材料科学
分解水
光电流
X射线光电子能谱
带材弯曲
单斜晶系
氧化物
氮化物
氮化镓
透射电子显微镜
分析化学(期刊)
光电子学
纳米技术
化学工程
光催化
结晶学
晶体结构
化学
催化作用
冶金
色谱法
工程类
图层(电子)
生物化学
作者
Maheswari Arunachalam,Kanase Rohini Subhash,Kwang‐Soon Ahn,Chung Soo Kim,Jun‐Seok Ha,Sang‐Wan Ryu,Soon Hyung Kang
出处
期刊:ACS applied energy materials
[American Chemical Society]
日期:2022-01-18
卷期号:5 (2): 2169-2183
被引量:4
标识
DOI:10.1021/acsaem.1c03725
摘要
This paper investigated the chemically surface-modified gallium nitride (GaN) films used as photoanodes for photoelectrochemical (PEC) water splitting. Here, the porous GaN is prepared by a simple chemical etching process (referred to as β–Ga2O3/GaN–10 s, β–Ga2O3/GaN–30 s, and β–Ga2O3/GaN–1 min) and then annealed in an air ambient atmosphere at 600 °C to introduce the crystalline monoclinic β–Ga2O3 oxide into the GaN surface. X-ray photoelectron spectroscopy and focused ion beam-high-resolution-transmission electron microscopy studies confirmed the chemically robust Ga–O bonds as well as the formation of highly crystalline β–Ga2O3 with a thickness of 15 nm. Notably, the 15-nm-thick β–Ga2O3-integrated GaN photoelectrode provided a large photovoltage of ∼1.2 VRHE, resulting in extended band bending for efficient charge separation, leading to efficient PEC water oxidation. This phenomenon reduces the charge recombination in the surface state, protecting semiconductors from chemical corrosion of the pristine GaN film. As expected, the engineered β–Ga2O3/GaN–30 s photoanode displayed an excellent photocurrent density (Jph) of 1.2 mA·cm–2 at 1.23 V versus a reversible hydrogen electrode (VRHE) under a stable working condition, up to 25, 21, and 34% greater than those of the bare GaN, β–Ga2O3/GaN–10 s, and β–Ga2O3/GaN–1 min of 0.95, 0.99, and 0.86 mA/cm2, respectively, in 0.5 M NaOH alkaline solution. Moreover, nickel phosphate (Ni–Pi) electrocatalysts were supported on the β–Ga2O3/GaN–30 s photoanode film by a simple photoelectrodeposition method, revealing a Jph of 1.4 mA·cm–2 at 0 VRHE. The superior performance of the Ni–Pi/β–Ga2O3/GaN photoanode system clearly demonstrates the possibility of highly stable water splitting by the modulation of the reaction kinetic parameters, such as passivation and surface kinetics.
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