Journal Archive

Johnson Matthey Technol. Rev., 2023, 67, (2), 219
doi: 10.1595/205651323X16759335257118

Challenges and Opportunities for Platinum in the Modern Three-Way Catalyst

Flexibility and performance in gasoline emissions control

  • Maria C. Vlachou*, Huw R. Marchbank, Emily Brooke, Amy Kolpin
  • Johnson Matthey, Blounts Court, Sonning Common, Reading, RG4 9NH, UK
  • *Email: 
    Received 1st December 2022; Revised 6th February 2023; Accepted 8th February 2023; Online 9th February 2023

Article Synopsis

Gasoline vehicles have generally relied upon a combination of palladium and rhodium for more than 25 years to facilitate the required oxidative and reductive reactions of carbon monoxide (CO), hydrocarbons (HCs), and nitrogen oxides (NOx). Recently, steady increases in the price of palladium relative to platinum have fuelled demand to reincorporate platinum into three-way catalysts (TWCs). However, the fundamental properties of platinum, including susceptibility toward sintering and inhibition under typical gasoline operating conditions, present significant challenges. This article presents an overview of the origins for these challenges, as well as select strategies for maximising platinum’s contribution to modern-day TWCs. Optimisation of ceria-zirconia supports is one route by which platinum’s performance can be significantly improved through tuning of the ceria-to-zirconia ratio. Additionally, alloying platinum with a secondary platinum group metal (pgm), such as rhodium, leverages complimentary properties of both metals, imparting stability and overall activity enhancements. Such routes not only enable pgm flexibility, but also provide opportunities to further improve TWC performance.

Historical Platinum Group Metal Use in Three-Way Catalysts

Automotive catalysts have been offsetting vehicular exhaust emissions for almost half a century. When Johnson Matthey began the design of automotive exhaust aftertreatment catalysts in the 1960s, it was platinum-based technology that steered the way, with the first-generation automotive catalyst introduced in the 1970s (13). More specifically, the primary gasoline exhaust aftertreatment system started out as a primitive ‘two-way’, rhodium-promoted-platinum oxidation catalyst (13). By the 1980s, the technology had developed into a dual component platinum-rhodium ‘three-way catalyst’, so-called for its ability to complete NOx reduction reactions simultaneously to oxidation reactions of CO and HCs with the help of engine calibration (14). Since the implementation of TWCs in commercial systems, there have been significant efforts in both industry and academia to explore cheaper alternatives to pgm based systems, but without widespread adoption in commercial applications. Ultimately, only three metals from the platinum group achieve the required performance, are sufficiently abundant and stand up to the harsh operating conditions of a gasoline engine: platinum, palladium and rhodium.

Research efforts have undoubtedly driven developments in TWC technology over time, but so too have external factors like pgm cost. Notably, the relatively high platinum prices of the 1990s, as seen in Figure 1(a), motivated efforts to substitute with the then cheaper palladium. However, while cost pressures drove these changes in the catalyst technology, it was ultimately external factors like improvements in fuel quality (4) that enabled them to be implemented successfully.

Fig. 1.

(a) Average monthly pgm price chart illustrating the cost pressures on the inclusion (or exclusion) of platinum and palladium in TWCs over the past three decades; (b) including rhodium. Note the order of magnitude scale difference between (a) and (b) (Johnson Matthey, December 2022)

The late 1990s saw a move towards desulfurisation of fuel as sulfur limits were beginning to be imposed by governments around the world with the intention of reducing both sulfur-containing emissions and catalyst deactivation (5). Sulfur is a major catalyst poison for pgms to contend with in commercial systems, with sensitivity to deactivation following the order of palladium>platinum>>rhodium (5), but once sulfur was effectively removed from gasoline, the performance of palladium was better able to compete with that of platinum.

