Related Experiment Video
Updated: Sep 19, 2025

CO2 Photoreduction to CH4 Performance Under Concentrating Solar Light
Published on: June 12, 2019
Releasing 8.0 wt.% H2 from the LiBH4-2LiNH2 Composite within 5 Min under Light Illumination
Haoyang Yu1,2, Zibo Cheng1,2, Hong Wen1
1Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, China.
None:
The absence of safe and efficient hydrogen storage technologies is the major bottleneck for widespread applications of hydrogen energy. Reactive hydride composites with high gravimetric and volumetric hydrogen densities are ideal hydrogen storage materials. However, their traditional dehydrogenation processes normally involving electric-thermal-chemical energy conversion require high operating temperatures and substantial energy inputs to heat the reactor and oven. In this study, using LiBH4-2LiNH2 as a model system, that rapid dehydrogenation via a photo-thermal-chemical and/or photo-chemical energy conversion initiated by direct light irradiation is demonstrated and can be fulfilled in the presence of a catalyst and a photothermal agent. The experimental results revealed that the non-thermal effect of UV light plays a critical role in reducing the desorption temperature and enhancing the dehydrogenation kinetics. The collective photothermal and non-thermal effects drove over 8.0 wt.% hydrogen desorption from LiBH4-2LiNH2 within 5 min, which is ≈60 times faster than the thermal dehydrogenation process at the same temperature.
More Related Videos
Related Concept Videos
Acid Halides to Alcohols: LiAlH4 Reduction
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
Electrophilic Addition of HX to 1,3-Butadiene: Thermodynamic vs Kinetic Control

