Metamorphic oxygen-evolving molecular Ru and Ir catalysts.

Today sustainable and clean energy conversion strategies are based on sunlight and the use of water as a source of protons and electrons, in a similar manner as it happens in Photosystem II. To achieve this, the charge separation state induced by light has to be capable of oxidising water by 4 protons and 4 electrons and generating molecular oxygen. This oxidation occurs by the intermediacy of a catalyst capable of finding low-energy pathways via proton-coupled electron transfer steps. The high energy involved in the thermodynamics of water oxidation reaction, coupled with its mechanistic complexity, is responsible for the difficulty of discovering efficient and oxidatively robust molecules capable of achieving such a challenging task. A significant number of Ru coordination complexes have been identified as water oxidation catalysts (WOCs) and are among the best understood from a mechanistic perspective. In this review, we describe the catalytic performance of these complexes and focus our attention on the factors that influence their performance during catalysis, especially in cases where a detailed mechanistic investigation has been carried out. The collective information extracted from all the catalysts studied allows one to identify the key features that govern the complex chemistry associated with the catalytic water oxidation reaction. This includes the stability of trans-O-Ru-O groups, the change in coordination number from CN6 to CN7 at Ru high oxidation states, the ligand flexibility, the capacity to undergo intramolecular proton transfer, the bond strain, the axial ligand substitution, and supramolecular effects. Overall, combining all this information generates a coherent view of this complex chemistry.

Reducing the Trap Density in MAPbI3 Based Perovskite Solar Cells via Bromide Substitution.

The past decade has witnessed tremendous advancement in the field of halide perovskite (PSK) as a choice of material for high-performing solar cells fabrication. Here, we investigate the impact of the halide exchange through N-bromosuccinimide (NBS) treatment in MAPbI3 based solar cells. We observed the partial halide exchange (I- to Br- ) or the filling of halide (X- ) vacancy upon treatment of different NBS concentrations experimentally by spectroscopic and diffractogram studies. We noted that halide exchange impacts the crystallization and is beneficial in improving the photovoltaic performance. The optimized 0.5 % NBS treated PSC exhibited a power conversion efficiency of 17.87 % due to an increment in open-circuit voltage (Voc ) and short circuit current (Jsc ). We noted improved perovskite crystal growth upon Br- substitution; eventually, it helps to lower the trap density, reducing non-radiative recombination and renders the enhancement of long-term stability of PSC.

Next generation of chemistry and biochemistry conference posters: Animation, augmented reality, visitor statistics, and visitors' attention.

Every branch of science needs visitors' attention during the poster presentation session at conferences, symposiums, seminars, etc. In particular, participants in the chemistry and biochemistry conference need more visual tools to explain their research work in detail. Presence of smartphones and the ability of 2D barcodes will allow chemical reactions or processes to be shown in the form of a movie, animation or augmented reality (AR). Therefore, the next generation of posters will be more interested in this view. Here, the ability of 2D barcodes or QR codes to help researchers to catch more attention in their research work was presented during a poster presentation session. In this way, the visitors showed positive attitudes to the applicability of such tools. Also, some information including the number of poster visitors and interesting topics in the conference can be collected easily which is useful for the scientific and organizing committee of conferences. As a result, biochemistry conference posters can be presented in new ways, based on animation images or video, to capture the attention of viewers and deepen their understanding of poster concepts.

A broad view on the complexity involved in water oxidation catalysis based on Ru-bpn complexes.

A new Ru complex with the formula [Ru(bpn)(pic)2]Cl2 (where bpn is 2,2'-bi(1,10-phenanthroline) and pic stands for 4-picoline) (1Cl2) is synthesized to investigate the true nature of active species involved in the electrochemical and chemical water oxidation mediated by a class of N4 tetradentate equatorial ligands. Comprehensive electrochemical (by using cyclic voltammetry, differential pulse voltammetry, and controlled potential electrolysis), structural (X-ray diffraction analysis), spectroscopic (UV-vis, NMR, and resonance Raman), and kinetic studies are performed. 12+ undergoes a substitution reaction when it is chemically (by using NaIO4) or electrochemically oxidized to RuIII, in which picoline is replaced by an hydroxido ligand to produce [Ru(bpn)(pic)(OH)]2+ (22+). The former complex is in equilibrium with an oxo-bridged species {[Ru(bpn)(pic)]2(µ-O)}4+ (34+) which is the major form of the complex in the RuIII oxidation state. The dimer formation is the rate determining step of the overall oxidation process (kdimer = 1.35 M-1 s-1), which is in line with the electrochemical data at pH = 7 (kdimer = 1.4 M-1 s-1). 34+ can be reduced to [Ru(bpn)(pic)(OH2)]2+ (42+), showing a sort of square mechanism. All species generated in situ at pH 7 have been thoroughly characterized by NMR, mass spectrometry, UV-Vis and electrochemical techniques. 12+ and 42+ are also characterized by single crystal X-ray diffraction analysis. Chemical oxidation of 12+ triggered by CeIV shows its capability to oxidize water to dioxygen.

