Catalytic Hydrogen Production Research Articles

Interplanar spacing and nanosheet thickness regulation of carbon nitride and its “cold” catalytic hydrogen production performance under 10 W LED irradiation

Investigation of hydrogen production catalysis under low-temperature and low-power light irradiation, such as LEDs, is important for energy conservation in cold natural conditions. Interlayer charge transfer in g-C3N4 nanosheets is influenced by the crystal face spacing and nanosheet thickness, due to rapid photogenerated carrier recombination and slow charge transfer, thus enhancing hydrogen production capabilities. Few studies have controlled both crystal face spacing and nanosheet thickness simultaneously. In this research, copper-phosphorus co-doped g-C3N4 was synthesized through one-step thermal polymerization, achieving both control over nanosheet thickness and crystal surface spacing. The hydrogen production rate of 0.5 %Cu/1 %P doped g-C3N4 was increased by 5.25 times and reached 958.98 μmol/g/h under 10 °C and 10 W LED illumination. Copper and phosphorus doping that reduced (002) surface spacing of g-C3N4, resulting in thinner nanosheets. This structural modification facilitated interlayer charge transfer and suppressed photogenerated carrier recombination. This research provides a novel insight and strategy for designing hydrogen production photocatalyst at low temperatures and with low energy consumption.

Pt atomic clusters/MoS2 nanosheets/Co-doped hollow carbon nanofibers for high-current–density alkaline hydrogen production

The application of layered molybdenum disulfide (MoS2) in catalytic hydrogen production has attracted great interest, while their catalytic properties are limited by poor electron conductivity and a few catalytically active sites. In this work, we demonstrated a highly active electrocatalyst for large-scale hydrogen production, consisting of two-dimensional (2D) Pt-MoS2 nanosheets along one-dimensional (1D) cobalt nanoparticle integrated carbon hollow nanofibers (Co@CHNF). The as-prepared Pt-MoS2-Co@CHNF had a large specific surface area (44.5 m2 g−1). X-ray photoelectron spectrometer (XPS) and spherical aberration corrected transmission electron microscope (AC-STEM) demonstrated that Pt atomic clusters (Pt ACs) were doped on MoS2 nanosheets by thermodynamically induced spontaneous interfacial redox between MoS2 and H₂PtCl₆. The Pt-MoS2-Co@CHNF based catalysts exhibited an overpotential as low as 91 mV for 10 mA cm−2 and 258 mV for 200 mA cm−2 in 1 M KOH electrolyte, and there is no significant floating for catalytic active with 14 h continuous operation, which demonstrates its excellent long-term operation durability, significantly superior to the previously reported state-of-the-art Co-based or Mo-based catalysts. In particular, the self-supporting binder-free Pt-MoS2-Co@CHNF catalyst-based electrode showed an ultra-high current density of 500 mA cm−2 at a low overpotential of 301 mV, without any decrease after 24 h operation at 500 mA cm−2 in 1 M KOH seawater electrolyte, representing a great potential for large-scale seawater hydrogen production.

Hydrogen production from chemical hydrogen storage materials over copper‐based catalysts

AbstractHydrogen, as a clean and efficient energy source, is one of the important energy carriers in the future. However, the safe storage and delivery of hydrogen is still a bottleneck in its practical applications. Chemical hydrides (such as NaBH4, NH3BH3, N2H4·H2O, N2H4BH3, and HCOOH) are considered as potential chemical hydrogen storage materials that can achieve rapid on‐site hydrogen production. At present, the most critical issue for them is to develop economic catalysts to achieve efficient hydrogen production from chemical hydrides. Copper (Cu) is considered as a promising catalyst that is one of the most reactive metals among the first‐row transition metals and economically cheap. In this review, we outline the recent advancements of Cu‐based catalysts in catalyzing hydrogen production from chemical hydrides. Moreover, the synthesis methods, characterization techniques, and hydrogen production catalytic activity of Cu‐based catalysts were also introduced. Finally, a brief conclusion and outlook are given for the application of Cu‐based catalysts in the dehydrogenation of chemical hydrides. We hope that this review will stimulate interest in the promising research area of Cu‐based catalysts for the dehydrogenation of chemical hydrides.

