...
首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >Phosphorus-doped porous carbon nitride for efficient sole production of hydrogen peroxide via photocatalytic water splitting with a two-channel pathway
【24h】

Phosphorus-doped porous carbon nitride for efficient sole production of hydrogen peroxide via photocatalytic water splitting with a two-channel pathway

机译:磷掺杂多孔碳氮化物,其通过光催化水分裂有效地产生过氧化氢,双通道路径

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The production of hydrogen peroxide (H2O2) by photocatalytic water splitting has attracted much attention due to the wide application of H2O2 as a multi-functional chemical. Most of the present photocatalysts require sacrificial agents and/or noble metal cocatalysts. Herein, we report that phosphorus-doped porous carbon nitride (CPN), as a metal-free photocatalyst, achieves the photocatalytic water splitting via a two-channel pathway (water oxidation reaction and oxygen reduction reaction) with high H2O2 yield of 1968 mu mol g(-1) h(-1) (highest yield in current records without sacrificial agent) under room temperature and normal pressure without sacrificial agent and cocatalyst. The quantum efficiency of the sole production of H2O2 was measured to be 1.57% under wavelength lambda = 420 nm and the solar energy conversion efficiency was determined to be 0.43%. In the present reaction system, the concentration of H2O2 can be up to 0.171% (wt%) in a one-batch reaction using 80 mg CPN catalyst (in 15 mL oxygen saturated H2O) after 36 h under visible light illumination. H2O2 obtained by this metal-free catalyst without adding a sacrificial agent is more conducive to subsequent purification in industrial production.
机译:由于H2O2作为多功能化学品的广泛应用,通过光催化水分裂产生过氧化氢(H2O2)的产生非常关注。大多数本发明的光催化剂需要牺牲剂和/或贵金属助催化剂。在此,我们报告说,作为无金属光催化剂,磷掺杂的多孔碳氮化物(CPN)通过双通道途径(水氧化反应和氧还原反应)实现了光催化水分,高H2O2产量为1968亩在室温和常压下,G(-1)H(-1)H(-1)(当前记录中的最高产量,没有牺牲剂和助催化剂。在波长λ= 420nm下测量H 2 O 2的唯一生产的量子效率为1.57%,确定太阳能转化效率为0.43%。在本反应体系中,在可见光照射下36小时后,在36小时后,在一次间歇反应中,H 2 O 2的浓度可高达0.171%(wt%),在36小时后,在36小时后,在36小时后在36小时后在36小时后。通过该无金属催化剂获得的H 2 O 2而不添加牺牲剂,更有利于工业生产的后续纯化。

著录项

  • 来源
  • 作者单位

    Soochow Univ Inst Funct Nano &

    Soft Mat FUNSOM Jiangsu Key Lab Carbon Based Funct Mat &

    Devices Suzhou Peoples R China;

    Soochow Univ Inst Funct Nano &

    Soft Mat FUNSOM Jiangsu Key Lab Carbon Based Funct Mat &

    Devices Suzhou Peoples R China;

    Soochow Univ Inst Funct Nano &

    Soft Mat FUNSOM Jiangsu Key Lab Carbon Based Funct Mat &

    Devices Suzhou Peoples R China;

    Soochow Univ Inst Funct Nano &

    Soft Mat FUNSOM Jiangsu Key Lab Carbon Based Funct Mat &

    Devices Suzhou Peoples R China;

    Soochow Univ Inst Funct Nano &

    Soft Mat FUNSOM Jiangsu Key Lab Carbon Based Funct Mat &

    Devices Suzhou Peoples R China;

    Soochow Univ Inst Funct Nano &

    Soft Mat FUNSOM Jiangsu Key Lab Carbon Based Funct Mat &

    Devices Suzhou Peoples R China;

    Soochow Univ Inst Funct Nano &

    Soft Mat FUNSOM Jiangsu Key Lab Carbon Based Funct Mat &

    Devices Suzhou Peoples R China;

    Soochow Univ Inst Funct Nano &

    Soft Mat FUNSOM Jiangsu Key Lab Carbon Based Funct Mat &

    Devices Suzhou Peoples R China;

    Soochow Univ Inst Funct Nano &

    Soft Mat FUNSOM Jiangsu Key Lab Carbon Based Funct Mat &

    Devices Suzhou Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 工程材料学;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号