Efficient electrocatalytic desulfuration and synchronous hydrogen evolution from H2S via anti-sulfuretted NiSe nanowire array catalyst

被引:44
作者
Duan, Chao [1 ,2 ]
Tang, Chun [2 ]
Yu, Shan [2 ]
Li, Lina [3 ]
Li, Jinjin [4 ]
Zhou, Ying [1 ,2 ]
机构
[1] Southwest Petr Univ, State Key Lab Oil & Gas Reservoir Geol & Exploitat, Chengdu 610500, Peoples R China
[2] Southwest Petr Univ, Sch New Energy & Mat, Chengdu 610500, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai Synchrotron Radiat Facil, Shanghai 201204, Peoples R China
[4] PetroChina Southwest Oil & Gas Field Co, Res Inst Nat Gas Technol, Lab Nat Gas Sweetening, Chengdu 610213, Sichuan, Peoples R China
来源
APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY | 2023年 / 324卷
基金
中国国家自然科学基金;
关键词
Electrocatalysis; Hydrogen evolution; Sulfur oxidation reaction; HER coupling reaction; SULFIDE; H2S; PHOTOCATALYST; PERFORMANCE; COMPOSITE; OXIDATION; DOTS; ION; H-2;
D O I
10.1016/j.apcatb.2022.122255
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
Decreasing energy consumption of water splitting strategy by replacing oxygen evolution reaction (OER) with more facile sulfide oxidation reaction (SOR) to H2 evolution and value-added sulfur products is a promising technology. Nevertheless, the unsatisfactory catalyst long-term stability and passivation issues substantially limit the overall productivity. Herein, we report an anti-sulfuretted NiSe nanowire array catalyst on nickel foam (NiSe/NF), this catalyst exhibits a significantly reduced anode potential of 0.49 V vs. RHE at 100 mA cm-2 compared to the oxygen evolution reaction (1.78 V vs. RHE) and remains admirable stability for more than 500 h without passivation. Particularly, the skillful combination of UV-vis, in situ Raman, and attenuated total reflection Fourier transform infrared spectra, we reveal that S2-/HS- has been selectively converted to Sn2-and by-product S2O32-rather than sulfur, which avoids long-perplexing passivation issue of solid sulfur. For the first time, we demonstrate the feasibility of the system (SOR + HER) in a commercial membrane electrode assembly stack, which affords 19.0 mL min-1 H2 at a low cell voltage of 1.0 V with consuming the electricity of 2.63 kWh Nm- 3 H2. This work provides a new avenue for low-cost H2 production by H2S electrooxidation desulfurization.
引用
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页数:8
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