Enhanced interfacial stability of Pt/TiO2/Ti via Pt-O bonding for efficient acidic electrolyzer

The development of efficient and stable integrated electrodes is crucial for the advancement of electrolyzer. Herein, the ultra-low platinum (12.7 μgPt cm−2) anchored TiO2 nano-polyhedrons protective titanium fibers paper (Pt/TiO2/Ti) is synthesized as an integrated electrode for gas diffusion, current collector and catalytic hydrogen production. The Pt/TiO2/Ti electrode exhibits remarkable activity (23 mV at 10 mA cm−2) and durability (180 mA cm−2 for 25 h) for hydrogen evolution reaction in acidic electrolyte, which is attributed to the enhanced interface via Pt-O bond between Pt and TiO2. Specifically, the optimizing electronic structure of Pt anchoring on the TiO2 enhances hydrogen adsorption energy to improve the intrinsic activity of HER. In addition, the relatively negative adsorption energy (Eads) of Pt atom on TiO2 significantly contributes to the structural stability of the Pt/TiO2/Ti electrode. Moreover, the complete encapsulation of titanium fibers by TiO2 layer enhances the structural stability of Pt/TiO2/Ti by preventing hydrogenation-induced breakage of the titanium substrate. The constructed electrolyzer of (−) Pt/TiO2/Ti || IrO2/TiO2/Ti (+) presents efficient water splitting performance (1.464 V at 10 mA cm−2) and long-term durability (∼100% retention for 30 h) in acidic electrolyte. This work highlights the importance of integrated electrodes and the feasibility of acidic electrolyzer.

ZnIn2S4-based multi-interface coupled photocatalyst for efficient photothermal synergistic catalytic hydrogen evolution

Photothermal synergistic catalysis is a novel technology that converts energy. In this study, ZnIn2S4 with S-vacancy (ZIS-Vs) is combined with Nickel, Nickle Oxide and Carbon Nanofiber aggregates (Ni-NiO@CNFs) to create a multi-interface coupled photocatalyst with double Schottky barrier, double channel and mixed photothermal conversion effect. Theoretical calculation confirms that the Gibbs free energy (ΔG*H) of the S-scheme heterojunction in the composite material is −0.07 eV, which is close to 0. This promotes the adsorption of H* and accelerates the formation of H2. Internal photothermal catalysis is achieved by visible-near infrared (Vis-NIR, RT) irradiation. The internal photothermal catalytic hydrogen production rate of the best sample (0.9Ni-NiO@CNFs/ZIS-Vs) is as high as 17.24 mmol·g−1·h−1, and its photothermal conversion efficiency (η) is as high as 61.42 %. Its hydrogen production efficiency is 20.52 times that of ZIS-Vs (0.84 mmol·g−1·h−1) under visible light (Vis, RT) conditions. When the Vis-NIR light source is combined with external heating (75 ℃), the hydrogen production efficiency is further improved, and the hydrogen production efficiency (29.16 mmol·g−1·h−1) is 26.75 times that of ZIS-Vs (1.09 mmol·g−1·h−1, Vis-NIR, RT). Further analysis shows that the increase in hydrogen production resulted from the apparent activation energy (Ea) of the catalyst decreasing from 16.7 kJ·mol−1 to 9.28 kJ·mol−1. This study provides a valuable prototype for the design of an efficient photothermal synergistic catalytic system.

