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.

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.

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.

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.

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.

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.

Robust, Highly Luminescent Au13 Superatoms Protected by N-Heterocyclic Carbenes.

Gold superatom nanoclusters stabilized entirely by N-heterocyclic carbenes (NHCs) and halides are reported. The reduction of well-defined NHC-Au-Cl complexes produces clusters comprised of an icosahedral Au13 core surrounded by a symmetrical arrangement of nine NHCs and three chlorides. X-ray crystallography shows that the clusters are characterized by multiple CH-π and π-π interactions, which rigidify the ligand and likely contribute to the exceptionally high photoluminescent quantum yields observed, up to 16.0%, which is significantly greater than that of the most luminescent ligand-protected Au13 superatom cluster. Density functional theory analysis suggests that clusters are 8-electron superatoms with a wide HOMO-LUMO energy gap of 2 eV. Consistent with this, the clusters have high stability relative to phosphine stabilized clusters.

Impact of Ferrocene Substitution on the Electronic Properties of BODIPY Derivatives and Analogues.

Bis(ferrocenyl)-functionalized boron dipyrromethene (BODIPY) compound 1 featuring direct Fc-B bonds was obtained via a "prefunctionalization strategy". UV-vis absorption, electrochemical, and transient absorption experiments were performed on compound 1 and its analogues to examine the impact of ferrocenyl substitution on the electronic properties. The ferrocene units were found to have little impact on the absorption spectrum of the BODIPY unit but significantly change the excited-state dynamics.

Experimental Evidence for a Triplet Biradical Excited-State Mechanism in the Photoreactivity of N,C-Chelate Organoboron Compounds.

N,C-chelate organoborates represent an emerging class of photoresponsive materials due to their photochromic switching at a boron center. Despite the promising applicability of such systems, little is known about the excited-state processes that lead to their unique photoreactivity, which is detrimental to the design of next-generation smart materials based on boron. As part of our ongoing effort to understand and improve the utility of these organoboron compounds, we report some of the first experimental evidence to support an excited-state mechanism for N,C-chelate organoborates. Femtosecond transient absorption spectroscopy combined with steady-state UV/vis and fluorescence measurements gives direct insight into their underlying photochemical processes, such as the formation of a common triplet charge-transfer state which either relaxes radiatively or undergoes the desired photoisomerization through a biradical intermediate. With this information, a complete mechanistic picture of the excited-state reactivity of N,C-chelate organoborates has been established, which is anticipated to lead to new smart materials with improved performance.

A Single Model for the Excited-State Dynamics of Au18(SR)14 and Au25(SR)18 Clusters.

Excited-state properties of photonic materials play an important part in dictating the photocatalytic activity. Thiol-protected gold clusters, like Au18(SR)14 and Au25(SR)18, are an emerging material of interest with unique optical and electronic properties. Au18(SR)14 clusters, in particular, have shown promise as one of the highest efficiency clusters in light harvesting, with a high emission quantum yield. In this work, the excited-state properties of Au18(SR)14 are studied in-depth by ultrafast pump/probe spectroscopy for the first time. A single model describing the optical characteristics of thiol-protected Au18(SR)14 and Au25(SR)18 clusters is offered. Excited-state dynamics analysis suggests that there are state-resolved relaxations due to the presence of multiple excited states. The populations of these excited states are shown to be solvent- and ligand-dependent.

Two Distinct Transitions in Cu(x)InS2 Quantum Dots. Bandgap versus Sub-Bandgap Excitations in Copper-Deficient Structures.

Cu-deficient CuInS2 quantum dots (QDs) synthesized by varying the [Cu]:[In] ratio allow modulation of optical properties as well as identification of the radiative emission pathways. Absorption and emission spectral features showed a strong dependence on the [Cu]:[In] ratio of CuxInS2 QDs, indicating two independent optical transitions. These effects are pronounced in transient absorption spectra. The bleaching of band edge absorption and broad tail absorption bands in the subpicosecond-nanosecond time scale provide further evidence for the dual optical transitions. The recombination process as monitored by photoemission decay indicated the involvement of surface traps in addition to the bandgap and sub-bandgap transitions. Better understanding of the origin of the optical transitions and their influence on the photodynamics will enable utilization of ternary semiconductor quantum dots in display and photovoltaic devices.

How Lead Halide Complex Chemistry Dictates the Composition of Mixed Halide Perovskites.

Varying the halide ratio (e.g., Br(-):I(-)) is a convenient approach to tune the bandgap of organic lead halide perovskites. The complexation between Pb(2+) and halide ions is the primary step in dictating the overall composition, and optical properties of the annealed perovskite structure. The complexation between Pb(2+) and Br(-) is nearly 7 times greater than the complexation between Pb(2+) and I(-), thus making Br(-) a dominant binding species in mixed halide systems. Emission and transient absorption measurements show a strong dependence of excited state behavior on the composition of halide ions employed in the precursor solution. When excess halide (X = Br(-) and I(-)) are present in the precursor solution (0.3 M PbX2 and 0.9 M CH3NH3X), the exclusive binding of Pb(2+) with Br(-) results in the formation of CH3NH3PbBr3 perovskites as opposed to mixed halide perovskite.

