氨硼烷
催化作用
硼烷
加速度
化学
水解
火山
氨
材料科学
组合化学
物理
地质学
地球化学
有机化学
脱氢
经典力学
作者
Naixin Kang,Xiaorong Wei,Ruofan Shen,Baojun Li,Eduardo Guisasola,Sergio Moya,Lionel Salmon,Changlong Wang,Emerson Coy,Muriel Berlande,Jean‐Luc Pozzo,Didier Astruc
标识
DOI:10.1016/j.apcatb.2022.121957
摘要
Production of hydrogen (H2) from H2 storage materials is very attractive as a source of sustainable energy. We report that [email protected] alloys are very efficient nanocatalysts for H2 evolution upon ammonia borane hydrolysis under visible-light illumination with turnover frequency 3.4 times higher than with the monometallic Ni catalyst in the dark. This improvement is attributed to dramatic volcano-type positive synergy optimized in Au0.5Ni0.5 @ZIF-8, for which ZIF-8 is by far the superior support, as well as to the localized surface plasmon resonance induced between 450 and 620 nm. Infrared spectra analysis and tandem reaction confirm the origin of the hydrogen atoms, reveal the reaction mechanism, and suggest how the cleavage of the B–H and O–H bonds proceeds in this reaction. Deuteration experiments with D2O including primary kinetic isotope effects and density functional theory calculation under both dark and visible light conditions show that activation of H2O always is the rate-determining step.
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