材料科学
光催化
阳极氧化
氢
贵金属
化学工程
制氢
无机化学
分解水
乙二胺四乙酸
纳米技术
金属
催化作用
螯合作用
冶金
铝
化学
生物化学
有机化学
工程类
作者
Jingtao Bi,Chengqian Li,Jie Ren,Yingying Zhao,Zhiyong Ji,Ting Wang,Xin Huang,Hongxun Hao
标识
DOI:10.1002/adfm.202407834
摘要
Abstract Achieving a high dispersity of deposited transition metal is crucial in the anodization preparation of noble‐metal‐free composites for photocatalytic hydrogen generation. Herein, for the first time, an in situ ion pumping anodization method is proposed to confine single‐atom Fe within the spatially ordered structure of anodized TiO 2 nanotubes (TNT), assisted by ferric sodium salt of ethylenediaminetetraacetic acid (EDTA) as an “ion pump” to deliver Fe 3+ toward anodes. Both experimental and theoretical calculations confirm that highly dispersed single‐atom Fe can interact with single‐electron‐trapped oxygen vacancies (SETOV), effectively reducing the oxygen vacancy concentration in TiO 2 nanotubes. This reduction promotes efficient charge carrier separation through the Fe(III)/Fe(II) pathway and enhances hydrogen desorption, ultimately boosting the photocatalytic hydrogen evolution performance.
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