 3 ) at a pH of 13.2. This study demonstrated that ultrasonic spray pyrolysis is a feasible approach for large-scale photocatalyst synthesis and corresponding doping modification.
“…Hydrogen (H2) is a clean fuel and it emits water upon utilization and it does not emit greenhouse gases, free from air pollution [3]. With the existing production mechanisms, cost and the under-developed technology, utilization of hydrogen fuel has many practical difficulties.…”
Fabrication of economically viable photocathode for hydrogen energy production through solar water splitting is a major research among the scientific community for a decade. P-type compound Cu2ZnSnS4 (CZTS) is very interesting material due to its absorption property, earth-abundant constituents and environmental friendliness that serves as a suitable candidate to act as a photocathode. In the present work, Cu2ZnSnS4 (CZTS) nanoparticles are synthesized by simple one-step chemical method and annealed at 350 °C for three different times (60 minutes, 90 minutes and 120 minutes). The effect of annealing time on the structural, optical and photoelectrochemical properties are investigated. XRD pattern indicates the formation of tetragonal crystal structure and the crystallinity increases according to the annealing time. 2-D nanoplate morphology is obtained for the sample that was annealed for 120 minutes. From the absorption spectra, it was found that the band gap decreases with increase of annealing time. Further, the prepared nanoparticle thin films are used as a cathode for photoelectrochemical water splitting application. Among these, the nanoparticles that are annealed for 120 minutes showed higher photocurrent density when compared to nanoparticles annealed for 60 minutes and 90 minutes.
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