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Amorphous p-type oxides are essential for next-generation flexible and scalable complementary metal-oxide semiconductor (CMOS) technologies. Among emerging candidates, tellurium-based oxides (Te-TeOx) show great promise due to their unique Te-Te conduction networks embedded within the amorphous TeO₂ matrix. However, controlled formation of these conduction channels remains challenging, limiting both hole transport and dopability under low thermal budgets. Here, we report a sulfur-mediated redox strategy that modulates the local bonding environment via TeO₂ dissociation and partial Te⁴⁺ reduction, promoting formation of short-chain Te-Te networks. This enables high-performance p-channel thin-film transistors processed at an ultralow temperature of 120°C, exhibiting an average hole mobility of 11.5 cm² V⁻¹ s⁻¹ and on/off current ratios around 10⁶ with high uniformity and reproducibility. Integration with n-type counterparts enables all-oxide CMOS circuits on both flexible and rigid substrates, including inverters with gain up to 1694, ring oscillators operating at 339 kHz, and large-scale functional circuits with rail-to-rail output.
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Wang et al. (2025) studied this question.
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