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Electrocatalytic activity of multi-valence metal oxides for oxygen evolution reaction (OER) arises from various interactions among the constituent metal elements. Although the high-valence metal ions attract recent attentions due to the interactions with their neighboring 3d transition metal catalytic center, atomic-scale explanations for the catalytic efficiencies are still lacking. Here, by employing density functional theory predictions and experimental verifications, unprecedented electronic isolation of the catalytic 3d center (M 2+ ) induced by the surrounding high-valence ions such as W 6+ is discovered in multivalent oxides MWO 4 (M = Ti, V, Cr, Mn, Fe, Co, Ni, Cu, and Zn). Due to W 6+ 's extremely high oxidation state with the minimum electron occupations (d 0 ), the surrounding W 6+ blocks electron transfer toward the catalytic M 2+ ions and completely isolates the ions electronically. Now, the isolated M 2+ ions solely perform OER without any assistant electron flow from the adjacent metal ions, and thus the original strong binding energies of Cr with OER intermediates are effectively moderated. Through exploiting "electron isolators" such as W 6+ surrounding the catalytic ion, exploring can be done beyond the conventional materials such as Ni- or Co-oxides into new candidate groups such as Cr and Mn on the left side of the periodic table for ideal OER., (© 2024 The Authors. Small published by Wiley‐VCH GmbH.)

Despite intensive studies over decades, the development of electrocatalysts for acidic water splitting still relies on platinum group metals, especially Pt and Ir, which are scarce, expensive, and poorly sustainable. Because such problems can be alleviated, Ru-based bifunctional catalysts such as rutile RuO 2 have recently emerged. However, RuO 2 has a relatively low activity for hydrogen evolution reactions (HER) and low stability for oxygen evolution reactions (OER) under acidic conditions. In this study, the synthesis of a RuO x -based bifunctional catalyst (RuSiW) for acidic water splitting via the electrochemical evolution from Ru-based polyoxometalates at cathodic potentials is reported. RuSiW consists of the nanocrystalline RuO 2 core and Si,W-codoped RuO x shell. RuSiW exhibits outstanding HER and OER activity comparable to Pt/C and RuO 2 , respectively, with high stability. Computational analysis suggests that the codoping of RuO x with W and Si synergistically improves the HER activity of otherwise poor RuO 2 by shifting the d-band center and optimizing atomic configurations beneficial for proper hydrogen adsorption. This study provides insights into the design and synthesis of unprecedented bifunctional electrocatalysts using catalytically inactive and less explored elements, such as Si and W., (© 2023 Wiley-VCH GmbH.)

Efficient electrochemical hydrogen production and biomass refinery are crucial for the decarbonization of various sectors. However, their energy-intensive nature and low efficiency have hindered their practical application. In this study, earth-abundant and non-toxic photocatalysts that can produce hydrogen and reform biomass efficiently, utilizing unlimited solar energy, are presented. The approach involves using low-bandgap Si flakes (SiF) for efficient light-harvesting, followed by modification with Ni-coordinated N-doped graphene quantum dots (Ni-NGQDs) to enable efficient and stable light-driven biomass reforming and hydrogen production. When using kraft lignin as a model biomass, SiF/Ni-NQGDs facilitate record-high hydrogen productivity at 14.2 mmol g cat -1  h -1 and vanillin yield of 147.1 mg g lignin -1 under simulated sunlight without any buffering agent and sacrificial electron donors. SiF/Ni-NQGDs can be readily recycled without any noticeable performance degradation owing to the prevention of deactivation of Si via oxidation. This strategy provides valuable insights into the efficient utilization of solar energy and practical applications of electro-synthesis and biomass refinement., (© 2023 The Authors. Advanced Materials published by Wiley-VCH GmbH.)

