Xiaoqing Yan, Zihao Chen, Yufei Yue, Ruijie Chai, Honghui Ou, Yang Li, Guidong Yang
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引用次数: 0
摘要
调节双活性位点对于提高载流子定向迁移效率和缩短中间产物的传质距离至关重要,尤其是在光催化整体水分离中。本文采用原位水热耦合气相化学还原法在 g-CN 上合成了 janus 钴催化剂。实验测量和密度泛函理论计算表明,破环钴催化剂可以微调 g-CN 的局部电子结构,从而大大降低能垒,缩短反应中间产物的传质距离。同时,CoP 和 CoO 的内置电场也进一步有效地促进了催化剂界面载流子的快速定向分离。这项研究阐明了整体水分离的原子级机制,为合理设计用于整体水分离的高性能催化剂提供了宝贵的见解。结果表明,CoP/CoO@g-CN 样品显著提高了整体水分离活性(133.2 μmol g h H 和 67.2 μmol g h O),分别是 CoP@g-CN 和 CoO@g-CN 样品的 1.4 倍和 3.8 倍。
Janus cobalt sites on carbon nitride for efficient photocatalytic overall water splitting
Regulating the dual active sites is crucial for enhancing the carrier-directed migration efficiency and shortening mass transfer distance of intermediates, particularly in photocatalytic overall water splitting. In this paper, we adopt in situ hydrothermal coupled gas phase chemical reduction methods to synthesize janus cobalt cocatalysts on g-CN. Experimental measurement and density functional theory calculations show that the janus cobalt cocatalysts fine-tunes the local electronic structure of g-CN, which can greatly reduce energy barriers and shorten mass transfer distance of intermediates for reactions. And while the built-in electric field of CoP and CoO also further efficiently facilitates rapid directional separation of interface carriers of the cocatalysts. This study elucidates atom-level mechanisms underlying overall water splitting and offers valuable insights for rational design of high-performance catalysts for overall water splitting. As a result, the CoP/CoO@g-CN samples exhibit a remarkable enhancement in overall water splitting activity (133.2 μmol g h H and 67.2 μmol g h O), surpassing that of the CoP@g-CN and CoO@g-CN samples by 1.4 and 3.8 times, respectively.