Rational design of an acceptor-chromophore-relay-catalyst tetrad assembly for water oxidation.

We report the step-by-step synthesis of a precious metal-free acceptor-chromophore-relay-catalyst tetrad assembly that exhibits a turnover frequency (TOF) of 7.5 × 10-3 s-1 under neutral conditions. Transient absorption spectroscopic studies indicate that upon fullerenol incorporation into the investigated complexes, charge separation efficiency increases considerably.

"Plug and Play" Photosensitizer-Catalyst Dyads for Water Oxidation.

We present a simple and easy-to-scale synthetic method to plug common organic photosensitizers into a cyanide-based network structure for the development of photosensitizer-water oxidation catalyst (PS-WOC) dyad assemblies for the photocatalytic water oxidation process. Three photosensitizers, one of which absorbs red light similar to P680 in photosystem II, were utilized to harvest different regions of the solar spectrum. Photosensitizers are covalently coordinated to CoFe Prussian blue structures to prepare PS-WOC dyads. All dyads exhibit steady water oxidation catalytic activities throughout a 6 h photocatalytic experiment. Our results demonstrate that the covalent coordination between the PS and WOC group not only enhances the photocatalytic activity but also improves the robustness of the organic PS group. The photocatalytic activity of "plug and play" dyads relies on several structural and electronic parameters, including the position of the energy levels of the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) of the PS with respect to the HOMO level of the catalytic site, the intensity and wavelength of the absorption band of the PS, and the number of catalytic sites.

Light-Driven Water Oxidation with Ligand-Engineered Prussian Blue Analogues.

The elucidation of the ideal coordination environment of a catalytic site has been at the heart of catalytic applications. Herein, we show that the water oxidation activities of catalytic cobalt sites in a Prussian blue (PB) structure could be tuned systematically by decorating its coordination sphere with a combination of cyanide and bidentate pyridyl groups.  K0.1[Co(bpy)]2.9[Fe(CN)6]2 ([Cobpy-Fe]), K0.2[Co(phen)]2.8[Fe(CN)6]2 ([Cophen-Fe]), {[Co(bpy)2]3[Fe(CN)6]2}[Fe(CN)6]1/3 ([Cobpy2-Fe]), and {[Co(phen)2]3[Fe(CN)6]2}[Fe(CN)6]1/3 Cl0.11 ([Cophen2-Fe]) were prepared by introducing bidentate pyridyl groups (phen: 1,10-phenanthroline, bpy: 2,2'-bipyridine) to the common synthetic protocol of Co-Fe Prussian blue analogues. Characterization studies indicate that [Cobpy2-Fe] and [Cophen2-Fe] adopt a pentanuclear molecular structure, while [Cobpy-Fe] and [Cophen-Fe] could be described as cyanide-based coordination polymers with lower-dimensionality and less crystalline nature compared to the regular Co-Fe Prussian blue analogue (PBA), K0.1Co2.9[Fe(CN)6]2 ([Co-Fe]). Photocatalytic studies reveal that the activities of [Cobpy-Fe] and [Cophen-Fe] are significantly enhanced compared to those of [Co-Fe], while molecular [Cobpy2-Fe] and [Cophen2-Fe] are inactive toward water oxidation. [Cobpy-Fe] and [Cophen-Fe] exhibit upper-bound turnover frequencies (TOFs) of 1.3 and 0.7 s-1, respectively, which are ∼50 times higher than that of [Co-Fe] (1.8 × 10-2 s-1). The complete inactivity of [Cobpy2-Fe] and [Cophen2-Fe] confirms the critical role of aqua coordination to the catalytic cobalt sites for oxygen evolution reaction (OER). Computational studies show that bidentate pyridyl groups enhance the susceptibility of the rate-determining Co(IV)-oxo species to the nucleophilic water attack during the critical O-O bond formation. This study opens a new route toward increasing the intrinsic water oxidation activity of the catalytic sites in PB coordination polymers.

Electrodeposited cobalt hexacyanoferrate electrode as a non-enzymatic glucose sensor under neutral conditions.

A CoFe Prussian blue analogue (CoFe PB) modified FTO electrode, prepared via a facile electrodeposition method, is investigated as a non-enzymatic glucose sensor under neutral conditions. The electrode exhibits a linear detection of glucose in the 0.1-8.2 mmol/L range with a detection limit of 67 µM, a sensitivity of 18.69 µA/mM.cm2, and a fast response time of less than 7 s under neutral conditions. Its stability is confirmed with both electrochemical experiments and characterization studies performed on the pristine and post-mortem electrode. We also conducted a comprehensive electrochemical analysis to elucidate the identity of the active site and the glucose oxidation mechanism on the Prussian blue surface.

Photocatalytic water oxidation with a Prussian blue modified brown TiO2.

A recently emerging visible light-absorbing semiconductor, brown TiO2 (b-TiO2), was coupled with a CoFe Prussian blue (PB) analogue to prepare an entirely earth-abundant semiconductor/water oxidation catalyst hybrid assembly. PB/b-TiO2 exhibits a sevenfold higher photocatalytic water oxidation activity compared to b-TiO2. An elegant band alignment unified with the optical absorption of b-TiO2 and excellent electronic dynamics of PB yield a high-performance photocatalytic system.

