Efficient Hydrogen Generation Research Articles

Cobalt Phosphide-Supported Single-Atom Pt Catalysts for Efficient and Stable Hydrogen Generation from Ammonia Borane Hydrolysis.

Ammonia borane (AB) has emerged as a promising chemical hydrogen storage material. The development of efficient, stable, and cost-effective catalysts for AB hydrolysis is the key to achieving hydrogen energy economy. Here, cobalt phosphide (CoP) is used to anchor single-atom Pt species, acting as robust catalysts for hydrogen generation from AB hydrolysis. Thanks to the high Pt utilization and the synergy between CoP and Pt species, the optimized Pt/CoP-100 catalyst exhibits an unprecedented hydrogen generation rate, giving a record turnover frequency (TOF) value of 39911 and turnover number of 2926829 at room temperature. These metrics surpass those of all existing state-of-the-art supported metal catalysts by an order of magnitude. Density functional theory calculations reveal that the integration of single-atom Pt onto the CoP substrate significantly enhances adsorption and dissociation processes for both water and AB molecules, thereby facilitating hydrogen production from AB hydrolysis. Interestingly, the TOF value is further elevated to 54878 under UV-vis light irradiation, which can be attributed to the efficient separation and mobility of photogenerated carriers at the Pt-CoP interface. The findings underscore the effectiveness of CoP as a support for single-atom metals in hydrogen production, offering insights for designing high-performance catalysts for chemical hydrogen storage.

The nature of photocatalytic hydrogen generation on silicon nanowires prepared by MAWC

Highly n-doped silicon nanowires (SiNWs) exhibit excellent hydrogen generation. Our results indicate three hydrogen generation possibilities, i.e. SiNWs oxidation, photocatalysis and the cleavage of dangling H bonds, are jointly responsible for the efficient hydrogen generation. Oxidation accounts for about 80% of total hydrogen, photocatalysis contributes less than 20% of total hydrogen, and about 0.1% of total hydrogen is from cleavage of dangling H bonds. SiNWs were oxidized in water and form SiOx (0 < X < 2) thin layer. Furthermore, the ratio of photo-generated hydrogen to photo-generated oxygen is about 2.4:1. It suggests that photocatalysis appears to be a process of water splitting. This study is significant to reveal the mechanism of hydrogen production on SiNWs prepared by Metal-Assisted Wet Chemical Etching (MAWC).

Recent Progress of Ion-Modified TiO2 for Enhanced Photocatalytic Hydrogen Production.

Harnessing solar energy to produce hydrogen through semiconductor-mediated photocatalytic water splitting is a promising avenue to address the challenges of energy scarcity and environmental degradation. Ever since Fujishima and Honda's groundbreaking work in photocatalytic water splitting, titanium dioxide (TiO2) has garnered significant interest as a semiconductor photocatalyst, prized for its non-toxicity, affordability, superior photocatalytic activity, and robust chemical stability. Nonetheless, the efficacy of solar energy conversion is hampered by TiO2's wide bandgap and the swift recombination of photogenerated carriers. In pursuit of enhancing TiO2's photocatalytic prowess, a panoply of modification techniques has been explored over recent years. This work provides an extensive review of the strategies employed to augment TiO2's performance in photocatalytic hydrogen production, with a special emphasis on foreign dopant incorporation. Firstly, we delve into metal doping as a key tactic to boost TiO2's capacity for efficient hydrogen generation via water splitting. We elaborate on the premise that metal doping introduces discrete energy states within TiO2's bandgap, thereby elevating its visible light photocatalytic activity. Following that, we evaluate the role of metal nanoparticles in modifying TiO2, hailed as one of the most effective strategies. Metal nanoparticles, serving as both photosensitizers and co-catalysts, display a pronounced affinity for visible light absorption and enhance the segregation and conveyance of photogenerated charge carriers, leading to remarkable photocatalytic outcomes. Furthermore, we consolidate perspectives on the nonmetal doping of TiO2, which tailors the material to harness visible light more efficiently and bolsters the separation and transfer of photogenerated carriers. The incorporation of various anions is summarized for their potential to propel TiO2's photocatalytic capabilities. This review aspires to compile contemporary insights on ion-doped TiO2, propelling the efficacy of photocatalytic hydrogen evolution and anticipating forthcoming advancements. Our work aims to furnish an informative scaffold for crafting advanced TiO2-based photocatalysts tailored for water-splitting applications.

