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
秋风完成签到 ,获得积分10
2秒前
shire完成签到,获得积分10
3秒前
Dorcas_M完成签到,获得积分10
3秒前
fanwei完成签到,获得积分10
4秒前
Hello应助一一采纳,获得10
5秒前
科研通AI6.4应助丸子采纳,获得10
5秒前
huyuan发布了新的文献求助30
6秒前
6秒前
李健应助车灵寒采纳,获得10
6秒前
7秒前
9秒前
JJDS发布了新的文献求助10
11秒前
ehsl完成签到,获得积分10
11秒前
12秒前
lbq123发布了新的文献求助10
12秒前
12秒前
13秒前
老迟到的曼文完成签到,获得积分10
13秒前
包远锋完成签到,获得积分10
14秒前
TIANEO完成签到,获得积分10
14秒前
虎啊虎啊发布了新的文献求助10
14秒前
乐观谷芹完成签到,获得积分10
14秒前
熊熊发布了新的文献求助10
15秒前
15秒前
菜菜完成签到 ,获得积分10
16秒前
16秒前
nikola发布了新的文献求助10
17秒前
科研通AI2S应助乔乔采纳,获得10
17秒前
MgSO4完成签到,获得积分20
17秒前
不以发布了新的文献求助10
18秒前
18秒前
cc完成签到,获得积分10
18秒前
上官若男应助OhOHOh采纳,获得10
19秒前
科研通AI6.3应助知韵墨客采纳,获得10
19秒前
8R60d8应助细腻戒指采纳,获得10
20秒前
香蕉觅云应助科研通管家采纳,获得10
20秒前
CipherSage应助积极无施采纳,获得10
20秒前
20秒前
lbq123完成签到,获得积分10
21秒前
汉堡包应助科研通管家采纳,获得10
21秒前
高分求助中
Markov Chain Monte Carlo 10000
(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
Common Foundations of American and East Asian Modernisation: From Alexander Hamilton to Junichero Koizumi 2000
Weaponeering: An Introduction Fourth Edition, Volume 1 1000
Advanced Weaponeering Fourth Edition, Volume 2 1000
悉尼大学博士学位论文,题目:Modelling and testing of one-sided stitched laminated composites. 作者:Kristopher P. Plain 700
Matrix Methods in Data Mining and Pattern Recognition Second Edition 610
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 7516201
求助须知:如何正确求助?哪些是违规求助? 9104196
关于积分的说明 19434787
捐赠科研通 7121235
什么是DOI,文献DOI怎么找? 3253755
关于科研通互助平台的介绍 2422511
邀请新用户注册赠送积分活动 2240547