S. Suárez

Development of alternative photocatalysts to TiO2: Challenges and opportunities

Since the early development of this technology in the 1970s, TiO2 constitutes the archetypical photocatalyst due to its relatively high efficiency, low cost and availability. However, during the last decade a considerable number of new photocatalytic materials, either semiconductor or not, have been proposed as potential substitutes of TiO2, particularly in the case of solar applications, for which this standard photocatalyst is not very suitable because of its wide band gap. Semiconductors based on cations with d0 configuration such Ta5+ or Nb5+, as well as oxides or nitrides of d10 elements such as Bi3+, In3+ or Ga3+ are among the most successful novel photocatalysts, but non-semiconductor solids like cation-interchanged zeolites also produce interesting results. In addition, some classical semiconductors like ZnO or CdS, initially discarded as a consequence of their poor stability under irradiation, have been reconsidered as feasible photocatalysts for particular applications. This growing body of data requires new analysis of the challenges and opportunities facing photocatalysis in order to assess which of the photoactive materials are best for each particular application. In this review, we summarize, with an historical perspective, the main achievements obtained with photocatalyst alternatives to TiO2 in the three main niches for this technology: water splitting for hydrogen production, decontamination and disinfection processes, and organic synthesis.

Photocatalytic materials: recent achievements and near future trends

Research on photocatalytic materials has been a field in continuous expansion in the recent decades, as it is evidenced by the large number of articles published every year. So far, more than 190 different semiconductors have been assayed as suitable photocatalysts. To this figure, it is necessary to add the combinations with other functional materials or between different semiconductors, as well as their morphological modifications. Summing up the outcome of these different preparation strategies eventually leads to the enormous number of photocatalytic systems that have been reported in the scientific literature. Dealing with such an amount of information requires updated and educated guidance to select the most significant realizations, and it also calls for critical assessments on how the expectations are being fulfilled. This perspective article intends to assess the state of the art of photocatalysis with regard to materials and systems, considering the well-established results, but also the emerging aspects, and the envisaged new directions of this technology in the near future. In the first part, the most relevant achievements in this area, some of them already in the market while others still in development, will be reviewed according to the current understanding. The second part of the article is devoted to the most innovative and promising photocatalysts and related systems described in the open literature.

Photocatalytic elimination of indoor air biological and chemical pollution in realistic conditions

The photocatalytic elimination of microorganisms from indoor air in realistic conditions and the feasibility of simultaneous elimination of chemical contaminants have been studied at laboratory scale. Transparent polymeric monoliths have been coated with sol-gel TiO(2) films and used as photocatalyst to treat real indoor air in a laboratory-scale single-step annular photocatalytic reactor. The analytical techniques used to characterize the air quality and analyze the results of the photocatalytic tests were: colony counting, microscopy and PCR with subsequent sequencing for microbial quantification and identification; automated thermal desorption coupled to gas chromatography with mass spectrometry detection for chemical analysis. The first experiments performed proved that photocatalysis based on UVA-irradiated TiO(2) for the reduction of the concentration of bacteria in the air could compete with the conventional photolytic treatment with UVC radiation, more expensive and hazardous. Simultaneously to the disinfection, the concentration of volatile organic compounds was greatly reduced, which adds value to this technology for real applications. The fungal colony number was not apparently modified.

Influence of Catalyst Properties and Reactor Configuration on the Photocatalytic Degradation of Trichloroethylene Under Sunlight Irradiation

In this work, the influence of the reactor configuration and the characteristics of the catalysts on the photodegradation of trichloroethylene (TCE) vapors are studied under sunlight illumination. The photocatalytic activity tests were carried out using two types of continuous flow reactors: (i) a compound parabolic collector (CPC) and (ii) a simple flat reactor. Three different photocatalysts based on TiO 2 were utilized: (i) commercial powders calcined at 500°C (ii) a Ti0 2-x N x sample synthesized by treating the commercial sample at 500°C in an NH 3 gas flow, and (iii) TiO 2 thin film coatings on differently shaped borosilicate glass supports prepared by a sol-gel procedure. The obtained data reveal that the photonic efficiency for the removal of TCE is quite high but slightly decreases with increasing the light intensity. The commercial TiO 2 sample presents the highest efficiency while nitrogen doping seems to be slightly detrimental for photoactivity, despite the fact that certain photoresponse in the visible can be envisaged. In contrast, transparent sol-gel TiO 2 coatings present the highest TCE degradation rate per mass of catalyst. Regarding the type of reactor, it is found that the use of CPCs can be advantageous, especially when dealing with high volumes of effluent and elevated concentration of TCE, although flat reactor also shows a considerable efficiency.