High-density Hydrogen Research Articles

Healable, Recyclable, and Ultra-Tough Waterborne Polyurethane Elastomer Achieved through High-Density Hydrogen Bonding Cross-Linking Strategy.

With the increasing popularity of elastomers in industry and daily life, their high performance and functionality have attracted widespread attention. However, it is a great challenge for them to possess both high mechanical properties and excellent healing and recovery capabilities due to the limitations of the preparation methods and the intrinsic microstructure of the elastomers. In this study, a strategy of ice-controlled interfacial stepwise cross-linking was proposed to prepare the waterborne polyurethane-based elastomers with ultrahigh-density hydrogen bonding interaction achieved by enhancing the utilization rate of phenol hydroxyl groups of tannic acid to the maximum extent. The elastomers have incredible mechanical properties, including ultrahigh toughness of 1.03 GJ m-3 (which represents the highest level among polyurethane elastomers prepared through common processing techniques to date), extremely high true fracture stress of ∼1.9 GPa, world-record fracture energy of 520 kJ m-2, and exciting multiple functional characteristics, such as highly efficient self-healing ability of 10 min, high resistance to physical damage and chemical corrosion, broad temperature and frequency damping effects, good shape memory effect, and excellent melt-processing recyclability and solvent recyclability. These robust multifunctional elastomers represent considerable potential in various fields, from defense and military industry and civil transportation to precision manufacturing, etc.

Polymerization-Induced Self-Assembly Providing PEG-Gels with Dynamic Micelle-Crosslinked Hierarchical Structures and Overall Improvement of Their Comprehensive Performances.

Polymer gels are fascinating soft materials and have become excellent candidates for wearable electronics, biomedicine, sensors, etc. Synthetic gels usually suffer from poor mechanical properties, and integrating good mechanical properties, adhesiveness, stability, and self-healing performances in one gel is more difficult. Herein, polymerization-induced self-assembly (PISA) providing PEG-gels with an overall improvement in their comprehensive performances is reported. PISA synthesis is carried out in PEG (solvent) to efficiently produce various nanoparticles, which are used as the nanofillers in the subsequent synthesis of PEG-gels with dynamic micelle-crosslinked hierarchical structures. Compared to hydrogels, PEG-gels show excellent long-term stability due to the nonvolatile feature of PEG solvent. The hierarchical PEG-gels (with nanofillers) exhibit better mechanical and adhesive properties than the homogeneous-gels (without nanofillers). The energy dissipation mechanism of the PEG-gels is analyzed via stress relaxation and cyclic mechanical tests. High-density hydrogen bonds between the micelles and PAA matrix can be broken and reformed, endowing better self-healing properties of the dynamic micelle-crosslinked PEG gels. This work provides a simple strategy for producing hierarchical structural gels with enhanced properties, which offers fundamentals and inspirations for the designing of various advanced functional materials.

Prospects for Long-Distance Cascaded Liquid—Gaseous Hydrogen Delivery: An Economic and Environmental Assessment

As an important energy source to achieve carbon neutrality, green hydrogen has always faced the problems of high use cost and unsatisfactory environmental benefits due to its remote production areas. Therefore, a liquid-gaseous cascade green hydrogen delivery scheme is proposed in this article. In this scheme, green hydrogen is liquefied into high-density and low-pressure liquid hydrogen to enable the transport of large quantities of green hydrogen over long distances. After long-distance transport, the liquid hydrogen is stored and then gasified at transfer stations and converted into high-pressure hydrogen for distribution to the nearby hydrogen facilities in cities. In addition, this study conducted a detailed model evaluation of the scheme around the actual case of hydrogen energy demand in Chengdu City in China and compared it with conventional hydrogen delivery methods. The results show that the unit hydrogen cost of the liquid-gaseous cascade green hydrogen delivery scheme is only 51.58 CNY/kgH2, and the dynamic payback periods of long- and short-distance transportation stages are 13.61 years and 7.02 years, respectively. In terms of carbon emissions, this scheme only generates indirect carbon emissions of 2.98 kgCO2/kgH2 without using utility electricity. In sum, both the economic and carbon emission analyses demonstrate the advantages of the liquid-gaseous cascade green hydrogen delivery scheme. With further reductions in electricity prices and liquefication costs, this scheme has the potential to provide an economically/environmentally superior solution for future large-scale green hydrogen applications.

