Preparing low-cost and highly efficient electrocatalysts for the hydrogen evolution reaction using a simple strategy still faces challenges. In this work, we proposed a facile phosphating process to successfully transform… Click to show full abstract
Preparing low-cost and highly efficient electrocatalysts for the hydrogen evolution reaction using a simple strategy still faces challenges. In this work, we proposed a facile phosphating process to successfully transform CoFe-BTC (BTC = 1,3,5-benzenetricarboxylate) precursors into carbon-incorporated bimetallic phosphide (CoFe-P/C) nanospheres. Due to the synergistic effect between bimetals and uniformly covered carbon shells outside, the as-synthesized porous bimetallic phosphide nanospheres exhibit superior HER activity, enhanced kinetics, and excellent cycle durability in both acidic and alkaline solutions. The optimized material could afford a current density of 10 mA cm-2 with overpotentials of 138 and 193 mV for the HER in acidic and alkaline solutions, respectively. Meanwhile, it delivered small Tafel slopes of 84 and 78 mV dec-1 for the HER in 0.5 M H2SO4 and 1.0 M KOH, respectively. Moreover, an assembled alkaline electrolyzer enabled a low voltage of 1.62 V to drive a current density of 10 mA cm-2 for overall water splitting. DFT calculations indicate that the CoP-Fe2P composite is supposed to exhibit better HER performance than each component, revealing the vital role of the interfacial site in catalyzing the HER.
               
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