Exploring Flower-Structured Bifunctional VCu Layered Double Hydroxide and its Nanohybrid with g-C3N4for Electrochemical and Photoelectrochemical Seawater Electrolysis.

Seawater electrolysis holds great promise for sustainable green hydrogen generation, but its implementation is hindered by high energy consumption and electrode degradation. Two dimensional (2D) layered double hydroxide (LDH) exhibits remarkable stability, high catalytic activity, and excellent corrosion resistance in the harsh electrolytic environment. The synergistic effect between LDH and seawater ions enhances the oxygen evolution reaction, enabling efficient and sustainable green hydrogen generation. Here, we report a synthesis of low cost, novel 2D Vanadium Copper (VCu) LDH first time in the series of LDH's as a highly efficient bifunctional electrocatalyst. The electrochemical (EC) and photoelectrochemical (PEC) study of VCu LDH and VCu LDH/Graphite Carbon Nitride (g-C3N4) nanohybrid was performed in 0.5 M H2SO4 (acidic), 1 M KOH (basic), 0.5 M NaCl (artificial seawater), 0.5 M NaCl + 1 M KOH (artificial alkaline seawater), real seawater and 1 M KOH + real seawater (alkaline real seawater) electrolyte medium. It was found that VCu LDH shows a remarkable lower overpotential of 72 mV hydrogen evolution reaction (HER) and 254 mV oxygen evolution reaction (OER) at current density of 10 mA/cm2 under alkaline real seawater electrolysis exhibiting bifunctional activity and also showing better stability.

Fe-Incorporated Metal-Organic Cobalt Hydroxide Toward Efficient Oxygen Evolution Reaction

AbstractMetal-organic cobalt hydroxide emerges as a cost-effective electrocatalyst for the oxygen evolution reaction (OER) in energy conversion. However, the limited active sites and poor conductivity hinder their large-scale application. This study employed salicylate as a bridging ligand to synthesize iron-incorporated metal-organic cobalt hydroxide. The influence of Fe intercalation on Co(OH)(Hsal) (where Hsal denotes o-HOC6H4COO−) was investigated using X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). Fe0.2Co0.8(OH)(Hsal) demonstrates remarkable electrocatalytic activity, displaying an OER overpotential of 298 mV at 10 mA cm−2 and a Tafel slope of 57.46 mV dec−1. This enhancement can be attributed to improved charge transfer kinetics and increased active sites. This work highlights the crucial role of Fe in improving the efficiency of Co-based oxygen-evolving catalysts (OECs) and its potential for boosting efficient hydrogen generation in alkaline environments. Graphical Abstract

Harnessing Dual-Functionality of N, F-Codoped SnO2 Material for Efficient Hydrogen Generation and Dye Degradation

Harnessing Dual-Functionality of N, F-Codoped SnO2 Material for Efficient Hydrogen Generation and Dye Degradation

Exploring Nanomaterials for Hydrogen Storage: Advances, Challenges, and Perspectives.

Hydrogen energy heralded for its environmentally friendly, renewable, efficient, and cost-effective attributes, stands poised as the primary alternative to fossil fuels in the future. Despite its great potential, the low volumetric density presents a formidable challenge in hydrogen storage. Addressing this challenge necessitates exploring effective storage techniques for a sustainable hydrogen economy. Solid-state hydrogen storage in nanomaterials (physically or chemically) holds promise for achieving large-scale hydrogen storage applications. Such approaches offer benefits, including safety, compactness, lightness, reversibility, and efficient generation of pure hydrogen fuel under mild conditions. This article presents solid-state nanomaterials, specifically nanoporous carbons (activated carbon, carbon fibers), metal-organic frameworks, covalently connected frameworks, nanoporous organic polymers, and nanoscale metal hydrides. Furthermore, new developments in hydrogen fuel cell technology for stationary and mobile applications have been demonstrated. The review outlines significant advancements thus far, identifies key barriers to practical implementation, and presents a perspective for future sustainable energy research. It concludes with recommendations to enhance hydrogen storage performance for cost-effective and long-lasting utilization.

