Determining the hydronium pK[Formula: see text] at platinum surfaces and the effect on pH-dependent hydrogen evolution reaction kinetics.

Electrocatalytic hydrogen evolution reaction (HER) is critical for green hydrogen generation and exhibits distinct pH-dependent kinetics that have been elusive to understand. A molecular-level understanding of the electrochemical interfaces is essential for developing more efficient electrochemical processes. Here we exploit an exclusively surface-specific electrical transport spectroscopy (ETS) approach to probe the Pt-surface water protonation status and experimentally determine the surface hydronium pKa [Formula: see text] 4.3. Quantum mechanics (QM) and reactive dynamics using a reactive force field (ReaxFF) molecular dynamics (RMD) calculations confirm the enrichment of hydroniums (H3O[Formula: see text]) near Pt surface and predict a surface hydronium pKa of 2.5 to 4.4, corroborating the experimental results. Importantly, the observed Pt-surface hydronium pKa correlates well with the pH-dependent HER kinetics, with the protonated surface state at lower pH favoring fast Tafel kinetics with a Tafel slope of 30 mV per decade and the deprotonated surface state at higher pH following Volmer-step limited kinetics with a much higher Tafel slope of 120 mV per decade, offering a robust and precise interpretation of the pH-dependent HER kinetics. These insights may help design improved electrocatalysts for renewable energy conversion.

Platinum Surface Water Orientation Dictates Hydrogen Evolution Reaction Kinetics in Alkaline Media.

The fundamental understanding of sluggish hydrogen evolution reaction (HER) kinetics on a platinum (Pt) surface in alkaline media is a topic of considerable debate. Herein, we combine cyclic voltammetry (CV) and electrical transport spectroscopy (ETS) approaches to probe the Pt surface at different pH values and develop molecular-level insights into the pH-dependent HER kinetics in alkaline media. The change in HER Tafel slope from ∼110 mV/decade in pH 7-10 to ∼53 mV/decade in pH 11-13 suggests considerably enhanced kinetics at higher pH. The ETS studies reveal a similar pH-dependent switch in the ETS conductance signal at around pH 10, suggesting a notable change of surface adsorbates. Fixed-potential calculations and chemical bonding analysis suggest that this switch is attributed to a change in interfacial water orientation, shifting from primarily an O-down configuration below pH 10 to a H-down configuration above pH 10. This reorientation weakens the O-H bond in the interfacial water molecules and modifies the reaction pathway, leading to considerably accelerated HER kinetics at higher pH. Our integrated studies provide an unprecedented molecular-level understanding of the nontrivial pH-dependent HER kinetics in alkaline media.

Amorphous nickel hydroxide shell tailors local chemical environment on platinum surface for alkaline hydrogen evolution reaction.

In analogy to natural enzymes, an elaborated design of catalytic systems with a specifically tailored local chemical environment could substantially improve reaction kinetics, effectively combat catalyst poisoning effect and boost catalyst lifetime under unfavourable reaction conditions. Here we report a unique design of 'Ni(OH)2-clothed Pt-tetrapods' with an amorphous Ni(OH)2 shell as a water dissociation catalyst and a proton conductive encapsulation layer to isolate the Pt core from bulk alkaline electrolyte while ensuring efficient proton supply to the active Pt sites. This design creates a favourable local chemical environment to result in acidic-like hydrogen evolution reaction kinetics with a lowest Tafel slope of 27 mV per decade and a record-high specific activity and mass activity in alkaline electrolyte. The proton conductive Ni(OH)2 shell can also effectively reject impurity ions and retard the Oswald ripening, endowing a high tolerance to solution impurities and exceptional long-term durability that is difficult to achieve in the naked Pt catalysts. The markedly improved hydrogen evolution reaction activity and durability in an alkaline medium promise an attractive catalyst material for alkaline water electrolysers and renewable chemical fuel generation.

Periodic Assembly of Diblock Pt-Au Heteronanowires for the Methanol Oxidation Reaction.