Influence of dislocation cells on hydrogen embrittlement in wrought and additively manufactured Inconel 718

Hydrogen embrittlement (HE) is a major issue for the mechanical integrity of high-strength alloys exposed to hydrogen-rich environments, with diffusion and trapping of hydrogen being critical phenomena. Here, the role of microstructure on hydrogen diffusion, trapping and embrittlement in additively manufactured (AM) and wrought Inconel 718 is compared, revealing the key role played by dislocation cells. Trapping behaviour in hydrogen-saturated alloys is analysed by thermal desorption spectroscopy and numerical simulations. A high density of hydrogen traps in cell walls, attributed to dense dislocations and Laves phases, are responsible for the local accumulation of hydrogen, causing significant loss in strength, and triggering cracking along dislocation cell walls. The influential role of dislocation cells alters fracture behaviour from intergranular in the wrought alloy to intragranular for the AM alloy, due to the large proportion of dislocation cells in AM alloys. In addition, the cellular network of dislocations accelerates hydrogen diffusion, enabling faster and deeper penetration of hydrogen in the AM alloy. These results indicate that the higher HE susceptibility of nickel superalloys is intrinsically associated with the interaction of hydrogen with dislocation walls.

Ultrafine Pd nanoparticles confined in naphthalene-based covalent triazine frameworks for efficient and stable hydrogen production from formic acid

Formic acid (FA) is considered as a kind of promising hydrogen storage materials due to its economic feasibility, safety, stability and high hydrogen density. Nevertheless, it is a challenge to design a high-performance catalyst with high activity, selectivity and stability for the dehydrogenation of FA to generate hydrogen (H2). Herein, a range of covalent triazine frameworks (CTFs including 1,8-CTF, 1,5-CTF and 2,3-CTF) with abundant nitrogen atoms are developed to support palladium nanoparticles for efficiently catalyzing FA dehydrogenation. Ultrasmall palladium nanoparticles with a size of 1.2 ± 0.3 nm showed near 100 % H2 selectivity and high catalytic activity in FA dehydrogenation supported by 1,8-CTF. The activation energy of FA dehydrogenation catalyzed by Pd/1,8-CTF reaches 26.17 kJ·mol−1. In addition, Pd/1,8-CTF exhibits high stability and easy recyclability, and the catalytic activity is maintained even after 6 cycles. This work gives a feasible strategy to develop high-efficiency and selective nanocatalysts for H2 production from FA dehydrogenation.

Supercooling-Driven Homogenization and Strengthening of Hydrogel Networks.

By leveraging principles from metal grain refinement, we introduce a transformative technique for fabricating poly(vinyl alcohol) (PVA) hydrogels via supercooling-coupled wet annealing, significantly enhancing their mechanical robustness and isotropy while maintaining their exceptionally high water content. Our methodology involves the dissolving PVA in water at elevated temperatures, mirroring the homogeneity achieved with a molten metal, in order to ensure a uniform distribution of polymer chains. This uniformity facilitates a rapid cooling phase that generates ultrafine ice crystals, setting the stage for a crucial solvent exchange with ethylene glycol (EG). The EG-mediated supercooling technique ensures the polymer homogeneity and structure integrity and induces the PVA chains to aggregate and form high-density hydrogen bonds, leading to a uniformly distributed, interconnected PVA network with high crystallinity. The process is further strengthened by EG-enabled wet annealing, which promotes the formation of densely packed crystalline domains within the polymer network. This rigorous process yields PVA hydrogels with superior mechanical properties, including a tensile strength of 13.65 MPa and a fracture toughness of 35.39 MJ m-3, alongside remarkable water content nearing 80%. These advances not only surpass the capabilities of conventional hydrogels but also broaden their application potential, highlighting the innovative integration of supercooling principles in polymer science.

