石墨烯
拉曼光谱
电子
离子
材料科学
紫外光电子能谱
费米能级
费米能量
X射线光电子能谱
紫外线
电子转移
原子物理学
化学物理
化学
光化学
电子结构
纳米技术
光电子学
物理
计算化学
光学
量子力学
有机化学
核磁共振
作者
Pingping Zhuang,Weiyi Lin,Bo Tian,Tien-Mo Shih,Weiwei Cai
出处
期刊:Carbon
[Elsevier]
日期:2017-10-01
被引量:3
标识
DOI:10.1016/j.carbon.2017.07.084
摘要
Abstract Outer-shell electrons of singly-charged anions are allowed to be detached by absorbing photons with appropriate energy that is larger than the corresponding atomic electron affinity. In an anion-graphene system, these escaped electrons face the possibility of travelling to graphene through the electron-exchanged path that originates from the anion-graphene orbital overlapping. Using electrical measurements, we observe that the hole concentration of gold-chloride-functionalized graphene decreases upon ultraviolet-light impingements, yet by contrast it persists under visible lights. Then we identify the governing mechanism in which chlorine anions are neutralized to gaseous molecules, thus donating electrons to graphene, subsequently elevating the Fermi level, and lowering the electrical conductivity in graphene. This mechanism is validated by field-effect-transistor-based Dirac-point-shift measurements that reveal Fermi-level and carrier-mobility variations of graphene. Raman statistical analyses and X-ray photoelectron spectroscopy measurements are employed to further confirm this electron-transfer-related process. Our study can be applied to designs of anion-graphene-embedded devices for sensing as well as energy harvesting.
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