Janus cobalt sites on carbon nitride for efficient photocatalytic overall water splitting

被引:1
|
作者
Yan, Xiaoqing [1 ]
Chen, Zihao [1 ]
Yue, Yufei [1 ]
Chai, Ruijie [1 ]
Ou, Honghui [1 ]
Li, Yang [1 ]
Yang, Guidong [1 ]
机构
[1] Xi An Jiao Tong Univ, Sch Chem Engn & Technol, XJTU Oxford Int Joint Lab Catalysis, Xian 710049, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Janus cobalt cocatalysts; Carbon nitride; Photocatalysis; Overall water splitting; HYDROGEN EVOLUTION;
D O I
10.1016/j.apcatb.2024.124527
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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-C3N4. Experimental measurement and density functional theory calculations show that the janus cobalt cocatalysts fine-tunes the local electronic structure of g-C3N4, 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-C3N4 samples exhibit a remarkable enhancement in overall water splitting activity (133.2 mu mol g(-1) h(-1) H-2 and 67.2 mu mol g(-1) h(-1) O-2), surpassing that of the CoP@g-C3N4 and CoO@g-C3N4 samples by 1.4 and 3.8 times, respectively.
引用
收藏
页数:10
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