AgBr Nanoparticles Anchored on CdS Nanorods as Photocatalysts for H2 Evolution

2021 ◽  
Vol 4 (9) ◽  
pp. 9274-9282
Author(s):  
Yuting Ren ◽  
Tianao Dong ◽  
Shuoping Ding ◽  
Xiufan Liu ◽  
Haizhao Zheng ◽  
...  
Keyword(s):  
Nano Letters ◽  
2017 ◽  
Vol 17 (6) ◽  
pp. 3803-3808 ◽  
Author(s):  
Hengming Huang ◽  
Baoying Dai ◽  
Wei Wang ◽  
Chunhua Lu ◽  
Jiahui Kou ◽  
...  

2021 ◽  
Vol 412 ◽  
pp. 128690
Author(s):  
Bo Wang ◽  
Chuanxia Chen ◽  
Yuanyuan Jiang ◽  
Pengjuan Ni ◽  
Chenghui Zhang ◽  
...  

2018 ◽  
Vol 43 (15) ◽  
pp. 7388-7396 ◽  
Author(s):  
Junmei Wang ◽  
Zhijian Wang ◽  
Peng Qu ◽  
Qinchao Xu ◽  
Jianfeng Zheng ◽  
...  

Nanomaterials ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 619 ◽  
Author(s):  
Rama Krishna Chava ◽  
Namgyu Son ◽  
Yang Soo Kim ◽  
Misook Kang

One dimensional (1D) metal sulfide nanostructures are one of the most promising materials for photocatalytic water splitting reactions to produce hydrogen (H2). However, tuning the nanostructural, optical, electrical and chemical properties of metal sulfides is a challenging task for the fabrication of highly efficient photocatalysts. Herein, 1D CdS nanorods (NRs) were synthesized by a facile and low-cost solvothermal method, in which reaction time played a significant role for increasing the length of CdS NRs from 100 nm to several micrometers. It is confirmed that as the length of CdS NR increases, the visible photocatalytic H2 evolution activity also increases and the CdS NR sample obtained at 18 hr. reaction time exhibited the highest H2 evolution activity of 206.07 μmol.g−1.h−1. The higher H2 evolution activity is explained by the improved optical absorption properties, enhanced electronic bandstructure and decreased electron-hole recombination rate.


2020 ◽  
Vol 508 ◽  
pp. 144869 ◽  
Author(s):  
Baiyan Zhang ◽  
Chaoqiu Chen ◽  
Jian Liu ◽  
Wei Qiao ◽  
Jixiao Zhao ◽  
...  

Author(s):  
Saikumar Manchala ◽  
Ambedkar Gandamalla ◽  
Vempuluru Navakoteswara Rao ◽  
Shankar Muthukonda Venkatakrishnan ◽  
Vishnu Shanker

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