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Conventional water purification technologies struggle to simultaneously address purification efficiency and energy consumption. Molecular orbital level surface micro-electric field (MEF)-driven water purification is an original and innovative concept conceived and developed by our group in recent years. The core idea involves creating electron-rich and electron-poor micro-areas on the nanomaterial surface, which drive pollutants or H2O molecules to provide electrons in the electron-poor micro-areas while other environmental factors (such as H2O2 and O2) obtain electrons in the electron-rich micro-areas. This process effectively utilizes the internal energy contained within wastewater and emerging contaminants (ECs). Centered on this core, this review systematically examines the discovery, construction, and characteristics of MEF and MEF-like systems and summarizes their application directions. The challenges, bottlenecks, and future development directions of MEF technology are also analyzed and discussed. Reviews of MEFs can facilitate the development of low-consumption, high-efficiency water purification technologies.

Conventional advanced oxidation processes (AOPs) require significant external energy consumption to eliminate emerging contaminants (ECs) with stable structures. Herein, a catalyst consisting of nanocube BiCeO particles (BCO‐NCs) prepared by an impregnation‐hydrothermal process is reported for the first time, which is used for removing ECs without light/electricity or any other external energy input in water and simultaneous in situ generation of H2O2. A series of characterizations and experiments reveal that dual reaction centers (DRC) which are similar to the valence band/conducting band structure are formed on the surface of BCO‐NCs. Under natural conditions without any external energy consumption, the BCO‐NCs self‐purification system can remove more than 80% of ECs within 30 min, and complete removal of ECs within 30 min in the presence of abundant electron acceptors, the corresponding second‐order kinetic constant is increased to 3.62 times. It is found that O2 can capture electrons from ECs through the Bi─O─Ce bond bridge during the reaction process, leading to the in situ production of H2O2. This work will be a key advance in reducing energy consumption for deep wastewater treatment and generating important chemical raw materials. [ABSTRACT FROM AUTHOR]

An innovative strategy for synthesizing novel dual-reaction-center (DRC) catalysts from chicken manure (CM) biochar to purify wastewater that contained emerging contaminants (ECs) is proposed to synchronously address the release of ECs and improper disposal of livestock manure. A series of characterization techniques reveal the formation of a special C-O-Ca bond bridge (cation-π) structure on resourcelized CM nanosheets (RCM NSs). RCM NSs exhibit distinct selectivity and anti-interference capability for various ECs removal in complex matrices, and the water purification system remains stable after 1735 hours (equivalent to 3470 cycles) of operation. Density Functional Tomography (DFT) calculations reveal that trace of peroxymonosulfate as an inducer initiates the continuous donation of electrons from electron-rich ECs and the C-O-Ca bond bridges provide a favorable pathway for electron transfer, which facilitates the electron capture effect of dissolved oxygen in the system. This study provides a novel strategy to convert livestock manure into DRC-catalysts for developing energy-saving and high-efficiency environmental remediation technologies. Highlights: • The chicken manure biochar was converted into a water purification catalyst through a graphitization process. • Resourcelized catalyst RCM NSs had superior removal capability for various ECs triggering by trace of PMS. • RCM NSs could quickly eliminate ECs and simultaneously drive NOM removal, even with NOM interference. • The key role of dissolved oxygen for water purification was illustrated in RCM NSs system. [ABSTRACT FROM AUTHOR]