副教授 博士生导师 硕士生导师
任职 : 辽宁省能源材料及器件重点实验室副主任
性别: 男
毕业院校: 大连理工大学
学位: 博士
所在单位: 材料科学与工程学院
学科: 材料物理与化学. 材料表面工程
办公地点: 新三束4#楼311室
联系方式: 0411-84706661-101
电子邮箱: aimin@dlut.edu.cn
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论文类型: 期刊论文
发表时间: 2017-01-01
发表刊物: DALTON TRANSACTIONS
收录刊物: SCIE、EI、PubMed
卷号: 46
期号: 8
页面范围: 2643-2652
ISSN号: 1477-9226
摘要: (GaN)(1-x)(ZnO)(x) solid solution has attracted extensive attention due to its feasible band-gap tunability and excellent photocatalytic performance in overall water splitting. However, its potential application in the photodegradation of organic pollutants and environmental processing has rarely been reported. In this study, we developed a rapid synthesis process to fabricate porous (GaN)(1-x)(ZnO)(x) solid solution with a tunable band gap in the range of 2.38-2.76 eV for phenol photodegradation. Under visible-light irradiation, (GaN)(0.75)(ZnO)(0.25) solid solution achieved the highest photocatalytic performance compared to other (GaN)(1-x)(ZnO)(x) solid solutions with x = 0.45, 0.65 and 0.85 due to its higher redox capability and lower lattice deformation. Slight Ag decoration with a content of 1 wt% on the surface of the (GaN)(0.75)(ZnO)(0.25) solid solution leads to a significant enhancement in phenol degradation, with a reaction rate eight times faster than that of pristine (GaN)(0.75)(ZnO)(0.25). Interestingly, phenol in aqueous solution (10 mg L-1) can also be completely degraded within 60 min, even under the direct exposure of sunlight irradiation. The photocurrent response indicates that the enhanced photocatalytic activity of (GaN)(0.75)(ZnO)(0.25)/Ag is directly induced by the improved transfer efficiency of the photogenerated electrons at the interface. The excellent phenol degradation performance of (GaN)(1-x)(ZnO)(x)/Ag further broadens their promising photocatalytic utilization in environmental processing, besides in overall water splitting for hydrogen production.