Tannic acid one-step induced quaternized chitin-based edible and easy-cleaning coatings with multifunctional preservation for perishable products

The development of biomass hydrogel coatings is significant for fruit preservation. This paper presents the facile development of a multifunctional polysaccharide-based hydrogel produced from quaternized chitin (QC) and tannic acid (TA) by in situ rapid cross-linking with high-density hydrogen bonding using the sample mixing method. The Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) spectra, and thermogravimetric analysis (TGA) proved that QC-TA hydrogel was formed by physical interactions (hydrogen bonding, electrostatic interaction, etc.). Moreover, the cross-linking density of the QC-TA hydrogels was analyzed by rheological property measurements and scanning electron microscope (SEM) morphology observations. This polysaccharide-based hydrogel, QC-TA, was evaluated as an edible coating for perishable food items, demonstrating significant improvements in physic-chemical properties, oxidation resistance, and antimicrobial activity against key pathogens (E. coli, S. aureus, and C. albicans). Notably, the hydrogel formed a protective film that effectively shields fruits from mechanical damage, maintaining freshness and extending shelf life, and also featuring with easy cleaning. Applied to cherry tomatoes, the QC-TA coating ensured a smooth, uniform surface, reducing dehydration and flavor loss while inhibiting microbial growth. These findings underscore the potential of employing polyphenol induced polysaccharide forming green hydrogel coatings as an economical, efficient strategy for enhancing the quality and safety of perishable foods, representing an advancement in the field of sustainable food packaging.

The study of design and performance improvement of catalysts for the stepwise production of bicyclohexane from benzene and cyclohexene

Bicyclohexane is a hydrogen storage reagent with high hydrogen density and low boiling point. Compared with the hydrogenation of biphenyl, the alkylation of benzene and cyclohexene to cyclohexylbenzene and hydrogenation is a promising way to prepare cyclohexane on a large scale. The research and development of high-efficiency cyclohexyl benzene hydrogenation catalyst should be further developed based on mature alkylation technology. This paper used an acidified USY molecular sieve to catalyze the alkylation of benzene and cyclohexene to cyclohexylbenzene, which achieved 100% conversion and selectivity. Furthermore, Pt/TiO2/γ-Al2O3 catalyst is prepared by pre-deposition TiO2 film of different thicknesses on γ-Al2O3 surface and then supported with platinum particles by Atomic layer deposition (ALD). The role of TiO2 film in improving the cyclohexylbenzene hydrogenation performance of the catalyst is studied. TEM, CO pulse chemisorption, CO-DRIFTs, quasi-in situ XPS, H-D exchange, and H2-TPR characterization show that compared with Pt/γ-Al2O3, TiO2 thin films on Pt/TiO2/γ-Al2O3 do not change the dispersion of Pt particles, but can form new Pt-TiO2 interactions. The hydrogenation performance of cyclohexylbenzene was improved by increasing the electron density and the proportion of planar active sites on the surface of platinum and reducing the energy barrier of hydrogen spillover. The research provides theoretical support for further bicyclohexane organic liquid hydrogen storage reagent development. The relevant metal-support interaction regulation strategy can be applied to the development of efficient catalysts for other aromatic molecules hydrogenation.

Facile synthesis of high-performance and self-healing polyurethane-urea nanocomposites reinforced with graphene

In this study, a facile method was employed to synthesize strong, yet highly elastic polyurethane-urea (PUU) with typical characteristics and 94 ​% optical transmittance. Graphene platelets (GNPs) were prepared and modified via a scalable and eco-friendly mechanochemical approach. The produced GNPs is at 1.6-nm thickness with high electrical conductivity of ∼950 ​S/m. The structure-property relations of PUU/GNP nanocomposites were comprehensively investigated through morphology and mechanical properties measurements. The strong interface and high-density hydrogen bonds between modified GNPs (M-GNPs) and PUU significantly enhanced the mechanical properties of the PUU nanocomposite. The PUU composite showed 66.7 ​% and 36.2 ​% increments in tensile and impact strengths, respectively, at 0.2 ​wt% M-GNPs. The reversible hydrogen bond between M-GNPs and PUU endowed the nanocomposite with self-healing properties achieving 97.8 ​% healing efficiency of the strength after 5 ​h at 120 ​°C. This study demonstrates the importance of surface modification and provides a simple yet robust approach for preparing high-performance and functional PUU/graphene composites.