Catalyzing hydrogen production: Exploring plasmonic effects in self-assembled CuO/Cu2O thin films via pulsed laser deposition

Plasmonic catalysis triggers the dissociation of H2 or adsorbed O2 (sluggish processes) under continuous wave excitation via plasmon decay. This is coupled to interband or intraband excitation of d-band or sp-band, respectively, to levels above fermi level of metals. Here, we have studied the plasmonic and photocatalytic behavior in an environment friendly medium with AM 1.5 G sunlight of CuO/Cu2O thin films fabricated by pulsed laser deposition technique in vacuum with varying thickness. We have achieved ∼0.59 kmol h−1g−1H2 production in the CuO/Cu2O film with a thickness of ∼27 nm. The role of plasmons with metal–dielectric and semiconductor–semiconductor interfaces is conducted through both experimental and theoretical approaches. The results suggest that the impact of plasmonic catalysis/synthesis is subject to the dimension, composition, and band alignment of two interface materials.

Computation-Driven Rational Design of Self-Assembled Short Peptides for Catalytic Hydrogen Production.

Self-assembling peptides represent a captivating area of study in nanotechnology and biomaterials. This interest is largely driven by their unique properties and the vast application potential across various fields such as catalytic functions. However, design complexities, including high-dimensional sequence space and structural diversity, pose significant challenges in the study of such systems. In this work, we explored the possibility of self-assembled peptides to catalyze the hydrolysis of hydrosilane for hydrogen production using ab initio calculations and carried out wet-lab experiments to confirm the feasibility of these catalytic reactions under ambient conditions. Further, we delved into the nuanced interplay between sequence, structural conformation, and catalytic activity by combining modeling with experimental techniques such as transmission electron microscopy and nuclear magnetic resonance and proposed a dual mode of the microstructure of the catalytic center. Our results reveal that although research in this area is still at an early stage, the development of self-assembled peptide catalysts for hydrogen production has the potential to provide a more sustainable and efficient alternative to conventional hydrogen production methods. In addition, this work also demonstrates that a computation-driven rational design supplemented by experimental validation is an effective protocol for conducting research on functional self-assembled peptides.

From Co-MOF to Co@carbon–comparison of needle-like catalysts in photo-driven hydrogen evolution

In response to the rising demand for catalytic hydrogen production, more attention is focused on noble-metal-free catalysts such as cobalt-based metal–organic frameworks (MOFs) and their derivatives. Due to the varying activity of cobalt forms in photocatalytic processes, the present study explores the performance of photo-driven hydrogen generation of cobalt nitrilotriacetate (Co-NTA) with metal ions and MOF-derived carbons containing Co/CoOx/CoNx. The needle-like morphology of the obtained Co-NTA template was preserved in carbon materials prepared through carbonization with and without furfuryl alcohol. Carbons featured nitrogen-containing graphitic structures and oxygen functional groups. They were also characterized by a more developed specific surface area and larger pore volume compared to their parent MOF. All materials evolved hydrogen under visible light in a photosensitized system. Owing to the high content of metallic cobalt on the surface of non-impregnated carbon, it produced three times more hydrogen (14.2 mmol g−1) than Co-NTA.

Ultrafine Ni-MoOx Nanoparticles Anchored on Nitrogen-Doped Carbon Nanosheets: A Highly Efficient Noble-Metal-Free Catalyst for Ammonia Borane Hydrolysis.

