Abstract

In recent years, the utilisation of oxygen-deficient zirconia (ZrO2-α), commonly referred to as black zirconia, has garnered considerable attention due to its potential applications for solid oxide fuel cells (SOFCs), gas sensors, biomedical implant materials, and photocatalysis. However, current methods employed to manufacture ZrO2-α exhibit noticeable limitations regarding their scalability, environmental sustainability, and cost-effectiveness. Our recent work has successfully demonstrated the feasibility for bulk conversion of conventional white zirconia into oxygen-deficient black zirconia through direct current (DC) plasma treatment (i.e. plasma blackening). This study elucidates the conditions for plasma blackening and provides a unique mechanism for the bulk transformation of zirconia. A systematic investigation of different plasma technologies (DC, active-screen plasma), treatment configurations (contact conditions, cathode material, and cathode potential), and treatment parameters (voltage, temperature, duration) uncover the crucial variables that influence the feasibility and rate of the reduction process. The reduction of zirconia is shown to initiate from localised contacting points at the cathode-facing surface and grow, with a hemispherical shape, towards the anode-facing surface. A series of development stages are proposed for the process, namely: bulk oxygen vacancy conductance, surface activation, oxygen vacancy generation and a moving cathode front. The findings of this study provide insights into the underlying mechanisms involved in the bulk-reduction of zirconia and help to pave the way towards future scalable and cost-effective generation of oxygen-deficient zirconia.

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