Selectively Adsorbed p-Aminothiophenol Molecules Improve the Electrocatalytic and Photo-Electrocatalytic Hydrogen Evolution on Au/TiO2

电催化剂 纳米材料基催化剂 材料科学 催化作用 吸附 分子 化学工程 异质结 光催化 密度泛函理论 纳米技术 光化学 电极 电化学 纳米颗粒 物理化学 化学 光电子学 计算化学 有机化学 工程类
作者
Jin Wang,Zhongyan Gong,Yulong Zhang,Yaxin Song,Xinya Chen,Zhihao Lü,Lu Jiang,Chengcheng Zhu,Kun Gao,Kaili Wang,Junjie Wang,Liuyingzi Yu,Soukaina Khayour,Haijiao Xie,Zhuoyao Li,Gang Lü
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:15 (47): 54550-54558 被引量:1
标识
DOI:10.1021/acsami.3c13974
摘要

Electrocatalytic hydrogen evolution reaction (HER) is receiving increasing attention as an effective process to produce clean energy. The commonly used precious metal catalysts can be hybridized with semiconductors to form heterostructures for the improvement of catalytic efficiency and reduction of cost. It will be promising to further improve the efficiency of heterostructure-based nanocatalysts in electrocatalytic and photocatalytic HER using a simple and effective method. Herein, we improve the efficiency of Au/TiO2 in electrocatalytic and photo-electrocatalytic HER by selectively adsorbing p-aminothiophenol (PATP) molecules. The PATP molecules are adsorbed on the gold surface by using a simple solution-based method and favor the charge separation at the Au-TiO2 interface. We also compare the PATP molecules with other thiophenol molecules in the enhancement of electrocatalytic HER. The PATP-induced enhancement in electrocatalysis is then further investigated by density functional theory (DFT) calculations, and this enhancement is attributed to a reduction in Gibbs energy of adsorbed hydrogen after surface adsorption of PATP molecules. This work provides a simple, cost-effective, and highly efficient approach to improve the electrocatalytic and photo-electrocatalytic efficiency of Au/TiO2, and this approach could be easily extended to other heterostructure-based nanocatalysts for performance enhancement and may be used in many other catalytic reactions.
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
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

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
小垃圾完成签到 ,获得积分10
2秒前
扭扭车完成签到,获得积分10
3秒前
jiangmj1990发布了新的文献求助10
3秒前
3秒前
毕业比耶完成签到,获得积分20
4秒前
华仔应助牙牙采纳,获得10
6秒前
7秒前
科研通AI5应助zhaoyichun采纳,获得10
8秒前
脑洞疼应助JerryZ采纳,获得10
8秒前
大模型应助陈佳祥采纳,获得10
8秒前
yangxiaoxu完成签到 ,获得积分10
9秒前
魁梧的小霸王完成签到,获得积分10
10秒前
10秒前
AaronDP完成签到,获得积分10
12秒前
14秒前
科研通AI5应助Emma采纳,获得10
15秒前
16秒前
16秒前
彭于晏应助科研通管家采纳,获得10
17秒前
天天快乐应助科研通管家采纳,获得10
17秒前
烟花应助科研通管家采纳,获得10
17秒前
科目三应助科研通管家采纳,获得10
17秒前
王子安应助科研通管家采纳,获得10
17秒前
赘婿应助科研通管家采纳,获得10
17秒前
ED应助科研通管家采纳,获得10
17秒前
18秒前
领导范儿应助科研通管家采纳,获得10
18秒前
大模型应助科研通管家采纳,获得10
18秒前
搜集达人应助科研通管家采纳,获得10
18秒前
完美世界应助科研通管家采纳,获得10
18秒前
完美世界应助科研通管家采纳,获得10
18秒前
18秒前
18秒前
18秒前
18秒前
18秒前
soso完成签到 ,获得积分10
18秒前
孔骁发布了新的文献求助10
21秒前
21秒前
21秒前
高分求助中
The Mother of All Tableaux: Order, Equivalence, and Geometry in the Large-scale Structure of Optimality Theory 3000
Social Research Methods (4th Edition) by Maggie Walter (2019) 1030
A new approach to the extrapolation of accelerated life test data 1000
Indomethacinのヒトにおける経皮吸収 400
基于可调谐半导体激光吸收光谱技术泄漏气体检测系统的研究 370
Phylogenetic study of the order Polydesmida (Myriapoda: Diplopoda) 370
Robot-supported joining of reinforcement textiles with one-sided sewing heads 320
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 3993587
求助须知:如何正确求助?哪些是违规求助? 3534299
关于积分的说明 11265206
捐赠科研通 3274074
什么是DOI,文献DOI怎么找? 1806303
邀请新用户注册赠送积分活动 883118
科研通“疑难数据库(出版商)”最低求助积分说明 809712