异质结
光催化
煅烧
非阻塞I/O
材料科学
层状结构
氢
制氢
光电流
分解水
化学工程
氢氧化物
氧化剂
催化作用
无机化学
光电子学
化学
复合材料
工程类
有机化学
生物化学
作者
Chaoyue Zheng,Guoping Jiang,Youji Li,Zhiliang Jin
标识
DOI:10.1016/j.jallcom.2022.164041
摘要
NiO and Co1.29Ni1.71O4 were generated in situ by oxidizing and calcining NiCo LDH (Layered Double Hydroxide) to erect an S-scheme heterojunction heterogeneous catalyst. After calcination, the lamellar structure of NiCo LDH becomes thinner and part of the lamellar porous, which can provide more active sites for hydrogen precipitation reaction. The amount of hydrogen released by the composite catalyst is 3 times that of NiCo LDH This in-situ generation method will allow NiO and Co1.29Ni1.71O4 to establish a close relationship, form a built-in electric field, and build an S-scheme heterojunction. NiO and Co1.29Ni1.71O4 have good band structure and band gap position matching. S-scheme heterojunction composite catalyst has the best light absorption intensity and photocurrent response, the smallest electronic impedance, and good electron and hole separation efficiency, thereby improving the performance of photocatalytic hydrogen evolution. It was confirmed by a large number of characterization studies.
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