The development of low-cost and high-efficiency catalysts for the hydrolytic dehydrogenation of ammonia borane (AB, NH3BH3) is still a challenging technology. Herein, ultrafine MoOx-doped Ni nanoparticles (~3.0 nm) were anchored on g-C3N4@glucose-derived nitrogen-doped carbon nanosheets via a phosphate-mediated method. The strong adsorption of phosphate-mediated nitrogen-doped carbon nanosheets (PNCS) for metal ions is a key factor for the preparation of ultrasmall Ni nanoparticles (NPs). Notably, the alkaline environment formed by the reduction of metal ions removes the phosphate from the PNCS surface to generate P-free (P)NCS so that the phosphate does not participate in the subsequent catalytic reaction. The synthesized Ni-MoOx/(P)NCS catalysts exhibited outstanding catalytic properties for the hydrolysis of AB, with a high turnover frequency (TOF) value of up to 85.7 min-1, comparable to the most efficient noble-metal-free catalysts and commercial Pt/C catalyst ever reported for catalytic hydrogen production from AB hydrolysis. The superior performance of Ni-MoOx/(P)NCS can be ascribed to its well-dispersed ultrafine metal NPs, abundant surface basic sites, and electron-rich nickel species induced by strong electronic interactions between Ni-MoOx and (P)NCS. The strategy of combining multiple modification measures adopted in this study provides new insights into the development of economical and high-efficiency noble-metal-free catalysts for energy catalysis applications.

Advances in the Homogeneously Catalyzed Hydrogen Production from Biomass Derived Feedstocks: a Review.

Biomass‐derived feedstocks for hydrogen production are crucial as an alternative to fossil fuel especially in those areas where green electricity and clean water are scarce. In this framework the transformation of simple (formic acid, alcohols) and more complex (polyalcohols, sugars and cellulose) bio‐derivatives in pure hydrogen is recognized as a promising approach. Parallel to great effort in heterogeneous catalysis, milder molecular systems represent a more selective eye for alternative solutions and mechanistic insights. In the present review the introduction summarizes the challenges in the catalytic utilization of biomass‐derived feedstocks, followed by the advances in homogeneously catalyzed hydrogen production from different substrates which will cover formic acid, with oustanding efficiency with noble metals and promising results with earth abundant ones and alcohols and polyalcohols, with particular emphasis to the development of heterogenized systems, ligand assisted catalysts and bi‐catalytic synergistic solutions which allow to avoid base and to promote catalyst stability and recyclability. In the last part, description of hydrogen production from more complex substrates, such as sugars and cellulose, will show the role of molecular complexes in main and side reactions. Critical comments on the reported advances are provided along the whole discussion.

High-performance heterometallic photocatalysts afforded by polyoxometalate synthons for efficient H2 production

MoS2-based materials have emerged as photoelectric semiconductors characterized by a narrow band gap, high capacity for absorbing visible light, and reduced H2 adsorption energy comparable to Pt. These attributes render them appealing for application in photocatalytic hydrogen production. Despite these advantages, the widespread adoption of MoS2-based materials remains hindered by challenges associated with limited exposure to active sites and suboptimal catalytic hydrogen production efficiency. To address these issues, we have designed and synthesized a new class of highly dispersed bimetallic/trimetallic sulfide materials. This was achieved by developing polyoxometalate synthons containing Ni-Mo elements, which were subsequently reacted with thiourea and CdS. The resulting Ni3S2-MoS2 and Ni3S2-MoS2-CdS materials achieve photocatalytic hydrogen production rates of 2770 and 2873 μmol g–1h−1, respectively. Notably, the rate of 2873 μmol g–1h−1 for Ni3S2-MoS2-CdS surpassed triple (3.23 times) the performance of CdS and nearly sextuple (5.77 times) that of single MoS2. These materials outperformed the majority of MoS2-based photocatalysts. Overall, this study introduces a straightforward methodology for synthesizing bimetallic/trimetallic sulfides with enhanced photocatalytic H2 evolution performance. Our findings underscore the potential of transition metal sulfide semiconductors in the realm of photocatalysis and pave the way for the development of more sustainable energy production systems.

