催化作用
光催化
氧化钴
钴
析氧
分解水
材料科学
氧化物
氧气
无机化学
吸收(声学)
化学
物理化学
电化学
电极
冶金
复合材料
生物化学
有机化学
作者
Lihua Lin,Valeria Polliotto,Junie Jhon M. Vequizo,Xiaoping Tao,Xizhuang Liang,Yiwen Ma,Takashi Hisatomi,Tsuyoshi Takata,Kazunari Domen
标识
DOI:10.1002/cptc.202200209
摘要
Abstract Y 2 Ti 2 O 5 S 2 (YTOS), an oxysulfide material, has attracted attention as a photocatalyst due to its optical absorption at wavelengths up to 650 nm, and its ability to split water into hydrogen and oxygen. However, the performance of YTOS in photocatalytic water splitting has remained low. One important factor accounting for this poor activity is the absence of highly efficient active sites. Surface modification with oxygen‐evolution co‐catalysts is indispensable for enhancing the activity and durability of non‐oxide narrow‐bandgap photocatalysts. Herein, we report the preparation of cobalt oxide (Co 3 O 4 )‐loaded YTOS for photocatalytic oxygen evolution. The Co 3 O 4 co‐catalyst was loaded by thermal decomposition of cobalt nitrate. The as‐obtained sample showed significantly enhanced activity in the oxygen evolution reaction compared with unmodified or IrO 2 ‐loaded YTOS. Transient absorption spectroscopy revealed that the Co 3 O 4 co‐catalyst captured holes and promoted charge separation, which accounted for the enhanced activity.
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