In theory, platinum and palladium are both capable of catalysing oxidation reactions to the level expected for modern three-way technology and thus should be interchangeable from this respect. However, their properties differ considerably as do their optimal operating conditions. For example, palladium’s greater sintering resistance enabled TWCs to be physically shifted closer to the engine when it largely replaced platinum as the dominant pgm by the late 1990s. This shift in position took advantage of faster catalyst warm up to reduce the slip of emissions at cold start. These two changes of desulfurisation and catalyst positioning led the way to today’s widespread TWC palladium-rhodium formula, which can realise greater than 99% emissions conversion.

Since the early 1990s, the cost of platinum has generally exceeded that of palladium, however a turning point was reached around 2018 when high demand for palladium and rhodium coincided with a stall in demand for platinum. Thorough accounts of supply and demand histories dating back to 1999 are offered through Johnson Matthey’s annual PGM Market Reports. As of 2022, the platinum price is less than half that of palladium (6). For this reason, impetus to shift the dominant pgm in commercial TWCs has returned as a key market demand, but the tides have turned with the push now to remove palladium and reincorporate platinum. As we enter a new era for the internal combustion engine, we are revisiting the origins of the technology. Can we simply shift back to the original platinum-rhodium TWC? And if not, what other options do TWCs have to make use of platinum once more?

Challenges for Platinum Incorporation in Today’s Three-Way Catalyst

Today’s TWC technology generally comprises a monolith with a catalytic coating containing palladium and rhodium supported on rare earth (RE) stabilised alumina and RE stabilised ceria-zirconia (CeZr) mixed oxides, usually with additional promotor elements like barium. In addition to catalytic activity, durability is a crucial property of TWCs with commercial systems needing to maintain high levels of performance after exposure to temperatures in the region of 950–1050°C for many hours, with regular and extreme fluctuations between reductive and oxidative atmospheres. These conditions present a greater challenge for platinum than palladium, in part due to platinum’s susceptibility to both types of sintering mechanisms experienced under TWC conditions: particle coalescence and Ostwald ripening (7).

The first of these mechanisms, particle coalescence, involves the diffusion of nanoparticles (NPs) over the support surface, causing them to collide and agglomerate into larger NPs. This process is more easily facilitated when pgm particles are reduced to their metallic form and oxygen bonds with the support are broken. Even for support materials which would usually afford pgm particles some sintering resistance through strong metal support interactions (8), the reducing conditions experienced during TWC operation can be sufficient to overcome these stabilising effects. Platinum exhibits a lower oxide decomposition temperature compared to palladium or rhodium as seen in Table I, which means that it is in its metallic form independent of the gas conditions, even when only operating at moderate TWC temperatures of ~600°C. Relative to palladium and rhodium, platinum particles therefore spend a greater proportion of time susceptible to coalescence effects.

Table I

Bulk Oxide Decomposition Temperatures in Air

Decomposition temperature, °C Reference
Rh2O3 ~1100 (9)
PdO ~850 (10)
PtO2 ~500–650 (11)

The second mechanism, Ostwald ripening, is far more detrimental to platinum dispersion. This process involves the oxygen-mediated movement of individual atoms across a support surface or through the gas phase. The loss and reincorporation of atoms between NPs leads to a net transfer of atoms from smaller particles to larger ones, resulting in sintering. The gas phase transport process is enabled through the formation of volatile gas-phase oxides when pgms are heated in an oxidising atmosphere at high temperature. Platinum in particular is known for its proclivity to form such volatile oxides to relatively high vapour pressure and well within the temperature range of TWC operation (12). Palladium, on the other hand, volatilises to an almost negligible degree in this temperature regime (13). The culmination of these properties is effectively demonstrated by comparing lanthanum-doped alumina-supported palladium and platinum catalysts that have been exposed to moderate calcination temperatures by transmission electron microscopy (TEM), shown in Figure 2. The average pgm particle size of the platinum catalyst is an order of magnitude greater than the palladium catalyst.

Fig. 2.

