Noble Metal Phosphides Supported on CoNi Metaphosphate for Efficient Overall Water Splitting.
Bingrong GuoJianying ZhaoYao XuXinxin WenXiaoqian RenXiaoxiao HuangSiqi NiuYulong DaiRuhai GaoPing XuSiwei LiPublished in: ACS applied materials & interfaces (2024)
Transition metal metaphosphates and noble metal phosphides prepared under similar conditions are potential hybrid catalysts for electrocatalytic water splitting, which is of great significance for H 2 production. Herein, the structure and electrocatalytic activity of different noble metal species (i.e., Rh, Pd, Ir) on CoNiP 4 O 12 nanoarrays have been systematically studied. Due to the different formation energies of noble metal phosphides, the phosphides of Rh (RhP x ) and Pd (PdP x ) as well as the noble metal Ir are obtained under the same phosphorylation conditions perspectively. RhP x /CoNiP 4 O 12 and PdP x /CoNiP 4 O 12 exhibit much better HER activity than Ir/CoNiP 4 O 12 due to the advantages of phosphides. Density functional theory (DFT) calculations reveal that the extraordinary activity of RhP x /CoNiP 4 O 12 originated from the strong affinity to H 2 O and optimal adsorption for H*. The best RhP x /CoNiP 4 O 12 only requires a low overpotential of 30 and 234 mV to deliver 10 mA cm -2 for HER and OER, respectively, and therefore is effective for overall water splitting (requiring 1.57 V to achieve a current density of 10 mA cm -2 ). This work not only develops a novel RhP x /CoNiP 4 O 12 electrocatalyst for overall water splitting but also provides deep insight into the formation mechanism of noble metal phosphides.