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作 者:Antony Charles Minja 王涛涛 曹虹云 杜平武[1] Antony Charles Minja;Taotao Wang;Hongyun Cao;Pingwu Du(Hefei National Laboratory for Physical Sciences at the Microscale,iChEM,CAS Key Laboratory of Materials for Energy Conversion,Department of Materials Science and Engineering,University of Science and Technology of China,Hefei 230026,China)
机构地区:[1]中国科学技术大学材料科学与工程系,中国科学院能量转换材料重点实验室,合肥微尺度物质科学国家研究中心,能源材料化学协同创新中心,合肥230026
出 处:《Chinese Journal of Chemical Physics》2023年第3期349-359,I0046-I0058,I0101,共25页化学物理学报(英文)
基 金:supported by the National Key Research and Development Program of China(No.2017YFA0402800);the National Natural Science Foundation of China(No.51772285 and No.21971229);the Fundamental Research Funds for the Central Universities,and CAS Belt and Road Scholarship for International Students.
摘 要:本文利用一种简单的化学配体控制氧化方法,将NiFeCoAlOOH纳米颗粒负载在钛掺杂的纳米多孔赤铁矿光阳极上(Ti-PH),并将其用于光电催化水分解、由于NiFeCoAlOOH能够帮助提升Ti-PH光阳极的析氧反应动力学并且降低表面电荷转移电阻,修饰后的光阳极相对于1.23 V us.RHE时具有2.46 mA/cm^(2)的光电流密度,并且与Ti-PH或空白赤铁矿光阳极相比具有更好的稳定性.此外,对比钛掺杂的纳米多孔赤铁矿光阳极,NiFeCoAlOOH修饰后的光电流的起始电位负移了~60 mV.这项工作为设计高性能、稳定、廉价的光电化学电池提供了一种具有潜力的催化剂修饰方法.Herein,we present the decoration of NiFeCoAlOOH nanoparticles onto titanium doped nanoporous hematite(Ti-PH)utilizing a simple electroless ligand-controlled oxidation method for photoelectrochemical water splitting.Owing to the improved oxygen evolution reaction kinetics and reduced charge transfer resistance,the resulting Ti-PH/NiFeCoAlOOH photoanode presents an excellent photocurrent density of 2.46 mA/cm2 at 1.23 V vs.RHE and good stability compared to Ti-PH or bare hematite.Furthermore,the onset potential of the photocurrent density is shifted cathodically by∼60 mV with reference to the titanium doped nanoporous hematite.This work offers a promising method for designing high-performance,stable,and inexpensive catalysts for photoelectrochemical applications.
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