2010
DOI: 10.1016/j.cattod.2009.12.002
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Product desorption limitations in selective photocatalytic oxidation

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Cited by 20 publications
(24 citation statements)
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“…In operando photocatalytic studies have been traditionally used to investigate reaction mechanisms using infrared spectroscopy (Rohmann et al, 2008 ; Renckens et al, 2010 ; Hauchecorne and Lenaerts, 2013 ; Zandi and Hamann, 2016 ). In the last decade, in operando analysis of the photocatalyst surface has been widely carried out using advanced (time-resolved) X-ray spectroscopy techniques, with emphasis into photoelectrochemical water splitting and hydrogen evolution processes (Braun et al, 2012 ; Bora et al, 2013 ; Crumlin et al, 2015 ; Baran et al, 2016 ; Li et al, 2016b ; Neppl et al, 2016 ; Lu et al, 2020 ).…”
Section: Qualitative Approaches For the Assessment Of Photocatalytic mentioning
confidence: 99%
“…In operando photocatalytic studies have been traditionally used to investigate reaction mechanisms using infrared spectroscopy (Rohmann et al, 2008 ; Renckens et al, 2010 ; Hauchecorne and Lenaerts, 2013 ; Zandi and Hamann, 2016 ). In the last decade, in operando analysis of the photocatalyst surface has been widely carried out using advanced (time-resolved) X-ray spectroscopy techniques, with emphasis into photoelectrochemical water splitting and hydrogen evolution processes (Braun et al, 2012 ; Bora et al, 2013 ; Crumlin et al, 2015 ; Baran et al, 2016 ; Li et al, 2016b ; Neppl et al, 2016 ; Lu et al, 2020 ).…”
Section: Qualitative Approaches For the Assessment Of Photocatalytic mentioning
confidence: 99%
“…Similart emperature dependencies reported in the literature were ascribed to adsorption-desorption equilibria. [9,10] Mul and co-workers [12,13] encountered ar elated issue for the photooxidation of cyclohexaneo ver TiO 2 .T he unfavorable desorption of water limited the adsorption capacity for cyclohexane at low temperature. This explanation maya lso hold for the Figure 1.…”
Section: Influence Of Temperaturementioning
confidence: 99%
“…But in selective formation, desorption of the desired product from the catalyst surface takes place, thus stopping it from undergoing the further oxidation steps to total mineralization, whereas, in selective degradation, the adsorbed contaminant and its oxygenated intermediates stick onto the catalyst surface until they are finally completely mineralized. Selectivity in NTO photocatalysis is achieved through one or more of the following approaches: (i) attraction of the targets towards the catalyst, 7,8,[20][21][22][23][24][25][26][27][28][29][30][31][32][33][34][35][36][37][38][39] (ii) adsorption of the targets on the catalyst surface, 8,22,24,28,[40][41][42][43][44][45][46] (iii) desorption of the products from the catalyst surface, [47][48][49][50][51][52][53][54] (iv) doping effect, [55][56][57][58]…”
Section: Selectivity In Nto Photocatalysismentioning
confidence: 99%
“…Hydrophilic/hydrophobic (polar/nonpolar) interactions play a crucial role in desorption of the desired product from the NTO catalyst surface. [47][48][49][50][51][52][53] NTO incorporated into clays can form hydrophobic surfaces, [47][48][49] which have been used for selective formation of different organic compounds. TiO 2 pillared on three different clays (mica, montmorillonite and saponite) produced only 3.2% CO 2 from an aqueous solution of benzene; the remainder of the products were oxygenated organic compounds: maleic acid (45.6%), hydroquinone (2.7%), resorcinol (15.7%), catechol (16%) and PL (16.6%).…”
Section: Adsorption On the Catalystmentioning
confidence: 99%