How to Build Prussian Blue Based Water Oxidation Catalytic Assemblies: Common Trends and Strategies.

Prussian blue (PB) and its analogues (PBAs) have at least a three-century-long history in coordination chemistry. Recently, cobalt-based PBAs have been acknowledged as efficient and robust water oxidation catalysts. Given the flexibility in their synthesis, the structure and morphology of cobalt-based PBAs have been modified for enhanced catalytic activity under electrochemical (EC), photocatalytic (PC), and photoelectrochemical (PEC) conditions. Here, in this review, the work on cobalt-based PBAs is presented in four sections: i) electrocatalytic water oxidation with bare PBAs, ii) photocatalytic processes in the presence of a photosensitizer (PS), iii) photoelectrochemical water oxidation by coupling PBAs to proper semiconductors (SCs), and iv) the utilization of PBA-PS assemblies coated on SCs for the dye-sensitized photoelectrochemical water oxidation. This review will guide readers through the structure and catalytic activity relationship in cobalt-based PBAs by describing the role of each structural component. Furthermore, this review aims to provide insight into common strategies to enhance the catalytic activity of PBAs.

A Robust, Precious-Metal-Free Dye-Sensitized Photoanode for Water Oxidation: A Nanosecond-Long Excited-State Lifetime through a Prussian Blue Analogue.

Herein, we establish a simple synthetic strategy affording a heterogeneous, precious metal-free, dye-sensitized photoelectrode for water oxidation, which incorporates a Prussian blue (PB) structure for the sensitization of TiO2 and water oxidation catalysis. Our approach involves the use of a Fe(CN)5 bridging group not only as a cyanide precursor for the formation of a PB-type structure but also as an electron shuttle between an organic chromophore and the catalytic center. The resulting hetero-functional PB-modified TiO2 electrode demonstrates a low-cost and easy-to-construct photoanode, which exhibits favorable electron transfers with a remarkable excited state lifetime on the order of nanoseconds and an extended light absorption capacity of up to 500 nm. Our approach paves the way for a new family of precious metal-free robust dye-sensitized photoelectrodes for water oxidation, in which a variety of common organic chromophores can be employed in conjunction with CoFe PB structures.

A Noble-Metal-Free Heterogeneous Photosensitizer-Relay Catalyst Triad That Catalyzes Water Oxidation under Visible Light.

An entirely earth-abundant chromophore-relay water oxidation catalyst triad system, which is robust and efficient at neutral pH, is presented. The synthesis involves the coordination of a porphyrin derivative to a bridging Fe(CN)5 group, which is then reacted with Co ions to prepare a covalently linked chromophore-Prussian blue analogue assembly. Light-driven water oxidation studies in the presence of an electron scavenger indicate that the triad is active and it maintains a steady activity for at least three hours. Transient absorption experiments and computational studies reveal that the Fe(CN)5 group is more than a linker as it takes part in electron-transfer and co-operates with porphyrin in the charge separation process.

Examination of gas and solid products during the preparation of activated carbon using phosphoric acid.

Activating agents play significant roles in the preparation of activated carbon (AC) from biomasses and their wastes, which are widely used in AC production. Application methods are also important for the production process. Products give remarkable ideas regarding the method and heat treatment process. The activated carbon was produced from waste tea in accordance with either the conventional method or microwave energy pretreated method using phosphoric acid (H3PO4) as activating agent. The yields of the activated carbons were 51.8% for conventional method and 46.0% for microwave pretreated method. The acid suppressed the formation of tar and promoted the amount of solid and aromatic structure accordance to sp2 hybridisation. Additionally, the waste tea was directly carbonised (without H3PO4) and the yield was 36.3%. Major gas (H2, CH4, C2H6, C2H4, CO2 and CO) products obtained during heat treatment process in a conventional furnace were examined in terms of quantity and quality. The solid products were characterised in terms of surface area, pore size and surface properties. The result of gas analysis showed that phosphoric acid affected formation of activated carbon mechanism and significant reactions occurred during microwave pretreatment process.

Catalytic Properties of Vanadium Diselenide: A Comprehensive Study on Its Electrocatalytic Performance in Alkaline, Neutral, and Acidic Media.

Here, we report the synthesis of vanadium diselenide (VSe2) three-dimensional nanoparticles (NPs) and two-dimensional (2D) nanosheets (NSs) utilizing nanosecond pulsed laser ablation technique followed by liquid-phase exfoliation. Furthermore, a systematic study has been conducted on the effect of NP and NS morphologies of VSe2 in their catalytic activities toward oxygen reduction reaction (ORR), oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) under alkaline, neutral, and acidic conditions. Research on VSe2 clearly demonstrates that these morphologies do not have a significant difference for ORR and OER; however, a drastic effect of morphology was observed for HER. The ORR activity of both NSs and NPs involves ∼2.85 numbers of electrons with the Tafel slope of 120 mV/dec in alkaline and neutral pH. In alkaline solution, NPs are proved to be an efficient catalyst for OER with an onset potential 1.5 V; however, for HER, NSs have a better onset potential of -0.25 V. Moreover, the obtained NPs have also better catalytic activity with a 400 mV anodic shift in the onset potential compared to NSs. These results provide a reference point for the future application of VSe2 in energy storage and conversion devices and mass production of other 2D materials.