A simple model to describe electrochemical promotion of catalysis

Author(s):  
Ian S. Metcalfe
Catalysts ◽  
2019 ◽  
Vol 9 (2) ◽  
pp. 157 ◽  
Author(s):  
Ioannis V. Yentekakis ◽  
Philippe Vernoux ◽  
Grammatiki Goula ◽  
Angel Caravaca

Recent studies have shown that the catalytic performance (activity and/or selectivity) of Pt-group metal (PGM) catalysts for the CO and hydrocarbons oxidation as well as for the (CO, HCs or H2)-SCR of NOx or N2O can be remarkably affected through surface-induced promotion by successful application of electropositive promoters, such as alkalis or alkaline earths. Two promotion methodologies were implemented for these studies: the Electrochemical Promotion of Catalysis (EPOC) and the Conventional Catalysts Promotion (CCP). Both methodologies were in general found to achieve similar results. Turnover rate enhancements by up to two orders of magnitude were typically achievable for the reduction of NOx by hydrocarbons or CO, in the presence or absence of oxygen. Subsequent improvements (ca. 30–60 additional percentage units) in selectivity towards N2 were also observed. Electropositively promoted PGMs were also found to be significantly more active for CO and hydrocarbons oxidations, either when these reactions occur simultaneously with deNOx reactions or not. The aforementioned direct (via surface) promotion was also found to act synergistically with support-mediated promotion (structural promotion); the latter is typically implemented in TWCs through the complex (Ce–La–Zr)-modified γ-Al2O3 washcoats used. These attractive findings prompt to the development of novel catalyst formulations for a more efficient and cost-effective control of the emissions of automotives and stationary combustion processes. In this report the literature findings in the relevant area are summarized, classified and discussed. The mechanism and the mode of action of the electropositive promoters are consistently interpreted with all the observed promoting phenomena, by means of indirect (kinetics) and direct (spectroscopic) evidences.


2002 ◽  
Vol 56 (4) ◽  
pp. 137-142 ◽  
Author(s):  
György Fóti ◽  
Ivan Bolzonella ◽  
Justyna Eaves ◽  
Christos Comninellis

Catalysts ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 1276
Author(s):  
Angel Caravaca ◽  
Jesús González-Cobos ◽  
Philippe Vernoux

The phenomenon of “Non-Faradaic Electrochemical Modification of Catalytic Activity (NEMCA)” or “Electrochemical Promotion of Catalysis (EPOC)” has been extensively studied for the last decades. Its main strength, with respect to conventionally promoted catalytic systems, is its capability to modify in-situ the activity and/or selectivity of a catalyst by controlling the supply and removal of promoters upon electrical polarization. Previous reviews have summarized the main achievements in this field from both the scientific and technological points of view. However, to this date no commercial application of the EPOC phenomenon has been developed, although numerous advances have been made on the application of EPOC on catalyst nanostructures (closer to those employed in conventional catalytic systems), and on the development of scaled-up reactors suitable for EPOC application. The main bottleneck for EPOC commercialization is likely the choice of the right chemical process. Therefore, from our point of view, future efforts should focus on coupling the latest EPOC advances with the chemical processes where the EPOC phenomenon offers a competitive advantage, either from an environmental, a practical or an economic point of view. In this article, we discuss some of the most promising cases published to date and suggest future improvement strategies. The considered processes are: (i) ethylene epoxidation with environmentally friendly promoters, (ii) NOx storage and reduction under constant reaction atmosphere, (iii) CH4 steam reforming with in-situ catalyst regeneration, (iv) H2 production, storage and release under fixed temperature and pressure, and (v) EPOC-enhanced electrolysers.


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