A perspective on three sustainable hydrogen production technologies with a focus on technology readiness level, cost of production and life cycle environmental impacts.

Hydrogen will play an indispensable role as both an energy vector and as a molecule in essential products in the transition to climate neutrality. However, the optimal sustainable hydrogen production system is not definitive due to challenges in energy conversion efficiency, economic cost, and associated marginal abatement cost. This review summarises and contrasts different sustainable hydrogen production technologies including for their development, potential for improvement, barriers to large-scale industrial application, capital and operating cost, and life-cycle environmental impact. Polymer electrolyte membrane water electrolysis technology shows significant potential for large-scale application in the near-term, with a higher technology readiness level (expected to be 9 by 2030) and a levelized cost of hydrogen expected to be 4.15-6 €/kg H2 in 2030; this equates to a 50% decrease as compared to 2020. The four-step copper-chlorine (Cu-Cl) water thermochemical cycle can perform better in terms of life cycle environmental impact than the three- and five-step Cu-Cl cycle, however, due to system complexity and high capital expenditure, the thermochemical cycle is more suitable for long-term application should the technology develop. Biological conversion technologies (such as photo/dark fermentation) are at a lower technology readiness level, and the system efficiency of some of these pathways such as biophotolysis is low (less than 10%). Biomass gasification may be a more mature technology than some biological conversion pathways owing to its higher system efficiency (40%-50%). Biological conversion systems also have higher costs and as such require significant development to be comparable to hydrogen produced via electrolysis.

A review of water electrolysis-based systems for hydrogen production using hybrid/solar/wind energy systems.

Hydrogen energy, as clean and efficient energy, is considered significant support for the construction of a sustainable society in the face of global climate change and the looming energy revolution. Hydrogen is one of the most important chemical substances on earth and can be obtained through various techniques using renewable and nonrenewable energy sources. However, the necessity for a gradual transition to renewable energy sources significantly hampers efforts to identify and implement green hydrogen production paths. Therefore, this paper's objective is to provide a technological review of the systems of hydrogen production from solar and wind energy utilizing several types of water electrolyzers. The current paper starts with a short brief about the different production techniques. A detailed comparison between water electrolyzer types and a complete illustration of hydrogen production techniques using solar and wind are presented with examples, after which an economic assessment of green hydrogen production by comparing the costs of the discussed renewable sources with other production methods. Finally, the challenges that face the mentioned production methods are illuminated in the current review.

Rewiring cyanobacterial photosynthesis by the implementation of an oxygen-tolerant hydrogenase.

Molecular hydrogen (H2) is considered as an ideal energy carrier to replace fossil fuels in future. Biotechnological H2 production driven by oxygenic photosynthesis appears highly promising, as biocatalyst and H2 syntheses rely mainly on light, water, and CO2 and not on rare metals. This biological process requires coupling of the photosynthetic water oxidizing apparatus to a H2-producing hydrogenase. However, this strategy is impeded by the simultaneous release of oxygen (O2) which is a strong inhibitor of most hydrogenases. Here, we addressed this challenge, by the introduction of an O2-tolerant hydrogenase into phototrophic bacteria, namely the cyanobacterial model strain Synechocystis sp. PCC 6803. To this end, the gene cluster encoding the soluble, O2-tolerant, and NAD(H)-dependent hydrogenase from Ralstonia eutropha (ReSH) was functionally transferred to a Synechocystis strain featuring a knockout of the native O2 sensitive hydrogenase. Intriguingly, photosynthetically active cells produced the O2 tolerant ReSH, and activity was confirmed in vitro and in vivo. Further, ReSH enabled the constructed strain Syn_ReSH+ to utilize H2 as sole electron source to fix CO2. Syn_ReSH+ also was able to produce H2 under dark fermentative conditions as well as in presence of light, under conditions fostering intracellular NADH excess. These findings highlight a high level of interconnection between ReSH and cyanobacterial redox metabolism. This study lays a foundation for further engineering, e.g., of electron transfer to ReSH via NADPH or ferredoxin, to finally enable photosynthesis-driven H2 production.

Ultralong Nanostructured Carbon Nitride Wires and Self-Standing C-Rich Filters from Supramolecular Microspheres.

The rational design of ultralong carbon nitride nanostructures is highly attractive due to their high aspect ratio alongside their high surface-to-bulk ratio, which make them suitable candidates for various applications such as photocatalysts, water treatment, and sensors. However, the synthesis of ultralong, continuous carbon nitride wires is highly challenging. Here we report the synthesis of 4 cm long and large lateral size carbon nitride wires by utilizing unique supramolecular spheres composed of graphitic carbon nitride (g-CN) monomers as the reactants. In situ scanning electron microscopy studies reveal that upon calcination the g-CN wires spontaneously start to grow from the spheres, while the remaining assembly which acts as a substrate creates self-standing carbon-rich g-CN porous films. The different morphology, chemical composition, and electronic properties of the wires and carbon-rich g-CN allow their utilization as both photocatalyst and water cleaning materials. The g-CN wires exhibit excellent photoactivity for hydrogen production whereas the porous carbon-rich g-CN porous film can be efficiently used for water cleaning applications. The reported work opens opportunities for tailored design of g-CN nanostructures and their use as multifunctional materials for photocatalysis, sensing, and other energy-related applications.