Boosting the Photovoltage of Dye-Sensitized Solar Cells with Thiolated Gold Nanoclusters.

Glutathione-capped gold nanoclusters (Aux-GSH NCs) are anchored along with a sensitizing squaraine dye on a TiO2 surface to evaluate the cosensitizing role of Au(x)-GSH NCs in dye-sensitized solar cells (DSSCs). Photoelectrochemical measurements show an increase in the photoconversion efficiency of DSSCs when both sensitizers are present. The observed photoelectrochemical improvements in cosensitized DSSCs are more than additive effects as evident from the increase in photovoltage (ΔV as high as 0.24 V) when Au(x)-GSH NCs are present. Electron equilibration and accumulation within gold nanoclusters increase the quasi-Fermi level of TiO2 closer to the conduction band and thus decrease the photovoltage penalty. A similar beneficial role of gold nanoclusters toward boosting the V(oc) and enhancing the efficiency of Ru(II) polypyridyl complex-sensitized solar cells is also discussed.

Synergistic Effects in the Coupling of Plasmon Resonance of Metal Nanoparticles with Excited Gold Clusters.

When molecules or clusters are within the proximity of metal particles, their electronic transitions can be drastically enhanced. We have now probed the off-resonance excitation of molecule-like, glutathione-capped gold clusters (Au-GSH) in the close proximity of larger (plasmonic) Au and Ag nanoparticles. The excited state absorption spectrum of Au-GSH* is obtained with monophotonic excitation. The characteristic absorption of Au-GSH* allows us to probe the influence of excited plasmonic nanoparticles coupled with the clusters. Although infrared (775 nm) lasers pulses do not produce Au-GSH*, the excited states of these clusters are formed when coupled with metal (Au, Ag) nanoparticles. Interestingly, the coupled excitation of Au-GSH/AgNP with 775 nm laser pulses also results in an enhanced field effect, as seen from increased plasmon response of the metal nanoparticles. Transient absorption measurements confirm the synergy between these two inherently different nanomaterials, causing them to display greater excitation features. Better understanding of metal cluster-metal nanoparticle interactions will have important implications in designing light harvesting systems, and optoelectronic devices.

Photochemical synthesis of biocompatible and antibacterial silver nanoparticles embedded within polyurethane polymers.

In situ light initiated synthesis of silver nanoparticles (AgNP) was employed for AgNP incorporation within the polymeric matrices of medical grade polyurethane. The resulting materials showed improved antibacterial and antibiofilm activity against Pseudomonas aeruginosa with negligible toxicity for human primary skin cells and erythrocytes.

Facile SILAR approach to air-stable naked silver and gold nanoparticles supported by alumina.

A synthetically convenient and scalable SILAR (successive ion layer adsorption and reaction) method is used to make air-stable films of silver and gold nanoparticles supported on alumina scaffolds. This solution-based deposition technique yields particles devoid of insulating capping agents or ligands. The optical properties of the nanoparticle films were investigated using femtosecond transient absorption spectroscopy. A linear absorption arising from intraband excitation (775 nm laser pulse) is seen only for Au nanoparticles at low intensity. However, both Au and Ag particles exhibit plasmon resonance responses at high excitation intensity via two photon absorption of the 775 nm pump pulse. The difference in optical response to near-IR laser excitation is rationalized based on the known density of states for each metal. To demonstrate the potential applications of these films, alumina-supported Ag nanoparticles were utilized as substrates for surface enhanced Raman spectroscopy, resulting in a 65-fold enhancement in the Raman signal of the probe molecule rhodamine 6G. The exceptional stability and scalability of these SILAR films opens the door for further optical and photocatalytic studies and applications, particularly with ligand-free Ag nanoparticles that typically oxidize under ambient conditions. Additionally, isolating plasmonic and interband electronic excitations in stable AgNP under visible light irradiation could enable elucidation of the mechanisms that drive noble metal-assisted photocatalytic processes.

Size-dependent excited state behavior of glutathione-capped gold clusters and their light-harvesting capacity.

Glutathione-protected gold clusters exhibit size-dependent excited state and electron transfer properties. Larger-size clusters (e.g., Au25GSH18) with core-metal atoms display rapid (<1 ps) as well as slower relaxation (~200 ns) while homoleptic clusters (e.g., Au(10-12)GSH(10-12)) exhibit only slower relaxation. These decay components have been identified as metal-metal transition and ligand-to-metal charge transfer, respectively. The short lifetime relaxation component becomes less dominant as the size of the gold cluster decreases. The long-lived excited state and ability to participate in electron transfer are integral for these clusters to serve as light-harvesting antennae. A strong correlation between the ligand-to-metal charge-transfer excited state lifetime and photocatalytic activity was evidenced from the electron transfer to methyl viologen. The photoactivity of these metal clusters shows increasing photocatalytic reduction yield (0.05-0.14) with decreasing cluster size, Au25 < Au18 < Au15 < Au(10-12). Gold clusters, Au18GSH14, were found to have the highest potential as a photosensitizer on the basis of the quantum yield of electron transfer and good visible light absorption properties.