N-Heterocyclic Carbene-Stabilized Atomically Precise Metal Nanoclusters.

This perspective highlights advances in the preparation and understanding of metal nanoclusters stabilized by organic ligands with a focus on N-heterocyclic carbenes (NHCs). We demonstrate the need for a clear understanding of the relationship between NHC properties and their resulting metal nanocluster structure and properties. We emphasize the importance of balancing nanocluster stability with the introduction of reactive sites for catalytic applications and the importance of a better understanding of how these clusters interact with their environments for effective use in biological applications. The impact of atom-scale simulations, development of atomic interaction potentials suitable for large-scale molecular dynamics simulations, and a deeper understanding of the mechanisms behind synthetic methods and physical properties (e.g., the bright fluorescence displayed by many clusters) are emphasized.

Accelerated size-focusing light activated synthesis of atomically precise fluorescent Au22(Lys-Cys-Lys)16 clusters.

Atomically precise metal nanoclusters are promising candidates for various biomedical applications, including their use as photosensitizers in photodynamic therapy (PDT). However, typical synthetic routes of clusters often result in complex mixtures, where isolating and characterizing pure samples becomes challenging. In this work, a new Au22(Lys-Cys-Lys)16 cluster is synthesized using photochemistry, followed by a new type of light activated, accelerated size-focusing. Fluorescence excitation-emission matrix spectroscopy (EEM) and parallel factor (PARAFAC) analysis have been applied to track the formation of fluorescent species, and to assess optical purity of the final product. Furthermore, excited state reactivity of Au22(Lys-Cys-Lys)16 clusters is studied, and formation of type-I reactive oxygen species (ROS) from the excited state of the clusters is observed. The proposed size-focusing procedure in this work can be easily adapted to conventional cluster synthetic methods, such as borohydride reduction, to provide atomically precise clusters.

Photophysical investigation into room-temperature emission from xanthene derivatives.

The photophysical consequences of replacing the nitrogen heteroatom in phenothiazine with methylene are investigated for both solutions and crystalline solids. We analysed the excited state dynamics of four xanthene derivatives and observed an anomalous fluorescence from an energy level higher than the S1 state with lifetimes between 2.8 ns and 5.8 ns in solution and as solids. Additionally, the solid-state xanthene derivatives exhibited long-lived emission consistent with a triplet excited state, displaying millisecond lifetimes that ranged from 0.1 ms to 3.4 ms at ambient temperature in air. Our findings were supported by optical studies, crystallographic structural analyses, and DFT computations, which corroborated the photophysical measurements. It was concluded that the presence of the nitrogen atom in phenothiazine is crucial for achieving ultra-long emission lifetimes and that these results contribute to a deeper understanding of excited state dynamics which have potential implications for applications, such as display technologies, anticounterfeiting technologies, and sensors.

Photochemical synthesis of fluorescent Au16(RGDC)14 and excited state reactivity with molecular oxygen.

Aqueous metal nanoclusters have emerged as effective materials for biomedical imaging and therapy. Among them, gold nanoclusters (AuNCs) have been widely studied due to their unique electronic structures. These nanoclusters are often optically impure, comprising a mixture of fluorescent clusters with different metal/ligand compositions. The polydispersity of nanoclusters makes it challenging to isolate the most stable structure, and poses further risks for eventual clinical applications. Herein, Au16L14 clusters are reported which are optically pure as assessed by fluorescence excitation-emission matrix (EEM) spectroscopy and parallel factor (PARAFAC) analysis. The reactivity of their excited state with molecular oxygen was also probed, demonstrating that the Au16L14 clusters generate type I reactive oxygen species (ROS), which can make them effective sensitizers for photodynamic therapy.

Hybrid plasmonic metasurface as enhanced Raman hot-spots for pesticide detection at ultralow concentrations.

A surface-enhanced Raman scattering (SERS) active metasurface composed of metallic nanohole arrays and metallic nanoparticles is developed. The metasurface can operate in aqueous environments, achieves an enhancement factor of 1.83 × 109 for Rhodamine 6G, and enables the detection of malachite green at a concentation of 0.46 ppb.

Tuning the Functionalization of Graphite for Hydrovoltaic Power Generation.