Synergistic, dual energy source production of hydrogen using Ru-promoted nitrogen-doped carbon nanotubes

In this work, ruthenium-promoted nitrogen-doped carbon nanotubes (Ru/NCN) composite materials were synthesized and utilized for the dual thermo-photo catalytic production of hydrogen using biomass-derived reactants. A spectroscopic and microscopy-based characterization showed that the composites contain rather small metallic ruthenium entities uniformly distributed and stabilized through interaction with the carbon-containing component. A highly active and (under reaction conditions) stable Ru/NCN material maximized hydrogen output under continuous operation, showing outstanding reaction rates up to ca. 30 mmol g−1 h−1 and quantum efficiencies of ca. 7.5 %. The synergy reached by the combined use of two energy sources was studied quantitatively and analyzed in the temperature range going from room temperature to 300 °C. The combination of heat and light triggers a mechanism by which the bio-molecule, methanol, is activated by light-triggered hydroxyl-type radical species and promotes the reaction up to temperatures close to 300 °C. The new composite materials based on nitrogen-doped carbon nanotubes show thus high potential to improve classic, thermal-based processes for hydrogen production.

Ultrasound-assisted preparation of PdCo bimetallic nanoparticles loaded on beta zeolite for efficient catalytic hydrogen production from dodecahydro-N-ethylcarbazole

Research and development of high-performance catalysts is a key technology to realize hydrogen energy storage and transportation based on liquid organic hydrogen carriers. Co/beta was prepared using beta zeolite as a carrier via an electrostatic adsorption (ESA)-chemical reduction method, and it was used as the template and reducing agent to prepare bimetallic catalysts via an ultrasonic assisted galvanic replacement process (UGR). The fabricated PdCo/beta were characterized by TEM, XPS, FT-IR, XRD, H2-TPR, and H2-TPD. It was shown that the ultrafine PdCo nanoparticles (NPs) are evenly distributed on the surface of the beta zeolite. There is electron transfer between metal NPs and strong-metal-support-interaction (SMSI), which results in highly efficient catalytic dodecahydro-N-ethylcarbazole (12H-NEC) dehydrogenation performance of PdCo bimetallic catalysts. The dehydrogenation efficiency reached 100 % in 4 h at 180 °C and 95.3 % in 6 h at 160 °C. The TOF of 146.22 min−1 is 7 times that of Pd/beta. The apparent activation energy of the reaction is 66.6 kJ/mol, which is much lower than that of Pd/beta. Under the action of ultrasonic waves, the galvanic replacement reaction is accelerated, and the intermetal and metal-carrier interactions are enhanced, which improves the catalytic reaction performance.

Au decorated chemically exfoliated g-C3N4 as highly efficient visible light catalyst for hydrogen production

The demand for photocatalytic hydrogen production through water splitting is continuously increasing as the world is seeking cleaner and sustainable energy solutions. Herein, we report a comparative study of the as-fabricated Bulk g-C3N4 (BCN), chemically exfoliated g-C3N4 (ECN) and Au-decorated chemically exfoliated g-C3N4 (Au/ECN) photocatalysts for visible light-driven catalytic hydrogen production. To understand the structural, morphological, chemical, and electronic properties of the as-fabricated photocatalysts, XRD, TEM, Raman, PL, XPS, FTIR, UV and EPR analysis was performed. The as-prepared Au/ECN photocatalyst revealed exceptional visible light catalytic performance by producing 410 μmol·g−1 of hydrogen, which is 27.3- and 9.3-fold enhanced compared to those of the CN (15 μmol·g−1) and ECN (44 μmol·g−1) photocatalysts, respectively. This improved visible light-driven catalytic performance of the Au/ECN photocatalyst for hydrogen production is due to the enhanced specific surface area via the chemically exfoliated layered sheets, promoted light absorption due to the decrease in band gap via the effect of surface plasmon resonance attributable to decorated Au nanoparticles, and efficient separation of charge carriers at the interfacial contact. The photocatalytic recyclable experiments indicate excellent stability of the Au/ECN photocatalyst for H2 evolution. These findings reveal the effect of chemical exfoliation and Au decorating on the catalytic efficiency of g-C3N4-based photocatalysts, revealing potential functions for green hydrogen production under the standard visible light illumination.

