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Nick Serpone

Bio: Nick Serpone is an academic researcher from University of Pavia. The author has contributed to research in topics: Photodegradation & Microwave. The author has an hindex of 85, co-authored 474 publications receiving 30532 citations. Previous affiliations of Nick Serpone include Saint Petersburg State University & Meisei University.


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Book
01 Oct 1989
TL;DR: In this paper, the reader is first introduced to the meaning of photocatalysis and subsequently taken through the essentials of photochemistry towards bridging it to semiconductor materials, followed by thermodynamic and kinetic aspects.
Abstract: The book is devoted to the study of photocatalysis, a very popular area of modern-day chemistry. The various chapters will cover aspects of the field that are of particular interest to those at the top in research expertise. Among the subjects discussed are: the theory and preparation of semiconductor mate- rials, the various types of heterogeneous photocatalysis methods, absorption and desorption in photocatalysis, and applied photoca- talysis in energy production. A knowledge of photochemistry is not essential as the format and selection of topics make the field evolve naturally. The student is first introduced to the meaning of photocatalysis and subsequently taken through the essentials of photochemistry towards bridging it to semiconductor materials. The reader is also introduced to the colloidal state of semiconductors followed by thermodynamic and kinetic aspects of photocatalysis. The book is aimed at professional, faculty and graduate students in inorganic and physical chemistry, organic chemistry, oganometallic chemistry, and catalysis.

1,660 citations

Journal ArticleDOI
TL;DR: Heterogeneous photocatalysis is a process in which the illumination of an oxide semiconductor, usually the anatase form of titanium dioxide, produces photoexcited electrons (e{sup {minus}}) and holes (h{sup +}). These can migrate to the oxide surface and participate in halfcell reactions that are part of a closed, catalytic cycle as mentioned in this paper.
Abstract: Heterogeneous photocatalysis is a process in which the illumination of an oxide semiconductor, usually the anatase form of titanium dioxide, produces photoexcited electrons (e{sup {minus}}) and holes (h{sup +}). These can migrate to the oxide surface and participate in half-cell reactions that are part of a closed, catalytic cycle. In the aqueous phase, the illuminated surface is widely regarded as a producer of hydroxyl radicals (e.g., h{sup +} + OH{sup {minus}} {yields} {center dot}OH), and these and other highly oxidizing initial products of this indirect photochemistry go on to attack oxidizable contaminants. This article highlights recent developments in photocatalysis that are applicable to water treatment. Topics discussed include the generality of photocatalysis for complete contaminant destruction (mineralization); some specific contaminant classes of interest (chlorinated aromatics, surfactants, herbicides, and pesticides); the use of solar versus artificial illumination; the influence of additional oxidants such as H{sub 2}O{sub 2}; catalyst forms (suspended vs. immobilized); and related potential applications of photocatalysis (metal recovery and total organic carbon (TOC) analyses).

1,115 citations

Journal ArticleDOI
Nick Serpone1
TL;DR: It is argued that the red-shift of the absorption edge is in fact due to formation of the color centers, and that while band gap narrowing is not an unknown occurrence in semiconductor physics it does necessitate heavy doping of the metal oxide semiconductor, thereby producing materials that may have completely different chemical compositions from that of TiO(2) with totally different band gap electronic structures.
Abstract: Second-generation TiO2-xDx photocatalysts doped with either anions (N, C, and S mostly) or cations have recently been shown to have their absorption edge red-shifted to lower energies (longer wavelengths), thus enhancing photonic efficiencies of photoassisted surface redox reactions. Some of the studies have proposed that this red-shift is caused by a narrowing of the band gap of pristine TiO2 (e.g., anatase, Ebg = 3.2 eV; absorption edge ca. 387 nm), while others have suggested the appearance of intragap localized states of the dopants. By contrast, a recent study by Kuznetsov and Serpone (J. Phys. Chem. B, in press) has proposed that the commonality in all these doped titanias rests with formation of oxygen vacancies and the advent of color centers (e.g., F, F+, F++, and Ti3+) that absorb the visible light radiation. This article reexamines the various claims and argues that the red-shift of the absorption edge is in fact due to formation of the color centers, and that while band gap narrowing is not an...

999 citations

Journal ArticleDOI
TL;DR: In this article, the inverse photosensitized oxidative transformation of tetraethylated rhodamine (RhB) under visible illumination of aqueous titania dispersions is demonstrated.
Abstract: Chemical oxygen demand (CODCr) and proton NMR, UV−vis, and spin trapping EPR spectroscopic evidence is presented to demonstrate the inverse photosensitized oxidative transformation of tetraethylated rhodamine (RhB) under visible illumination of aqueous titania dispersions. Both de-ethylation and oxidative degradation take place with the former proceeding in a stepwise manner to yield mono-, di-, tri-, and tetra-de-ethylated rhodamine species. Intermediates present after each de-ethylation step remain in a fast dynamic equilibrium between the titania particle surface and the bulk solution. The concentration of •OH radicals, formed from the inverse photosensitization process through the superoxide radical anion, increases upon addition of the anionic dodecylbenzene sulfonate surfactant (DBS) because a larger number of RhB excited states are able to inject an electron into the conduction band of the TiO2 particles. Also, intermediates that can no longer absorb the visible light, (i.e., once the dye solution ...

