ZnxCd1-xS/bacterial cellulose bionanocomposite foams with hierarchical architecture and enhanced visible-light photocatalytic hydrogen evolution activity
ZnxCd1-xS/bacterial cellulose bionanocomposite foams with hierarchical architecture and enhanced visible-light photocatalytic hydrogen evolution activity
复制标题
具有分层结构和增强可见光催化析氢活性的ZnxCd1-xS/细菌纤维素生物纳米复合泡沫
DOI:
10.1039/c4ta05722h
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发表时间:
2015
影响因子:
11.9
通讯作者:
Y. Xu
中科院分区:
文献类型:
--
作者:
P. P. Wang;Z. B. Geng;J. X. Gao;R. F. Xuan;P. Liu;Y. Wang;K. K. Huang;Y. Z. Wan;Y. Xu
Visible-light photocatalytic H2 production by water splitting is of great importance for its promising potential in converting solar energy to chemical energy. ZnxCd1−xS-based systems are intrinsic visible-light photocatalysts with appropriate electronic band structure and negative reduction potential of photoexcited electrons; however, the H2 evolution rate is far from satisfactory. A common strategy for improving the photocatalytic activity includes the incorporation of expensive cocatalysts such as noble metals and graphene. Here, we report, for the first time, that high visible-light photocatalytic H2 production activity can be achieved by organizing ZnxCd1−xS nanoparticles into the hierarchical architecture of bacterial cellulose (BC). This is achieved by templated mineralization and ion exchange/seeded growth. The bionanocomposite foams of ZnxCd1−xS/BC are flexible, monolithic and hierarchically porous. The optimized Zn0.09Cd0.91S/BC exhibits a high H2 evolution rate of 1450 μmol h−1 g−1 and an excellent apparent quantum efficiency of 12% at 420 nm. The monolithic nature of ZnxCd1−xS/BC makes catalyst recovery and recycling possible. The current work manifests that the integration of intrinsic chemical properties with multilength scale structural hierarchy affords performance optimization.