Self-healing cellulose nanocrystals/fluorinated polyacrylate with double dynamic interactions of coumarin groups and multiple hydrogen bonds

In this work, self-healing cellulose nanocrystals/fluorinated polyacrylate with dual dynamic networks of photoreversible crosslinking network and high-density hydrogen bonds was prepared by Pickering emulsion polymerization. The main work was to study the effects of 7-(2-methacryloyloxy)-4-methylcoumarin (CMA) and 2-ureido-4[1H]-pyrimidinone methyl methacrylate (UPyMA) monomer dosage on emulsion polymerization and latex film properties. The monomer conversion increased first and then decreased as the CMA and UPyMA monomer dosage increased, while a reverse trend was noted for the particle size and particle size distribution. Incorporating UPyMA allowed the rapid formation of hydrogen bonds at the crosslinking sites, which increased the interaction force between the healing surfaces. Besides, reversible photocrosslinking reaction of coumarin groups provided another support for self-healing performance. Moreover, the influence of self-healing temperature, self-healing time and UV irradiation on the self-healing ability was also systematically investigated The tensile strength of the prepared cellulose nanocrystals/fluorinated polyacrylate latex film exhibited a self-healing efficiency of 91.4 % under 365 nm UV irradiation and 80 °C for 12 h. The latex film had excellent thermal stability as was shown by TG and DTG analyses. The outstanding self-healing capability of latex film was attributed to the reversible photodimerization of coumarin groups and multiple hydrogen bonds. In addition, the water-oil repellent and mechanical properties of the latex films were improved as the CMA and UPyMA monomer dosage increased.

Strategic integration of metamaterials properties and topology optimization of gyroid metal hydride reactor for high-density hydrogen storage

Metal hydride (MH) is considered to be one of the potential materials for storing hydrogen. It has a substantial limitation to wide use in the mobility sector, which is its low gravimetric hydrogen storage density. A novel canister design utilizing the optimization of gyroid structure for MH-based hydrogen storage is proposed to enhance reactor strength and capacity, increasing the favor of using it outside stationary applications. Topology optimization (TO) of the reactor increases the capacity by 49 % while maintaining the capability of this reactor to sustain 5000 N of bending case. On top of that, changing the metamaterial properties of the gyroid results in a larger chamber size for storing a larger amount of MH by the maximum amount of 30 %. However, increasing the chamber size comes with a cost of a lower charging rate and a considerable area of non-reacted hydride at the same charging time compared to the non-modified structure. By evaluating the MH bed that consists of lanthanum nickel (LaNi5), the topologically optimized reactor design is varied with different chamber offsets of 0, 2, and 4 mm. The results show that using a 2 mm offset in this study case can increase hydrogen storage capacity by 22 % while maintaining the same charging time of less than 4500 s. The combination of both proposed methods can increase the overall MH bed chamber by 66.22 % compared to previous initial research that acts as proof of concept.

[N x H3x+1 +][BH4 −] (x = 1−5): role of polynuclear superalkalis in chemical hydrogen storage

Ammonium borohydride, [NH4 +][BH4 −], despite its high gravimetric hydrogen density, can not be used for hydrogen storage due to its instability against dehydrogenation. In this paper, we have replaced NH4 + with polynuclear N x H3x+1 + cations and studied the resulting [N x H3x+1 +][BH4 −] complexes for x = 2–5 using density functional theory. N x H3x+1 + are superalkali cations, whose vertical electron affinity is lower than the ionisation energy of alkali cations. Their binding energy, dehydrogenation energy and enthalpy, being higher than that of [NH4 +][BH4 −], increase with an increase in x. Thus, these complexes are more stable than [NH4 +][BH4 −], which comes at the cost of slightly decreased gravimetric hydrogen density. The enhanced stability of [N x H3x+1 +][BH4 −] complexes is a consequence of the lower vertical electron affinity, i.e. the superalkali properties of N x H3x+1 + cations. Further, their stability against the loss of ammonia suggests a possible route of synthesis of these complexes. Thus, the superalkalis play an important role in the design of more stable and novel borohydrides for hydrogen storage.

Delayed ammonia release of ammonia borane hydrolysis by citric acid

Ammonia borane (AB), with high hydrogen density and stability under ambient conditions, readily releases hydrogen via catalyzed hydrolysis. However, ammonia, a byproduct of hydrogen release, limits its utilization. Citric acid, a safe and cost-effective acid catalyst, for the acid catalyst of AB hydrolysis was investigated in this study to mitigate ammonia emissions while enhancing hydrogen release. Maximal hydrogen release (3 eq.H2) and ammonia emission suppression (<0.5 ppm) were achieved using a 2-mol/L AB aqueous solution adding into citric acid powder (molar ratio of AB: citric acid = 1:1). In contrast, the amount of hydrogen release at other concentrations and/or using the mixing method was below 2.7 mol/mol AB within several hours. Ammonia re-released even after hydrogen release in the case of high AB concentration (e.g. >4 mol/L AB aqueous solution with citric acid powder (molar ratio of AB: citric acid = 1:1)) in the solution because of formation of borate ester (1:2 borate–diol molar ratio) via mono-ammonium citrate (a borate-ester precursor), which was revealed by the solution NMR. These results reveal a cost-effective and simple on-way method for hydrogen release with suppressed impurities. Furthermore, understanding impurity generation mechanisms can contribute to utilizing AB-derived hydrogen.

