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Efficient visible light-driven hydrogen generation on g-C3N4 coupled with iron phosphide
摘要: Transition metal phosphides as promising noble-metal-free cocatalysts are gaining increasing interest for hydrogen generation and other energy conversion reactions. Herein, the present study reports a new Fe2P/g-C3N4 hybrid for efficient photocatalytic hydrogen generation by water splitting under visible light irradiation, whose H2 production rate is ~15 times higher than that of pure g-C3N4, and is comparable with that of Pt/g-C3N4 at the same condition. According to the detailed analyses of UV-vis diffuse reflectance, photoluminescence spectra, and photoelectrochemical measurements, the reason for the high efficiency of Fe2P/g-C3N4 hybrid is due to highly effective separation and low recombination rate of photo-generated electrons and holes rather than absorption light. The present study shows a promising photocatalyst with non-toxicity, low cost, and natural abundance for improving photocatalytic H2 generation.
关键词: photocatalysis,g-C3N4,hydrogen generation,noble metal-free,Fe2P
更新于2025-11-19 16:51:07
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Ultra-small colloidal heavy-metal-free nanoplatelets for efficient hydrogen generation
摘要: Metal chalcogenide semiconducting nanoplatelets exhibit a broad absorption spectrum, as well as thickness-dependent optical and electronic properties. As such, they may be used as building blocks in a variety of optoelectronic devices. The direct synthesis of heavy-metal-free ultra-small sized nanoplatelets is still challenging, due to the inherent limits in existing synthetic approaches. Here, we report an efficient template-assisted cation-exchange route to synthesize heavy metal free metal chalcogenide nanoplatelets that are optically active in the near infrared. The SnSe nanoplatelets, whose lateral dimension is 6-10 nm, exhibit a quantum yield of 20%. The nanoplatelets are applied as light absorbers in a photoelectrochemical (PEC) system for hydrogen generation, leading to a saturated photocurrent density of 7.4 mA/cm2, which is a record for PEC devices using heavy metal-free colloidal quantum dots or nanoplatelets under identical measurement conditions. Our results indicate that quasi-zero-dimensional SnSe nanoplatelets hold great potential as efficient light absorbers for emerging optoelectronic technologies.
关键词: nanoplatelets,cation exchange,optoelectronic technologies,SnSe,hydrogen generation
更新于2025-11-19 16:51:07
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Visible light active CZTS sensitized CdS/TiO2 tandem photoanode for highly efficient photoelectrochemical hydrogen generation
摘要: A tandem photoanode consisting of Cu2ZnSnS4 (CZTS) nanoparticles layer over CdS/TiO2 heterostructure thin film on FTO substrate has been fabricated for photoelectrochemical hydrogen generation. CdS thin film has been deposited by chemical bath deposition over the spin-coated TiO2 thin film, which is followed by the deposition of CZTS nanoparticles layer by spray coating technique resulting in a CZTS/CdS/TiO2/FTO photoanode. The coating of CZTS nanoparticles layer over CdS/TiO2 films resulted in the tandem structure of different band level positions, which enhances the optical absorption in the visible region and also leads to higher separation of the photogenerated charge carriers. A substantial enhancement (39 times) in the PEC activity has been demonstrated for the CZTS/CdS/TiO2/FTO photoanode as compared to TiO2/FTO photoanode, which is due to cascade band gap from 3.2 eV to 1.7 eV and formation of heterojunction at interfaces. The enhancement in the charge transport properties of CZTS/CdS/TiO2/FTO photoanode has been confirmed from the electrochemical impedance spectroscopy (EIS) measurement. The EIS results confirm that the CZTS/CdS/TiO2/FTO photoanode exhibited lowest charge transfer resistance (Rct = 302 Ω/cm2) as compared to CdS/TiO2 (Rct = 615 Ω/cm2) and TiO2 (Rct = 1700 Ω/cm2) photoanode. A mechanism depicting the enhanced the performance of photoelectrochemical (PEC) CZTS/CdS/TiO2/FTO photoanode has been proposed.
