Light‐Induced Adaptive Structural Evolution in Gallium Nitride Nanowire/Nickel Hydroxide Symbiotic System in Photoelectrochemical Environment

纳米线 材料科学 半导体 纳米结构 纳米技术 光催化 氮化镓 异质结 氮化物 光电子学 图层(电子) 生物化学 催化作用 化学
作者
Yang Kang,Danhao Wang,Anyang Wang,Wei Chen,Boyang Liu,Shi Fang,Xin Liu,Liuan Li,Binghui Ge,Zhenghui Liu,Chengjie Zuo,Lan Fu,Yuzheng Guo,Kang Liang,Sheng Liu,Haiding Sun
出处
期刊:Advanced Functional Materials [Wiley]
卷期号:34 (7) 被引量:6
标识
DOI:10.1002/adfm.202311223
摘要

Abstract The adaptability of living organisms to dynamically adjust their biological behavior in response to fluctuating surroundings is a prerequisite for their evolutionary success. However, artificially‐synthesized materials, especially semiconductors, have not been able to replicate such adaptability due to their inherent physical rigidity and lack of intrinsic structural responsiveness to external stimuli. Herein, an adaptive structural evolution in group‐III‐nitride semiconductors is demonstrated by constructing an AlGaN‐nanowire/Ni(OH) 2 symbiotic‐system, resulting in self‐improved optoelectronic characteristics. The mutualistic interplay between AlGaN and Ni(OH) 2 nanostructure leads to the adaptive evolution of crystalline‐facets of AlGaN‐nanowires, along with self‐optimization of Ni(OH) 2 nanocrystals upon photon‐irradiation during its operation. Specifically, the nanowire‐surfaces dynamically evolve during Ni(OH) 2 photo‐deposition, removing the (000) plane while exposing the (10), which facilitates carrier transport at AlGaN/Ni(OH) 2 interface. Moreover, light‐induced electrons generated from AlGaN‐nanowires then partially reduce Ni 2+ ions in the Ni(OH) 2 nanostructure into Ni 0 nanometals, which further boosts the proton reduction thermodynamics, generating an unusual self‐improving photocurrent from −59.6 to −101.6 µA cm −2 . Such a “symbiotic system,” which is barely observed in conventional semiconductors, provides a promising avenue toward realizing smart adaptive semiconductors that are capable of dynamic structural evolution to fully unleash their potential for emerging optoelectronic and artificial‐photocatalysis applications.
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