TEM images of: (a) palladium; and (b) platinum supported on lanthanum-doped alumina following calcination at 650°C in air. Average particle sizes dav are given in the images

The result shown in Figure 2 is in agreement with other studies which show that platinum sinters in air from ~580°C (1416). As previously mentioned, the average operating temperatures of TWCs are commonly upwards of 600°C (post light-off). Platinum therefore cannot redisperse via practical pgm redispersion routes, i.e., the oxidising conditions of the gasoline engine and air, without further measures put in place to inhibit sintering via Ostwald ripening, such as atom traps. Palladium on the other hand can undergo some redispersion in oxidising gasoline conditions below the palladium oxide decomposition temperature and following relevant TWC ageing conditions (17, 18). Sintering prevention is therefore key to preventing the permanent loss of platinum dispersion. There are many pgm stabilisation strategies, but an example which has recently received more attention in the literature is that of atom-trapping support technology (19). When applied to platinum-based catalysts, such strategies utilise the otherwise problematic issue of platinum volatility to capture and stabilise mobile molecular species on undercoordinated surface sites of a support material, which then show increased resistance to re-agglomeration (2025). These specialised sites are maximised on high surface area materials with highly defective surface topographies, such as ceria. Studies that successfully employ atom-trap materials use mild conditions of heating at 800°C in air, i.e. diesel ageing conditions, to volatilise the platinum (2025). However, materials such as pure ceria (which have the greatest potential for use in such a strategy) lack the stabilisers and dopants which are generally considered essential to endure TWC ageing conditions (26, 27). Preparing stable, atom trapping materials that inherently have the high energy surfaces required is therefore a paradoxically challenging research area for pgm stabilisation in TWC applications.

Another challenging consideration of note in the drive to reincorporate platinum into TWCs which is often ignored is the greater atomic mass of platinum (195 u) compared to that of palladium (106 u). Palladium sold on a weight basis contains almost twice the number of atoms as the equivalent mass of platinum. Considering the relative prices of the two metals as of 2022, the cost of palladium and platinum atoms are quite comparable. Successful palladium replacement on a weight basis therefore demands that each platinum atom be essentially twice as active as a palladium atom.

Strategies for Overcoming Platinum’s Challenging Properties

Direct Exchange of Palladium for Platinum

There are clearly challenges that must be addressed when considering platinum incorporation into modern TWCs. As a starting point, a brief exercise in swapping out palladium for platinum on representative TWC support materials was explored. Catalysts were compared through simulated activity testing of pelletised powders in a plug flow reactor under a gasoline-type rich/lean perturbed gas mix with the temperature ramped from room temperature to 500°C. Descriptions of experimental and ageing conditions can be found elsewhere (28). Where appropriate, the T50 light off temperature (temperature at which 50% conversion is reached) was selected for comparisons of catalyst activity. Prior to evaluation, catalysts were hydrothermally aged at 950°C under a simulated gasoline-type rich/lean perturbed gas mix. Whether supported on RE-doped CeZr or RE-doped alumina, platinum shows a substantial loss of light-off activity compared to palladium when substituted on a 1 wt% loading basis, as shown in Figure 3. Given the aforementioned challenges platinum faces under typical gasoline operating and ageing conditions, it is perhaps unsurprising this switch results in decreased activity. More notably, this data elucidates palladium’s similar light-off activity irrespective of its support whereas platinum has a significant activity difference; the platinum catalyst exhibits a considerable detriment to light-off activity when supported on alumina. Note that the CeZr based catalysts (which have oxygen storage capacity) achieve high final conversions of >85% by buffering the perturbing gas conditions of the test.

Fig. 3.

