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作 者:于文丽 王子璇 董斌[1] 吴则星 柴永明[1] 王磊[2] YU Wenli;WANG Zixuan;DONG Bin;WU Zexing;CHAI Yongming;WANG Lei(State Key Laboratory of Heavy Oil Processing,College of Chemistry and Chemical Engineering,China University of Petroleum(East China),Qingdao 266580,China;Key Laboratory of Eco-chemical Engineering,Ministry of Education,International Science and Technology Cooperation Base of Eco-chemical Engineering and Green Manufacturing,College of Chemistry and Molecular Engineering,Qingdao University of Science and Technology,Qingdao 266042,China)
机构地区:[1]中国石油大学(华东)化学化工学院,重质油国家重点实验室,青岛266580 [2]青岛科技大学化学与分子工程学院,生态化工国家重点实验室培育基地,生态化工与绿色制造国际科技合作基地,青岛266042
出 处:《高等学校化学学报》2024年第12期69-78,共10页Chemical Journal of Chinese Universities
基 金:国家自然科学基金(批准号:52272222,52072197);泰山学者青年人才计划项目(批准号:tsqn201909114);中国石油大学(华东)研究生创新基金;中央高校基本科研业务费专项资金(批准号:24CX04025A)资助.
摘 要:金属与载体的相互作用会引起金属与载体之间的电荷转移,从而优化催化剂的催化性能,是设计高效、高稳定性电催化剂的关键.本文利用抗坏血酸辅助的方法,将超细Pt纳米颗粒锚定在金属有机框架材料(MOF)表面合成了催化剂Pt-Vc-MOF.由于Pt-Vc-MOF具有较强的界面相互作用,MOF载体可以将电子转移至Pt,从而形成丰富且有效的催化活性位点,有助于增加催化析氢反应活性.所合成的催化剂在酸性、碱性和中性电解液中分别表现出17,45和32 mV(10 mA/cm^(2))的低过电位,更小的Tafel斜率和12 h的连续操作稳定性,优于商用Pt/C催化剂.The metal-support interactions can induce the charge transfer between the metal and the support,changing the catalytic performance of the catalyst,which is the key to design an efficient and durable electrocatalyst to promote the electrocatalytic reaction.In this work,the ultrafine Pt nanoparticles were anchored on the surface of MOF(Pt-Vc-MOF)by ascorbic acid assisted treatment.Due to the strong interfacial interaction of Pt-Vc-MOF,MOF-support can donate electrons to Pt,contributing to abundant catalytic active sites to effectively promote hydrogen evolution reaction.The electron-enriched Pt exhibits a low overpotential of 17,45 and 32 mV at 10 mA/cm^(2) in acidic,alkaline and neutral electrolytes,respectively,which was superior to commercial Pt/C catalysts.
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