Destruction of a Copper Metal-Organic Framework to Induce CuPt Growth as a Heterojunction Catalyst for Hydrogen Peroxide Sensing.

Assembling bimetallic alloys (BAs) with metal-organic frameworks (MOFs) to form heterojunctions has emerged as a promising strategy for the construction of highly active electrocatalysts. However, the current approaches to prepare BA@MOF heterojunctions suffer from poor controllability. In this work, a fascinating method involving partial thermal reduction and galvanic replacement to induce CuPt growth on a CuHHTP MOF (HHTP=2,3,6,7,10,11-hexahydroxytriphenylene) is reported in order to construct a CuPt@CuHHTP heterojunction. The size of the CuPt nanoparticles can be effectively regulated by modifying the reduction temperature. The resultant CuPt NP@CuHHTP heterojunction nanoarrays exhibit high electrocatalytic activity and potential as an electrochemical H2 O2 sensor with a low detection limit (5 nM), high sensitivity (6.942 mA ⋅ mM-1 ⋅ cm-2 ), and outstanding selectivity. This in situ approach provides not only new insights into the preparation of BA@MOF-based heterojunctions but also an effective approach for the optimization of the catalytic performance of MOFs and related materials.

Catalytic Hydrogenation of Nitroarenes over Ag33 Nanoclusters: The Ligand Effect.

Using ligand-protected metallic nanoclusters with atomic precision as catalysts and elucidating its ligand effect in the catalysis are the prerequisites to deepen the structure-catalysis relationship of nanoclusters at the molecular level. Herein, a series of Ag33 nanoclusters protected with different thiolate ligands (2-phenylethanethiol, 4-chlorobenzyl mercaptan, and 4-methoxybenzyl mercaptan as precursors) were synthesized and used as heterogeneous catalysts for the conversion of nitroarenes to arylamine with NaBH4 as reductant. The obtained nanoclusters exhibited ligand-dependent catalytic activity, with benzyl thiolate ligands distinctly superior to the phenethyl thiolate ligands. DFT calculations revealed that the ligand regulated catalytic activity of the nanoclusters was ascribed to the H-π and π-π interactions between the ligands and the substrates, owing to the presence of phenyl rings in these structures. This work highlighted the importance of the ligands on the metallic nanoclusters in catalysis and provides a strategy to regulate the catalytic activity by utilizing weak interactions between the catalysts and the substrates.

Galvanic Replacement-Driven Transformations of Atomically Intermixed Bimetallic Colloidal Nanocrystals: Effects of Compositional Stoichiometry and Structural Ordering.

Galvanic replacement reactions dictated by deliberately designed nanoparticulate templates have emerged as a robust and versatile approach that controllably transforms solid monometallic nanocrystals into a diverse set of architecturally more sophisticated multimetallic hollow nanostructures. The galvanic atomic exchange at the nanoparticle/liquid interfaces induces a series of intriguing structure-transforming processes that interplay over multiple time and length scales. Using colloidal Au-Cu alloy and intermetallic nanoparticles as structurally and compositionally fine-tunable bimetallic sacrificial templates, we show that atomically intermixed bimetallic nanocrystals undergo galvanic replacement-driven structural transformations remarkably more complicated than those of their monometallic counterparts. We interpret the versatile structure-transforming behaviors of the bimetallic nanocrystals in the context of a unified mechanistic picture that rigorously interprets the interplay of three key structure-evolutionary pathways: dealloying, Kirkendall diffusion, and Ostwald ripening. By deliberately tuning the compositional stoichiometry and atomic-level structural ordering of the Au-Cu bimetallic nanocrystals, we have been able to fine-maneuver the relative rates of dealloying and Kirkendall diffusion with respect to that of Ostwald ripening through which an entire family of architecturally distinct complex nanostructures are created in a selective and controllable manner upon galvanic replacement reactions. The insights gained from our systematic comparative studies form a central knowledge framework that allows us to fully understand how multiple classic effects and processes interplay within the confinement by a colloidal nanocrystal to synergistically guide the structural transformations of complex nanostructures at both the atomic and nanoparticulate levels.