CO light-off activity curves from simulated activity testing for 1 wt% palladium and platinum catalysts supported on RE-doped CeZr and RE-doped alumina supports. Prior to testing, catalysts were hydrothermally redox aged at 950°C and cooled to room temperature in 1.3% oxygen in nitrogen

Optimising the Ceria-to-Zirconia Ratio for Platinum Three-Way Catalysts

The above results highlighted a potential pathway by which platinum’s activity can be improved and prompted a study to examine 1 wt% platinum and palladium catalysts supported on a range of CeZr mixed oxides of differing ceria-to-zirconia ratios. All catalysts were hydrothermally redox aged at 950°C. Descriptions of experimental and ageing conditions can be found elsewhere (28). As seen in Figure 4, there is a strong dependence of the CO T50 value on the ceria-to-zirconia ratio for the platinum catalysts, whereas evaluation of the palladium catalysts reveals no relationship. This observation emphasises the very different catalytic properties of these two pgms which must be considered when trying to use them interchangeably for TWC applications. At low temperatures, and hence during catalyst light-off, platinum particles can be inhibited by rich gas conditions, i.e. platinum is temporarily poisoned by CO (29, 30). The initial light-off ‘hump’ seen in Figure 3 for the platinum-alumina catalyst illustrates this inhibitory behaviour. Interactions between platinum and ceria appear to reduce these inhibition effects. Many studies have explored the phenomenon of reverse oxygen spillover across the support-metal boundary from ceria to platinum at low temperatures. It is suggested that this ‘activated oxygen’ initiates lower temperature CO oxidation and keeps catalytic sites clear at the pgm-support interface, thus alleviating some inhibition effects (29, 30). Whilst there are certainly activity and durability benefits to be gained from optimising the ceria content to help overcome some of platinum’s inherent challenges, an alternative strategy discussed in the final section of this paper actually seeks to turn these challenges into an advantage for promotion of overall TWC performance.

Fig. 4.

CO T50 light-off values for 1 wt% platinum catalysts supported on RE-doped CeZr supports plotted as a function of the ceria mol% content in the support (shown in blue) reveal a positive trend toward lower light-off temperature. T50 values for 1 wt% palladium catalysts reveal a relatively flat trend (shown in pink). Prior to testing, catalysts were hydrothermally redox aged at 950°C and cooled to room temperature in 1.3% oxygen in nitrogen

Partial Platinum Substitution: Rhodium-Platinum Alloys

As clearly laid out in previous sections of this paper, platinum has a number of inherent properties which make wholescale replacement of palladium in TWCs a challenging prospect. One alternative strategy for achieving this goal is designing ‘trimetal’ TWCs by partially replacing some of the more expensive palladium or rhodium with platinum; specifically through co-location of platinum with palladium or rhodium on a support material. Given the relatively high cost of rhodium as of 2022 as well as general price volatility, illustrated in Figure 1(b), partial replacement of rhodium with platinum has been chosen as a case study to illustrate this strategy considering the dual potential benefits of platinum incorporation and rhodium thrifting.

Rhodium catalysts partially replaced with platinum were prepared at a pgm loading of 0.2 wt% and supported on a RE-doped CeZr with ~38 mol% ceria. In addition to the monometallic platinum-only and rhodium-only reference catalysts, bimetallic rhodium-platinum catalysts with rhodium-platinum weight ratios of 5:1, 2:1 and 1:1 were prepared. These ratios were chosen to maintain an overall rhodium character and activity. All catalysts were hydrothermally redox aged at 950°C. Descriptions of experimental and ageing conditions can be found elsewhere (28). In order to emphasise the themes of rhodium thrifting and stabilisation alongside platinum substitution, an oxidising cooldown step was chosen for the ageing procedure. Such shutdown conditions are particularly stressful for rhodium performance given its susceptibility to form inactive oxides under oxidising conditions until exposed to sufficiently reducing conditions to recover the metallic state. Catalysts were evaluated through simulated activity testing as described previously, with the nitric oxide (NO) T40 value chosen for comparison as the rhodium component of a TWC is especially important for controlling NO emissions. T40 (and not T50) values were chosen to enable comparison to the two ≤0.13% rhodium-only references which had not reached 50% conversion by the end of the test at 500°C. The results presented in Figure 5 reveal that activity is maintained upon replacing rhodium with platinum up to the maximum substitution of 50%. Comparison of the activities of the 0.1 wt% and 0.2 wt% rhodium-only references with the 1:1 rhodium-platinum catalyst reveals the strong interaction that low rhodium loadings can have with a support following ageing (31, 32). A synergistic interaction between rhodium and platinum is evidently able to limit this deactivation mechanism.