Effect of multi-cusp magnetic fields to generate a high-density hydrogen plasma inside a low pressure H2 cylindrical hollow cathode discharge

Based on probe measurements, the plasma density in a low pressure H2 radio-frequency (RF) magnetized cylindrical hollow-cathode capacitively coupled plasma (CCP) is demonstrated to be enhanced by applying a multi-cusp magnetic field (MCMF). CCPs can be used for fabricating functional thin-films, but are currently limited by low plasma densities of less than or about 1016 m−3. It is found that a maximum plasma density of 2.51, 2.88, and 3.14 × 1016 m−3 is obtained at 3, 4 and 5 Pa, respectively. The employed MCMF arrangement contributes to achieving superior plasma uniformity, both in axial and radial direction, at an RF power of 50 W.

Visible-Light-Driven Hydrogen Release from Dye-Sensitized Hydrogen Boride Nanosheets.

Hydrogen boride (HB) nanosheets are expected to be safe and lightweight hydrogen carriers because of their high gravimetric hydrogen density (8.5 wt %) and photon-driven hydrogen release under mild conditions. However, previously reported HB nanosheets respond only to ultraviolet (UV) light to release hydrogen. In this study, we develop dye-modified HB nanosheets that can release hydrogen under visible light irradiation (>470 nm) without heat input. Hydrogen generation is initiated by electron injection from excited dye molecules into the conduction band of the HB nanosheets. The conduction band of the HB nanosheets is formed by the antibonding states of the B 2py and H 1s atomic orbitals, and the electrons injected from the dye molecules react with the protons of the HB nanosheets to release gaseous hydrogen molecules. Although the hydrogen production is terminated after long-term light irradiation owing to dye oxidation and/or loss of protons in HB nanosheets, the total amount of the released hydrogen molecules corresponds to approximately 25% of the protons in HB nanosheets even under the extra mild conditions. The addition of a sacrificial agent like iodine ions and a proton source like formic acid sustained the H2 generation from the dye-modified HB nanosheets under visible light irradiation for long term.

Phase manipulating toward Ni catalysts via lattice nitrogen endows high energy density hydrogen gas battery

Metastable structures commonly generate unique catalytic effects. However, it is challenging to prepare due to thermodynamic limitations. Here, we first propose a nitrogen insertion strategy for Ni phase manipulating in alkaline hydrogen oxidation reaction (HOR). With the incremental lattice nitrogen, face centered cubic (fcc), bi-mixed fcc and N-induced an unconventional hexagonal close packed (N-u-hcp), tri-mixed fcc-Ni/N-u-hcp-Ni/Ni3N and Ni3N phase evolves successively, with corresponding volcanic HOR activities. Specifically, the biphasic fcc-Ni/N-u-hcp-Ni shows highest activity of 67 A g−1. Theoretical calculations show that lattice nitrogen reduce the formation energy of biphasic Ni, and this biphasic structure could provide electron rich interface to optimize the adsorption of H* and OH*. As a proof-of-concept for Ni-H2 battery, the gas diffusion electrode prepared with this biphasic Ni catalyst achieves an 8 Ah Ni-H2 battery with 163 Wh kg−1. This study provides an inspiration for the controllable synthesis of metastable nano-catalysts and demonstrates the efficient catalysis in practical hydrogen energy applications.