Nanoscale Surface Curvature Effects on Ligand-Nanoparticle Interactions: A Plasmon-Enhanced Spectroscopic Study of Thiolated Ligand Adsorption, Desorption, and Exchange on Gold Nanoparticles.

The interfacial adsorption, desorption, and exchange behaviors of thiolated ligands on nanotextured Au nanoparticle surfaces exhibit phenomenal site-to-site variations essentially dictated by the local surface curvatures, resulting in heterogeneous thermodynamic and kinetic profiles remarkably more sophisticated than those associated with the self-assembly of organothiol ligand monolayers on atomically flat Au surfaces. Here we use plasmon-enhanced Raman scattering as a spectroscopic tool combining time-resolving and molecular fingerprinting capabilities to quantitatively correlate the ligand dynamics with detailed molecular structures in real time under a diverse set of ligand adsorption, desorption, and exchange conditions at both equilibrium and nonequilibrium states, which enables us to delineate the effects of nanoscale surface curvature on the binding affinity, cooperativity, structural ordering, and the adsorption/desorption/exchange kinetics of organothiol ligands on colloidal Au nanoparticles. This work provides mechanistic insights on the key thermodynamic, kinetic, and geometric factors underpinning the surface curvature-dependent interfacial ligand behaviors, which serve as a central knowledge framework guiding the site-selective incorporation of desired surface functionalities into individual metallic nanoparticles for specific applications.

Residual Silver Remarkably Enhances Electrocatalytic Activity and Durability of Dealloyed Gold Nanosponge Particles.

Percolation dealloying of multimetallic alloys entangles the selective dissolution of the less-noble elements with nanoscale restructuring of the more-noble components, resulting in the formation of spongelike, nanoporous architectures with a unique set of structural characteristics highly desirable for heterogeneous catalysis. Although the dealloyed nanoporous materials are compositionally dominated by the more-noble elements, they inevitably contain residual less-noble elements that cannot be completely removed through the percolation dealloying process. How to employ the less-noble elements to rationally guide the structural evolution and optimize the catalytic performances of the dealloyed noble metal nanocatalysts still remains largely unexplored. Here, we have discovered that incorporation of Ag into Au-Cu binary alloy nanoparticles substantially enhances the Cu leaching kinetics while effectively suppressing the ligament coarsening during the nanoporosity-evolving percolation dealloying of the alloy nanoparticles. The controlled coleaching of Ag and Cu from Au-Ag-Cu ternary alloy nanoparticles provides a unique way to optimize both the surface area-to-mass ratios and specific activities of the dealloyed nanosponge particles for the electrocatalytic oxidation of alcohols. The residual Ag in the fully dealloyed nanosponge particles plays crucial roles in stabilizing the surface active sites and maintaining the nanoporous architectures during the electrocatalytic reactions, thereby greatly enhancing the durability of the electrocatalysts. The insights gained from this work shed light on the underlying roles of residual less-noble elements that are crucial to the rational optimization of electrocatalysis on noble-metal nanostructures.

General synthesis and atomic arrangement identification of ordered Bi-Pd intermetallics with tunable electrocatalytic CO2 reduction selectivity.

Intermetallic compounds (IMCs) with fixed chemical composition and ordered crystallographic arrangement are highly desirable platforms for elucidating the precise correlation between structures and performances in catalysis. However, diffusing a metal atom into a lattice of another metal to form a controllably regular metal occupancy remains a huge challenge. Herein, we develop a general and tractable solvothermal method to synthesize the Bi-Pd IMCs family, including Bi2Pd, BiPd, Bi3Pd5, Bi2Pd5, Bi3Pd8 and BiPd3. By employing electrocatalytic CO2 reduction as a model reaction, we deeply elucidated the interplay between Bi-Pd IMCs and key intermediates. Specific surface atomic arrangements endow Bi-Pd IMCs different relative surface binding affinities and adsorption configuration for *OCHO, *COOH and *H intermediate, thus exhibiting substantially selective generation of formate (Bi2Pd), CO (BiPd3) and H2 (Bi2Pd5). This work provides a comprehensive understanding of the specific structure-performance correlation of IMCs, which serves as a valuable paradigm for precisely modulating catalyst material structures.