The recent discovery of hydrovoltaic devices for power generation has led to a rapid growth into new materials for harvesting energy specifically for this research field. Of the materials investigated, carbon materials have dominated, and graphene oxide (GO) has emerged as the leader. While graphite is conductive, it does not have functional groups to strongly interact with water, and highly functionalized GO forms strong interaction with water to generate necessary surface charges but does not typically have high conductivity. Herein, we report the fabrication and functionalization of a graphite-based structure, controlling the extent of oxidation to balance the effects of conductivity and functionalization to achieve high power outputs in hydrovoltaics. Devices prepared using the functionalized graphite achieve a power output of 53.3 µW/g. High power output and good film stability are key advances toward the practical application of hydrovoltaic devices for renewable energy.

Enhanced Charge Carrier Separation in WO3/BiVO4 Photoanodes Achieved via Light Absorption in the BiVO4 Layer.

Photoelectrochemical (PEC) water splitting converts solar light and water into oxygen and energy-rich hydrogen. WO3/BiVO4 heterojunction photoanodes perform much better than the separate oxide components, though internal charge recombination undermines their PEC performance when both oxides absorb light. Here we exploit the BiVO4 layer to sensitize WO3 to visible light and shield it from direct photoexcitation to overcome this efficiency loss. PEC experiments and ultrafast transient absorption spectroscopy performed by frontside (through BiVO4) or backside (through WO3) irradiating photoanodes with different BiVO4 layer thickness demonstrate that irradiation through BiVO4 is beneficial for charge separation. Optimized electrodes irradiated through BiVO4 show 40% higher photocurrent density compared to backside irradiation.

Empowerment of Water-Evaporation-Induced Electric Generators via the Use of Metal Electrodes.

As water rises in the pores of a partially immersed porous film due to capillary action, it carries along ions that are dissociated from the pore walls, generating a streaming current and potential. The water and current flows are sustained due to water evaporation from the unsubmerged surfaces. Traditionally, inert graphite (C) electrodes are used to construct water-evaporation-induced generators (WEIGs) that harness this electricity. WEIGs are environmentally friendly but have weak power outputs. Herein, we report on C/metal WEIGs that feature C top electrodes and metal bottom electrodes, as well as metal/metal WEIGs. Operating in a NaCl solution that facilitates the Galvanic corrosion of the metal (Cu, steel, and Al) electrodes, these Galvanic WEIGs outperform a C/C WEIG by thousands of times in power output. Equally interestingly, the asymmetric environments and potential differences between the two electrodes of a WEIG facilitate metal corrosion and fabrication of compact Galvanic WEIGs. This study clearly shows that one should choose electrodes with caution for the construction of true WEIGs.

NHC-Stabilized Au10 Nanoclusters and Their Conversion to Au25 Nanoclusters.

Herein, we describe the synthesis of a toroidal Au10 cluster stabilized by N-heterocyclic carbene and halide ligands via reduction of the corresponding NHC-Au-X complexes (X = Cl, Br, I). The significant effect of the halide ligands on the formation, stability, and further conversions of these clusters is presented. While solutions of the chloride derivatives of Au10 show no change even upon heating, the bromide derivative readily undergoes conversion to form a biicosahedral Au25 cluster at room temperature. For the iodide derivative, the formation of a significant amount of Au25 was observed even upon the reduction of NHC-Au-I. The isolated bromide derivative of the Au25 cluster displays a relatively high (ca. 15%) photoluminescence quantum yield, attributed to the high rigidity of the cluster, which is enforced by multiple CH-π interactions within the molecular structure. Density functional theory computations are used to characterize the electronic structure and optical absorption of the Au10 cluster. 13C-Labeling is employed to assist with characterization of the products and to observe their conversions by NMR spectroscopy.

FDTD Analysis of Hotspot-Enabling Hybrid Nanohole-Nanoparticle Structures for SERS Detection.

Metallic nanoparticles (MNPs) and metallic nanostructures are both commonly used, independently, as SERS substrates due to their enhanced plasmonic activity. In this work, we introduce and investigate a hybrid nanostructure with strong SERS activity that benefits from the collective plasmonic response of the combination of MNPs and flow-through nanohole arrays (NHAs). The electric field distribution and electromagnetic enhancement factor of hybrid structures composed of silver NPs on both silver and gold NHAs are investigated via finite-difference time-domain (FDTD) analyses. This computational approach is used to find optimal spatial configurations of the nanoparticle positions relative to the nanoapertures and investigate the difference between Ag-NP-on-Ag-NHAs and Ag-NP-on-Au-NHAs hybrid structures. A maximum GSERS value of 6.8 × 109 is achieved with the all-silver structure when the NP is located 0.5 nm away from the rim of the NHA, while the maximum of 4.7 × 1010 is obtained when the nanoparticle is in full contact with the NHA for the gold-silver hybrid structure. These results demonstrate that the hybrid nanostructures enable hotspot formation with strong SERS activity and plasmonic enhancement compatible with SERS-based sensing applications.

