Constructing Electron- and Surface-Structure-Controlled Crystalline/Amorphous Hierarchical NiTe/NiFeCe-LDH Nanoarrays for Efficient Overall Water Splitting

材料科学 过电位 析氧 异质结 分解水 纳米棒 碲化物 密度泛函理论 双功能 纳米技术 兴奋剂 无定形固体 电子结构 催化作用 光电子学 电导率 电流密度 合理设计
作者
Yu-Chan Liu,Wenjing Gao,Qintong Huang,Chenyao Chen,Rongkai Ye,Xiaoxiong Liu,Jian-Qiang Hu
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
标识
DOI:10.1021/acsami.5c12742
摘要

Constructing nonprecious metal-based telluride heterointerfaces provides an effective strategy for developing efficient bifunctional catalysts for overall water splitting. However, there still remain major challenges for catalysts that rely on constructing heterojunction interfaces to obtain high-active sites with optimized electronic structures to achieve an efficient oxygen evolution reaction (OER). Herein, hierarchical NiTe/NiFeCe-LDH core-shell heterojunction nanoarrays with crystalline/amorphous interfaces were synthesized based on the Ce doping and interface engineering strategy. Benefiting from the high conductivity of crystalline NiTe nanorods and abundant active sites in amorphous NiFeCe-LDHs, the NiTe/NiFeCe-LDH heterojunction nanoarrays exhibited an excellent OER performance and long-term stability of more than 120 h in an alkaline medium, achieving a low overpotential of ∼247 mV at 100 mA·cm-2, which was ∼44% lower than commercial RuO2 (∼443 mV). Moreover, the NiTe/NiFeCe-LDHs achieved a current density of 10 mA·cm-2 at a low voltage of 1.45 V in overall water splitting. Density functional theory calculations revealed that Ce doping and the strong electronic interaction at the crystalline/amorphous interface of the NiTe/NiFeCe-LDHs could modulate its electronic structure by upward-shifting the d-band center of the Ni sites. This modulation optimized the binding energies of oxygen intermediates and consequently enhanced the OER performance of the NiTe/NiFeCe-LDHs. This research presents a novel approach for designing efficient overall water-splitting electrocatalysts through the synergistic doping-interface strategy.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
ada发布了新的文献求助10
刚刚
刚刚
1秒前
1秒前
2秒前
2秒前
科研通AI2S应助科研通管家采纳,获得10
2秒前
2秒前
2秒前
顾矜应助科研通管家采纳,获得10
2秒前
3秒前
3秒前
机灵柚子应助科研通管家采纳,获得20
3秒前
科研通AI6.2应助安详苠采纳,获得30
3秒前
doudou发布了新的文献求助10
3秒前
情怀应助科研通管家采纳,获得10
3秒前
田様应助科研通管家采纳,获得10
3秒前
今后应助科研通管家采纳,获得10
3秒前
爆米花应助科研通管家采纳,获得10
3秒前
无花果应助科研通管家采纳,获得10
4秒前
Owen应助科研通管家采纳,获得10
4秒前
Hello应助科研通管家采纳,获得10
4秒前
4秒前
4秒前
科研通AI6.4应助昊昊采纳,获得10
4秒前
小蘑菇应助科研通管家采纳,获得10
4秒前
隐形曼青应助科研通管家采纳,获得10
5秒前
Lucas应助科研通管家采纳,获得10
5秒前
anna1992发布了新的文献求助10
5秒前
充电宝应助科研通管家采纳,获得10
5秒前
yaya完成签到,获得积分10
5秒前
5秒前
5秒前
仇文琪完成签到,获得积分10
5秒前
lili应助着急帅采纳,获得10
6秒前
科研通AI6.4应助周一更采纳,获得10
6秒前
聪慧紫蓝完成签到,获得积分20
6秒前
ju00发布了新的文献求助10
7秒前
CCC完成签到,获得积分10
7秒前
7秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
HYDROLYSE ACIDE DE QUELQUES DIOXASPIROCYCLANES 1000
Navigating Normative Orders. Interdisciplinary Perspectives 800
1 Peter and Christ's Descent to the Dead in Its Early Christian Reception 700
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 600
Organizational Behavior 510
Management and the Arts 510
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7741073
求助须知:如何正确求助?哪些是违规求助? 9289608
关于积分的说明 20196565
捐赠科研通 7319281
什么是DOI,文献DOI怎么找? 3306554
关于科研通互助平台的介绍 2458896
邀请新用户注册赠送积分活动 2316904