Coupling plasmon and catalytic-active hotspots of Au@Pt core-satellite nanoparticles for in-situ spectroscopic observation of plasmon-promoted decarboxylation.

Plasmon-induced hot carriers are a promising "active" energy source, attracting increasing attention for their potential applications in photocatalysis and photodetection. Here, we hybridize plasmonic Au spherical nanoparticles (SNPs) with catalytically active Pt nanocrystals to form Au@Pt core-satellite nanoparticles (CSNPs), which act as both an efficient catalyst for plasmon-promoted decarboxylation reaction and a robust surface-enhanced Raman scattering (SERS) substrate for plasmon-enhanced molecular spectroscopic detection. By regulating the coverage of Pt nanocrystals on the Au SNPs, we modulated the "hotspot" structures of the Au@Pt CSNPs to optimize the SERS detecting capability and catalytic decarboxylation performance. The coupling functionalities enable us with unique opportunities to in-situ SERS monitor universal reactions catalyzed by active catalysts (e.g. Pt, Pd) in the chemical industry in real-time. The decarboxylation rate of 4-mercaptophenylacetic acid was dynamically controlled by the surface catalytic decarboxylation step, following first-order overall reaction kinetics. Moreover, the reaction rate exhibited a strong correlation with the local field enhancement |E/E0|4 of the hotspot structure. This work provides spectroscopic insights into the molecule-plasmon interface under the plasmon-promoted catalytic reactions, guiding the rational design of the plasmonic interface of nanocatalysts to achieve desired functionalities.

Plasmon-Switched Kinetics for Formic Acid Dehydrogenation: Selective Adsorption Driven by Local Field and Hot Carriers.

Understanding illumination-mediated kinetics is essential for catalyst design in plasmon catalysis. Here we prepare Pd-based plasmonic catalysts with tunable electronic structures to reveal the underlying illumination-enhanced kinetic mechanisms for formic acid (HCOOH) dehydrogenation. We demonstrate a kinetic switch from a competitive Langmuir-Hinshelwood adsorption mode in dark to a non-competitive type under irradiation triggered by local field and hot carriers. Specifically, the electromagnetic field induces a spatial-temporal separation of dehydrogenation-favorable configurations of reactant molecule HCOOH and HCOO- due to their natural different polarities. Meanwhile, the generated energetic carriers can serve as active sites for selective molecular adsorption. The hot electrons act as adsorption sites for HCOOH, while holes prefer to adsorb HCOO-. Such unique non-competitive adsorption kinetics induced by plasmon effects serves as another typical characteristic of plasmonic catalysis that remarkably differs from thermocatalysis. This work unravels unique adsorption transformations and a kinetic switching driven by plasmon nonthermal effects.

M/BiOCl-(M = Pt, Pd, and Au) Boosted Selective Photocatalytic CO2 Reduction to C2 Hydrocarbons via *CHO Intermediate Manipulation.

Selective CO2 photoreduction to C2 hydrocarbons is significant but limited by the inadequate adsorption strength of the reaction intermediates and low efficiency of proton transfer. Herein, an ameliorative *CO adsorption and H2O activation strategy is realized via decorating bismuth oxychloride (BiOCl) nanostructures with different metal (Pt, Pd, and Au) species. Experimental and theoretical calculation results reveal that distinct *CO binding energies and *H acquisition abilities of the metal cocatalysts mediate the CO2 reduction activity and hydrocarbon selectivity. The relatively moderate *CO adsorption and *H supply over Pd/BiOCl endows it with the lowest free energy to generate *CHO, leading to its highest activity of hydrocarbon production. Specifically, the Pt cocatalyst can efficiently participate in H2O dissociation to deliver more *H for facilitating the protonation of the *CHO and *CHOH, thereby favoring CH4 production with 76.51% selectivity. A lower *H supply over Pd/BiOCl and Au/BiOCl results in a large energy barrier for *CHO or *CHOH protonation and thus a more thermodynamically favored OC─CHO coupling pathway, which endows them with vastly increased C2 hydrocarbon selectivity of 81.21% and 92.81%, respectively. The understanding of efficient C2 hydrocarbon production in this study sheds light on how materials can be engineered for photocatalytic CO2 reduction.

