电催化剂
塔菲尔方程
过电位
交换电流密度
材料科学
原电池
双金属片
催化作用
合金
化学工程
成核
电流密度
纳米颗粒
纳米技术
冶金
电极
化学
电化学
物理化学
金属
工程类
有机化学
生物化学
物理
量子力学
作者
Ankur Kumar,Sasanka Deka
标识
DOI:10.1016/j.apcata.2020.117575
摘要
Herein, a novel nanostructured hollow bimetallic alloy system is introduced as highly efficient and stable electrocatalyst to produce H2 through water splitting reaction. Hollow nanospheres of Pd1-xSnx (x = 0.0–1.0) alloy having large electrochemically active sites was developed in an autoclave by taking the advantage of different redox potentials of Pd and Sn and of auto-galvanic replacement process. Maximum synergistic electron coupling or special conjunct effects in Pd0.6Sn0.4, hollow morphology and high electrochemically active surface area (488 cm2) were accounted towards the robust electrocatalysis during hydrogen evolution reaction at a low overpotential of 68 mV to reach a current density of 10 mA/cm2 in 1.0 M H2SO4. The catalyst showed long cycling stability and extended durability at high constant current density (100 mA/cm2) anticipating negligible degradation of the catalyst. A lower Tafel slope (58 mV/dec), high exchange current density (114.63 mA/cm2), and higher mass activity demonstrated faster reaction kinetics of Pd0.6Sn0.4 electrocatalyst.
科研通智能强力驱动
Strongly Powered by AbleSci AI