光催化
制氢
材料科学
光化学
可见光谱
量子点
共价键
三嗪
催化作用
纳米技术
化学工程
化学
光电子学
有机化学
高分子化学
工程类
作者
Yueling Chen,Guocheng Huang,Yanxin Gao,Qiaoshan Chen,Jinhong Bi
标识
DOI:10.1016/j.ijhydene.2021.12.220
摘要
Photocatalytic hydrogen production holds great promise for alleviating the energy shortage through effective photo-to-chemical conversion, and the development of visible-light responsive, low-cost and sustainable photocatalysts remains key priority. In this study, carbon quantum dots/covalent triazine-based framework (CQDs/CTF) non-metallic photocatalyst was constructed through a simple impregnation method for photocatalytic H2 evolution. Upon 0.24% CQDs loading, a three-fold enhanced H2 production activity of 102 μmol∙g−1∙h−1 was achieved compared with pristine CTF-1 (34.5 μmol∙g−1∙h−1). Photoluminescence and photoelectrochemical study revealed carbon quantum dots served as the electron libraries, which was conducive to facilitate electron capture and promote the separation of photoinduced electron-hole pairs in CTF-1. Notably, the excitation-independent up-conversion fluorescent characteristics of CQDs endowed the catalysts broadened visible-light response range and higher solar energy utilization efficiency. This study deepens insights into the mechanism of CQDs modification and paves a trustworthy strategy for harvesting visible-light-driven metal-free photocatalyst with highly-active and robust performance.
科研通智能强力驱动
Strongly Powered by AbleSci AI