Modulation of copper sites in porphyrin metal-organic frameworks for electrochemical ascorbic acid sensing.

Two metal-organic frameworks (MOFs) with different Cu-centered coordination structures were synthesized. By introducing 4,4-bipyridine as a linker in the Cu-MOFs, we have discovered that Cu-O, instead of Cu-N, is the active site with higher electrocatalytical activity towards ascorbic acid, which is essential to understand and develop Cu-based ascorbic acid sensors.

Effect of alloying element content on anaerobic microbiologically influenced corrosion sensitivity of stainless steels in enriched artificial seawater.

Stainless steels (SS) are not immune to microbiologically influenced corrosion (MIC) especially in the presence of sulfate reducing bacteria (SRB). It is necessary to study the influence of alloying elements on the MIC. SRB MIC behaviors of four stainless steels (2205 SS, 316L SS, 304 SS, and 410 SS), with different alloying element compositions were compared after 14 days of incubation at 37°C in enriched artificial seawater inoculated with Desulfovibrio sp. The sessile cell sequence was 410 SS > 316L SS > 304 SS > 2205 SS, inversely proportional to Cr content. The uniform corrosion rate (based on weight loss) sequence was 410 SS > 304 SS > 316L SS > 2205 SS, which matches the pitting resistance equivalent number (PREN) sequence inversely. 410 SS with the lowest Cr and Mo contents suffered the most severe pitting, with pit depth of 35 µm and weight loss of 0.75 mg/cm2 (0.91 mm/a pitting rate and 25 µm/a uniform corrosion rate). The other three stainless steels with higher Cr and Mo contents suffered only metastable pits. The semiconductor characteristics and the re-passivation abilities of the passive films were found to be affected by Cr and Mo contents.

Cobalt Nanoparticles Anchored on N-Doped Porous Carbon Derived from Yeast for Enhanced Electrocatalytic Oxygen Reduction Reaction.

Biomass-derived carbon materials have received extensive attention for use in high-performance electrocatalysts. In this study, a highly efficient electrocatalyst is developed with Co nanoparticles anchored on N-doped porous carbon material (CoNC) by using yeast as a biomass precursor through a facial activation and pyrolysis process. CoNC exhibits comparable catalytic activity with commercial 20 % Pt/C for the oxygen reduction reaction (ORR) with a half-wave potential of 0.854 V. A home-made primary Zn-air battery exhibited an open circuit potential of 1.45 V and a peak power density of 188 mW cm-2 . Moreover, the discharge voltage of the primary battery maintained at a stable value up to 9 days. The enhanced performance of CoNC was probably ascribed to its high content of pyridinic-N and graphitic-N species, extra Co loading and porous structure, which provided sufficient active sites and channels to promote mass/electron transfer for ORR. This work provides a promising strategy to develop an efficient non-noble metal carbon-based electrocatalyst for fuel cells and metal-air batteries.

Photo-enhanced dehydrogenation of formic acid on Pd-based hybrid plasmonic nanostructures.

Coupling visible light with Pd-based hybrid plasmonic nanostructures has effectively enhanced formic acid (FA) dehydrogenation at room temperature. Unlike conventional heating to achieve higher product yield, the plasmonic effect supplies a unique surface environment through the local electromagnetic field and hot charge carriers, avoiding unfavorable energy consumption and attenuated selectivity. In this minireview, we summarized the latest advances in plasmon-enhanced FA dehydrogenation, including geometry/size-dependent dehydrogenation activities, and further catalytic enhancement by coupling local surface plasmon resonance (LSPR) with Fermi level engineering or alloying effect. Furthermore, some representative cases were taken to interpret the mechanisms of hot charge carriers and the local electromagnetic field on molecular adsorption/activation. Finally, a summary of current limitations and future directions was outlined from the perspectives of mechanism and materials design for the field of plasmon-enhanced FA decomposition.

