Water electrolysis generating green hydrogen will play a vital role in achieving the net-zero 2050 goal; however, freshwater electrolysis will further strain an already strained supply of clean freshwater.1 If seawater electrolysis can be scaled successfully, it would provide an important source of green hydrogen. Current research on untreated, direct seawater electrolysis is limited, and only recently have studies emerged analyzing catalyst performance at near-neutral pH.2 At industrially-relevant current densities, the formation of corrosive hypochlorite must be considered as a secondary reaction.3 Hypochlorite forms through the chloride oxidation reaction (ClOR), which competes with the oxygen evolution reaction (OER) in seawater electrolysis.2 In this work, we discuss the limitations of the current methods for determining anodic catalyst selectivity between OER and ClOR. The short lifetime of hypochlorite can cause faradaic efficiency measurement methods such as titration or oxygen gas capture to become unreliable, as these tests require that the hypochlorite remain stable. Using a rotating ring-disc electrode (RRDE), we measure the selectivity of common OER catalysts in-situ (Figure 1a). Real-time hypochlorite sensing overcomes the challenge of measuring catalyst selectivity posed by the short lifetime of hypochlorite. Remarkably, a PtRu catalyst outperformed more common OER catalysts with the best in OER selectivity and low overpotential, a novel development in the field of near-neutral water electrolysis. We also determine that elevated heat and low chlorine concentration are conducive to improved OER selectivity on an IrO2 catalyst (Figure 1b). We hope this work will set the standard in catalyst benchmarking for seawater electrolysis catalysts and could lead to the development of catalysts for efficient, scalable, and sustainable hydrogen production from seawater. H. Jin et al., Sci Adv, 9, eadi7755 (2023) https://www.science.org/doi/10.1126/sciadv.adi7755.F. Dionigi, T. Reier, Z. Pawolek, M. Gliech, and P. Strasser, ChemSusChem, 9, 962–972 (2016) https://onlinelibrary.wiley.com/doi/full/10.1002/cssc.201501581.J. Guo et al., Nature Energy 2023, 1–9 (2023) https://www.nature.com/articles/s41560-023-01195-x. Figure 1. a) LSV profiles of common OER catalysts (solid line) and the corresponding faradaic efficiency (dashed line) for the OER, measured using the ring current of the rotating ring-disc electrode. Catalysts were tested in 0.5 M NaCl and buffered with KHCO3 to pH 8.5. b) A ternary plot depicting the effect of varying Cl concentrations and temperatures on the selectivity of an IrO2 catalyst at pH 8.5. Figure 1
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