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机构地区:[1]国家纳米科学中心中国科学院纳米系统与多级次制造重点实验室,北京100190 [2]中国科学院大学,北京100049
出 处:《物理化学学报》2016年第2期543-550,共8页Acta Physico-Chimica Sinica
基 金:国家科技部国际合作司(2015DFG62610)资助项目~~
摘 要:利用水热法合成了形貌可控的氧化锌(ZnO)微纳材料。利用X射线衍射(XRD),扫描电子显微镜(SEM),透射电子显微镜(TEM),紫外-可见(UV-Vis)分光光谱和比表面积分析(BET)等技术对所制备的ZnO材料进行了表征。不同酸碱度(pH值)条件下,经过500℃退火2h制备的ZnO均为纤锌矿结构。随着前驱液pH值的增加,所得ZnO从片状晶体变为棒状晶体。片状ZnO主要暴露极性晶面,棒状ZnO主要暴露非极性晶面。从生长角度考虑,在溶液为弱酸性条件下(pH 6.5),溶液中游离的氯离子(CI^-)抑制了ZnO在锌极性面({Zn^(2+)}_(crystal surface))的生长,水热反应产物为片状Zn_5(OH)_8Cl_2·H_2O,退火后得到微孔片状ZnO;当溶液中添加氢氧根(OH^-)后,锌离子(Zn^(2+))被络合为四羟基锌络合离子(Zn(OH)_4^(2-)),该络离子促进了ZnO在Zn^(2+)}_(crystal surface)的生长,从而得到棒状晶体。利用上述催化剂,在氙灯照射下进行光催化还原二氧化碳实验,发现极性面较多的片状ZnO具有更高的光催化性能。ZnO microstructures and nanostructures with controlled-morphology were synthesized by the hydrothermal method.All samples were prepared using precursors at different pH values and then annealed at 500 ℃ for 2 h.The samples were characterized by X-ray diffraction(XRD) patterns,scanning electron microscopy(SEM),transmission electron microscopy(TEM),ultraviolet-visible spectroscopy(UV-Vis),and BET specific surface area measurement.All samples were confirmed by XRD to be wurtzite ZnO.As the pH value of the precursor increased,sheet-like ZnO disappeared and rod-like ZnO was produced.The major surfaces of sheet-like and rod-like ZnO were polar and nonpolar crystal faces,respectively.At pH 6.5,Cl- was adsorbed onto the(002) polar face and inhibited the growth along the polar crystal face({Zn2+}(crystal surface)).A microporous sheet ZnO was formed by annealing the obtained sheet-like Zn5(OH)8Cl2·H2O.When OH^- was added into the precursor,Zn(OH)4^(2-) was generated via coordination with Zn^(2+),which was adsorbed onto the(002) polar face and promoted growth along the polar crystal face.Rod-like ZnO was thus produced.The obtained ZnO could photocatalytically reduce CO2 under illumination.Sheet-like ZnO exhibited better photocatalytic performance than rod-like ZnO.This may be because the polar crystal face shows better photocatalytic activity than the unpolar crystal face.
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