Fig. 5.

NO T40 light-off values for 0.2 wt% pgm catalysts supported on a RE-doped CeZr with ~38% ceria demonstrating synergistic activity enhancements for rhodium-platinum (shown in light blue) as compared to rhodium-only reference catalysts (shown in pink). Platinum-only activity (shown in dark blue) confirms that the enhanced activity for the rhodium-platinum catalysts is not governed by platinum alone. Prior to testing, catalysts were hydrothermally redox aged at 950°C and cooled to room temperature in 1.3% oxygen in nitrogen

Physical characterisation methods were employed to probe the synergistic relationship apparently underpinning the enhanced catalytic behaviour, with the pgm loading increased to 3 wt% to emphasise observable effects. Both X-ray diffraction (XRD) and energy-dispersive X-ray spectroscopy analysis via TEM (EDX TEM) results clearly evidence the presence of bulk rhodium-platinum alloy particles as seen in Figure 6. This observation aligns with expectations from literature based on the phase diagrams (33) of rhodium-platinum (and palladium-platinum), which indicate the ageing temperature employed, and thus the extreme operating temperatures of TWCs, are sufficient to induce rhodium-platinum (and palladium-platinum) alloy formation.

Fig. 6.

Physical characterisation of a 3 wt% rhodium-platinum 1:1 catalyst supported on a RE-doped CeZr with ~38 wt% ceria evidencing the formation of rhodium-platinum alloyed particles by: (a) XRD, where the inset confirms the primary presence of a rhodium-platinum alloy; (b) high-resolution TEM image; and (c) EDX linescan profile through two pgm particles which show a uniform distribution of rhodium and platinum. Counts are shown for the Lα lines of rhodium, cerium, zirconium and platinum. The catalyst had been hydrothermally redox aged at 950°C and cooled to room temperature in 1.3% oxygen in nitrogen

CO probe Fourier transform infrared spectroscopy (CO-FTIR) was employed to examine the nature of the catalytically active rhodium-platinum surface. Figure 7 shows the first scan data taken immediately following the introduction of CO at room temperature and compares rhodium-only and platinum-only references with the rhodium-platinum 1:1 alloyed catalyst at 0.2 wt% pgm loading. Prior to CO introduction, self-supporting pellets of catalyst of 13 mm diameter were subjected to a 5% hydrogen pretreatment for 10 min at 250°C. CO-probe data was collected at 30°C in a flow of 500 ppm CO in helium. Difference spectra were obtained by using t = 0 as the background for subsequent spectra under CO flow. Difference spectra were normalised by the weight of the pellet used. The difference spectra shown here are at t = 5 min. Note that the negative band at ~2127 cm–1 is ascribed to Ce3+ defects induced by the hydrogen pretreatment. As CO is introduced over the catalysts, this band is steadily lost due to direct interaction of CO with the defect (3437). The rhodium and rhodium-platinum catalysts present major bands at 2003 cm–1 and 2073 cm–1, assigned to the symmetric and antisymmetric stretching modes of gem-dicarbonyl Rh+(CO)2 (38, 39), i.e. CO adsorbed to dispersed, oxidic rhodium species. It is apparent that the spectrum of the rhodium-platinum catalyst closely resembles that of the rhodium-only reference, and in fact, reveals similar intensity in the Rh+(CO)2 bands, indicating similar rhodium surface area despite there being half the amount of rhodium present in the catalyst overall. Platinum, therefore, is able to promote a similar accessible rhodium surface area (compared to the addition of the same weight percentage of rhodium as seen in the rhodium-only reference) during exposure to the excess-oxygen conditions at high temperatures. This accounts for the equivalent light-off activity seen for the rhodium-platinum catalysts.

Fig. 7.