Photothermal catalytic hydrogen production coupled with thermoelectric waste heat utilization and thermal energy storage for continuous power generation

Photothermal catalytic water splitting is a potential way to produce renewable hydrogen. However, low-grade heat converted from solar energy in the photochemical process is inevitably dissipated to the environment and often wasted. Besides, the intermittency of solar energy causes the devices unable to work continuously. Here, a novel integrated solar to hydrogen-electricity and thermal storage system (STHET) is proposed to solve above problems. STHET consists of a photothermal catalytic system and a thermoelectric generator (TEG) system, which can realize hydrogen-electricity co-production and thermal self-storage. Photothermal effect in STHET is increased by recycling scattered light, leading to an enhancement of 22.7% in hydrogen production than the traditional system without TEG. Meanwhile, the maximum power of waste heat utilization by TEG is 193.53 μW. Furthermore, since strengthened heat exchange in STHET with forced cooling, the output power of TEG can improve to 1578.13 μW, and hydrogen production is reduced by only 1.4% than the traditional system without TEG. Additionally, STHET can continuously generate power using stored thermal by the liquid reaction system to achieve continuous working in the dark, in which 19% (maximum proportion) of the electrical energy output can be obtained at night. The heat exchange methods in STHET can be flexibly selected according to the requirement for hydrogen energy and electric power. As a conceptual model, STHET can also be promoted in other solid-liquid reaction systems.

The g-ZnO/PtSe2 S-scheme heterojunction with controllable band structure for catalytic hydrogen production

The structural, photo-electronic catalytic properties, and the biaxial strain modulation of band structure for the g-ZnO/PtSe2 S-scheme heterojunction are studied by First-principles calculation. The stability for the heterojunction is verified by negative generation energy and ab-initio molecular dynamic simulation. The photo-generated carrier motion and band structure are in accordance with the S-scheme, and the electron mobility of up to 2023 cm2/Vs is obtained in the Zigzag direction. The absorption of visible light is improved, and an absorption peak of 2.893 × 105 cm−1 at 434.337 nm is observed. Due to a higher redox potential, photocatalytic water splitting can occur in the pH range of 0∼14, and a high solar to hydrogen (STH) efficiency of 30.7 % is obtained. The over-potential of hydrogen evolution reaction (HER) (3.719 V) is lower than oxygen evolution reaction (4.128 V), which tends to proceed at the g-ZnO interface. When the strain ≥4 %, the bandgap alignment of the g-ZnO/PtSe2 heterojunction changes from a staggered gap (Type-Ⅱ) to straddling gap (Type-Ⅰ). The g-ZnO/PtSe2 heterojunction exhibits high electron mobility, high STH efficiency, strong absorption of visible light, strong HER ability, and a tunable band structure, expecting as a promising candidate material for catalytic water splitting.

Significant hydrogen generation via photo-mechanical coupling in flexible methylammonium lead iodide nanowires.

The flexoelectric effect, which refers to the mechanical-electric coupling between strain gradient and charge polarization, should be considered for use in charge production for catalytically driving chemical reactions. We have previously revealed that halide perovskites can generate orders of higher magnitude flexoelectricity under the illumination of light than in the dark. In this study, we report the catalytic hydrogen production by photo-mechanical coupling involving the photoflexoelectric effect of flexible methylammonium lead iodide (MAPbI3) nanowires (NWs) in hydrogen iodide solution. Upon concurrent light illumination and mechanical vibration, large strain gradients were introduced in flexible MAPbI3 NWs, which subsequently induced significant hydrogen generation (at a rate of 756.5 μmol g-1 h-1, surpassing those values from either photo- or piezocatalysis of MAPbI3 nanoparticles). This photo-mechanical coupling strategy of mechanocatalysis, which enables the simultaneous utilization of multiple energy sources, provides a potentially new mechanism in mechanochemistry for highly efficient hydrogen production.

