Department of Chemical & Materials Engineering, The University of Auckland, 20 Symonds Street, Auckland 1010, New Zealand.
J Hazard Mater. 2010 Jun 15;178(1-3):115-22. doi: 10.1016/j.jhazmat.2010.01.050. Epub 2010 Jan 18.
Potential dissolution and photo-dissolution are important concerns for zinc oxide (ZnO) photocatalysts due to the possible results of catalyst inactivation and secondary pollution from free Zn(2+). In this study, magnetron-sputtered ZnO thin films were prepared and exposed under a series of corrosive conditions. ZnO films suffered rapid dissolution under: (a) extreme pH levels (< or =5 or > or =11); (b) 1mM ethylenediaminetetraacetic acid (EDTA) solution; (c) UV (lambda=254 nm). The dissolution rate of ZnO films was moderate at pH=6 and decreased markedly as pH increased to 7. It continued to decrease as pH increased from 7 to 10, then the trend quickly reversed as pH increased further. The lowest dissolution rate was obtained at pH=10, with only 1.2% ZnO dissolved after 24h of exposure. Minimal dissolution was observed on ZnO films in alkalised 1mM oxalate and acetate solutions. Pitting corrosion was observed on ZnO films after UV irradiation, which was ascribed to photo-generated holes on surface defect sites. The presence of hole scavengers (Na(2)SO(3)) caused significant suppression on ZnO photo-dissolution. This suppression effect remained in place until hole scavengers were completely consumed, from where the photo-dissolution rates accelerated.
由于可能导致催化剂失活和游离 Zn(2+) 造成二次污染,氧化锌 (ZnO) 光催化剂的潜在溶解和光溶解是重要的关注点。在这项研究中,采用磁控溅射法制备了 ZnO 薄膜,并将其暴露在一系列腐蚀性条件下。ZnO 薄膜在以下情况下会迅速溶解:(a) 极端 pH 值(< 或 =5 或 > 或 =11);(b) 1mM 乙二胺四乙酸(EDTA)溶液;(c) UV(lambda=254nm)。在 pH=6 时,ZnO 薄膜的溶解速率适中,随着 pH 增加到 7 时显著下降。当 pH 从 7 增加到 10 时,其继续下降,随后随着 pH 进一步增加,趋势迅速逆转。在 pH=10 时,溶解速率最低,暴露 24 小时后仅溶解 1.2%的 ZnO。在碱性 1mM 草酸盐和乙酸盐溶液中,ZnO 薄膜的溶解最小。在紫外线照射后,ZnO 薄膜上观察到点蚀,这归因于表面缺陷部位光生空穴。光生空穴清除剂(Na(2)SO(3))的存在对 ZnO 光溶解有显著抑制作用。这种抑制作用一直存在,直到空穴清除剂完全消耗,此后光溶解速率加快。