Transmission CO-FTIR difference spectra of 0.2 wt% pgm catalysts (rhodium, platinum and rhodium-platinum) supported on a RE-doped CeZr with ~38% ceria content which have been hydrothermally redox aged at 950°C and cooled to room temperature in 1.3% oxygen in nitrogen

As previously discussed, platinum is easily sintered by TWC conditions. Moreover, it does not recover a bulk reoxidised form following sintering of its metallic state. It reforms a passivating oxygen layer at its surface only (40) and by this definition, is the most noble of the three pgms used for TWC applications. It is proposed that when alloyed with rhodium or palladium, platinum lends some of its nobility to form more metallic particles that show greater resistance to severe deactivation with the support during oxidising conditions, enabling the use of, in the case examined here, lower rhodium loadings. It is further suggested that the oxidic rhodium seen via the CO-FTIR results, i.e. Rh+(CO)2, resides at the surface of stabilised bulk rhodium-platinum alloyed particles, demonstrated by the XRD and EDX TEM measurements. This proposed structure is illustrated in Figure 8.

Fig. 8.

Proposed structure of rhodium-platinum particles following high temperature (950°C) ageing and shutdown procedure under oxidising conditions

This rhodium-platinum alloy technology demonstrates not only a route by which platinum can be incorporated into TWCs, but also one where the challenging properties of platinum can be repurposed towards promoting the activity and durability of one of the most important, and costly, TWC components. As previously stated, the first generation TWCs were rhodium-promoted platinum oxidation catalysts. This study has shown that platinum has the potential to return the favour by promoting today’s rhodium TWCs to mitigate rhodium’s less-desirable properties.


The requirements of the TWC over the past ~25 years have evolved far beyond the capabilities of the original platinum-rhodium formulations. Today’s palladium-rhodium TWC has been fine-tuned to achieve current emission limits, including optimisation of supports and promotors. While pgm price fluctuations take place over a relatively fast timescale, prompting the requirement for pgm flexibility, similar platinum TWC optimisation efforts should be expected in order to see platinum reinstated in palladium’s place. Non-equivalent performance from straight exchange to the otherwise unchanged TWC technology is the beginning of the story, not the end! It is evident that there are options and furthermore, opportunities for platinum in returning to the TWC. Results shown here demonstrate that platinum activity and stability are enhanced by increasing the ceria-to-zirconia ratio, with further optimisation opportunities to hone platinum’s ultimate TWC performance. Moreover, it was shown that platinum can be effectively substituted for a portion of the other pgms in the system due to the synergistic nature of the alloys formed. And beyond this substitution achievement, it was demonstrated that mixing the properties of platinum with those of rhodium can positively impact the TWC performance of these existing components.