Recent studies have found that green hydrogen production and biomass utilization technologies can be combined to efficiently produce both hydrogen and value-added chemicals using biomass as an electron and proton source. However, the majority of them have been limited to proof-of-concept demonstrations based on batch systems. Here the authors report the design of modular flow systems for the continuous depolymerization and valorization of lignin and low-voltage hydrogen production. A redox-active phosphomolybdic acid is used as a catalyst to depolymerize lignin with the production of aromatic compounds and extraction of electrons for hydrogen production. Individual processes for lignin depolymerization, byproduct separation, and hydrogen production with catalyst reactivation are modularized and integrated to perform the entire process in the serial flow. Consequently, this work enabled a one-flow process from biomass conversion to hydrogen gas generation under a cyclic loop. In addition, the unique advantages of the fluidic system (i.e., effective mass and heat transfer) substantially improved the yield and efficiency, leading to hydrogen production at a higher current density (20.5 mA cm -2 ) at a lower voltage (1.5 V) without oxygen evolution. This sustainable eco-chemical platform envisages scalable co-production of valuable chemicals and green hydrogen for industrial purposes in an energy-saving and safe manner., (© 2022 The Authors. Advanced Science published by Wiley-VCH GmbH.)

The functionalization of graphene has been extensively used as an effective route for modulating the surface property of graphene, and enhancing the dispersion stability of graphene in aqueous solutions via functionalization has been widely investigated to expand its use for various applications across a range of fields. Herein, an effective approach is described for enhancing the dispersibility of graphene in aqueous solutions at different pH levels via non-covalent zwitterion functionalization. The results show that a surfactant with electron-deficient carbon atoms in its backbone structure and large π-π interactive area enables strong interactions with graphene, and the zwitterionic side terminal groups of the molecule support the dispersibility of graphene in various pH conditions. Experimental and computational studies confirm that perylene diimide amino N-oxide (PDI-NO) allows efficient functionalization and pH-independent dispersion of graphene enabled by hydration repulsion effects induced by PDI-NO. The PDI-NO functionalized graphene is successfully used in the oxygen evolution reaction as an electron mediator for boosting the electrocatalytic activity of a Ru-based polyoxometalate catalyst in an acidic medium. The proposed strategy is expected to bring significant advances in producing highly dispersible graphene in aqueous medium with pH-independent stability, thus broadening the application range of graphene., (© 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

We report the development of semiconducting melanin-based organic/inorganic hybrid photoanodes for solar water oxidation. Synthetic melanin thin-film incorporating polyoxometalate (POM) water oxidation catalysts (WOCs) are readily deposited on the surface of various n-type inorganic semiconductors (e.g., Fe 2 O 3 , BiVO 4 , and TiO 2 ) by electropolymerization. The deposition of melanin and POM hybrid (MP) thin-film results in the remarkably improved performance of an underlying semiconductor photoanode for solar water oxidation with a significantly increased photocurrent density and decreased onset potential for water oxidation through the formation of a melanin-based p-n heterojunction structure. We believe that this study can provide insights into the design and fabrication of various melanin-based optoelectronic devices by utilizing its unique physicochemical properties., (© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Efficient harvesting of unlimited solar energy and its conversion into valuable chemicals is one of the ultimate goals of scientists. With the ever-increasing concerns about sustainable growth and environmental issues, numerous efforts have been made to develop artificial photosynthetic process for the production of fuels and fine chemicals, thus mimicking natural photosynthesis. Despite the research progress made over the decades, the technology is still in its infancy because of the difficulties in kinetic coupling of whole photocatalytic cycles. Herein, we report a new type of artificial photosynthesis system that can avoid such problems by integrally coupling biocatalytic redox reactions with photocatalytic water splitting. We found that photocatalytic water splitting can be efficiently coupled with biocatalytic redox reactions by using tetracobalt polyoxometalate and Rh-based organometallic compound as hole and electron scavengers, respectively, for photoexcited [Ru(bpy)3](2+). Based on these results, we could successfully photosynthesize a model chiral compound (L-glutamate) using a model redox enzyme (glutamate dehydrogenase) upon in situ photoregeneration of cofactors., (© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Breaking the mold: Self-assembled peptide nanowires were used as a template for the synthesis of hollow polyaniline (PANI) nanotubes (see scanning electron microscopy images). The thickness and the morphology of the PANI nanostructures could be controlled readily either by varying the reaction time or by applying multiple PANI coatings.