A Ru-bda Complex with a Dangling Carboxylate Group: Synthesis and Electrochemical Properties.

Ruthenium complexes containing the tetradentate 2,2'-bipyridine-6,6'-dicarboxylato (bda2-) equatorial ligand and ortho-subsituted pyridines in the axial position have been prepared and characterized using spectroscopic, crystallographic and electrochemical techniques. Complexes [Ru(Hbda)(DMSO)(pyC)] (1) and [Ru(bda)(DMSO)(pyA)] (2) (where pyC is 2-pyridinecarboxylate, pyA is pyridine-2-ylmethanol and DMSO is dimethyl sulfoxide) have been isolated in moderate to high yields. The solid state structures of (1-H)- and 2 reveal the strong chelate effect of the axial pyridine ligand that coordinates in a bidentate fashion leaving the bda2- equatorial ligand coordinating in a tridentate mode. In solution, compound 2 shows a dynamic equilibrium between different coordination modes of the bda2- and pyA ligands. This phenomenon does not occur for 1 because the carboxylate binds stronger than the labile alcohol in 2. Cyclic voltammetry analysis of 1 reveals a complex behavior with a pH-independent wave at E1/2 = 1.12 V that is tentatively associated with the two-electron RuIV/II couple. In sharp contrast, complex 2 shows a pH-dependent one-electron wave at E1/2 = 0.83 V (pH 1), assigned to the proton-coupled electron transfer process of the RuIII/II couple and a pH-independent wave at E1/2 = 1.06 V assigned to the RuIV/III couple. Compound 2 is used to prepare complex [Ru(bda)(pic)(pyA)] (4). This complex is air sensitive and converts to complex [Ru(bda)(pic)(pyE)] (5) (where pyE is methyl 2-pyridine carboxylate) in the presence of methanol. This oxidation also occurs by applying a positive potential to an aqueous solution of 4, producing the derivative [Ru(bda)(pic)(pyC)] (3). Cyclic voltammetry of 3 shows two pH-independent one-electron oxidation waves at E1/2 = 0.64 V and E1/2 = 1.0 V, corresponding to the RuIII/II and RuIV/III couples, respectively. In addition, a water oxidation catalytic wave appears at Eonset ≈ 1.4 V. Foot-of-the-wave analysis of this catalytic wave based on a water nucleophilic attack accounts for a TOFmax = 0.63-0.74 s-1.

Behavior of Ru-bda Water-Oxidation Catalysts in Low Oxidation States.

The Ru complex [RuII (bda-κ-N2 O2 )(N-NH2 )2 ] (1; bda2- =2,2'-bipyridine-6,6'-dicarboxylate, N-NH2 =4-(pyridin-4-yl)aniline) was used as a synthetic intermediate to prepare new RuII and RuIII bda complexes that contain NO+ , MeCN, or H2 O ligands. In acidic solution complex 1 reacts with an excess of NO+ (generated in situ from sodium nitrite) to form a new Ru complex in which the aryl amine ligand N-NH2 is transformed into a diazonium salt [N-N2+ =4-(pyridin-4-yl)benzenediazonium)] together with the formation of a new Ru(NO) moiety in the equatorial zone, to generate [RuII (bda-κ-N2 O)(NO)(N-N2 )2 ]3+ (23+ ). Here the bda2- ligand binds in a κ-N2 O tridentate manner with a dangling carboxylate group. Similarly, complex 1 can also react with a coordinating solvent, such as MeCN, at room temperature to give [RuII (bda-κ-N2 O)(MeCN)(N-NH2 )2 ] (3). In acidic aqueous solutions, a related reaction occurs in which solvent water coordinates to the Ru center to form {[RuII {bda-κ-(NO)3 }(H2 O)(N-NH3 )2 ](H2 O)n }2+ (42+ ) and is strongly hydrogen-bonded with additional water molecules in the second coordination sphere. Furthermore, under acidic conditions the aniline ligands are also protonated to form the corresponding anilinium cationic ligands N-NH3+ . Additionally, the one-electron oxidized complex {[RuIII {bda-κ-(NO)3.5 }(H2 O)(N-NH3 )2 ](H2 O)n }3+ (53+ ) was characterized, in which the fractional value in the κ notation indicates the presence of an additional contact to the pseudo-octahedral geometry of the Ru center. The coordination modes of the complexes were studied in the solid state and in solution through single-crystal XRD, X-ray absorption spectroscopy, variable-temperature NMR spectroscopy, and DFT calculations. While κ-N2 O is the main coordination mode for 23+ and 3, an equilibrium that involves isomers with κ-N2 O and κ-NO2 coordination modes and neighboring hydrogen-bonded water molecules is observed for 42+ and 53+ .