  1. 1.
    C. Morgan, Johnson Matthey Technol. Rev., 2014, 58, (4), 217 LINK
  2. 2.
    G. J. K. Acres and B. Harrison, Top. Catal., 2004, 28, (1–4), 3 LINK
  3. 3.
    M. V. Twigg, Platinum Metals Rev., 1999, 43, (4), 168 LINK
  4. 4.
    H. S. Gandhi, G. W. Graham and R. W. McCabe, J. Catal., 2003, 216, (1–2), 433 LINK
  5. 5.
    T. J. Truex, ‘Interaction of Sulfur with Automotive Catalysts and the Impact on Vehicle Emissions – A Review’, SAE Technical Paper 1999-01-1543, SAE International, Warrendale, USA, 1999 LINK
  6. 6.
  7. 7.
    T. W. Hansen, A. T. DeLaRiva, S. R. Challa and A. K. Datye, Acc. Chem. Res., 2013, 46, (8), 1720 LINK
  8. 8.
    Y. Cao, R. Ran, X. Wu, Z. Si, F. Kang and D. Weng, J. Environ. Sci., 2023, 125, 401 LINK
  9. 9.
    K. T. Jacob, T. Uda, T. H. Okabe and Y. Waseda, High Temp. Mater. Process., 2000, 19, (1), 11 LINK
  10. 10.
    C. Mallika, O. M. Sreedharan and J. B. Gnanamoorthy, J. Less Common Met., 1983, 95, (2), 213 LINK
  11. 11.
    N. Seriani, W. Pompe and L. C. Ciacchi, J. Phys. Chem. B, 2006, 110, (30), 14860 LINK
  12. 12.
    K. Leistner, C. Gonzalez Braga, A. Kumar, K. Kamasamudram and L. Olsson, Appl. Catal. B: Environ., 2019, 241, 338 LINK
  13. 13.
    J. C. Chaston, Platinum Metals Rev., 1965, 9, (4), 126 LINK
  14. 14.
    R. M. J. Fiedorow and S. Wanke, J. Catal., 1976, 43, (1–3), 34 LINK
  15. 15.
    G. Straguzzi, J. Catal., 1980, 66, (1), 171 LINK
  16. 16.
    M. F. L. Johnson and C. D. Keith, J. Phys. Chem., 1963, 67, (1), 200 LINK
  17. 17.
    X. Chen, Y. Cheng, C. Y. Seo, J. W. Schwank and R. W. McCabe, Appl. Catal. B: Environ., 2015, 163, 499 LINK
  18. 18.
    Q. Wang, B. Zhao, G. Li and R. Zhou, Environ. Sci. Technol., 2010, 44, (10), 3870 LINK
  19. 19.
    A. Datye and Y. Wang, Natl. Sci. Rev., 2018, 5, (5), 630 LINK
  20. 20.
    J. Jones, H. Xiong, A. T. DeLaRiva, E. J. Peterson, H. Pham, S. R. Challa, G. Qi, S. Oh, M. H. Wiebenga, X. I. P. Hernández, Y. Wang and A. K. Datye, Science, 2016, 353, (6295), 150 LINK
  21. 21.
    Y. Nagai, T. Hirabayashi, K. Dohmae, N. Takagi, T. Minami, H. Shinjoh and S. Matsumoto, J. Catal., 2006, 242, (1), 103 LINK
  22. 22.
    H. N. Pham, A. DeLaRiva, E. J. Peterson, R. Alcala, K. Khivantsev, J. Szanyi, X. S. Li, D. Jiang, W. Huang, Y. Sun, P. Tran, Q. Do, C. L. DiMaggio, Y. Wang and A. K. Datye, ACS Sustain. Chem. Eng., 2022, 10, (23), 7603 LINK
  23. 23.
    D. Kunwar, C. Carrillo, H. Xiong, E. Peterson, A. DeLaRiva, A. Ghosh, G. Qi, M. Yang, M. Wiebenga, S. Oh, W. Li and A. K. Datye, Appl. Catal. B: Environ., 2020, 266, 118598 LINK
  24. 24.
    S. Xie, W. Tan, C. Wang, H. Arandiyan, M. Garbrecht, L. Ma, S. N. Ehrlich, P. Xu, Y. Li, Y. Zhang, S. Collier, J. Deng and F. Liu, J. Catal., 2022, 405, 236 LINK
  25. 25.
    Z. Zhang, Y. Zhu, H. Asakura, B. Zhang, J. Zhang, M. Zhou, Y. Han, T. Tanaka, A. Wang, T. Zhang and N. Yan, Nat. Commun., 2017, 8, (1), 16100 LINK
  26. 26.
    “Catalysis by Ceria and Related Materials”, 2nd Edn., eds. A. Trovarelli and P. Fornasiero, Catalytic Science Series, Vol. 12, Imperial College Press, London, UK, 2013, 908 pp LINK
  27. 27.
    E. Aneggi, M. Boaro, C. de Leitenburg, G. Dolcetti and A. Trovarelli, Catal. Today, 2006, 112, (1–4), 94 LINK
  28. 28.
    P. Millington and M. C. Vlachou, Johnson Matthey Plc, ‘TWC Catalysts for Gasoline Engine Exhaust Gas Treatments’, US Patent Appl. 2021/451,352
  29. 29.
    F. C. Meunier, L. Cardenas, H. Kaper, B. Šmíd, M. Vorokhta, R. Grosjean, D. Aubert, K. Dembélé and T. Lunkenbein, Angew. Chem. Int. Ed., 2020, 60, (7), 3799 LINK
  30. 30.
    M. Di, K. Simmance, A. Schaefer, Y. Feng, F. Hemmingsson, M. Skoglundh, T. Bell, D. Thompsett, L. I. A. Jensen, S. Blomberg and P.-A. Carlsson, J. Catal., 2022, 409, 1 LINK
  31. 31.
    S. Rood, S. Eslava, A. Manigrasso and C. Bannister, Proc. Inst. Mech. Eng. Part D: J. Automob. Eng., 2019, 234, (4), 936 LINK
  32. 32.
    E. A. Alikin and A. A. Vedyagin, Top. Catal., 2016, 59, (10–12), 1033 LINK
  33. 33.
    G. Rakhtsaum, Platinum Metals Rev., 2013, 57, (3), 202 LINK
  34. 34.
    S. Afrin and P. Bollini, J. Phys. Chem. C, 2023, 127, (1), 234 LINK
  35. 35.
    C. Binet, A. Badri and J.-C. Lavalley, J. Phys. Chem., 1994, 98, (25), 6392 LINK
  36. 36.
    C. Binet, M. Daturi and J.-C. Lavalley, Catal. Today, 1999, 50, (2), 207 LINK
  37. 37.
    F. Bozon-Verduraz and A. Bensalem, J. Chem. Soc. Faraday Trans., 1994, 90, (4), 653 LINK
  38. 38.
    X. Yin, S. Li, J. Deng, Y. Wang, M. Li, Y. Zhao, W. Wang, J. Wang and Y. Chen, Ind. Eng. Chem. Res., 2022, 61, (35), 13011 LINK
  39. 39.
    E. Ivanova and K. Hadjiivanov, Phys. Chem. Chem. Phys., 2002, 5, (3), 655 LINK
  40. 40.
    J. C. Chaston, Platinum Metals Rev., 1964, 8, (2), 50 LINK

