Sushant Sahu

Carbon Nanoparticles as Visible-Light Photocatalysts for Efficient CO2 Conversion and Beyond

Increasing atmospheric CO(2) levels have generated much concern, driving the ongoing carbon sequestration effort. A compelling CO(2) sequestration option is its photocatalytic conversion to hydrocarbons, for which the use of solar irradiation represents an ultimate solution. Here we report a new strategy of using surface-functionalized small carbon nanoparticles to harvest visible photons for subsequent charge separation on the particle surface in order to drive the efficient photocatalytic process. The aqueous solubility of the catalysts enables photoreduction under more desirable homogeneous reaction conditions. Beyond CO(2) conversion, the nanoscale carbon-based photocatalysts are also useful for the photogeneration of H(2) from water under similar conditions.

Carbon “quantum” dots for optical bioimaging

Carbon dots, generally referring to small carbon nanoparticles with various levels of surface passivation, have emerged as a new class of quantum dot-like fluorescent nanomaterials. Since the original report in 2006, carbon dots have been investigated by many research groups worldwide, with major advances already made in their syntheses, structural and mechanistic understandings, and evaluations for biocompatibilities and potential bio-applications. In this article, representative studies responsible for these advances in the development and understanding of carbon dots are reviewed, and those targeting the use of carbon dots as high-performance yet nontoxic fluorescence agents for optical bioimaging in vitro and in vivo are highlighted and discussed.

Carbon Quantum Dots and Applications in Photocatalytic Energy Conversion

Quantum dots (QDs) generally refer to nanoscale particles of conventional semiconductors that are subject to the quantum-confinement effect, though other nanomaterials of similar optical and redox properties are also named as QDs even in the absence of strictly defined quantum confinement. Among such nanomaterials that have attracted tremendous recent interest are carbon dots, which are small carbon nanoparticles with some form of surface passivation, and graphene quantum dots in various configurations. In this article, we highlight these carbon-based QDs by focusing on their syntheses, on their photoexcited state properties and redox processes, and on their applications as photocatalysts in visible-light carbon dioxide reduction and in water-splitting, as well as on their mechanistic similarities and differences.

Competitive performance of carbon "quantum" dots in optical bioimaging.

Carbon-based “quantum” dots or carbon dots are surface-functionalized small carbon nanoparticles. For bright fluorescence emissions, the carbon nanoparticles may be surface-doped with an inorganic salt and then the same organic functionalization. In this study, carbon dots without and with the ZnS doping were prepared, followed by gel-column fractionation to harvest dots of 40% and 60% in fluorescence quantum yields, respectively. These highly fluorescent carbon dots were evaluated for optical imaging in mice, from which bright fluorescence images were obtained. Of particular interest was the observed competitive performance of the carbon dots in vivo to that of the well-established CdSe/ZnS QDs. The results suggest that carbon dots may be further developed into a new class of high-performance yet nontoxic contrast agents for optical bioimaging.

Carbon dots of different composition and surface functionalization: cytotoxicity issues relevant to fluorescence cell imaging

Nanoscale carbon particles have emerged as versatile precursors for a new class of highly fluorescent nanomaterials that resemble semiconductor quantum dots. The surface-passivated fluorescent carbon nanoparticles, dubbed ‘carbon dots’, were already demonstrated for their potential optical bioimaging applications in vitro and in vivo. In this study, we conducted a systematic cytotoxicity evaluation on the carbon dots prepared by various combinations of precursor carbon nanoparticles and molecules for the particle surface functionalization. The results suggested that the cytotoxicity of carbon dots was dependent on the selection of surface passivation molecules. Those dots showing more significant cytotoxicity at higher concentrations were also evaluated for their effects on the fluorescence imaging of live cells. The implications of the results on the eventual use of carbon dots as cell imaging agents are discussed.

