Photocatalytic H2Evolution from Ammonia Borane: Improvement of Charge Separation and Directional Charge Transmission

被引:28
作者
Zhang, Sishi [1 ]
Xu, Jie [1 ]
Cheng, Hongmei [1 ]
Zang, Cuicui [1 ]
Bian, Fengxia [1 ]
Sun, Bin [1 ]
Shen, Yu [1 ,2 ]
Jiang, Heyan [1 ]
机构
[1] Chongqing Technol & Business Univ, Chongqing Key Lab Catalysis & New Environm Mat, Coll Environm & Resources, Natl Base Int Sci & Technol Cooperat Intelligent, Chongqing 400067, Peoples R China
[2] Chongqing South To Thais Environm Protect Technol, Chongqing 400060, Peoples R China
基金
中国国家自然科学基金;
关键词
cobalt; hydrogen evolution; hydrogen storage; layered double hydroxides; photocatalysis; CATALYZED HYDROLYTIC DEHYDROGENATION; DOUBLE HYDROXIDE NANOSHEETS; LAYERED DOUBLE HYDROXIDES; VISIBLE-LIGHT; HYDROGEN EVOLUTION; HIGHLY EFFICIENT; H-2; EVOLUTION; NANOPARTICLES; LDH; INSIGHT;
D O I
10.1002/cssc.202001536
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Co/(MFe)-Fe-II layered double hydroxide (LDH) LDH photocatalysts have been designed from the aspect of employing stable half-filled Fe(3+)to trap photogenerated electrons, adjusting the M-II-O-Fe oxo-bridged structure to optimize the short-range directional charge transmission and intercalating oxometallate anions into the LDH to further improve light absorption along with electron-hole separation and non-noble metal Co NP loading and reduction to form a heterojunction. These LDH-based photocatalysts are employed for photocatalytic H(2)evolution from ammonia borane in aqueous solution under visible light at 298 K. The photocatalytic H(2)evolution activity is greatly improved through adjustment of the M-II-O-Fe oxo-bridged structure and molybdate intercalation into the LDH. Turnover frequencies of up to 113.2 min(-1)are achieved with Co/CoFe-Mo. Alongside the experimental results and materials characterization, capture experiments and in situ DRIFTS analysis are carried out to study the photocatalytic hydrogen production mechanism.
引用
收藏
页码:5264 / 5272
页数:9
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