首页> 外文期刊>European journal of inorganic chemistry >Al-Modified Zinc Oxide Nanorods for Photoelectrochemical Water Oxidation
【24h】

Al-Modified Zinc Oxide Nanorods for Photoelectrochemical Water Oxidation

机译:铝修饰的氧化锌纳米棒用于光电化学水氧化

获取原文
获取原文并翻译 | 示例
           

摘要

The photoassisted water oxidation by a range of electrodeposited Al-modified zinc oxide nanorod arrays (NRAs) has been explored in a standardised photoelectrochemical cell. The nanorods were prepared by electrodeposition onto fluorinedoped tin oxide glass substrates from warm aqueous solutions of zinc nitrate and aluminium nitrate. Photoluminescence measurements suggested that the nanorods have a very low concentration of defects that could act as centres for undesired charge recombination. The effect of NRA aluminium modification, morphology and optical properties as well as the presence of sputtered i-ZnO and aluminium-doped ZnO seeding layers on the catalytic performance of the films were investigated. Water oxidation was observed under 1 Sun illumination even at very low applied potentials (0 V vs. Ag/AgCl at pH 9.2). The pure ZnO nanorods yielded a relatively high photocurrent of 0.52 mAcm~(-2) (at 1 V vs. Ag/ AgCl). Al modification of the sputtered seeding layer and/or the NRAs did not change the performance significantly. The photocurrent was further increased by exchanging the sputtered ZnO seeding layer for a galvanostatically deposited seeding layer. In this case the photocurrent increased to 0.74 mAcm~(-2) (at 1 V bias). Light absorbance and IPCE measurements indicated that although all NRAs absorb well in the UV region, light conversion does not extend greatly into the visible region. To address the issue of rapid photodegradation during water oxidation catalysis, the effect of electrolyte pH was explored by using phosphate and borate buffers with a view to improving photocurrent and long-term stability. A borate buffer at pH 9.2 was found to be the most suitable. In this case, the photocurrent of undoped ZnO and aluminium-doped ZnO NRA films was sustained at a high level on continuous illumination with a reduction of less than 10 and 30%, respectively, over 1 hour, as opposed to almost complete deactivation after 20 min as observed in 0.1 M Na_2SO_4 (pH 6). These results indicate that the ZnO NRAs presented here have the potential to become viable photoelectrocatalysts for water oxidation.
机译:在标准的光电化学电池中,已经探索了通过一系列电沉积的Al-修饰的氧化锌纳米棒阵列(NRA)进行的光辅助水氧化。通过从温暖的硝酸锌和硝酸铝水溶液中电沉积到掺氟的氧化锡玻璃基板上来制备纳米棒。光致发光测量表明,纳米棒具有非常低的缺陷浓度,这些缺陷可以充当不良电荷复合的中心。研究了NRA铝的改性,形态和光学性能以及溅射的i-ZnO和铝掺杂的ZnO晶种层对薄膜催化性能的影响。即使在极低的施加电势下(pH值为9.2,0 V对Ag / AgCl),也能在1阳光照射下观察到水氧化。纯的ZnO纳米棒产生的相对较高的光电流为0.52 mAcm〜(-2)(在1 V下相对于Ag / AgCl)。溅射种子层和/或NRA的Al改性不会显着改变性能。通过将溅射的ZnO晶种层交换为恒电流沉积的晶种层,可以进一步增加光电流。在这种情况下,光电流增加到0.74 mAcm〜(-2)(在1 V偏压下)。光吸收率和IPCE测量表明,尽管所有NRA在紫外线区域吸收良好,但光转换并没有很大程度地扩展到可见光区域。为了解决水氧化催化过程中快速光降解的问题,通过使用磷酸盐和硼酸盐缓冲液来探索电解质pH的影响,以改善光电流和长期稳定性。发现pH 9.2的硼酸盐缓冲液是最合适的。在这种情况下,未掺杂的ZnO和掺铝的ZnO NRA薄膜的光电流在连续照明下持续保持较高的水平,在1小时内分别降低了不到10%和30%,与之相反,在20小时后几乎完全失活在0.1 M Na_2SO_4(pH 6)中观察到的最小时间。这些结果表明,此处提出的ZnO NRA具有成为水氧化可行的光电催化剂的潜力。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号