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首页> 外文期刊>Journal of Colloid and Interface Science >Lowering the onset potential of Zr-doped hematite nanocoral photoanodes by Al co-doping and surface modification with electrodeposited Co-Pi
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Lowering the onset potential of Zr-doped hematite nanocoral photoanodes by Al co-doping and surface modification with electrodeposited Co-Pi

机译:通过Al Co-掺杂和表面改性降低Zr掺杂的赤铁矿纳米陶瓷光胰岛的发病电位,用电沉积Co-Pi

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Herein, in situ zirconium-doped hematite nanocoral (Zr-Fe2O3 (I) NC) photoanode was prepared via a specially designed diluted hydrothermal approach and modified with Al3+ co-doping and electrodeposited cobalt-phosphate ("Co-Pi") cocatalyst. Firstly, an unintentional in situ Zr-Fe2O3 (I)) NC photoanode was synthesized, which achieved an optimum photocurrent density of 0.27 mA/cm(2) at 1.0 V vs. RHE but possessed a more positively shifted onset potential than conventionally prepared hematite nanorod photoelectrodes. An optimized amount of aluminum co-doping suppresses the bulk as well as surface defects, which causes a negative shift in the onset potential from 0.85 V to 0.8 V vs. RHE and enhances the photocurrent density of Zr-Fe2O3 (I) NC from 0.27 mA/cm(2) to 0.7 mA/cm(2) at 1.0 V vs. RHE. The electrodeposited Co-Pi modification further reduce the onset potential of Al co-doped Zr-Fe2O3 (I) NC to 0.58 V vs. RHE and yield a maximum photocurrent of 1.1 mA/cm(2) at 1.0 V vs. RHE (1.8 mA/cm(2) at 1.23 V vs RHE). The improved photocurrent at low onset potential can be attributed to synergistic effect of Al co-doping and Co-Pi surface modification. Further, during photoelectrochemical water-splitting, a 137 and 67 mu mol of hydrogen (H-2) and oxygen (O-2) evolution was achieved over the optimum Co-Pi-modified Al-co-doped Zr-Fe2O3 (l) NC photoanode within 6 h. The proposed charge transfer mechanism in optimum Co-Pi-modified Al-co-doped Zr-Fe2O3 (I) NC photoanodes during the photoelectrochemical water splitting was also studied. (C) 2020 Elsevier Inc. All rights reserved.
机译:在此,通过特殊设计的稀释水热方法制备了原位掺锆赤铁矿纳米珊瑚(Zr-Fe2O3(I)NC)光阳极,并用Al3+共掺杂和电沉积磷酸钴(co-Pi)助催化剂进行了改性。首先,合成了一种非故意的原位Zr-Fe2O3(I))NC光阳极,在1.0V vs.RHE下获得了0.27mA/cm(2)的最佳光电流密度,但与传统制备的赤铁矿纳米棒光电电极相比,具有更正位移的起始电位。优化的铝共掺杂量抑制了体缺陷和表面缺陷,这会导致起始电位从0.85 V到0.8 V相对于RHE的负偏移,并在1.0 V相对于RHE时将Zr-Fe2O3(I)NC的光电流密度从0.27 mA/cm(2)提高到0.7 mA/cm(2)。电沉积的Co-Pi改性进一步将Al共掺杂Zr-Fe2O3(I)NC的起始电势降低至0.58 V vs.RHE,并在1.0 V vs.RHE(1.23 V vs.RHE)下产生1.1 mA/cm(2)的最大光电流。低起始电位下光电流的改善可归因于铝共掺杂和co-Pi表面改性的协同效应。此外,在光电化学水分解过程中,最佳Co-Pi改性Al共掺杂Zr-Fe2O3(l)NC光电阳极在6h内产生137和67μmol的氢(H-2)和氧(O-2)。还研究了最佳Co-Pi改性Al共掺杂Zr-Fe2O3(I)NC光电化学水分解过程中提出的电荷转移机制。(C) 2020爱思唯尔公司版权所有。

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