Effect of ionic surfactants on the settling behavior of silt.

Ionic surfactants are easily adsorbed by silt and clay particles, thus affecting the flocculation characteristics and settling behavior. The settling velocity, typical size, Zeta potential and surface tension of silt flocs were measured in the presence of two different kinds of ionic surfactants. The results indicated that the cetyltrimethylammonium bromide (CTAB, a typical cationic surfactant) can dramatically accelerate the settling of slit particles, while the linear alkylbenzene sulfonate (LAS, a typical anionic surfactant) slightly retarded silt sedimentation to some extent. In still water, the representative settling velocity dramatically increased from 0.36 cm s-1 to 0.43 cm s-1 with the increase of CTAB concentration, which increased by more than 20%. Oppositely, the sedimentation rate decreased from 0.36 cm s-1 to 0.33 cm s-1 with the increase of LAS concentration. In flowing water, as the flow rate increased from 0 to 20 cm s-1 and the ionic surfactant concentration increased from 0 to 10 mg L-1, the sedimentation rate decreased to 57% and 89% in the presence of CTAB and LAS respectively, which was due to an enhanced dispersion of silt particles and a breaking of flocs. The SEM image test shows that the floc particle size increased 1.5 times of the primary particle size under the high CTAB concentration. The flocculation induced by ionic surfactants greatly influences the sediment size as well as the law of settling velocity. The intrinsic influence mechanism was also discussed based on the variations of silt particle properties. This systematic study can be used for further development of flocculation models and particle size distribution of fine-grained soil.

Synergistic Combination of Fermi Level Equilibrium and Plasmonic Effect for Formic Acid Dehydrogenation.

Developing an efficient catalyst for formic acid (FA) dehydrogenation is a promising strategy for safe hydrogen storage and transportation. Herein, we successfully developed trimetallic NiAuPd heterogeneous catalysts through a galvanic replacement reaction and a subsequent chemical reduction process to boost hydrogen generation from FA decomposition at room temperature by coupling Fermi level engineering with plasmonic effect. We demonstrated that Ni worked as an electron reservoir to donate electrons to Au and Pd driven by Fermi level equilibrium whereas plasmonic Au served as an optical absorber to generate energetic hot electrons and a charge-redistribution mediator. Ni and Au worked cooperatively to promote the charge heterogeneity of surface-active Pd sites, leading to enhanced chemisorption of formate-related intermediates and eventually outstanding activity (342 mmol g-1 h-1 ) compared with bimetallic counterpart. This work offers excellent insight into the rational design of efficient catalysts for practical hydrogen energy exploitation.

Template-free fabrication of Bi2O3 and (BiO)2CO3 nanotubes and their application in water treatment.

Uniform bismuth oxide (Bi(2)O(3)) and bismuth subcarbonate ((BiO)(2)CO(3)) nanotubes were successfully synthesized by a facile solvothermal method without the need for any surfactants or templates. The synergistic effect of ethylene glycol (EG) and urea played a critical role in the formation of the tubular nanostructures. These Bi(2)O(3) and (BiO)(2)CO(3) nanotubes exhibited excellent Cr(VI)-removal capacity. Bi(2)O(3) nanotubes, with a maximum Cr(VI)-removal capacity of 79 mg g(-1), possessed high removal ability in a wide range of pH values (3-11). Moreover, Bi(2)O(3) and (BiO)(2)CO(3) nanotubes also displayed highly efficient photocatalytic activity for the degradation of RhB under visible-light irradiation. This work not only demonstrates a new and facile route for the fabrication of Bi(2)O(3) and (BiO)(2)CO(3) nanotubes, but also provides new promising adsorbents for the removal of heavy-metal ions and potential photocatalysts for environmental remediation.