Cu-MOF Modified ZnIn2S4 Nanosheet Composite Catalyst for Photocatalytic Hydrogen Production

In the realm of photocatalysis, the creation of clean and pollution-free composite material catalysts is critical. Electrostatic self-assembly techniques were used in this study to construct ZnIn2S4 nanosheets onto the surface of Cu-MOF, culminating in the development of a unique Cu-MOF/ZnIn2S4 composite catalyst. Cu-MOF was shown to have a strong interface impact with ZnIn2S4, which resulted in a large increase in the number of active sites and, consequently, the efficiency of hydrogen generation. This was demonstrated by a number of parameters. The Cu-MOF/ZnIn2S4-10 composite material's optimum hydrogen evolution rate was 0.3 mmol h-1g-1, which was 2.14 times larger than that of pure ZnIn2S4 nanosheets (0.14 mmol h-1g-1). Furthermore, the development of Cu-MOF/ZnIn2S4 heterojunctions considerably improved ZnIn2S4's deficiencies in photocatalytic hydrogen production, increasing charge separation rates and providing a viable approach to improve ZnIn2S4's hydrogen production efficiency.

Investigating the potential of ZrO2/MoO3 nanocomposites for efficient hydrogen generation through NaBH4 methanolysis

This work investigates the potential of ZrO2/MoO3 nanocomposites as catalysts for hydrogen production through NaBH4 methanolysis. The samples were prepared by controlled thermal calcination and characterized using various techniques like XRD, FTIR, Raman, SEM, and surface area BET analysis. Rietveld refinements verified the presence of the ZrO2 monoclinic phase with the space group P21/c in all samples and a second orthorhombic MoO3 phase with the space group Pnma. The average crystal size decreased from 44 to 40 nm. FTIR and Raman spectroscopy confirmed the successful preparation of ZrO2/MoO3 nanocomposites. SEM analysis showed ZrO2 particles and MoO3 nanoparticles adhered to the ZrO2 surface, potentially creating a rougher texture. The results confirmed the formation of ZrO2/MoO3 nanocomposites with increasing MoO3 content, leading to an increased surface area of 19–23 m2/g. The catalytic performance evaluation revealed that the sample containing 30 % MoO3 (ZM3) exhibited the highest hydrogen generation rate of 18,451 mL/g. min at 30 °C. The calculated activation energy for ZM3 was 18.78 kJ/mol, suggesting efficient hydrogen generation at moderate temperatures.

Enhanced photocatalytic hydrogen generation using UiO-66(Zr) MOF with tailored modifications: A review

The utilization of UiO-66 MOF-based photocatalytic materials has achieved significant attention for their potential in hydrogen generation, owing to their remarkable stability and porous crystalline structure. Recent studies have disclosed enhanced light absorption capabilities in UiO-66 through both pre and post-synthetic modifications. These modifications also play a significant role in mitigating the recombination of photogenerated charge carriers by facilitating electron transfer in hybrid or derived materials. Designing of MOF-based modified improved photocatalyst includes, integration with other low band gap semiconductors, incorporation of noble metals as co-catalysts, surface engineering, inclusion of defects or introduction of heteroatom in the framework. MOF-COF hybridization, dye sensitization etc., further reinforced photocatalytic hydrogen yield. The above-mentioned comprehensive investigations have researched into aspects such as morphology, hydrogen generation efficiency, and the underlying mechanisms. It reveals that the creation of heterojunctions at interface channelizes the separation and smooth flow of electrons resulting in suppression of recombination reaction and favorable photocatalytic properties. The synergy between the components often results in enhanced performance. The present article provides a comprehensive review of modified UiO-66 MOF-based materials investigated for photocatalytic hydrogen generation.

Highly efficient photocatalytic hydrogen generation of PtPdy nanoframe/2D-CdS: Shape-controlled preparation and property modulation

This work focuses on the structure design of Pt-based alloys, and their influences on 2D-CdS semiconductor photocatalyst in hydrogen (H2) generation reaction from water-splitting under visible light, using traditional experimental techniques and DFT calculations as Pd concave nanocube (Pd CNCs) as a template, PtPdx alloy with cuboctahedron core-shell structure (PtPdx NPs) and cuboctahedron nanoframe (PtPdy NFs) were successfully synthesized via wet chemical routes. The structure of Pt-based alloys was certified by XRD, HRTEM, XPS, and ICP. The Pt-based co-catalysts were photo-deposited on 2D-CdS in an aqueous solution of (NH4)2SO3 while the reaction for photo-generating of H2 occurred. The obtained photocatalysts show excellent activity towards hydrogen generation, i.e., in ascending order, Pd CNCs/2D-CdS (46.1 mmol/h/g) < PtPd1.8 NPs/2D-CdS (55.4 mmol/h/g) < PtPd0.2 NFs/2D-CdS (71.7 mmol/h/g, QE=61.46%, λ=420 nm). Photoelectrochemical tests, ESR, and work functions results indicate that PtPd0.2 NFs have excellent photoelectrochemical performance, the longest lifetime of electrons, and the highest work function, respectively. Moreover, DFT calculations unveil that PtPd0.2 has the largest surface energy and the lowest activation energy ΔGH* which results in the fast charge transfer rate at the PtPd0.2/2D-CdS interface. This work offers a novel thought into the structural design of Pt-based co-catalysts applied in photocatalytic hydrogen generation from water-splitting.