Combination of chemometrics and mass spectrometric methods for the data mining of molecular structure information of coal and biomass

The combination of mass spectrometry (MS) data and chemometrics methods is conducive to obtaining more comprehensive molecular information and evaluating the transfer behavior of O and N atoms during the conversion of biomass and coal. In this work, 12 thermal dissolution (TD) extracts of coal/biomass samples and the catalytic hydrogenation products of TD extracts were analyzed by Orbitrap MS using spectral stitching and in-source collision-activated dissociation (ISCAD) methods. Spectral stitching improves the detection ability towards minor and trace species, enhancing the number of identified compounds by two times. Meanwhile, ISCAD provides more comprehensive molecular structure information, which can illustrate the transfer patterns of heteroatoms and deepen the understanding of the structural characteristics of aromatic rings during the conversion of biomass and coal. Two chemometrics methods, principal component analysis (PCA) and hierarchical cluster analysis (HCA), were introduced to dig out the detailed similarities and differences between O-containing and N-containing compounds in coal and biomass. HCA method not only recognized the category of O-containing and N-containing compounds in each sample, but also showed the removal behavior of O and N atoms in biomass and coal. Thus, the combination of MS methods and chemometrics method is expected to provide methodological support to elucidate the molecular structure and conversion pathways for complex coal and biomass.

Synthesis of FeOOH/Zn(OH)2/CoS Ferromagnetic Nanocomposites and the Enhanced Mechanism of Magnetic Field for Their Electrochemical Performances.

The FeOOH/Zn(OH)2/CoS (FZC) nanocomposites are synthesized and show the outstanding electrochemical properties in both supercapacitor and catalytic hydrogen production. The specific area capacitance reaches 17.04 Fcm-2, which is more than ten times higher than that of FeOOH/Zn(OH)2 (FZ) substrate: 1.58 Fcm-2). FZC nanocomposites also exhibit the excellent cycling stability with an initial capacity retention rate of 93.6% after 10000 long-term cycles. The electrolytic cell (FZC//FZC) assembled with FZC as both anode and cathode in the UOR (urea oxidation reaction)|| HER (hydrogen evolution reaction) coupled system requires a cell voltage of only 1.453V to drive a current density of 10mAcm-2. Especially, the electrochemical performances of FZC nanocomposites are enhanced in magnetic field, and the mechanism is proposed based on Stern double layer model at electrode-electrolyte interface (EEI). More electrolyte ions reach the surface of FZC electrode material under Kelvin force, moreover, the warburg impedance of FZC nanocomposites decrease under magnetic field action, which results in the enhanced behaviors for both the energy storage and urea oxidation reaction .

Catalytic reforming of polypropylene to produce hydrogen: Influence of support characteristics and active metal type in catalyst

Hydrogen production by catalytic pyrolysis of waste plastics has attracted extensive attention in recent years. This paper takes hydrogen production as the starting point. A variety of supported nickel catalysts were developed for the catalytic pyrolysis of polypropylene using a two-stage fixed bed reactor. Based on the better characteristics of bimetallic catalysts, calcium, magnesium, iron doped nickel bimetallic catalysts were prepared to explore the improvement effect of catalytic hydrogen production performance. The micromorphology, structure composition and active substance distribution of different supported catalysts and bimetallic catalysts were measured. The experimental results show that the catalyst with powdered activated carbon as the support has the best catalytic performance of hydrogen production. In a series of molecular sieve catalysts, the smaller the Si/Al ratio of the support, the higher the catalytic performance. Among the bimetallic catalysts, Fe-Ni bimetallic catalysts have better catalytic advantages than Ca-Ni and Mg-Ni bimetallic catalysts, which is closely related to the stable Fe-Ni alloy structure formed on the catalyst surface. In conclusion, the differences in catalytic performance between catalyst support and active metal discussed in this paper will provide theoretical support for the catalytic pyrolysis technology of plastics to produce hydrogen.