Wang Ping, Xu Shunqiu, Xia Yang, Wang Xuefei, Yu Huogen, Yu Jiaguo
School of Chemistry, Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan 430070, People's Republic of China.
Phys Chem Chem Phys. 2017 Apr 19;19(16):10309-10316. doi: 10.1039/c7cp01043e.
Recently, AgPO has been demonstrated to be a new kind of material with high visible-light photocatalytic performance for the decomposition of various organic species. To further improve the photocatalytic activity of AgPO, hole cocatalyst modification is a promising approach via the rapid transfer of photogenerated holes for effective oxidation reaction. In this work, Co-Pi as a hole cocatalyst was successfully modified on the AgPO surface by an in situ photodeposition method (referred to as CoPi/AgPO). The results showed that the photocatalytic activity of CoPi/AgPO was greatly improved compared with that of AgPO. Especially, CoPi/AgPO (0.3 wt%) reached the highest photocatalytic rate constant (k = 9.2 × 10 min), a value larger than that of AgPO (k = 1.4 × 10 min) by a factor of 6.6. However, it was further found that more accumulated electrons resulted in an obvious deactivation of AgPO due to the rapid transfer of holes by the Co-Pi cocatalyst, resulting in an obviously decreased photocatalytic performance during repeated tests. To enhance the performance stability of CoPi/AgPO, the Cu(ii) electron-cocatalyst was further loaded onto its surface to prepare the CoPi-Cu(ii)/AgPO photocatalyst. The resultant CoPi-Cu(ii)/AgPO not only indicated a much higher photocatalytic activity than CoPi/AgPO, but also maintained the excellent stability, which was ascribed to the synergistic effect of Co-Pi as a hole cocatalyst and Cu(ii) as an electron cocatalyst. This work may provide new insight for the development of highly stable and efficient photocatalysts for the degradation of organic pollutants.
最近,磷酸银已被证明是一种新型材料,具有高可见光光催化性能,可用于分解各种有机物质。为了进一步提高磷酸银的光催化活性,空穴助催化剂改性是一种很有前景的方法,通过光生空穴的快速转移来进行有效的氧化反应。在这项工作中,通过原位光沉积法成功地在磷酸银表面修饰了作为空穴助催化剂的磷酸钴(简称CoPi/AgPO)。结果表明,与磷酸银相比,CoPi/AgPO的光催化活性有了很大提高。特别是CoPi/AgPO(0.3 wt%)达到了最高的光催化速率常数(k = 9.2×10⁻³ min⁻¹),该值比磷酸银(k = 1.4×1⁻³ min⁻¹)大6.6倍。然而,进一步发现,由于磷酸钴助催化剂使空穴快速转移,更多积累电子导致磷酸银明显失活,并导致重复测试期间光催化性能明显下降。为了提高CoPi/AgPO的性能稳定性,进一步在其表面负载铜(II)电子助催化剂,制备了CoPi-Cu(II)/AgPO光催化剂。所得的CoPi-Cu(II)/AgPO不仅显示出比CoPi/AgPO更高的光催化活性,而且保持了优异的稳定性,这归因于作为空穴助催化剂的磷酸钴和作为电子助催化剂的铜(II)的协同效应。这项工作可能为开发用于降解有机污染物的高稳定性和高效光催化剂提供新的思路。