Periodic assembly of heterogeneous nanoparticles provides a strategy for integrating distinct nanocatalyst blocks where their synergic effects can be explored for diverse applications. To achieve the synergistic enhancement, an intimate clean interface is preferred which however is usually plagued by the bulky surfactant molecules used in the synthesis and assembly process. Herein, we showed the creation of one-dimensional Pt-Au nanowires (NWs) with periodic alternating Pt and Au nanoblocks, by assembling Pt-Au Janus nanoparticles with the assistance of peptide T7 (Ac-TLTTLTN-CONH2). It is demonstrated that the Pt-Au NWs showed much-improved performance in the methanol oxidation reaction (MOR), exhibiting 5.3 times higher specific activity and 2.5 times higher mass activity than the current state-of-the-art commercial Pt/C catalyst. In addition, the periodic heterostructure also improves the stability of Pt-Au NWs in the MOR, where the Pt-Au NWs retained 93.9% of their initial mass activity much higher than commercial Pt/C (30.6%).

New aspects of C2 selectivity in electrochemical CO2 reduction over oxide-derived copper.

The electrocatalytic CO2 reduction to yield C2 products is of particular interest in solar-to-fuel conversion schemes. The nanocrystalline oxide derived copper (ODCu) electrodes are specifically attractive due to their high faradaic efficiency towards C2 hydrocarbons like ethylene, ethane, acetate and ethanol. However, the mechanistic understanding of this special selectivity is still an impediment. In this work, ODCu is obtained from Cu2O nanowires and employed for electrocatalytic CO2 reduction, during which ethylene is found to be the major product with a faradaic efficiency of 65% at -0.8 V (vs. RHE). By in situ photoresponse measurement, combined with the ex situ structure and composition analysis, Cu2O is demonstrated to be persistent on the surface of ODCu throughout the CO2 reduction reaction (CO2RR) even at high applied bias (-1.0 V vs. RHE), while Cu2O is not present on the bulk Cu foil. Density functional theory calculations are employed to further investigate the correlation between the surface Cu2O on ODCu and its C2 selectivity performance, which is attributed to the orbital interactions between the persistent oxide and CO2 reduction intermediates. It should be noted that uncovering the active sites is the initial step to understand the surface reaction chemistry in CO2RR; here, we propose that the presence of Cu2O is the key for C2 selectivity during CO2RR in the ODCu system, which may facilitate the development of highly efficient catalysts.

Tripeptide Derivative-Modified Glassy Carbon Electrode: A Novel Electrochemical Sensor for Sensitive and Selective Detection of Cd2+ Ions.

A N-[(Benzyloxy)carbonyl]-l-alanyl-l-prolyl-l-leucine-N-cyclohexylcyclohexanamine (Cbz-APL) tripeptide-coated glassy carbon electrode (GCE)-based sensor was used for sensitive and selective recognition of cadmium ions in environmental water. Detailed cyclic voltammetric and electrochemical impedance spectroscopic studies were performed to investigate the charge transfer and sensing activity of the developed electrochemical sensor. Square wave anodic stripping voltammetry (SWASV) was employed to further investigate the sensitivity, selectivity, validity, and applicability of the developed sensor. A sharp electrochemical signal of oxidized Cd at -0.84 V versus Ag/AgCl provides evidence for the higher sensing ability of Cbz-APL/GCE than bare GCE at -0.79 V. Moreover, on Cbz-APL/GCE, extraordinary low detection limits of 4.34 fM and linearity range of 15 nM to 0.1 pM with coefficients of correlation higher than 0.99 for Cd2+ were achieved. Besides, the influence of inorganic and organic interferents on the targeted analyte signals was examined, and high selectivity of Cbz-APL/GCE for Cd2+ ions was observed. Lastly, the validity and applicability of the developed electrochemical sensor for the detection of Cd2+ ions were checked in real water samples, and 100% recovery was obtained.

Calix[4]arene Derivative-Modified Glassy Carbon Electrode: A New Sensing Platform for Rapid, Simultaneous, and Picomolar Detection of Zn(II), Pb(II), As(III), and Hg(II).