Efficient Fluorescence Quenching in Carbon Dots by Surface-Doped Metals - Disruption of Excited State Redox Processes and Mechanistic Implications

The carbon dots in this study were small carbon nanoparticles with the particle surface functionalized by oligomeric poly(ethylene glycol) diamine molecules. Upon photoexcitation, the brightly fluorescent carbon dots in aqueous solution served the function of excellent electron donors to reduce platinum(IV) and gold(III) compounds into their corresponding metals to be deposited on the dot surface. The deposited metals even in very small amounts were found to have dramatic quenching effects on the fluorescence emission intensities, but essentially no effects on the observed fluorescence decays. The obviously exclusive near-neighbor static quenching could be attributed to the disruption of electron-hole radiative recombinations (otherwise responsible for the fluorescence emissions in carbon dots). The results provide important evidence for the availability of photogenerated electrons that could be harvested for productive purposes, which in turn supports the current mechanistic framework on fluorescence emission and photoinduced redox properties of carbon dots.

Versatility with carbon dots – from overcooked BBQ to brightly fluorescent agents and photocatalysts

Carbon soot from overcooked barbecue meat was used as a precursor for brightly fluorescent carbon dots and for their serving as potent visible-light photocatalysts, similar to those from other nanoscale carbon sources, thus demonstrating the versatility of carbon dots in terms of structure, composition, and properties.

Carbon nanoparticles as chromophores for photon harvesting and photoconversion.

Carbon nanomaterials have generated a tremendous amount of attention in the scientific community. While most of the research and development efforts have been on fullerenes, carbon nanotubes, and graphene sheets, carbon nanoparticles (which are often considered as impurities or unwanted complications in the other carbon nanomaterials) have recently emerged as a unique class of highly fluorescent nano-dots. However, little or no attention has been paid to potential uses of carbon nanoparticles as chromophores in photochemical reactions or for photon harvesting and photoconversion in general. In the study reported herein we demonstrate the chromophore-equivalent functions of aqueous-suspended small carbon nanoparticles in harvesting visible photons for the reductive coating of the nanoparticles with silver and gold and, as a result, the preparation of unique carbon-noble-metal core-shell nanostructures.

Carbon-core silver-shell nanodots as sensitizers for phototherapy and radiotherapy

Spherical carbon nanoparticles (carbon nanodots) with a silver shell were investigated as potential sensitizing agents. The cytotoxicity of the combination of ultraviolet radiation or x-rays with the nanodots was examined in cancer cells in vitro. The cell viability decreased following the exposure to the radiation. The carbon nanodots enhanced the radiation effects by significantly reducing the amount of surviving cells compared to that of the cells exposed only to the radiation. Carbon-core silver-shell nanodots can be proposed as a bimodal sensitization platform for biological and medicinal applications employing non-ionizing or ionizing radiation.

The Myth of Visible Light Photocatalysis Using Lanthanide Upconversion Materials

Upconversion luminescence is a nonlinear optical process achieved by certain engineered materials, which allows conversion of low energy photons into higher energy photons. Of particular relevance to environmental technology, lanthanide-based upconversion phosphors have appeared in dozens of publications as a tool for achieving visible light activation of wide-band gap semiconductor photocatalysts, such as TiO2, for degradation of water contaminants. Supposedly, the phosphor particles act to convert sub-band gap energy photons (e.g., solar visible light) into higher energy ultraviolet photons, thus driving catalytic aqueous contaminant degradation. Herein, however, we reexamined the photophysical properties of the popular visible-to-UV converters Y2SiO5:Pr3+ and Y3Al5O12:Er3+, and found that their efficiencies are not nearly high enough to induce catalytic degradations under the reported excitation conditions. Furthermore, our experiments indicate that the false narrative of visible-to-UV upconversion-sensitized photocatalysis likely arose due to coincidental enhancements of dye degradation via direct electron injection that occur in the presence of dielectric-semiconductor (phosphor-catalyst) interfaces. These effects were unrelated to upconversion and only occurred for dye solutions illuminated within the chromophore absorption bands. We conclude that upconversion using Pr3+ or Er3+-activated systems is not a technologically appealing mechanism for visible light photocatalysis, and provide experimental guidelines for avoiding future misinterpretation of these phenomena.