‘Report Archive’, Johnson Matthey Plc, London, UK, 1999–2017 LINK

PGM Prices and Trading, Johnson Matthey Plc, London, UK LINK


We would like to thank the following members from Johnson Matthey: Gregory Goodlet for the TEM measurements and David Thompsett, Paul Millington and Nicola Collis for their intellectual contributions.

The Authors

Maria Vlachou joined Johnson Matthey in 2017 after completing a Johnson Matthey funded PhD at the University of Warwick, UK, in solid state nuclear magnetic resonance researching ceria-containing materials. She is now a Senior Scientist for the gasoline team in the emissions control group and among other activities, oversees projects related to the reincorporation of platinum into TWCs.

Huw Marchbank became a member of the analytical department at Johnson Matthey in 2016 after gaining a PhD in chemistry from University College London (UCL), UK, where he investigated binary and ternary metal oxides using synchrotron and neutron-based techniques. He is currently senior scientist based in the X-ray diffraction analytical team supporting scientists with understanding materials by X-ray diffraction, X-ray absorption spectroscopy and powder diffraction techniques.

Emily Brooke joined Johnson Matthey in 2015 after completing an Engineering and Physical Sciences Research Council (EPSRC) funded PhD on the physical vapour deposition growth and electron microscopy characterisation of metallic nanoparticles in the Materials Science Department at Imperial College London, UK. She is now a Senior Electron Microscopist offering characterisation using transmission electron microscopy, scanning electron microscopy and focused ion beam.

Amy Kolpin joined Johnson Matthey in 2014 after completing a Johnson Matthey funded PhD at the University of Oxford, UK, in inorganic chemistry researching electronic and geometric modification of pgm nanoparticles. She is now a Principal Scientist and leader of the Gasoline team in the Emissions Control group.

Related articles

In the Lab: Artificial Metalloenzymes for Sustainable Chemical Production

In the Lab: Heterogeneous Catalysis Mediated Interconversion between NAD(P)+ and NAD(P)H Accompanied by Consumption and Generation of Hydrogen

Find an article