NiB as a Substitute for the Pt Cocatalyst in CdS with Enhanced Visible-Light Photocatalytic H2 Production

被引:9
|
作者
Lv, Zhiguo [1 ]
Wang, Yilin [1 ]
Liu, Ying [1 ]
Wang, Jinming [1 ]
Qin, Guohui [1 ]
Guo, Zhenmei [1 ]
Zhang, Chao [1 ,2 ,3 ,4 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Chem Engn, Prov & Minist Coconstruct Collaborat Innovat Ctr, State Key Lab Base Ecochem Engn, Qingdao 266042, Peoples R China
[2] Anhui Univ, AnHui Prov Key Lab Chem Inorgan Organ Hybrid Func, Hefei 230601, Peoples R China
[3] South Cent Univ Nationalities, Key Lab Catalysis & Energy Mat Chem, Minist Educ, Wuhan 430074, Peoples R China
[4] South Cent Univ Nationalities, Hubei Key Lab Catalysis & Mat Sci, Wuhan 430074, Peoples R China
基金
中国博士后科学基金;
关键词
HYDROGEN-PRODUCTION; NANOPARTICLES; PERFORMANCE; GENERATION; HETEROJUNCTION; CONSTRUCTION; NANORODS; TIO2;
D O I
10.1021/acs.jpcc.2c01755
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
It is necessary to find a low-cost cocatalyst as a substitute for Pt in the CdS-based photocatalytic area. Hence, NiB was proposed to replace Pt for high H-2 production. CdS@NiB presented an excellent H-2 generation rate of 28,112 mu mol h(-1) g(-1) (lambda > 420 nm), which was 11 and 5.7 times higher than that of CdS and CdS@Pt, respectively. Different characterization methods (e.g., electron paramagnetic resonance, photoluminescence spectra, photoelectric responsiveness, etc.) proved that the synergistic effect between NiB and CdS could improve the photogenerated charge carrier separation of CdS. According to density functional theory results, a strong electronic coupling effect between CdS and NiB induced more electrons to participate in H-2 production. When adsorbed with H2O, the d-band center of Ni atoms in CdS@NiB shifted from -1.84 to -1.96 eV, leading to the migration of more electrons across the Fermi level. From the electron density redistribution in CdS@NiB-H2O, the electron transfer path of NiB -> CdS -> H2O was achieved, which could extend the H-O bond of H2O from 0.975 to 0.986 A and increase the H-O-H bond angle from 104.274 to 105.365 degrees, thereby activating H2O and promoting H-2 production.
引用
收藏
页码:9041 / 9050
页数:10
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