The glassy carbon electrode was fabricated with multifunctional bis-triazole-appended calix[4]arene and then used for the simultaneous detection of Zn(II), Pb(II), As(III), and Hg(II). Before applying the square-wave anodic stripping voltammetry, the sensitivity and precision of the modified electrode was assured by optimizing various conditions such as the modifier concentration, pH of the solution, deposition potential, accumulation time, and supporting electrolytes. The modified glassy carbon electrode was found to be responsive up to picomolar limits for the aforementioned heavy metal ions, which is a concentration limit much lower than the threshold level permitted by the World Health Organization. Importantly, the designed sensing platform showed anti-interference ability, good stability, repeatability, reproducibility, and applicability for the detection of multiple metal ions. The detection limits obtained for Zn(II), Pb(II), As(III), and Hg(II) are 66.3, 14.6, 71.9, and 28.9 pM, respectively.

Radical-Triggered Chemiluminescence of Phenanthroline Derivatives: An Insight into Radical-Aromatic Interaction.

The hitherto unknown influence of 1,10-phenonthroline (1,10-phen) and its derivatives on the weak chemiluminescence (CL) of periodate-peroxide has been investigated, and a novel method for CL catalysis is described. Herein, we have deconvoluted the variation in CL intensity arising from the addition of various derivatives of 1,10-phen. Interestingly, similar derivatives of 1,10-phen show interesting differences in their reactivity toward CL. Electron-withdrawing substituents on 1,10-phen boosted the CL signals, indicating a negative charge buildup on 1,10-phen in the rate-determining step. The 1,10-phen derivatives having substitution at the C5=C6 position resulted in no CL signals due to the blockage of the reactive site. Mechanistic investigations are interpreted in terms of free radical (H2O2 reaction), followed by the oxygen atom transfer via an electrophilic attack of IO4 - (IO4 - reaction) on 1,10-phen resulting in dioxetane with enhanced CL emission. Additionally, the relationship between electronic structures and photophysical properties was investigated using density functional theory. Our results are expected to open up promising application of 1,10-phen as a molecular catalyst, providing a new strategy for metal-free catalytic CL enhancement reaction. We believe that this would foster in gleaning more detailed information on the nature of these reactions, thereby leading to a deeper understanding of the CL mechanism.

Synthesis, pH dependent photometric and electrochemical investigation, redox mechanism and biological applications of novel Schiff base and its metallic derivatives.

A novel Schiff base, 1-((2, 4-dimethylphenylimino)methyl)naphthalen-2-ol abbreviated as (HL) and its four metallic complexes were synthesized and confirmed by 1H and 13C NMR, FTIR, TGA and UV-Visible spectroscopy. Schiff base was also characterized by X-ray analysis. The photometric and electrochemical responses of all the synthesized compounds were investigated in a wide pH range. Structures of the compounds were optimized computationally for the evaluation of different physico-chemical parameters. On the basis of electrochemical results the redox mechanistic pathways of the compounds were proposed. The cytotoxicity analysis on Hela cells revealed that HL and its complexes inhibit cell growth as revealed from their IC50 values (HL):106.7µM, (L2VO): 40.66µM, (L2Sn): 5.92µM, (L2Zn): 42.82 and (L2Co): 107.68µM. The compounds were tested for anti-diabetic, triglyceride, cholesterol, anti-microbial, anti-fungal and enzyme inhibition activities. The results revealed that HL and its complexes are promising new therapeutic options as these compounds exhibit strong activity against cancer cells, diabetics, fungal and microbial inhibition.

Biological activity, pH dependent redox behavior and UV-Vis spectroscopic studies of naphthalene derivatives.

Two naphthalene derivatives, naphthalene-2,3-dicarboxylic acid (NDA) and 1,8-dimethoxynaphthalene (DMN) were screened for antioxidant and anti-diabetic activities. Biological antioxidant studies revealed NDA as more effective antioxidant as compared to DMN. Both compounds significantly increased the cholesterol level but showed varied biological activities as regards glucose and triglyceride concentrations. The cytotoxicity results evidenced DMN to significantly inhibit the cell proliferation in a dose dependent manner with IC50 of 0.13 mM. Like the biological antioxidant studies, the electrochemical results also witnessed NDA as stronger antioxidant than DMN. The pH dependent spectrophotometric and electrochemical behavior was investigated in order to provide useful mechanistic insights about the biological role of the selected compounds.