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磷化镍钼电催化剂的制备及其析氢性能研究

张松竹 萧礼标 曹丽云 聂光临 闫振华 赵勇 李嘉胤

陕西科技大学学报2026,Vol.44Issue(2):124-133,10.
陕西科技大学学报2026,Vol.44Issue(2):124-133,10.

磷化镍钼电催化剂的制备及其析氢性能研究

Study on preparation of nickel-molybdenum phosphide electrocatalysts and its hydrogen evolution performance

张松竹 1萧礼标 2曹丽云 3聂光临 2闫振华 2赵勇 2李嘉胤3

作者信息

  • 1. 蒙娜丽莎集团股份有限公司,广东佛山 528211||广东省大尺寸陶瓷薄板企业重点实验室,广东佛山 528211||高安市蒙娜丽莎新材料有限公司,江西宜春 300800
  • 2. 蒙娜丽莎集团股份有限公司,广东佛山 528211||广东省大尺寸陶瓷薄板企业重点实验室,广东佛山 528211
  • 3. 陕西科技大学材料科学与工程学院,陕西西安 710021
  • 折叠

摘要

Abstract

Currently,commercially available electrolytic water catalysts are primarily precious metal catalysts represented by platinum and iridium.However,issues such as limited global reserves and high cost of precious metal catalysts hinder their large-scale application.This study successfully synthesized a NiMoP electrocatalyst via a one-step calcination method and investigated the effects of varying metal phosphorus and molybdenum source additions on the material's morphology and electrocatalytic hydrogen production performance.The results in-dicate that the synergistic interaction between Mo and Ni in the bimetallic catalyst enhances charge transfer.The coupling between these two metals yields a richer electronic and geomet-ric structure compared to single-metal phase catalysts(MoP and Ni2P),effectively addressing issues such as the unstable catalytic performance of single transition metal phosphides.At a current density of 10 mn A/cmn2 in 1.0 M KOH,the NiMoP electrocatalyst exhibited an over-potential 206 mV and 121 mV lower than MoP and Ni2P catalysts,respectively,while main-taining stable operation for at least 40 hours.This research provides significant guidance for developing novel transition bimetallic electrocatalysts.

关键词

耦合作用/金属磷化物/电催化剂

Key words

coupling action/metal phosphide/electrocatalyst

分类

化学化工

引用本文复制引用

张松竹,萧礼标,曹丽云,聂光临,闫振华,赵勇,李嘉胤..磷化镍钼电催化剂的制备及其析氢性能研究[J].陕西科技大学学报,2026,44(2):124-133,10.

基金项目

国家自然科学基金项目(52572110) (52572110)

广东省大尺寸陶瓷薄板企业重点实验室开放基金项目(kFkT2026001) (kFkT2026001)

陕西省西安市秦创原科技成果转化项目(202401) (202401)

陕西科技大学学报

2096-398X

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