Orbital-resolved visualization of single-molecule photocurrent channels

光电流 激发态 等离子体子 量子隧道 扫描隧道显微镜 分子轨道 原子轨道 材料科学 光电子学 化学 分子物理学 原子物理学 电子 分子 纳米技术 物理 有机化学 量子力学
作者
Miyabi Imai-Imada,Hiroshi Imada,Kuniyuki Miwa,Yusuke Tanaka,Kaname Kimura,Inhae Zoh,Rafael Jaculbia,Hiroko Yoshino,Atsuya Muranaka,Masanobu Uchiyama,Yousoo Kim
出处
期刊:Nature [Nature Portfolio]
卷期号:603 (7903): 829-834 被引量:20
标识
DOI:10.1038/s41586-022-04401-0
摘要

Given its central role in utilizing light energy, photoinduced electron transfer (PET) from an excited molecule has been widely studied1-6. However, even though microscopic photocurrent measurement methods7-11 have made it possible to correlate the efficiency of the process with local features, spatial resolution has been insufficient to resolve it at the molecular level. Recent work has, however, shown that single molecules can be efficiently excited and probed when combining a scanning tunnelling microscope (STM) with localized plasmon fields driven by a tunable laser12,13. Here we use that approach to directly visualize with atomic-scale resolution the photocurrent channels through the molecular orbitals of a single free-base phthalocyanine (FBPc) molecule, by detecting electrons from its first excited state tunnelling through the STM tip. We find that the direction and the spatial distribution of the photocurrent depend sensitively on the bias voltage, and detect counter-flowing photocurrent channels even at a voltage where the averaged photocurrent is near zero. Moreover, we see evidence of competition between PET and photoluminescence12, and find that we can control whether the excited molecule primarily relaxes through PET or photoluminescence by positioning the STM tip with three-dimensional, atomic precision. These observations suggest that specific photocurrent channels can be promoted or suppressed by tuning the coupling to excited-state molecular orbitals, and thus provide new perspectives for improving energy-conversion efficiencies by atomic-scale electronic and geometric engineering of molecular interfaces.

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
Jzhaoc580完成签到 ,获得积分10
1秒前
胡思乱响完成签到,获得积分10
2秒前
hahaha6789y完成签到,获得积分10
2秒前
想毕业的猫猫完成签到,获得积分10
3秒前
oy完成签到,获得积分10
3秒前
愤怒的水绿完成签到,获得积分10
4秒前
xiaowang发布了新的文献求助10
5秒前
浮尘完成签到 ,获得积分0
5秒前
舒心的夜完成签到,获得积分10
5秒前
hahaha2完成签到,获得积分10
5秒前
syltharion完成签到,获得积分10
5秒前
maybe完成签到,获得积分10
6秒前
sheep完成签到,获得积分10
6秒前
James完成签到,获得积分10
6秒前
simon666完成签到,获得积分10
7秒前
Miya完成签到 ,获得积分10
7秒前
徐彬荣完成签到,获得积分10
7秒前
LGA1700完成签到,获得积分10
8秒前
Paff完成签到,获得积分10
8秒前
Tom2077完成签到,获得积分10
8秒前
Walton完成签到,获得积分10
8秒前
MaxwellZH完成签到,获得积分10
8秒前
fate完成签到,获得积分10
9秒前
量子咸鱼K完成签到,获得积分10
9秒前
清风徐来完成签到,获得积分10
9秒前
PaperCrane完成签到,获得积分10
9秒前
执着柏柳完成签到,获得积分10
9秒前
霡霂完成签到,获得积分10
9秒前
qqqdewq完成签到,获得积分10
10秒前
surlamper完成签到,获得积分10
10秒前
molihuakai应助科研通管家采纳,获得10
10秒前
lilycat完成签到,获得积分10
11秒前
活泼学生完成签到 ,获得积分10
13秒前
xiaowang完成签到,获得积分10
14秒前
cgl155410完成签到 ,获得积分10
18秒前
隐形跳跳糖完成签到 ,获得积分10
18秒前
公冶愚志完成签到 ,获得积分10
18秒前
lily完成签到,获得积分10
20秒前
风中的向卉完成签到 ,获得积分10
24秒前
辻诺完成签到 ,获得积分10
26秒前
高分求助中
Adhesion Science: Principles & Practice 1234
Signals, Systems, and Signal Processing 610
Burger's Medicinal Chemistry and Drug Discovery 400
A Step-by-Step Guide to Qualitative Data Coding 2nd Edition 400
Impact of Storage Orientation and Duration on Prefilled Syringe Performance: Break-Loose and Glide Forces, and Injection Time Across Multiple Time Points 360
Programming for Chemical Engineers Using C, C++, and MATLAB 300
Upland Kenya wild flowers and ferns: a flora of the flowers, ferns, grasses, and sedges of highland Kenya 300
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 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6663148
求助须知:如何正确求助?哪些是违规求助? 8413192
关于积分的说明 17984478
捐赠科研通 5867254
什么是DOI,文献DOI怎么找? 2975010
邀请新用户注册赠送积分活动 1950898
关于科研通互助平台的介绍 1876727