关键词: EIS,Hydrothermal,PEC,Hydrogen generation,CZTS nanoparticles
更新于2025-10-22 19:40:53
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Electronic Structure and Room Temperature Ferromagnetism in Gd-doped Cerium Oxide Nanoparticles for Hydrogen Generation via Photocatalytic Water Splitting
摘要: Enhanced visible light photocatalytic activity of Gd-doped CeO2 nanoparticles (NPs) is experimentally demonstrated, whereas there are very few reports on this mechanism with rare earth doping. All-pure and Gd-doped CeO2 NPs are synthesized using a coprecipitation method and characterized using X-ray diffraction (XRD), absorption spectroscopy, surface-enhanced Raman Spectroscopy (SERS), X-ray photoelectron spectroscopy (XPS), and superconducting quantum interference device (SQUID). The effect of Gd-doping on properties of CeO2 is discussed along with defects and oxygen vacancies generation. The XRD confirms the incorporation of Gd3+ at the Ce3+/Ce4+ site by keeping the crystal structure same. The average particle size from transmission electron microscopy (TEM) images is in the range of 5–7 nm. The XPS spectra of Ce 3d, O 1s, and Gd 4d exhibits the formation of oxygen vacancies to maintain the charge neutrality when Ce4+ changes to Ce3+. The gradual increase in hydrogen production is observed with increasing Gd concentration. The observed results are in good correlation with the characterization results and a mechanism of water splitting is proposed on the basis of analyses. The absorption spectra reveal optical band gap (2.5–2.7 eV) of samples, showing band gap narrowing leads to desired optical absorbance and photoactivity of NPs.
关键词: water splitting,hydrogen generation,SERS,XPS
更新于2025-09-23 15:23:52
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Photocathodic hydrogen evolution from catalysed nanoparticle films prepared from stable aqueous dispersions of P3HT and PCBM
摘要: Photo-assisted hydrogen evolution is achieved on photocathodes comprising of nanoparticles of poly(3-hexylthiophene) (npP3HT) and nanoparticles of phenyl-C61-butyric acid methyl ester (npPCBM) onto which ultra-low loadings of Pt nanoparticles are deposited. The nanoparticles, npP3HT and npPCBM, are prepared individually via miniemulsion using surfactants of opposite head group polarity. Aqueous dispersions of npP3HT:npPCBM, devoid of organic solvent, are cast conformally onto ITO-coated glass to yield water-insoluble bulk-heterojunction films. Pt is deposited photoelectrochemically onto ITO/npP3HT:npPCBM photocathodes and found to nucleate preferentially on PCBM nanoparticles. ITO/npP3HT:npPCBM/Pt photocathodes produce 65 μA/cm2 photocurrent under 100 mW/cm2 of visible light at 0.0 VSHE and liberate H2 gas. The photocurrents observed for electrodes prepared using npP3HT:npPCBM are twice as large, and the onset potential is ~0.4 V more positive than analogous photocathodes cast from nanoparticles each comprising an intimate blend of P3HT and PCBM. These are encouraging results for large scale synthesis of organic photoelectrochemical devices, given the simplicity of the photoelectrode, i.e., prepared from aqueous solutions and devoid of vacuum-deposited films such as charge transport layers and protective films.
关键词: Polymer nanoparticle,Photoelectrochemistry,P3HT: PCBM bulk-heterojunction,Solar hydrogen generation,Organic semiconductor,Mini-Emulsion
更新于2025-09-23 15:23:52
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Liquid exfoliation of g-C3N4 nanosheets to construct 2D-2D MoS2/g-C3N4 photocatalyst for enhanced photocatalytic H2 production activity
摘要: Although graphitic carbon nitride (g-C3N4) is an attractive photocatalyst for solar H2 generation, the preparation of g-C3N4 nanosheets via a “green” and simple method as well as the construction of highly-efficient g-C3N4-based photocatalysts are still challenges. In this study, g-C3N4 nanosheets prepared by a simple probe sonication assisted liquid exfoliation method were used to construct 2D-2D MoS2/g-C3N4 photocatalyst for photocatalytic H2 production. The 2D-2D MoS2/g-C3N4 photocatalyst containing 0.75% MoS2 showed the highest H2 evolution rate of 1155 μmol·h-1·g-1 with an apparent quantum yield of 6.8% at 420 nm monochromatic light, which is much higher than that of the optimized 0D-2D Pt/g-C3N4 photocatalyst. The high photocatalytic H2 production activity of 2D-2D MoS2/g-C3N4 photocatalyst can be attributed to the large surface area and the formed 2D interfaces between MoS2 and g-C3N4 nanosheets. As demonstrated by photoluminescence quenching and time-resolved fluorescence decay studies, the 2D interfaces can accelerate the photoinduced charge transfer, resulting in the high photocatalytic H2 production performance. This study provides a new strategy in developing highly-efficient g-C3N4-based photocatalysts for H2 production via using 2D nanojunction as a bridge to promote the photoinduced charge separation and transfer.