A new modelling approach for in-situ hydrogen production from heavy oil reservoirs: Sensitivity analysis and process mechanisms

The increasing demand for eco-friendly and renewable energy has positioned hydrogen as a viable solution for global energy and environmental challenges. In-situ combustion gasification of heavy oil reservoirs offers potential for large-scale hydrogen production, injecting steam and air (or alternative gases) to trigger complex chemical reactions leading to hydrogen and syngas generation. However, a research gap exists due to the lack of a comprehensive numerical model for accurately simulating hydrogen production under SARA-based (saturate, aromatic, resin, asphaltene) hydrocarbon characterization in experiments and field study. This study addresses the gap by investigating in-situ combustion gasification for hydrogen generation in heavy oil reservoirs. A novel model based on SARA characterization is proposed, showing fidelity with experimental and numerical results. Different injection strategies, like pure oxygen and CO2, impact hydrogen production. Oxygen injection yields less hydrogen than air injection, highlighting the importance of oxygen control. CO2 injection reduces hydrogen but aids carbon management. The oxygen to nitrogen ratio (61/39) demonstrates the highest hydrogen-to-syngas ratio. Practical implementation requires economic feasibility, operational practicality, safety, and environmental considerations. This study advances in-situ combustion gasification technology, facilitating efficient and sustainable hydrogen generation from heavy oil reservoirs.

Electrochemical treatment coupled with solar light-driven photocatalytic approach: a challenging process in cascade for hydrogen production and wastewater remediation

This study presents an innovative approach for simultaneous hydrogen production and wastewater remediation, integrating electrochemical treatment with solar light-driven photocatalysis. The research focuses on the use of a noble metal-free cathode, based on a electrodeposited composite of Co2P and elemental P, for efficient hydrogen generation from simulated wastewater through water splitting. This composite is characterized, in its optimized form, by an overpotential equal to 133.6mV (at 10mAcm-2) and by a Tafel slope of 60.5mV dec-1. Challenges like the high potential required for the Oxygen Evolution Reaction (OER) and the use of expensive noble metals in electrodes are addressed by employing earth-abundant compounds for electrode fabrication. Additionally, the study explores the degradation of diclofenac (DCF) in wastewater, demonstrating that electrochemical treatment alone is insufficient for organic matter removal. Therefore, a coupled process involving a first electrochemical treatment step followed by a photocatalytic process using BiOCl is proposed. Thanks to the exposure of the (110) active face, BiOCl possesses excellent photocatalytic performances even under solar light irradiation. This hybrid approach not only enhances the efficiency of DCF degradation (about 90%) and reaches an organic matter removal of 59%, but it also improves hydrogen production, offering a sustainable solution for energy generation and water purification in the face of increasing global industrialization and water scarcity.

Enhanced photocatalytic hydrogen generation efficiency through molybdenum-sulfur dual sites synergistic catalysis

Photocatalysis has gained significant attention in recent years for water splitting, with graphitic carbon nitride (g-C3N4) emerging as a promising candidate. However, the low carrier mobility and the lack of active sites for hydrogen evolution limit photocatalytic hydrogen evolution performance. Herein, this work presents a facile approach to achieve single Mo sites with a unique local coordination structure featuring one Mo atom coordinated with two nitrogen atoms and one sulfur atom. Among the prepared photocatalysts, 6wt% Mo/SCN exhibits the highest photocatalytic hydrogen evolution activity with a yield rate of 4.05mmolg-1 h-1, which is 13 times higher than that of pure g-C3N4 and superior to most of the g-C3N4 series photocatalysts. Experimental results and density functional theory calculations confirm that the Mo single-atom and S atom have synergistic catalysis under the co-modification, and the formed Mo-S bonds will enhance the ability of the substrate to anchor the Mo single-atom to enhance the stability of the photocatalyst. This work offers insights into transition metal single-atom and synergistic catalysis design for photocatalytic hydrogen evolution.

