过电位
析氧
材料科学
分解水
磷化物
硫化物
阴极
电化学
阳极
过渡金属
催化作用
硒化物
无机化学
化学工程
纳米技术
金属
电极
物理化学
冶金
化学
硒
工程类
光催化
生物化学
作者
Chuqiang Huang,Sihang Cheng,Yu Luo,W. Zhang,Haiqing Zhou,Y. Zhang,Ying Yu
标识
DOI:10.1016/j.mtphys.2019.100162
摘要
Transition metal sulfide (TMS) and phosphide (TMP) have been considered as efficient catalysts for electrochemical water splitting. Here, we have reported an effective strategy to synthesize TMS- and TMP-assembled hierarchical anode ([email protected]2) and cathode (Cu3[email protected]2P) for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER), respectively. It is found that the three-dimensional (3D) hierarchical electrodes not only provide a large number of active sites to promote the apparent catalytic activity, but also present tuned valence state of Co, which enhances the intrinsic activity of the active sites. Therefore, the [email protected]2 anode possesses excellent OER activity with an overpotential of 230 mV at a current density of 10 mA/cm2, and the Cu3[email protected]2P cathode exhibits good HER performance with a low overpotential of 95 mV at a current density of 10 mA/cm2. Impressively, the [email protected]2//Cu3[email protected]2P electrolyzer deliver a current density of 10 mA/cm2 at a cell voltage of 1.55 V for overall water splitting, which is better than most reported TMS and TMP based catalysts.
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