针对AZ31镁合金作为镁电池负极时存在自腐蚀速率大、阳极极化、电位滞后等问题,寻找合适的缓蚀剂及其用量调配电解液以提高电池的放电性能。通过腐蚀浸泡试验表征了缓蚀剂Li_(2)CrO_(4)的缓蚀效果,然后通过极化曲线、电化学阻抗谱研究了...针对AZ31镁合金作为镁电池负极时存在自腐蚀速率大、阳极极化、电位滞后等问题,寻找合适的缓蚀剂及其用量调配电解液以提高电池的放电性能。通过腐蚀浸泡试验表征了缓蚀剂Li_(2)CrO_(4)的缓蚀效果,然后通过极化曲线、电化学阻抗谱研究了Mg(ClO_(4))_(2)溶液中Li_(2)CrO_(4)用量对AZ31镁合金电化学性能的影响,最后通过组装水系镁锰电池进行恒流放电作为应用端测试。结果表明:Li_(2)CrO_(4)能够使AZ31镁合金的腐蚀电位正移,最大正移量达到150 m V,在水系镁锰电池应用中能够提高镁电池的放电平台,当Li_(2)CrO_(4)质量分数为0.7%时放电平台提高0.15 V左右;当Li_(2)CrO_(4)质量分数为1.2%时,其能够显著改善AZ31镁合金在Mg(ClO_(4))_(2)溶液中的腐蚀,水系镁锰电池放电容量达最大,为196.9 m A·h,相对空白溶液,电池的放电容量提高约64%,工作电压高达1.39 V且放电曲线稳定。展开更多
Photodeposition is widely adopted for implanting metal/metal oxide cocatalysts on semiconductors.However,it is prerequisite that the photon energy should be sufficient to excite the host semiconductor.Here,we report a...Photodeposition is widely adopted for implanting metal/metal oxide cocatalysts on semiconductors.However,it is prerequisite that the photon energy should be sufficient to excite the host semiconductor.Here,we report a lower-energy irradiation powered deposition strategy for implanting CrO_(x) cocatalyst on TiO_(2).Excitingly,CrO_(x)-400 implanted under visible-light irradiation significantly promotes the CH4 evolution rate on TiO_(2)to 8.4μmolg·^(-1)h^(-1) with selectivity of98%from photocatalytic CO_(2)reduction,which is 15 times of that on CrO_(x)-200 implanted under UV-visible-light irradiation.Moreover,CrO_(x)-400 is identified to be composed of higher valence Cr species compared to CrO_(x)-200.This valence states regulation of Cr species is indicated to provide more active sites for CO_(2) adsorption/activation and to modulate the reaction mechanism from single Cr site to Cr-Cr dual sites,thus endowing the superior CH_(4)production.This work demonstrates an alternative strategy for constructing efficient metal oxides cocatalysts on wide bandgap semiconductor.展开更多
文摘针对AZ31镁合金作为镁电池负极时存在自腐蚀速率大、阳极极化、电位滞后等问题,寻找合适的缓蚀剂及其用量调配电解液以提高电池的放电性能。通过腐蚀浸泡试验表征了缓蚀剂Li_(2)CrO_(4)的缓蚀效果,然后通过极化曲线、电化学阻抗谱研究了Mg(ClO_(4))_(2)溶液中Li_(2)CrO_(4)用量对AZ31镁合金电化学性能的影响,最后通过组装水系镁锰电池进行恒流放电作为应用端测试。结果表明:Li_(2)CrO_(4)能够使AZ31镁合金的腐蚀电位正移,最大正移量达到150 m V,在水系镁锰电池应用中能够提高镁电池的放电平台,当Li_(2)CrO_(4)质量分数为0.7%时放电平台提高0.15 V左右;当Li_(2)CrO_(4)质量分数为1.2%时,其能够显著改善AZ31镁合金在Mg(ClO_(4))_(2)溶液中的腐蚀,水系镁锰电池放电容量达最大,为196.9 m A·h,相对空白溶液,电池的放电容量提高约64%,工作电压高达1.39 V且放电曲线稳定。
基金supported by the National Key Research and Development Program of China(2016YFB0700205,2017YFA0403402,2019YFA0405602,2017YFA0204904)the National Natural Science Foundation of China(52002367,21673214,U1732272,U1632273,U1832165)+1 种基金the foundation from Users with Excellence Program of Hefei Science Center CAS(2020HSC-UE001)the Fundamental Research Funds for the Central Universities(WK2310000093)。
文摘Photodeposition is widely adopted for implanting metal/metal oxide cocatalysts on semiconductors.However,it is prerequisite that the photon energy should be sufficient to excite the host semiconductor.Here,we report a lower-energy irradiation powered deposition strategy for implanting CrO_(x) cocatalyst on TiO_(2).Excitingly,CrO_(x)-400 implanted under visible-light irradiation significantly promotes the CH4 evolution rate on TiO_(2)to 8.4μmolg·^(-1)h^(-1) with selectivity of98%from photocatalytic CO_(2)reduction,which is 15 times of that on CrO_(x)-200 implanted under UV-visible-light irradiation.Moreover,CrO_(x)-400 is identified to be composed of higher valence Cr species compared to CrO_(x)-200.This valence states regulation of Cr species is indicated to provide more active sites for CO_(2) adsorption/activation and to modulate the reaction mechanism from single Cr site to Cr-Cr dual sites,thus endowing the superior CH_(4)production.This work demonstrates an alternative strategy for constructing efficient metal oxides cocatalysts on wide bandgap semiconductor.
