21:I[432972,["/_next/static/chunks/bb923814e1f4d2e9.js","/_next/static/chunks/dd3ee9f5b7716ca6.js","/_next/static/chunks/4204a0ae82542ca8.js","/_next/static/chunks/30036bedc5269936.js","/_next/static/chunks/6e1aa89a642f40be.js","/_next/static/chunks/cd5e572bc3e4eb92.js","/_next/static/chunks/8ffd0b71567920d8.js","/_next/static/chunks/67ea6dfd21f16c5f.js","/_next/static/chunks/24eb4379f68013fd.js","/_next/static/chunks/b8cd775ffdf935bd.js","/_next/static/chunks/983103cd9eb7b428.js","/_next/static/chunks/d4ac9dcf27f6ff52.js","/_next/static/chunks/294b9525248c8e5f.js"],"default"] 22:T4c0,CoO/g-C₃N₄ hybrid catalyst is facilely prepared for application to photocatalytic H₂ evolution from water splitting by the vacuum rotation-evaporation and in situ thermal method. The physical and chemical properties of CoO/g-C₃N₄ are determined by a series of characterization methods. The g-C₃N₄ with 0.6 wt% Co loading exhibits superior photocatalytic hydrogen evolution activity with an H₂ evolution amount of 23.25 mmol g^-1 after 5 h. The obtained 0.6 wt% CoO/g-C₃N₄ can split water to generate 0.39 mmol g^-1 H₂ without sacrificial agent and noble metal, while the pure g-C₃N₄ is inactive under the same reaction conditions. The remarkable enhancement of photocatalytic H₂ evolution activity of CoO/g-C₃N₄ composites is mainly ascribed to the effective separation of electron-hole pairs and charge transfer. The work creates new opportunities for the design of low-cost g-C₃N₄-based photocatalysts with high photocatalytic H₂ evolution activity from overall water splitting.23:T80c,

#	Concept	H-Index	Publications	Citations
1	Engineering	3	3	71
2	Chemistry	2	2	38
3	Catalysis	2	2	38
4	Chemical Engineering	1	1	26
5	Materials Science	1	1	12

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