In this study,an ultra‐fast and simple solvent‐free microwave method was successfully demonstrated using a series of ultra‐small(~2.5 nm)surfactant‐free Ru_(2)P@Ru/CNT heterostructures for the first time.The struc...In this study,an ultra‐fast and simple solvent‐free microwave method was successfully demonstrated using a series of ultra‐small(~2.5 nm)surfactant‐free Ru_(2)P@Ru/CNT heterostructures for the first time.The structure has a high‐density Ru component and Ru_(2)P component interface,which accelerates the hydrogen evolution reaction(HER).The prepared Ru_(2)P@Ru/CNT demonstrated excellent catalytic effects for the HER in alkaline media and real seawater.The experimental results indicate that ratio‐optimized Ru_(2)P@Ru/CNT(Ru_(2)P:Ru=66:34)requires only 23 and 29 mV to reach 10 mA cm^(-2)in 1.0 mol/L KOH and real seawater,respectively.These values are 10 and 24 mV lower than those of commercial Pt/C in 1.0 mol/L KOH(33 mV)and real seawater(53 mV),respectively,making it among the best non‐Pt HER reported in the literature.Additionally,the TOF of Ru_(2)P@Ru/CNT in alkaline freshwater and seawater were 13.1 and 8.5 s^(-1),respectively.These exceed the corresponding values for Pt/C,indicating that the catalyst has excellent intrinsic activity.The high current activity of Ru_(2)P@Ru/CNT in 1.0 mol/L KOH was explored,and only 77 and 104 mV were required to reach 500 and 1000 mA cm^(-2),respectively.After 100 h of durability testing,the catalyst retained excellent catalytic and structural stability in low current density,high current density,and seawater.展开更多
Molybdenum disulfide(MoS_(2))has become a competitive candidate for efficient and economical hydrogen evolution reaction(HER).Compared with 1T-MoS_(2),2H-MoS_(2) possesses exceptional thermodynamic stability but still...Molybdenum disulfide(MoS_(2))has become a competitive candidate for efficient and economical hydrogen evolution reaction(HER).Compared with 1T-MoS_(2),2H-MoS_(2) possesses exceptional thermodynamic stability but still suffers from low active site density,poor conductivity,and weak hydrogen bonding in the wide pH range.Herein,2H-MoS_(2) nanoflowers with phosphorus doping,sulfur vacancies and crystalline-amorphous heterojunction were synthesized via phosphorus-assisted rapid calcination method.Benefiting from the cooperative interaction of multiple strategies,the prepared 2H-MoS_(2) nanoflowers firstly achieve efficient pH-universal HER at high current densities.Experimental results show that in alkaline,acidic,and neutral media,MoS_(2)-P2 requires only 332,302,and 417 mV to drive the current density of 500 mA cm^(−2) and obtains 932,1100,and 472 mA cm^(−2) at the potential of−0.4 V vs.RHE,respectively.Moreover,MoS_(2)-P2 shows excellent stability of low and high current density in the full pH range.展开更多
文摘In this study,an ultra‐fast and simple solvent‐free microwave method was successfully demonstrated using a series of ultra‐small(~2.5 nm)surfactant‐free Ru_(2)P@Ru/CNT heterostructures for the first time.The structure has a high‐density Ru component and Ru_(2)P component interface,which accelerates the hydrogen evolution reaction(HER).The prepared Ru_(2)P@Ru/CNT demonstrated excellent catalytic effects for the HER in alkaline media and real seawater.The experimental results indicate that ratio‐optimized Ru_(2)P@Ru/CNT(Ru_(2)P:Ru=66:34)requires only 23 and 29 mV to reach 10 mA cm^(-2)in 1.0 mol/L KOH and real seawater,respectively.These values are 10 and 24 mV lower than those of commercial Pt/C in 1.0 mol/L KOH(33 mV)and real seawater(53 mV),respectively,making it among the best non‐Pt HER reported in the literature.Additionally,the TOF of Ru_(2)P@Ru/CNT in alkaline freshwater and seawater were 13.1 and 8.5 s^(-1),respectively.These exceed the corresponding values for Pt/C,indicating that the catalyst has excellent intrinsic activity.The high current activity of Ru_(2)P@Ru/CNT in 1.0 mol/L KOH was explored,and only 77 and 104 mV were required to reach 500 and 1000 mA cm^(-2),respectively.After 100 h of durability testing,the catalyst retained excellent catalytic and structural stability in low current density,high current density,and seawater.
基金supported by the National Natural Science Foundation of China(51772162,22001143 and 52072197)the Youth Innovation and Technology Foundation of Shandong Higher Education Institutions,China(2019KJC004)+4 种基金the Outstanding Youth Foundation of Shandong Province,China(ZR2019JQ14)the Taishan Scholar Young Talent Program(tsqn201909114,tsqn201909123)the Natural Science Foundation of Shandong Province(ZR2020YQ34)the Major Scientific and Technological Innovation Project(2019JZZY020405)the Major Basic Research Program of Natural Science Foundation of Shandong Province(ZR2020ZD09)。
文摘Molybdenum disulfide(MoS_(2))has become a competitive candidate for efficient and economical hydrogen evolution reaction(HER).Compared with 1T-MoS_(2),2H-MoS_(2) possesses exceptional thermodynamic stability but still suffers from low active site density,poor conductivity,and weak hydrogen bonding in the wide pH range.Herein,2H-MoS_(2) nanoflowers with phosphorus doping,sulfur vacancies and crystalline-amorphous heterojunction were synthesized via phosphorus-assisted rapid calcination method.Benefiting from the cooperative interaction of multiple strategies,the prepared 2H-MoS_(2) nanoflowers firstly achieve efficient pH-universal HER at high current densities.Experimental results show that in alkaline,acidic,and neutral media,MoS_(2)-P2 requires only 332,302,and 417 mV to drive the current density of 500 mA cm^(−2) and obtains 932,1100,and 472 mA cm^(−2) at the potential of−0.4 V vs.RHE,respectively.Moreover,MoS_(2)-P2 shows excellent stability of low and high current density in the full pH range.