Related Experiment Video
Updated: Apr 12, 2026

10:35
Novel Techniques for Observing Structural Dynamics of Photoresponsive Liquid Crystals
Published on: May 29, 2018
8.7K
Palladium-Doped Cs2AgBiBr6 with 1300 nm Near-Infrared Photoresponse
Hongwei Lei1,2, Utkarsh Singh2, Fuxiang Ji2
1College of Engineering, Huazhong Agricultural University, Wuhan, 430070, China.
Small (Weinheim an Der Bergstrasse, Germany)
|September 20, 2024
Summary
Palladium doping extends the light absorption of lead-free halide double perovskites (HDPs) to 1400 nm. This creates a sub-bandgap state, enabling HDPs for near-infrared optoelectronics.
Area of Science:
- Materials Science
- Solid-State Physics
- Optoelectronics
Background:
- Lead-free halide double perovskites (HDPs) like Cs2AgBiBr6 offer promising optoelectronic properties.
- A key limitation of Cs2AgBiBr6 is its narrow light absorption range, restricting its applications.
Purpose of the Study:
- To enhance the absorption range of Cs2AgBiBr6 using palladium (Pd) doping.
- To investigate the mechanism of absorption extension and its impact on photoelectric applications.
Main Methods:
- Palladium (Pd) doping into Cs2AgBiBr6 host lattice.
- Spectroscopical measurements to analyze material properties.
- Theoretical calculations to understand doping effects and electronic structure.
Main Results:
- Pd doping significantly extends the absorption spectrum of Cs2AgBiBr6 to approximately 1400 nm.
- Pd2+ ions substitute Ag atoms, introducing a sub-bandgap state within the host bandgap.
- The sub-bandgap state enables a photoresponse up to 1300 nm (NIR-II region), a record for HDPs.
Conclusions:
- Palladium is an effective dopant for broadening the absorption of large bandgap HDPs.
- Utilizing sub-bandgap states is a viable strategy for tailoring HDPs for near-infrared optoelectronics.
- This research opens new avenues for developing HDPs in NIR optoelectronic devices.
Related Concept Videos
Photoelectric Effect
41.3K
When light of a particular wavelength strikes a metal surface, electrons are emitted. This is called the photoelectric effect. The minimum frequency of light that can cause such emission of electrons is called the threshold frequency, which is specific to the metal. Light with a frequency lower than the threshold frequency, even if it is of high intensity, cannot initiate the emission of electrons. However, when the frequency is higher than the threshold value, the number of electrons ejected...
41.3K
The Photochemical Reaction Center
5.9K
Reaction centers are pigment-protein complexes that initiate energy conversion from photons to chemical entities. Therefore, photochemical reaction center is a more appropriate term that describes these complexes. The Nobel laureates Robert Emerson and William Arnold provided the first experimental evidence of photochemical reaction centers by demonstrating the participation of nearly 2,500 chlorophyll molecules for the release of just one molecule of oxygen. Despite thousands of photosynthetic...
5.9K
Photochemical Electrocyclic Reactions: Stereochemistry
2.4K
The absorption of UV–visible light by conjugated systems causes the promotion of an electron from the ground state to the excited state. Consequently, photochemical electrocyclic reactions proceed via the excited-state HOMO rather than the ground-state HOMO. Since the ground- and excited-state HOMOs have different symmetries, the stereochemical outcome of electrocyclic reactions depends on the mode of activation; i.e., thermal or photochemical.
Selection Rules: Photochemical Activation
Selection Rules: Photochemical Activation
2.4K

