Trapping [PMo ₁₂O ₄₀] ^3– clusters into pre-synthesized ZIF-67 toward Mo _x Co _x C particles confined in uniform carbon polyhedrons for efficient overall water splitting†

Abstract

A new trapping route has been used to synthesize Mo _x Co _x C confined in carbon polyhedrons, through trapping PMo ₁₂ clusters into pre-synthesized ZIF-67 polyhedrons. The catalysts showed excellent performance for water splitting.

Abstract

Bi-transition metal carbides (BTMCs) are promising in catalytic fields, but the synthesis of small-sized BTMCs remains a challenge. Here, Mo _x Co _x C (mainly below 20 nm in size) confined in uniform carbon polyhedrons (Mo _x Co _x C@C) was synthesized based on trapping [PMo ₁₂O ₄₀] ^3– (PMo ₁₂) clusters into pre-synthesized, uniform ZIF-67 (PMo/ZIF-67). The opening of the windows (0.34 nm) of ZIF-67 cages through heating is essential to allow the trapping of PMo ₁₂ into the cages. This trapping route provides a new method to successfully combine POMs and MOFs that can not be effectively combined via traditional POMOF-based (simultaneous assembly) routes. It also has advantages in controlling the uniformity and components of the materials. The size matching of PMo ₁₂ (1 nm) and the cages (1.16 nm) of ZIF-67 enables effective contact of the Co and Mo sources, thus giving small-sized Mo _x Co _x C protected by carbon via calcination. The optimized catalysts showed good performance for water splitting with a low η10 of 83 mV (295 mV) for the hydrogen (oxygen) evolution reaction, which is superior to those derived from ZIF-67 and precursors from POMOF-based routes. Our results also indicated that the HER activity is determined by the kind of BTMC, and the activity for the OER is relative to the oxygen-containing species formed during the initial OER test.

Notes

†Electronic supplementary information (ESI) available. See DOI: 10.1039/c8sc01454j