A vinylogous Norrish reaction as a strategy for light-mediated ring expansion.

The reactions of bicyclic divinyl ketones display wavelength-dependent changes in product formation. UV irradiation results in the formation of competitive [6,3,5] and [7,3,5] tricyclic unsaturated ketones that subsequently undergo ring expansion and reaction with a range of nucleophiles. DFT calculations and transient absorption experiments were completed that are consistent with a vinylogous Type II Norrish pathway.

All-Weather-Compatible Hydrovoltaic Cells Based on Al2O3 TLC Plates.

Electrical power can be extracted from interactions at the interface of water/materials, known as the "hydrovoltaic" phenomenon. Devices based on this emerging technology hold a lot of promise for meeting renewable energy demands, but materials reported to date largely require specific weather conditions, such as low humidity (∼10-30%), thus hindering widespread application. Herein, we report a new use of plates for thin layer chromatography (TLC) that provide a continuous support of capillary-driven water flow. When coated with α-Al2O3, this simple 8 cm2 device can produce a continuous voltage of ∼0.33 V and a short circuit current of ∼0.85 µA over a wide range of humidity (10-90%). Low cost, stability against surface reactions, ease of fabrication, and power output under varied weather conditions make this device a realistic possibility for use in renewable power generation applications.

Water-Evaporation-Induced Electric Generator Built from Carbonized Electrospun Polyacrylonitrile Nanofiber Mats.

Electricity has been generated from evaporation-driven water flow in films of carbon soot particles and other porous media. This paper reports the placement of carbon nanofiber mats (CNMs) on fiberglass screens for the construction of efficient water-evaporation-induced generators (WEIGs). These CNMs are prepared from carbonizing electrospun polyacrylonitrile nanofiber mats and then treating them with oxygen plasma. After electrode attachment to the two ends of a CNM, one electrode is immersed into water. Water rises in the mat due to capillary action and evaporates from the mat surface due to thermal energy provided by the environment. The steady rise of water pushes the dissociated ions of the surface functionalities upward, resulting in a streaming current and an electric potential. This paper investigates how the generated short-circuit current, Is, and open-circuit voltage, Vo, of the WEIG change with structural parameters of the CNMs. Under optimized conditions, these CNMs produce electricity at an areal power density of 83 nW/cm2, which is almost 10 times those offered by some existing ones. Thus, the easy-to-handle CNMs are an attractive porous scaffold for WEIGs.

Photophysics of Ag and Au alloys of M25(SR)18 clusters.

Superatom clusters, Au25(SR)18, and the silver analog and alloys of the two metals have been extensively investigated for their structure, stability, photoluminescence, and electronic properties. One can readily tune the physicochemical properties by varying the ratio of Au/Ag or the thiol ligand to attain desired properties, such as enhanced emission, increased stability, and catalytic activity. Herein, excitation emission matrix spectroscopy and pump-probe transient absorption spectroscopy are used to show that the excited state dynamics of Au25(SR)18, Ag25(SR)18, and their alloys differ significantly despite having similar structures. State-resolved excited state behavior that is well documented for gold clusters is largely affected by the metal composition, becoming less pronounced for silver analogs, resulting in diversity in terms of their excited state energy and relaxation dynamics and resultant photophysical properties, such as emission.

Exciting clusters, what does off-resonance actually mean?

Noble metal clusters have unique photophysical properties, especially as a new class of materials for multiphoton biomedical imaging. The previously studied Au25SR18 exhibits "giant" two-photon absorbance cross sections. Herein, we investigate the origins of the large two photon absorption for Au25SR18, as well as 10 other Au and Ag clusters using femtosecond pump/probe transient absorption spectroscopy (fsTAS). Excited state absorbance (ESA) ubiquitous to thiolated Au and Ag clusters is used herein as an optical signature of two-photon absorbances of the 11 different Au and Ag clusters, which does not require high quantum yields of emission. The large selection of clusters, studied with a single laser system, allows us to draw conclusions on the role of the particular metal, cluster size/structure, and the effects of the ligands on the ability to absorb multiple NIR photons. The use of a laser with a 1028 nm excitation also allows us to investigate the dramatic effect of excitation wavelength and explain why laser wavelength has led to large variances in the non-linear responses reported for clusters to date. We discuss the double resonance mechanism, responsible for giant two photon absorbance cross-sections, helping match properties of metal clusters with experimental conditions for maximizing signal/response in multiphoton applications.