First-principles calculations to investigate Mg3XH8 (X = Ca, Sc, Ti, V, Cr, Mn) materials for hydrogen storage

An ideal hydrogen storage material is a key topic in efficient hydrogen energy utilization. We have explored several potential hydrogen storage materials Mg3XH8 (X = Ca, Sc, Ti, V, Cr, Mn) by first-principles calculations. The studied materials all belong to lightweight hydrogen storage materials. The normal phonon dispersion spectrum indicates, without regard to other materials, at least Mg3TiH8 and Mg3VH8 are completely stable in dynamics, which is also demonstrated by elastic stability criteria. The elastic properties show that they are all ductile materials with the applicable potential in flexible fields. Besides, they are gapless and metallic in band structures. With the correction of Hubbard values, all transition metal based Mg3XH8 materials are magnetic materials with magnetic moments of 0.34 μB for Mg3ScH8, and 2.14 μB for Mg3TiH8, 1.29 μB for Mg3TiH8, 2.65 μB for Mg3TiH8 and 4.86 μB for Mg3MnH8, respectively. Whereas Mg3CrH8 and Mg3MnH8 exhibit highly light active in infrared and visible region. Considering overall structural stability, excellent mechanical properties, high gravimetric hydrogen density (6.21% and 6.07%) and moderate hydrogen desorption temperature (∼350 K), Mg3TiH8 and Mg3VH8 are considered as the candidates for promising hydrogen storage materials. Besides, Due to half-metallic nature, they are also potential in spin electronic devices.

Non-covalently crosslinked networks MXene-doped poly(eutectic) conductive elastomers with antimicrobial, self-healing, tunable mechanical properties, and wide temperature durability

Poly(eutectic) elastomers, as an emerging category of flexible electronic materials, have garnered growing interest for their cost-effectiveness, non-volatility, and biocompatibility. Nonetheless, they encounter challenges including limited functionalities, sensitivity, durability, and mechanical properties. This study involved synthesizing various MXene-doped poly(eutectic) elastomers using robust acrylamide and soft acrylic acid as organic monomers, minor MXene nanosheets as inorganic fillers and physical crosslinkers, and a rapid in-situ photopolymerization method within 2 min. Owing to the synergistic effect of thermodynamic self-assembly, high-density hydrogen bonding, and cation-dipole interactions in the matrix networks, the resulting non-covalently crosslinked elastomers exhibited remarkable mechanical strength (up to ∼ 16.2 MPa) and impressive tensile properties (nearly 700 %), along with rapid electrical self-healing (within 0.046 s) and the ability to withstand loads up to 2500 times their weight following self-healing without fracturing. Notably, these elastomers also demonstrated excellent microstrain (1 %–10 %) sensitivity with a gauge factor of 2.02, wide temperature tolerance (−20 °C ∼ 60 °C), outstanding harsh temperature durability (−20 °C) exceeding 22,000 cycles, and antibacterial properties. Furthermore, these elastomers-assembled strain sensors displayed real-time and rapid response in human motion detection and wireless signal transmission, presenting a promising approach for designing functionally integrated elastomeric materials.

Development of Ti–V–Cr–Mn–Mo–Ce high-entropy alloys for high-density hydrogen storage in water bath environments

Development of Ti–V–Cr–Mn–Mo–Ce high-entropy alloys for high-density hydrogen storage in water bath environments

Metal hydroxide hybridized Pd catalysts via in-situ etching for high current density and pH-universal hydrogen evolution reaction

The development of highly efficient and innovative electrocatalysts is crucial for the commercialization of the hydrogen evolution reaction (HER) at high current densities. An electrocatalyst consisting of Pd nanoparticles electrodeposited on nickel foam (NF) treated with ferric chloride etching, yielding a Pd content of 0.53 wt%, was synthesized. This PdFe/NF-24 h catalyst demonstrated outstanding HER performance across a wide pH range, requiring overpotentials of only 302 mV, 96.4 mV and 637.9 mV to achieve a current density of 1000 mA/cm2 in 1 M KOH, 0.5 M H2SO4 and 1 M Phosphate Buffer Saline (PBS) electrolytes, respectively. The ferric chloride etching increased the active surface area, while iron doping optimized the hydrogen adsorption free energy on Pd. Furthermore, the presence of metal hydroxides facilitated the dissociation of water into adsorbed hydrogen, which then bound to active sites on the Pd surface to produce hydrogen, thereby enhancing the efficiency of hydrogen production. The catalyst operated at 1000 mA/cm2 in 1 M KOH solution for 222 h without degradation; it maintained stability for 124 h in 30 % KOH solution; in 0.5 M H2SO4 solution, it retained 99.6 % performance for 77 h and it remained stable for 230 h in 1 M PBS solution.