This investigation, which is motivated by promising pseudocapacitive properties of Mn3O4 for energy storage in cathodes of supercapacitors, addresses the need to understand both the activation and the charge storage...

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Soft X-ray Scanning Transmission X-ray microscopy (STXM) is a synchrotron-based technique which can provide both spectroscopic characterization (near edge X-ray absorption fine structure, NEXAFS) and chemically selective imaging with high spatial resolution (~30 nm). Recently, we have developed in situ flow electrochemical devices [1,2] which allow control of the electrochemical environment while conducting STXM measurements, thus providing a platform for in-situ studies of electrochemical oxidation and reduction processes. This presentation reports results of in situ flow electrochemical STXM studies on three different systems to demonstrate the present capabilities. First, the ability to rapidly exchange the electrolyte is demonstrated by a STXM Fe 2p and in situ electrochemical study of the ferro/ferricyanide solution redox system. Second Cu and Ag-doped Cu catalysts for CO2 electrochemical reduction (CO2R) were successfully prepared using in situ electrodeposition. Third, the electrolyte was changed from CuSO4 to NaHCO3 (as substrate for CO2R) and the cell was operated under electrochemical CO2 reduction conditions, while monitoring the changes to the Cu deposited layer at various potentials, including –0.5 V where CO2 reduction is expected [3]. The figure shows a cyclic voltammogram (CV) and color-coded Cu oxidation state maps which were derived from Cu 2p stacks measured under chronoamperometric conditions at the indicated potentials. These results demonstrate that in situ flow electrochemical STXM measurements can be performed in our device under varying electrochemical reaction conditions, enabling visualization of the morphology changes from selective energy imaging, and quantitative tracking of electrochemical transformations from spectromicroscopy. This system will be used for in situ studies of CO2 electrochemical reduction catalysis with the goal of obtaining mechanistic insights to guide the development of catalysts with improved efficiency and selectivity. In addition, the system will be used to study a variety of material science, chemistry and environmental science related questions associated with oxidation or reduction processes, such as mechanisms of extra-cellular electron transport in marine sediment microbial biofilms [4]. This research is supported by NSERC (Canada). STXM measurements were performed at the ambient STXM facility at the Canadian Light Source, which is funded by the Canadian Foundation for Innovation. [1] V. Prabu et al., Rev. Sci. Inst. 89 (2018) 063702. [2] P. Ingino, et al., in preparation [3] L. Wang, D.C. Higgins, et al., Proc. Nat. Acad. Sci. (2020) 01821683. DOI: 10.1073/pnas.1821683117 [4] M. Obst, et al., Microsc. Microanal. 24 (S-2) (2018) 502-504. Figure 1

Atomically dispersed metal–nitrogen–carbon (M–N–C) materials are a class of electrocatalysts for fuel cell and electrochemical CO2 reduction (CO2R) applications. However, it is challenging to characterize the identity and concentration of catalytically active species owing to the structural heterogeneity of M–N–C materials. We utilize scanning transmission X-ray microscopy (STXM) as a correlative spectromicroscopy approach for spatially resolved imaging, identification, and quantification of structures and chemical species in mesoscale regions of nickel–nitrogen–carbon (Ni–N–C) catalysts, thereby elucidating the relationship between Ni content/speciation and CO2R activity/selectivity. STXM results are correlated with conventional characterization approaches relying on either bulk average (X-ray absorption spectroscopy) or spatially localized (scanning transmission electron microscopy with electron energy loss spectroscopy) measurements. This comparison illustrates the advantages of soft X-ray STXM to provide spatially resolved identification and quantification of active structures in Ni–N–C catalysts. The active site structures in these catalysts are identified to be atomically dispersed NiN x /C sites distributed throughout entire catalyst particles. The NiN x /C sites were notably demonstrated by spectroscopy to possess a variety of chemical structures with a spectroscopic signature that most closely resembles nickel­(II) tetraphenylporphyrin molecules. The quantification and spatial distribution mapping of atomically dispersed Ni active sites achieved by STXM address a target that was elusive to the scientific community despite its importance in guiding advanced material designs.

A micro-chip based three-electrode electrochemical reactor enabling controlled, variable electrolyte flow, rapid electrolyte change and applied electrode potentials was used for in-situ soft X-ray spectro-ptychography of Cu particle catalysts under electrochemical CO2 reduction (CO2R) conditions. In comparison to scanning transmission X-ray microscopy (STXM), the spatial resolution was improved by a factor of three through measuring patterns of diffracted photons via spectro-ptychography. We present here a detailed study of how individual cubic Cu particles change morphology and oxidation state as a function of applied potential during CO2R. Quantitative chemical mapping by in-situ spectro-ptychography demonstrated that as-deposited, primarily mixed Cu(I) and Cu(0) particles were completely reduced to pure Cu(0) at an electrode potential of -0.2 VRHE, above the potential at which CO2R commences. At increasingly negative potentials, in the regime of CO2R, these Cu(0) particles underwent morphological changes, losing the initial cubic structure and forming irregular dendritic-like structures. This initial demonstration of in-situ soft X-ray spectro-ptychography sheds insight on the morphological and chemical structural changes of Cu particles in the CO2R regime and paves the way for more detailed in-situ studies of electrochemical materials and processes.