Photoelectrocatalytic generation of H2 and S from toxic H2S by using a novel BiOI/WO3 nanoflake array photoanode

被引:6
作者
Bai, Jing [1 ]
Zhang, Bo [1 ]
Li, Jinhua [1 ]
Zhou, Baoxue [1 ,2 ,3 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Environm Sci & Engn, Shanghai 200240, Peoples R China
[2] Shanghai Inst Pollut Control & Ecol Secur, Shanghai 200090, Peoples R China
[3] Shanghai Jiao Tong Univ, Key Lab Thin Film & Microfabricat Technol, Shanghai 200240, Peoples R China
关键词
bismuth oxyiodide (BiOI); tungsten trioxide (WO3) nano-flake arrays (NFA); photoelectrocatalytic (PEC); H2S splitting; H-2; S; LIGHT PHOTOCATALYTIC ACTIVITY; FACILE SYNTHESIS; FILMS; HETEROJUNCTION; DEGRADATION; COMPOSITES; REDUCTION; OXIDATION; SURFACE; CO2;
D O I
10.1007/s11708-021-0775-7
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
In this paper, a photoelectrocatalytic (PEC) recovery of toxic H2S into H-2 and S system was proposed using a novel bismuth oxyiodide (BiOI)/ tungsten trioxide (WO3) nano-flake arrays (NFA) photoanode. The BiOI/ WO3 NFA with a vertically aligned nanostructure were uniformly prepared on the conductive substrate via transformation of tungstate following an impregnating hydroxylation of BiI3. Compared to pure WO3 NFA, the BiOI/WO3 NFA promotes a significant increase of photocurrent by 200%. Owing to the excellent stability and photoactivity of the BiOI/WO3 NFA photoanode and I-/I-3(-) catalytic system, the PEC system toward splitting of H2S totally converted S2- into S without any polysulfide (S-x(n)) under solar-light irradiation. Moreover, H-2 was simultaneously generated at a rate of about 0.867 mL/(h.cm). The proposed PEC H2S splitting system provides an efficient and sustainable route to recover H-2 and S.
引用
收藏
页码:744 / 751
页数:8
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