摘要
Hydrovoltaic devices, capable of harvesting energy from water of moisture, hold great potential for decentralized and sustainable electricity generation. However, their current density remains limited by unidirectional, single-ion transport, leaving nearly half of available charge carriers unused. Here, we propose a dual-interfacial gating (DIG) strategy that spatially separates cation and anion pathways, enabling simultaneous and bidirectional ion migration to fully exploit the ionic flux. This configuration significantly enhances current density, achieving a record value of 1.48 mA cm−3—one order of magnitude higher than those of typical hydrovoltaic systems (0.01–0.1 mA cm−3) and surpassing previously reported state-of-the-art results. Mechanistic insights from finite-element analysis and charge-injection experiments reveal that spatially segregated ion pathways effectively enhance ionic transport through simultaneous counter-directional ion migration. The scalable DIG architecture allows practical large-area integration; a 468 cm2 module generates 353 mA of short-circuit current, powering miniature fans continuously for over 3 hours and driving wearable sweat-based biosensors. These advances address the long-standing bottleneck of single-ion transport and establish a practical pathway toward high-performance, scalable moisture-driven power sources for sustainable energy, IoT and healthcare applications.
危险品化学品经营许可证(带存储)