Photophysics of J-Aggregating Porphyrin-Lipid Photosensitizers in Liposomes: Impact of Lipid Saturation.

Porphyrin aggregates have attractive photophysical properties for phototherapy and optical imaging, including quenched photosensitization, efficient photothermal conversion, and unique absorption spectra. Although hydrophobic porphyrin photosensitizers have long been encapsulated into liposomes for drug delivery, little is known about the membrane properties of liposomes with large amphiphilic porphyrin compositions. In this paper, a porphyrin-lipid conjugate was incorporated into liposomes formed of saturated or unsaturated lipids to study the membrane composition-dependent formation of highly ordered porphyrin J-aggregates and disordered aggregates. Porphyrin-lipid readily phase-separates in saturated membranes, forming J-aggregates that are destabilized during the ripple phase below the main thermal transition. Porphyrin-lipid J-aggregates are photostable with a photothermal efficiency of 54 ± 6%, comparable to gold. Even at high porphyrin-lipid compositions, porphyrin J-aggregates coexist with a minority population of disordered aggregates, which are photodynamically active despite being fluorescently quenched. For photothermal applications, liposome formulations that encourage porphyrin-lipid phase separation should be explored for maximum J-aggregation.

Electrokinetically-Driven Assembly of Gold Colloids into Nanostructures for Surface-Enhanced Raman Scattering.

Surface-enhanced Raman scattering (SERS) enables the highly sensitive detection of (bio)chemical analytes in fluid samples; however, its application requires nanostructured gold/silver substrates, which presents a significant technical challenge. Here, we develop and apply a novel method for producing gold nanostructures for SERS application via the alternating current (AC) electrokinetic assembly of gold nanoparticles into two intricate and frequency-dependent structures: (1) nanowires, and (2) branched "nanotrees", that create extended sensing surfaces. We find that the growth of these nanostructures depends strongly on the parameters of the applied AC electric field (frequency and voltage) and ionic composition, specifically the electrical conductivity of the fluid. We demonstrate the sensing capabilities of these gold nanostructures via the chemical detection of rhodamine 6G, a Raman dye, and thiram, a toxic pesticide. Finally, we demonstrate how these SERS-active nanostructures can also be used as a concentration amplification device that can electrokinetically attract and specifically capture an analyte (here, streptavidin) onto the detection site.

Light-Activated Peptide-Based Materials for Sutureless Wound Closure.

Using chemically modified extracellular matrix proteins, such as collagen, in combination with light for tissue bonding reduces inflammation and minimizes scarring. However, full length animal or recombinant human collagen proteins are difficult to isolate/produce. Thus, short biomimetic collagen peptides with properties equivalent to collagen at both structural and functional levels may be ideal building blocks for the development of remotely triggered adhesives and fillers. In this work, the conjugation of self-assembling collagen-like peptides to acrylate functionalized polyethylene glycol units yielded adhesive filler materials activated by visible light through the incorporation of a photosensitizer. When tested in a murine skin wound model, the photoactivated adhesives showed reduced scar formation and promoted epithelial regeneration.

Light activated synthesis of the atomically precise fluorescent silver cluster Ag18(Capt)14.

Metal clusters of gold and silver with highly tunable optical and electronic properties are attractive candidates for next generation medical imaging and therapy. Of these two most commonly studied metals, silver clusters often exhibit superior optical properties (i.e. stronger absorbance and higher emission quantum yield). The atomically precise synthesis of these clusters is essential before their use in biological applications can be realized. However, most cluster synthetic routes result in complex mixtures, where isolation and/or characterization can become incredibly challenging. Using photochemistry, we demonstrate a synthetic route for silver thiolate clusters resulting in the isolation of a pure eighteen-atom silver cluster capped by fourteen captopril ligands, Ag18(Capt)14. The facile control over the reduction of Ag(i) salt that this photochemical route affords can be readily applied as a general synthesis for isolating other new, atomically precise clusters.