948 citations


Cited by
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Journal ArticleDOI
TL;DR: The slow pace of hazardous waste remediation at military installations around the world is causing a serious delay in conversion of many of these facilities to civilian uses as discussed by the authors, which is a serious problem.
Abstract: The civilian, commercial, and defense sectors of most advanced industrialized nations are faced with a tremendous set of environmental problems related to the remediation of hazardous wastes, contaminated groundwaters, and the control of toxic air contaminants. For example, the slow pace of hazardous waste remediation at military installations around the world is causing a serious delay in conversion of many of these facilities to civilian uses. Over the last 10 years problems related to hazardous waste remediation have emerged as a high national and international priority.

17,188 citations

Journal ArticleDOI
TL;DR: In this article, the authors focus on interfacial processes and summarize some of the operating principles of heterogeneous photocatalysis systems, including the electron transfer and energy transfer processes in photocatalytic reactions.
Abstract: In 1972, Fujishima and Honda discovered the photocatalytic splitting of water on TiO{sub 2} electrodes. This event marked the beginning of a new era in heterogeneous photocatalysis. Since then, research efforts in understanding the fundamental processes and in enhancing the photocatalytic efficiency of TiO{sub 2} have come from extensive research performed by chemists, physicists, and chemical engineers. Such studies are often related to energy renewal and energy storage. In recent years, applications to environmental cleanup have been one of the most active areas in heterogeneous photocatalysis. This is inspired by the potential application of TiO{sub 2}-based photocatalysts for the total destruction of organic compounds in polluted air and wastewaters. There exists a vast body of literature dealing with the electron transfer and energy transfer processes in photocatalytic reactions. A detailed description of these processes is beyond the scope of this review. Here, the authors tend to focus on interfacial processes and to summarize some of the operating principles of heterogeneous photocatalysis. In section 2, the authors first look at the electronic excitation processes in a molecule and in a semiconductor substrate. The electronic interaction between the adsorbate molecule and the catalyst substrate is discussed in terms of the catalyzed ormore » sensitized photoreactions. In section 3, thermal and photocatalytic studies on TiO{sub 2} are summarized with emphasis on the common characteristics and fundamental principles of the TiO{sub 2}-based photocatalysis systems. In section 4, they address the research effort in the electronic modification of the semiconductor catalysts and its effect on the photocatalytic efficiency. Several representative examples will be presented including the Schottky barrier formation and modification at metal-semiconductor interfaces. Some concluding remarks and future research directions will be given in the final section. 160 refs.« less

10,719 citations

Journal ArticleDOI
10 Sep 1998-Nature
TL;DR: In this article, a host material doped with the phosphorescent dye PtOEP (PtOEP II) was used to achieve high energy transfer from both singlet and triplet states.
Abstract: The efficiency of electroluminescent organic light-emitting devices1,2 can be improved by the introduction3 of a fluorescent dye. Energy transfer from the host to the dye occurs via excitons, but only the singlet spin states induce fluorescent emission; these represent a small fraction (about 25%) of the total excited-state population (the remainder are triplet states). Phosphorescent dyes, however, offer a means of achieving improved light-emission efficiencies, as emission may result from both singlet and triplet states. Here we report high-efficiency (≳90%) energy transfer from both singlet and triplet states, in a host material doped with the phosphorescent dye 2,3,7,8,12,13,17,18-octaethyl-21H,23H-porphine platinum(II) (PtOEP). Our doped electroluminescent devices generate saturated red emission with peak external and internal quantum efficiencies of 4% and 23%, respectively. The luminescent efficiencies attainable with phosphorescent dyes may lead to new applications for organic materials. Moreover, our work establishes the utility of PtOEP as a probe of triplet behaviour and energy transfer in organic solid-state systems.

7,023 citations

Journal ArticleDOI
TL;DR: A review of the current progress in the area of TiO 2 photocatalysis, mainly photocatalytic air purification, sterilization and cancer therapy is discussed in this paper.
Abstract: Scientific studies on photocatalysis started about two and a half decades ago. Titanium dioxide (TiO 2 ), which is one of the most basic materials in our daily life, has emerged as an excellent photocatalyst material for environmental purification. In this review, current progress in the area of TiO 2 photocatalysis, mainly photocatalytic air purification, sterilization and cancer therapy are discussed together with some fundamental aspects. A novel photoinduced superhydrophilic phenomenon involving TiO 2 and its applications are presented.

6,802 citations