Rapid CO2 laser treatment of Pt–Fe MOF for efficient electrochemical hydrogen evolution reaction

The quest for efficient hydrogen production via electrochemical water splitting has led to extensive research on catalytic materials. This work focuses on enhancing the catalytic functionality of metal-organic frameworks (MOFs) by incorporating platinum (Pt) to improve the performance of the hydrogen evolution reaction (HER). Fe-based MOFs mixed with platinum precursors were altered through laser treatment, which caused considerable changes in their structure and catalytic activity in just 3 min. This was achieved without the need for vacuum or an inert atmosphere. Characterization techniques including X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, and electrochemical measurements were used to characterize the synthesized materials. The laser-treated Pt–Fe MOF demonstrated outstanding HER performance with 3.5 wt% Pt content, outperforming commercial 20 wt% Pt/C catalysts, and exhibiting good stability even after prolonged cycling. These results highlight the potential of laser-treated MOFs for efficient and cost-effective electrochemical hydrogen generation.

Catalysing a sustainable future: Harnessing solar energy with novel Co3O4@VO2 nanocomposites for enhanced photocatalytic hydrogen generation and dye degradation

This study focuses on the hydrothermal synthesis and characterization of Concentration dependent Co3O4@VO2 nanocomposites with varying molar ratios of Co3O4 to VO2 (2:1, 1:1, and 1:2) for efficient hydrogen generation and dye degradation. The structural and morphological characteristics of the prepared nanocomposites were analysed using x-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). Crystallographic analysis using XRD confirmed the formation of crystalline Co3O4 with a monoclinic structure, while the presence of VO2 was identified by characteristic peaks in the XPS. Microscopic analysis using SEM and TEM revealed well-dispersed nanocomposites with nanoscale dimensions. Photocatalytic activities were evaluated for hydrogen evolution and dye degradation, with the nanocomposite featuring a 2:1 ratio of Co3O4 to VO2 (CV-21) demonstrating significantly enhanced performance. CV-21 exhibited a lower onset potential and higher current density for hydrogen evolution (2270μmol/h/g), indicating improved photocatalytic activity. Additionally, it displayed rapid and superior dye degradation (93% within 10 min) under sunlight compared to Victoria blue B (VBB) dye. The Co3O4@VO2 nanocomposites, particularly CV-21, demonstrate enhanced photocatalytic performance for hydrogen generation and dye degradation compared to pristine VO2 and Co3O4. This improvement possibly due to synergistic effects between Co3O4 and VO2, optimized structural characteristics, and improved interfacial properties in the nanocomposite structure. These findings highlight the promising potential of Co3O4@VO2 nanocomposites, particularly CV-21, for environmental remediation applications.

Intramolecular Quaternary Carbon Nitride Homojunction for Enhanced Visible Light Hydrogen Production.

In this work, an intramolecular carbon nitride (CN)-based quaternary homojunction functionalized with pyridine rings is prepared via an in situ alkali-assisted copolymerization strategy of bulk CN and 2-aminopyridine for efficient visible light hydrogen generation. In the obtained structure, triazine-based CN (TCN), heptazine-based CN (HCN), pyridine unit incorporated TCN, and pyridine ring inserted HCN constitute a special multicomponent system and form a built-in electric field between the crystalline semiconductors by the arrangement of energy band levels. The electron-withdrawing function of the conjugated heterocycle can trigger the skeleton delocalization and edge induction effect. Highly accelerated photoelectron-hole transfer rates via multi-stepwise charge migration pathways are achieved by the synergistic effect of the functional group modification and molecular quaternary homojunction. Under the addition of 5mg 2-aminopyridine, the resulting homojunction framework exhibits a significantly improved hydrogen evolution rate of 6.64mmol g-1 h-1 with an apparent quantum efficiency of 12.27% at 420nm. Further, the catalyst verifies its potential commercial value since it can produce hydrogen from various real water environments. This study provides a reliable way for the rational design and fabrication of intramolecular multi-homojunction to obtain high-efficient photocatalytic reactions.

Photoilluminated Redox-Processed Rh2P Nanoparticles on Photocathodes for Stable Hydrogen Production in Acidic Environments.