关键词: Hydrogen generation,Molybdenum disulfide,Graphitic carbon nitride,Photocatalysis,2D photocatalyst
更新于2025-09-23 15:22:29
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Analysis of power efficient compressor with fuzzy logic MPPT-based PV/FC system
摘要: In this paper, a hybrid photovoltaic (PV)/fuel cell (FC) power generation system is considered, where the hydrogen generated by the electrolysis process is used for subsequent FC operation. A novel induction motor-based compressor is proposed to boost up the pressure of hydrogen, and hence to improve the performance of the FC system. A fuzzy logic-based maximum power point tracking (MPPT) system is designed for the considered PV system. Finally, a coordinated control scheme is applied for controlling the power supplied to the load by integrating both the sources. The complete model is realised in the MATLAB/Simulink environment. Extensive simulation studies are conducted to verify the developed model. The performance of the complete system is found satisfactory under different conditions.
关键词: electrolyzer system,coordinated control,fuzzy logic-based MPPT,hydrogen generation,solar PV system
更新于2025-09-23 15:22:29
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Flexible TiO2-coated nanocellulose membranes incorporated with CdTe as electrodes in photoelectrochemical cells
摘要: Incorporation of quantum dots (QDs) into porous matrices has triggered the development of novel optical devices. In this work, TiO2 sensitized by CdTe incorporated into bacterial nanocellulose (BNC) membranes were tested as photoelectrodes in a photoelectrochemical cell directed to the water splitting for hydrogen generation. The flexible membranes were produced by immersing BNC membranes in an aqueous solution of CdTe capped with glutathione (CdTe–GSH) and further deposited over a thin layer of TiO2. Incorporation of CdTe–GSH into BNC membranes was confirmed by infrared spectroscopy. Fluorescence spectroscopy revealed that the luminescence intensity increased with the immersion time in the CdTe–GSH solution. Field-emission gun scanning electron microscopy (FEG-SEM) images revealed that the CdTe/QDs (5 nm) were homogeneously dispersed on the cellulose nanofibers. BNC/CdTe–GSH membranes was tested as photoelectrodes. Photoelectrochemical cells exhibited a significant photocurrent in wavelengths ranging from 400 to 800 nm, which indicates their potential for applications as flexible electrodes, sensors and photovoltaic systems.
关键词: Photoelectrochemical cell,Quantum dots,Bacterial nanocellulose,Water splitting,Hydrogen generation
更新于2025-09-23 15:21:21
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Visible-Light Driven Photocatalytic Hydrogen Generation by Water-Soluble All-Inorganic Core-Shell Silicon Quantum Dots
摘要: The photocatalytic hydrogen (H2) generation by boron (B) and phosphorus (P) codoped silicon quantum dots (Si QDs) with diameters in the quantum confinement regime is investigated. The codoped Si QDs have an amorphous shell made from B, Si and P. The shell induces negative potential on the surface and makes codoped Si QDs dispersible in water. The hydrophilic shell offers enhanced stability and efficiency in the photocatalytic H2 generation and provides the opportunity to study the size dependence of the H2 generation rate. A drastic increase of the H2 generation rate with decreasing the QD size is observed. Analyses based on the Marcus theory reveal that the upper shift of the lowest unoccupied molecular orbital level of Si QDs by the quantum confinement effect is responsible for the enhanced photocatalytic activity.
关键词: silicon quantum dots,quantum confinement,Marcus theory,photocatalytic hydrogen generation
更新于2025-09-23 15:21:01
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Urchin-like TiO2 structures decorated with lanthanide-doped Bi2S3 quantum dots to boost hydrogen photogeneration performance
摘要: The formation of heterojunctions between wide- and narrow-bandgap photocatalysts is commonly employed to boost the efficiency of photocatalytic hydrogen generation. Herein, the photoactivity of urchin-like rutile particles is increased by decorating with pristine as well as Er- or Yb-doped Bi2S3 quantum dots (QDs) at varied QD loadings (1–20 wt%) and doping degrees (1–15 mol%), and the best hydrogen evolution performance is achieved at Er and Yb contents of 10 mol%. Specifically, a hydrogen productivity of 1576.7 μmol?gcat?1 is achieved after 20-h irradiation for TiO2 decorated by 10 mol% Yb-doped Bi2S3 QDs. Theoretical calculations show that the introduction of defects into the Bi2S3 lattice through Er/Yb doping promotes the creation of the levels and facilitates transport of photogenerated charges during the photocatalytic process.
关键词: quantum dots,photocatalysis,TiO2,lanthanide doping,Bi2S3,hydrogen generation
更新于2025-09-23 15:21:01