采用水热法制备了高分散碳载Pt/C和Pt-SnO2/C电催化剂。采用XRD、SEM、TEM和激光粒度仪等方法对制得的纳米催化剂进行了表面微观结构分析。采用电化学工作站测试循环伏安曲线(CV)等表征Pt/C和Pt-SnO2/C纳米催化剂电催化活性。测试结果表...采用水热法制备了高分散碳载Pt/C和Pt-SnO2/C电催化剂。采用XRD、SEM、TEM和激光粒度仪等方法对制得的纳米催化剂进行了表面微观结构分析。采用电化学工作站测试循环伏安曲线(CV)等表征Pt/C和Pt-SnO2/C纳米催化剂电催化活性。测试结果表明,Pt-SnO2/C纳米催化剂的峰电流密度(131.05 m A·cm-2)是Pt/C催化剂的峰电流密度(65.48 m A·cm-2)的2倍;Pt-SnO2/C催化的电化学表面积(108.4 m2·g-1)远高于Pt/C催化剂的电化学表面积(99.14 m2·g-1);Pt-SnO2/C纳米粒子比Pt/C纳米粒子具有更强的抗CO中毒能力和更高的电催化活性。展开更多
One of the most primary challenges to achieve large-scale hydrogen generation from water electrolysis is the sluggish kinetics and noble metal dependence of cathodic hydrogen evolution reaction(HER).By considering the...One of the most primary challenges to achieve large-scale hydrogen generation from water electrolysis is the sluggish kinetics and noble metal dependence of cathodic hydrogen evolution reaction(HER).By considering the excellent water dissociation catalytic activity of Mo2C, abundant Pt/Mo2C interfaces were facilely engineered via galvanic replacement(gr) by using Mo/Mo2C nanosheets as self-sacrificed templates to alter the alkaline HER mechanism on Pt based catalyst. The rational designed interface-rich gr-Pt/Mo2C catalyst exhibited excellent activity with the overpotential to drive 10 mA/cm2 current density decreased by 18.5 mV compared with the commercial Pt/C catalyst. 34.3 mV/dec Tafel slope confirms the Volmer-Tafel HER route on gr-Pt/Mo2C in alkaline condition. Platinum utilization is calculated to be improved by 9.7 times by considered the low Pt loading in the gr-Pt/Mo2C catalyst. With its satisfied stability, the scalable gr-Pt/Mo2C catalyst shows promising application potential in industrial electrolysis systems.展开更多
文摘采用水热法制备了高分散碳载Pt/C和Pt-SnO2/C电催化剂。采用XRD、SEM、TEM和激光粒度仪等方法对制得的纳米催化剂进行了表面微观结构分析。采用电化学工作站测试循环伏安曲线(CV)等表征Pt/C和Pt-SnO2/C纳米催化剂电催化活性。测试结果表明,Pt-SnO2/C纳米催化剂的峰电流密度(131.05 m A·cm-2)是Pt/C催化剂的峰电流密度(65.48 m A·cm-2)的2倍;Pt-SnO2/C催化的电化学表面积(108.4 m2·g-1)远高于Pt/C催化剂的电化学表面积(99.14 m2·g-1);Pt-SnO2/C纳米粒子比Pt/C纳米粒子具有更强的抗CO中毒能力和更高的电催化活性。
基金financial support from the National Natural Science Foundation of China (Nos.21875224 and 21703211)the Natural Science Foundation of Zhejiang Province (No.LGG19B030001)。
文摘One of the most primary challenges to achieve large-scale hydrogen generation from water electrolysis is the sluggish kinetics and noble metal dependence of cathodic hydrogen evolution reaction(HER).By considering the excellent water dissociation catalytic activity of Mo2C, abundant Pt/Mo2C interfaces were facilely engineered via galvanic replacement(gr) by using Mo/Mo2C nanosheets as self-sacrificed templates to alter the alkaline HER mechanism on Pt based catalyst. The rational designed interface-rich gr-Pt/Mo2C catalyst exhibited excellent activity with the overpotential to drive 10 mA/cm2 current density decreased by 18.5 mV compared with the commercial Pt/C catalyst. 34.3 mV/dec Tafel slope confirms the Volmer-Tafel HER route on gr-Pt/Mo2C in alkaline condition. Platinum utilization is calculated to be improved by 9.7 times by considered the low Pt loading in the gr-Pt/Mo2C catalyst. With its satisfied stability, the scalable gr-Pt/Mo2C catalyst shows promising application potential in industrial electrolysis systems.