While photoelectrochemical (PEC) cells show promise for solar-driven green hydrogen production, exploration of various light-absorbing multilayer coatings has yet to significantly enhance their hydrogen generation efficiency. Acidic conditions can enhance the hydrogen evolution reaction (HER) kinetics and reduce overpotential losses. However, prolonged acidic exposure deactivates noble metal electrocatalysts, hindering their long-term stability. Progress requires addressing catalyst degradation to enable stable, efficient, and acidic PEC cells. Here, we proposed a process design based on the photoilluminated redox deposition (PRoD) approach. We use this to grow crystalline Rh2P nanoparticles (NPs) with a size of 5-10 on 30 nm-thick TiO2, without annealing. Atomically precise reaction control was performed by using several cyclic voltammetry cycles coincident with light irradiation to create a system with optimal catalytic activity. The optimized photocathode, composed of Rh2P/TiO2/Al-ZnO/Cu2O/Sb-Cu2O/ITO, achieved an excellent photocurrent density of 8.2 mA cm-2 at 0 VRHE and a durable water-splitting reaction in a strong acidic solution. Specifically, the Rh2P-loaded photocathode exhibited a 5.3-fold enhancement in mass activity compared to that utilizing just a Rh catalyst. Furthermore, in situ scanning transmission electron microscopy (STEM) was performed to observe the real-time growth process of Rh2P NPs in a liquid cell.

High‐Efficiency Iridium‐Yttrium Alloy Catalyst for Acidic Water Electrolysis

AbstractProton exchange membrane (PEM) water electrolysis holds great promise in revolutionizing clean energy production by enabling the efficient generation of hydrogen. Nevertheless, a formidable challenge persists in the realm of designing electrocatalysts that are both highly active and acid‐resistant during the oxygen evolution reaction (OER), thereby mitigating the substantial kinetic barrier. In this study, the facile synthesis of iridium‐yttrium (IrY) alloy nanocatalysts via a thermal shock method is introduced, which exhibits exceptional activity in the context of acidic water oxidation. Through the strategic incorporation of dispersed Y into the lattice of Ir metal, the IrY catalyst demonstrates a notably low overpotential of 255 mV at a current density of 10 mA cm−2 and showcases remarkable catalytic stability in acidic electrolytes, enduring for over 500 h with a high current density of 100 mA cm−2. Through a comprehensive set of in situ characterizations and analytical methods, the formation of a surface Ir‐based oxide layer, induced by deprotonation and electrochemical oxidation is unveiled, which is notably stabilized by the presence of Y dopants. This stabilization of the active site imparts enhanced resistance to over‐oxidation and dissolution, underpinning the exceptional stability of the catalyst. Theoretical calculations suggest that the incorporation of Y into the catalyst structure has a significant impact on enhancing the reactivity of the oxygen intermediate (O*) at adjacent Ir sites, thus lowering the overpotential and promoting OER activity. The alloying approach presents a straightforward method for achieving atomic‐level modifications in catalyst design and can pave the way for the development of more effective and economically viable OER catalysts and beyond.

Rapid and robust hydrogen generation from sodium borohydride in optimum mixture of methanol and ethylene glycol using phosphorus-doped chitosan polymer matrix dispersed on alumina nanoparticles

Here, the highly efficient hydrogen (H2) generation by sodium borohydride (NaBH4) in a novel synergistic mixture of methanol and ethylene glycol using phosphorus-doped chitosan polymer matrix incorporated on alumina particles was investigated. The efficiency of P-doped chitosan-alumina hybride catalyst for H2 generation from NaBH4(NaBH4-HGR) in methanol, ethylene glycol, and methanol + ethylene glycol mixture showed significant differences. In particular, there is a very effective performance for NaBH4-HGR in a methanol + ethylene glycol mixture. The HGR values by mixture of methanol, ethylene glycol and methanol/ethylene glycol were 2342, 7364 and 13548 ml min-1g−1, respectively. Moreover, the H2 generation rate (HGR) value by NaBH4 using P-doped chitosan-alumina with the combination of methanol (8 ml) + ethylene glycol (2 ml) was 25,964 ml min-1g−1. Also, activation energy (Ea) was 30.62 kJmol−1. Additionally, the mechanism of H2 release by NaBH4 solvolysis reactions in the methanol + ethylene glycol mixture using P-doped chitosan-alumina was evaluated. In the methanol + ethylene glycol mixture, both the low viscosity of methanol and the high acidity of ethylene glycol are likely to have a positive synergistic effect on H2 production at the same time. Moreover, both the positivity of the P atoms and the increased acidity of the alumina become attractive to the negatively charged ions present in the reaction medium.