Ligand-Tuned Energetics for the Selective Synthesis of Ni2P and Ni12P5 Possessing Bifunctional Electrocatalytic Activity toward Hydrogen Evolution and Hydrazine Oxidation Reactions

• Published in: Inorganic chemistry Vol. 61; no. 10; pp. 4394 - 4403
• Main Authors: Praveen, Athma E, Ganguli, Sagar, Sarkar, Debashrita, Mahalingam, Venkataramanan
• Format: Journal Article
• Language: English
• Published: American Chemical Society 14-03-2022
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/acs.inorgchem.1c03801

The occurrence of many phases and stoichiometries of nickel phosphides calls for the development of synthetic levers to selectively produce phases with purity. Herein, thiol (−SH) and carboxylate (−COO–) functional groups in ligands were found to effectively tune the energetics of nickel phosphide phases during hydrothermal synthesis. The initial kinetic product Ni2P transforms into thermodynamically stable Ni12P5 at longer reaction times. The binding of carboxylate onto Ni2P promotes this phase transformation to produce pure-phase Ni12P5 within 5 h compared to previous reports (∼48 h). Thiol-containing ligands inhibit this transformation process by providing higher stability to the Ni2P phase. Cysteine-capped Ni2P showed excellent geometric and intrinsic electrocatalytic activity toward both hydrogen evolution and hydrazine oxidation reactions under alkaline conditions. This bifunctional electrocatalytic nature enables cysteine-capped Ni2P to promote hydrazine-assisted hydrogen generation that requires lower energy (0.46 V to achieve 10 mA/cmgeo 2) compared to the conventional overall water splitting (1.81 V to achieve 10 mA/cmgeo 2) for hydrogen generation.