Stability of Bimetallic PtxRuy - From Model Surfaces to Nanoparticulate Electrocatalysts.

Fundamental research campaigns in electrocatalysis often involve the use of model systems, such as single crystals or magnetron-sputtered thin films (single metals or metal alloys). The downsides of these approaches are that oftentimes only a limited number of compositions are picked and tested (guided by chemical intuition) and that the validity of trends is not verified under operating conditions typically present in real devices. These together can lead to deficient conclusions, hampering the direct application of newly discovered systems in real devices. In this contribution, the stability of magnetron-sputtered bimetallic PtxRuy thin film electrocatalysts (0 at. % to 100 at. % Ru content) along with three commercially available carbon-supported counterparts (50-67 at. % Ru content) was mapped under electrocatalytic conditions in acidic electrolytes using online ICP-MS. We found several differences between the two systems in the amount of metals dissolved along with the development of the morphology and composition. While the Pt-rich PtxRuy compositions remained unchanged, 30-50 nm diameter surface pits were detected in the case of the Ru-rich sputtered thin films. Contrastingly, the surface of the carbon-supported NPs enriched in Pt accompanied by the leaching of a significant amount of Ru from the alloy structure was observed. Change in morphology was accompanied by a mass loss reaching around 1-2 wt % in the case of the sputtered samples and almost 10 wt % for the NPs. Since PtxRuy has prime importance in driving alcohol oxidation reactions, the stability of all investigated alloys was screened in the presence of isopropanol. While Pt dissolution was marginally affected by the presence of isopropanol, several times higher Ru dissolution was detected, especially in the case of the Ru-rich compositions. Our results underline that trends in terms of electrocatalytic activity and stability cannot always be transferred from model samples to systems that are closer to the ones applied in real devices.

Electrolyte Engineering Stabilizes Photoanodes Decorated with Molecular Catalysts.

Invited for this month's cover is the group of Dunwei Wang from Boston College and Serhiy Cherevko from the Helmholtz Institute Erlangen-Nürnberg for Renewable Energy. The image illustrates the impact of different electrolyte environments on the stability of hematite decorated with an iridium molecular catalyst used for solar water splitting. The Research Article itself is available at 10.1002/cssc.202202319.

Electrolyte Engineering Stabilizes Photoanodes Decorated with Molecular Catalysts.

Molecular catalysts are promising oxygen evolution promoters in conjunction with photoanodes for solar water splitting. Maintaining the stability of both photoabsorber and cocatalyst is still a prime challenge, with many efforts tackling this issue through sophisticated material designs. Such approaches often mask the importance of the electrode-electrolyte interface and overlook easily tunable system parameters, such as the electrolyte environment, to improve efficiency. We provide a systematic study on the activity-stability relationship of a prominent Fe2 O3 photoanode modified with Ir molecular catalysts using in situ mass spectroscopy. After gaining detailed insights into the dissolution behavior of the Ir cocatalyst, a comprehensive pH study is conducted to probe the impact of the electrolyte on the performance. An inverse trend in Fe and Ir stability is found, with the best activity-stability synergy obtained at pH 9.7. The results bring awareness to the overall photostability and electrolyte engineering when advancing catalysts for solar water splitting.

High-throughput exploration of activity and stability for identifying photoelectrochemical water splitting materials.

The experimental high-throughput (HT) exploration for a suitable solar water splitting photoanode has greatly relied on photoactivity as the sole descriptor to identify a promising region within the searched composition space. Although activity is essential, it is not sufficient for describing the overall performance and excludes other pertinent criteria for photoelectrochemical (PEC) water splitting. Photostability in the form of (photo)electrocatalyst dissolution must be tracked to illustrate the intricate relation between activity and stability for multinary photoelectrocatalysts. To access these two important metrics simultaneously, an automated PEC scanning flow cell coupled to an inductively coupled plasma mass spectrometer (PEC-ICP-MS) was used to study an Fe-Ti-W-O thin film materials library. The results reveal an interrelation between composition, photocurrent density, and element-specific dissolution. These structure-activity-stability correlations can be represented using data science tools like principal component analysis (PCA) in addition to common data visualization approaches. This study demonstrates the importance of addressing two of the most important catalyst metrics (activity and stability) in a rapid and parallel fashion during HT experiments to adequately discover high-performing compositions in the multidimensional search space.

Accessing In Situ Photocorrosion under Realistic Light Conditions: Photoelectrochemical Scanning Flow Cell Coupled to Online ICP-MS.

High-impact photoelectrode materials for photoelectrochemical (PEC) water splitting are distinguished by synergistically attaining high photoactivity and stability at the same time. With numerous efforts toward optimizing the activity, the bigger challenge of tailoring the durability of photoelectrodes to meet industrially relevant levels remains. In situ photostability measurements hold great promise in understanding stability-related properties. Although different flow systems coupled to light-emitting diodes were introduced recently to measure time-resolved photocorrosion, none of the measurements were performed under realistic light conditions. In this paper, a photoelectrochemical scanning flow cell connected to an inductively coupled plasma mass spectrometer (PEC-ICP-MS) and equipped with a solar simulator, Air Mass 1.5 G filter, and monochromator was developed. The established system is capable of independently assessing basic PEC metrics, such as photopotential, photocurrent, incident photon to current efficiency (IPCE), and band gap in a high-throughput manner as well as the in situ photocorrosion behavior of photoelectrodes under standardized and realistic light conditions by coupling it to an ICP-MS. Polycrystalline platinum and tungsten trioxide (WO3) were used as model systems to demonstrate the operation under dark and light conditions, respectively. Photocorrosion measurements conducted with the present PEC-ICP-MS setup revealed that WO3 starts dissolving at 0.8 VRHE with the dissolution rate rapidly increasing past 1.2 VRHE, coinciding with the onset of the saturation photocurrent. The most detrimental damage to the photoelectrode is caused when subjecting it to a prolonged high potential hold, e.g., at 1.5 VRHE. By using standardized illumination conditions such as Air Mass 1.5 Global under 1 Sun, the obtained dissolution characteristics are translatable to actual devices under realistic light conditions. The gained insights can then be utilized to advance synthesis and design approaches of novel PEC materials with improved photostability.