2026/04/17 by Xudong Yang, Yuying Liu, Wei Chen +12 · 1 voice
Physics and Astronomy · Engineering · #GaN-based semiconductor devices and materials #Photocathodes and Microchannel Plates #Nanowire Synthesis and Applications
paper · pdf · doi:10.1007/s40820-026-02186-9
openalex publication_date 2026/04/17 · openalex created_date 2026/04/18 · openalex updated_date 2026/07/29
Abstract Efficient, durable, and scalable photocathodes are indispensable for large-scale solar-to-hydrogen production. Notably, single-junction semiconductor photocathodes are attractive due to their structural simplicity, cost-effectiveness, and mature fabrication, yet they usually exhibit intrinsically poor carrier extraction efficiency. To address this challenge, we propose a synergistic “dual-electron extraction” strategy that fully unleashes the hydrogen evolution potential of single-junction p-InGaN nanowires. Remarkably, the optimized p-InGaN photocathode achieves a photocurrent density of −3.40 mA cm −2 at 0 V vs. RHE—representing a 37.8-fold enhancement over the pristine device—with an onset potential of 0.82 V vs. RHE, while sustaining stable hydrogen generation for over 300 h without additional protective layers. Specifically, an electron-blocking layer was incorporated within p‑InGaN nanowires to suppress electron backflow toward the substrate and promote transport to the nanowire/electrolyte interface. Furthermore, surface anion doping in InGaN nanowires significantly enhances the band bending of InGaN, which promotes interfacial electron transfer while simultaneously optimizing hydrogen adsorption energy, thereby accelerating the hydrogen evolution reaction rate. The proposed synergistic dual-electron extraction strategy markedly improves the electron utilization efficiency of single-junction InGaN nanowires, providing a novel pathway to address the intrinsic limitations of wafer-scale III-V nitride photoelectrodes.