过电位
析氧
电催化剂
双功能
分解水
催化作用
氢氧化物
电解水
化学工程
电解
复合数
氧气
化学
电化学
氢
析因实验
电极
材料科学
碱性水电解
无机化学
中心组合设计
双功能催化剂
层状双氢氧化物
克拉克电极
制氢
纳米技术
电子效应
活动站点
作者
V. Sridevi,Komal Murugan,Pavithra Suresh,Arulmozhi Rajaram,Abirami Natarajan
出处
期刊:Langmuir
[American Chemical Society]
日期:2026-01-05
卷期号:42 (1): 482-493
标识
DOI:10.1021/acs.langmuir.5c04500
摘要
. Despite the fact that NCF-LDH/GCN4/CDs demonstrate a commendable overpotential of 230 mV for the HER and 250 mV for the OER, their diminished activity emphasizes the superior catalytic synergy in GCN5-based systems, which may be attributed to enhanced electronic transfer and active site availability. Furthermore, the chronoamperometric studies for overall water splitting reflect the good stability and catalytic activity of NCF-LDH/GCN5/CDs, with no significant loss over 50 h. This result signifies an interface engineered between triplex-LDH and GCN5, enabling significant charge migration and tunable electronic properties. The factorial design and function of the floret-like 2-fold electrocatalyst offer an innovative strategy to meet the critical demands in producing green hydrogen during the water electrolysis process.
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