Review of Graphitic Carbon Nitride and Its Composite Catalysts for Selective Reduction of CO2

复合数 石墨氮化碳 电催化剂 人工光合作用 催化作用 材料科学 碳纤维 氮化碳 可见光谱 二氧化碳电化学还原 甲醇 太阳能燃料 吸收(声学) 化学工程 纳米技术 化学 复合材料 光电子学 电极 一氧化碳 电化学 工程类 有机化学 物理化学 光催化
作者
Soumalya Bhowmik,Shankab J. Phukan,Neeraj K. Sah,Manas Roy,Somenath Garai,Parameswar Krishnan Iyer
出处
期刊:ACS applied nano materials [American Chemical Society]
卷期号:4 (12): 12845-12890 被引量:48
标识
DOI:10.1021/acsanm.1c02896
摘要

Influenced by "artificial photosynthesis", different energy mimetic fuels such as DME, methanol, formic acid, methane, etc. can be prepared by the reduction or hydrogenation of carbon dioxide (CO2), captured from the atmosphere while maintaining different reaction strategies, such as thermal catalysis, electrocatalysis, photocatalysis, and photoelectrocatalysis, and also by means of various enzymatic reactions. Harvesting ubiquitously inherent solar energy and applying the same in photopropagated CO2 reduction toward the generation of value-added energy feedstock using apposite semiconductor photocatalysts have proven to be a sustainable and greener process completing the carbon cycle. Graphitic carbon nitride (g-C3N4) has been recognized as a highly potent photo- as well as electrocatalyst for the CO2 reduction reaction (CRR), primarily due to its high chemical and thermal stability, low toxicity, cost-effectiveness, visible light absorption capacity, and ingeniously tunable synthetic routes as compared to other semiconductor platforms. Nevertheless, a lower specific surface area, lower electrical conductivity, fast recombination of phototriggered excitons, and narrow visible light absorption window hinder the application of this catalytic material for practical photocatalytic utilization. Adapting certain alteration approaches, such as structural modulation, elemental doping, attachment of metal complex motif, functional group modification of g-C3N4 etc., can dramatically reinforce the photocatalytic activity in the direction of efficient CO2 reduction. The present review explores the various perceptions of synthetic routes as well as individual optimization techniques of g-C3N4 promoting CO2 photoreduction adopted by the scientific community from the very outset to the latest findings. Predominantly, this review ruminates on the theoretical and experimental framework of practical photochemical CO2 reduction on g-C3N4-based hybrid platforms while elucidating the respective material optimization techniques employed to boost selectivity and efficiency along with their merits and demerits. The future scope of improvement and a comparative discussion are concluded in the form of an imminent panorama.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
www完成签到,获得积分10
1秒前
1秒前
1秒前
wzwz发布了新的文献求助10
2秒前
maybe完成签到,获得积分10
2秒前
huhuhu发布了新的文献求助10
2秒前
2秒前
贪玩的弱完成签到 ,获得积分10
2秒前
Orange应助tunacan采纳,获得20
2秒前
陈爱佳发布了新的文献求助10
2秒前
Freya完成签到 ,获得积分10
3秒前
夏天的风发布了新的文献求助10
3秒前
3秒前
似我发布了新的文献求助10
3秒前
知画春秋完成签到 ,获得积分10
3秒前
科研通AI6.2应助吴玉杰采纳,获得10
3秒前
Ming完成签到 ,获得积分10
3秒前
小邹完成签到,获得积分10
3秒前
Ljr123发布了新的文献求助10
3秒前
wyw完成签到,获得积分10
4秒前
木易发布了新的文献求助10
4秒前
4秒前
午木发布了新的文献求助10
4秒前
汉堡包应助浪费采纳,获得10
4秒前
入袍完成签到,获得积分10
4秒前
士多啤梨完成签到 ,获得积分10
4秒前
4秒前
4秒前
徐臣年发布了新的文献求助10
4秒前
Syu发布了新的文献求助10
4秒前
友好依风完成签到,获得积分10
4秒前
wzwz完成签到,获得积分10
6秒前
6秒前
无我完成签到,获得积分10
6秒前
李雪松完成签到,获得积分10
7秒前
7秒前
江屿发布了新的文献求助20
7秒前
7秒前
z同学完成签到,获得积分10
7秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Developing Genetic Editing Tools for Lysobacter 2000
Моделирование процессов самоорганизации в кристаллообразующих системах 1000
History of U.S. Space Surveillance and Satellite Cataloging 1000
Adhesion Science: Principles & Practice 800
Signals, Systems, and Signal Processing 610
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 600
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6524034
求助须知:如何正确求助?哪些是违规求助? 8317081
关于积分的说明 17798156
捐赠科研通 5625803
什么是DOI,文献DOI怎么找? 2928419
邀请新用户注册赠送积分活动 1905195
关于科研通互助平台的介绍 1765155