In situ electrochemical reductive construction of metal oxide/metal-organic framework heterojunction nanoarrays for hydrogen peroxide sensing.

Transition metal oxide/metal-organic framework heterojunctions (TMO@MOF) that combine the large specific surface area of MOFs with TMOs' high catalytic activity and multifunctionality, show excellent performances in various catalytic reactions. Nevertheless, the present preparation approaches of TMO@MOF heterojunctions are too complex to control, stimulating interests in developing simple and highly controllable methods for preparing such heterojunction. In this study, we propose an in situ electrochemical reduction approach to fabricating Cu2O nanoparticle (NP)@CuHHTP heterojunction nanoarrays with a graphene-like conductive MOF CuHHTP (HHTP is 2,3,6,7,10,11-hexahydroxytriphenylene). We have discovered that size-controlled Cu2O nanoparticles could be in situ grown on CuHHTP by applying different electrochemical reduction potentials. Also, the obtained Cu2O NP@CuHHTP heterojunction nanoarrays show high H2O2 sensitivity of 8150.6 µA·mM-1·cm2 and satisfactory detection performances in application of measuring H2O2 concentrations in urine and serum samples. This study offers promising guidance for the synthesis of MOF-based heterojunctions for early cancer diagnosis.

Engineering MOFs derived metal oxide nanohybrids: Towards electrochemical sensing of catechol in tea samples.

In this work, we have successfully developed Cu-MOF/CuO/NiO nanocomposites (NCs) and employed as a novel electrochemical sensing platform in catechol (CC) detection. The Scanning electron microscopy (SEM) along Energy dispersive X-ray Analysis (EDX), Transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS) are carried out to characterize the as-fabricated Cu-MOF/CuO/NiO NCs. Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) techniques have used to obtain oxidation peak currents of CC. Glassy carbon electrode (GCE) modified with Cu-MOF/CuO/NiO has exposed the superb EC properties representing low limit of detection (LOD) of 0.0078 µM (S/N = 3). To assess the practicability of Cu-MOF/CuO/NiO based sensing medium, it has been used to detect CC from two varieties of tea, namely black and green. Thus, we anticipate that this structural integration strategy possesses encouraging application potential in sensing podium and material synthesis.

Crevice corrosion of X80 carbon steel induced by sulfate reducing bacteria in simulated seawater.

Crevice corrosion of X80 carbon steel in simulated seawater with the presence of SRB was studied by surface analysis and electrochemical measurements. The electrode inside crevice was seriously corroded. Large amount of corrosion products accumulated along the crevice mouth. Galvanic current densities measurements confirmed that there was a galvanic effect between the carbon steel at the crevice interior and exterior during the crevice corrosion. The difference in the sessile SRB cells quantities and SRB biofilms developments inside and outside crevice caused the galvanic effect between the carbon steel inside and outside the crevice, which further induced crevice corrosion. Increased crevice width reduced the galvanic effect, resulting in less crevice corrosion in wider crevice.

Synergistic mediation of metallic bismuth and oxygen vacancy in Bi/Bi2WO6-x to promote 1O2 production for the photodegradation of bisphenol A and its analogues in water matrix.

Bi/Bi2WO6-x heterostructures has been successfully prepared by a facile one-step hydrothermal method. By maneuvering reaction time and Bi/W molar ratio of the precursors, we have been able to selectively introduce oxygen vacancy and metallic Bi into Bi2WO6 nanostructures. The obtained Bi/Bi2WO6-x heterostructures with more oxygen vacancy and moderate metallic Bi exhibit significantly improved photocatalytic activity for the photodegradation of bisphenol A (BPA) and its analogues due to its great ability for the generation of singlet oxygen (1O2), which has proven to work as the main reactive oxygen species during photocatalysis. It is also found the 1O2 concentration is highly depended on and modulated by the content of oxygen vacancy and metallic bismuth. Besides, we also demonstrate that the obtained Bi/Bi2WO6-x products display efficient photocatalytic performance toward BPA derivatives degradation and enhanced stability to resist the interferences in the water matrix.